Establishment of canine hemangiosarcoma xenograft models expressing endothelial growth factors, their receptors, and angiogenesis-associated homeobox genes
© Kodama et al; licensee BioMed Central Ltd. 2009
Received: 24 April 2009
Accepted: 14 October 2009
Published: 14 October 2009
Human hemangiosarcoma (HSA) tends to have a poor prognosis; its tumorigenesis has not been elucidated, as there is a dearth of HSA clinical specimens and no experimental model for HSA. However, the incidence of spontaneous HSA is relatively high in canines; therefore, canine HSA has been useful in the study of human HSA. Recently, the production of angiogenic growth factors and their receptors in human and canine HSA has been reported. Moreover, the growth-factor environment of HSA is very similar to that of pathophysiological angiogenesis, which some homeobox genes regulate in the transcription of angiogenic molecules. In the present study, we established 6 xenograft canine HSA tumors and detected the expression of growth factors, their receptors, and angiogenic homeobox genes.
Six primary canine HSAs were xenografted to nude mice subcutaneously and serially transplanted. Subsequently, the expressions of vascular endothelial growth factor (VEGF)-A, basic fibroblast growth factors (bFGF), flt-1 and flk-1 (receptors of VEGF-A), FGFR-1, and angiogenic homeobox genes HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1 were investigated in original and xenograft tumors by histopathology, immunostaining, and reverse transcription polymerase chain reaction (RT-PCR), using canine-specific primer sets.
Histopathologically, xenograft tumors comprised a proliferation of neoplastic cells that were varied in shape, from spindle-shaped and polygonal to ovoid; some vascular-like structures and vascular clefts of channels were observed, similar to those in the original tumors. The expression of endothelial markers (CD31 and vWF) was detected in xenograft tumors by immunohistochemistry and RT-PCR. Moreover, the expression of VEGF-A, bFGF, flt-1, flk-1, FGFR-1, HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1 was detected in xenograft tumors. Interestingly, expressions of bFGF tended to be higher in 3 of the xenograft HSA tumors than in the other tumors.
We established 6 xenograft canine HSA tumors in nude mice and found that the expressions of angiogenic growth factors and their receptors in xenograft HSAs were similar to those in spontaneous HSA. Furthermore, we detected the expression of angiogenic homeobox genes; therefore, xenograft models may be useful in analyzing malignant growth in HSA.
Hemangiosarcoma (HSA) is a malignant neoplasm that originates from vascular endothelial cells (ECs). In general, high-grade, aggressive tumors tend to recur locally and metastasize early, despite therapeutic modality [1–4]. However, the mechanisms of tumorigenesis in HSA have been barely elucidated, since these tumors comprise only approximately 2% of all cases of soft-tissue sarcoma in humans. In contrast, spontaneous HSA occurs more frequently in dogs than in any other species ; in fact, there are more occasions to gain new insights into canine HSA than into human HSA [6–8]. Knowledge obtained from the study of canine HSA is useful in understanding human HSA. In recent studies into canine and human HSA, expressions of both vascular endothelial growth factor A (VEGF-A) and their receptors, especially flk-1, were evident, and the presence of an autocrine or paracrine mechanism underpinning the growth factors might be associated with the malignant proliferation of canine HSA [9, 10]. Considering the similarities shared by human and canine HSAs, a canine HSA model may be useful in the study of human HSA.
Homeobox genes encode homeodomain-containing proteins, which regulate morphogenesis and cell differentiation as a transcription factor in embryonic development. Homeobox genes are highly conserved among various species, and thus they may serve a function similar to that of the corresponding genes in various animals, from simple organisms to vertebrates, including humans [11, 12]. Some homeobox genes tightly regulate the behavior of ECs during VEGF or bFGF-induced angiogenesis [13–18]. Regarding growth factor environments, HSA may have a growth mechanism similar to that of pathophysiological angiogenesis, and angiogenesis-associated homeobox genes may play a function in HSA. We hypothesized that angiogenic homeobox genes are also associated with the malignant behavior of HSA, which is rendered possible by the proliferation and invasion of neoplastic ECs.
Several in vitro models have been established and used to carry out biological and molecular characterization of canine HSA [19, 20]. On the other hand, experimental in vivo study models are essential for dynamic analysis of neoplasm. For instance, the pharmaceutical analysis of anticancer drugs with a consideration of drug metabolism is essential because the handling of clinical or fixed histopathological tumor samples is restricted. A transplantable neoplastic model is useful in the dynamic analysis of neoplasm in vivo; in human medical research, tumor xenografts have been widely used and have greatly contributed to advancements in the medical sciences [21–23].
In the present study, we attempted to transplant xenografts of canine HSA tumors into athymic nude mice. We were able to establish 6 xenograft tumors derived from 6 spontaneous canine HSAs and subsequently analyze the expression of VEGF-A, basic fibroblast growth factor (bFGF), their receptors, and angiogenesis-associated homeobox genes in established canine HSA xenograft tumors.
Sources of Canine Hemangiosarcoma Tumors
An information of original tumors
Liver and inguinal subcutis
After surgical removal or necropsy, these tumors were immediately prepared for histopathology and transplantation. For histopathological examination, these tumors were fixed in 10% neutral buffered formalin and embedded in paraffin, in a routine manner. Tissue sections from the original tumors were stained with hematoxylin and eosin (HE), as is customary. To transplant tumor to mice, tumor tissues were cut into 1-mm3 cubes under sterile conditions.
Nude Mice and Transplantations of Canine HSA Tissue to Nude Mice
Three-week-old male KSN Slc mice (Japan SLC, Inc., Hamamatsu, Japan) were anesthetized with pentobarbital and subcutaneously xenografted with tumor tissue flaps in the right or left dorsal area of the trunk. The skin was cleaned using 70% ethanol and a small skin incision was made. The tumor tissue flap was then introduced into the subcutaneous pocket with a transplantation needle (ϕ 2.0 mm). After injection, the tumor sizes were measured once a week. Putative tumor volume (V) was calculated as (width)2 × length/2 mm3. Tumor volumes were then expressed as fractional tumor volumes (V/V0), where V0 is the initial volume of the tumor immediately before treatment (day 0). When the tumors had increased to approximately 10 mm in diameter, tumors growing in nude mice were serially transplanted from mouse to mouse. The mice were scarified, and the tumor was immediately removed. Subsequently, several pieces of the xenografted tumor tissues were stored in a freeze-stock solution (Cell Banker; Nippon Zenyaku Kogyo Co., Fukushima, Japan) in a deep freezer at -80°C to confirm the tumorigenicity of frozen xenografted tumor tissues. All the excised tumors were treated the same as the spontaneous tumors for histopathological analyses. Snap-frozen samples were also collected for reverse transcriptase polymerase chain reaction (RT-PCR) and stored at -80°C until use. The experiments were performed according to the guidelines for the care and use of laboratory animals approved by the Animal Care and Use Committee of Gifu University.
Immunohistochemical Staining of Original or Xenograft Tumors
Immunohistochemical staining was performed for CD31 (anti-human CD31 mouse monoclonal antibody, prediluted; Dako Cytomation, Glostrup, Denmark), von Willebrand factor (anti-human von Willebrand factor rabbit monoclonal antibody [vWF], prediluted; Dako Cytomation), Ki-67 antigen (anti-human Ki-67 antigen mouse monoclonal antibody, clone MIB-1, 1:25; Dako Cytomation), VEGF-A (anti-human VEGF [C-1] mouse monoclonal antibody, 1:50; Santa Cruz Biotechnology, Santa Cruz, CA, USA), flt-1 (anti-human flt-1 [C-17] rabbit polyclonal antibody, 1:200; Santa Cruz Biotechnology), flk-1 (anti-mouse flk-1 [A-3] mouse monoclonal antibody, 1:200; Santa Cruz Biotechnology), bFGF (anti-human FGF-2  rabbit polyclonal antibody, 1:200; Santa Cruz Biotechnology), HoxA9 (anti-human HoxA9 [A-20] goat polyclonal antibody, 1:200; Santa Cruz Biotechnology), HoxB3 (anti-human HoxB3 [C-20] goat polyclonal antibody, 1:100; Santa Cruz Biotechnology), HoxB7 (anti-human HoxB7 rabbit polyclonal antibody, 1:1,000; CeMines, Golden, CO, USA), HoxD3 (anti-human HoxD3 rabbit polyclonal antibody, 1:400; Aviva Systems Biology, San Diego, CA, USA), Pbx1 (anti-human Pbx1 rabbit polyclonal antibody, 1:100; Novus Biologicals, Littleton, CO, USA), and Meis1 (anti-human Meis1 rabbit polyclonal antibody, 1:200; Abcam, Tokyo, Japan) for all the original tumor and xenograft samples that had been transplanted more than 5 times consecutively and then transplanted into frozen xenografted tumor tissues. These antibodies have been reported to be able to react with peptides of canine origin [10, 24–27]. Antibodies to HoxB7, Pbx1, and Meis1 are purified against a synthetic peptide whose sequence is identical to the canine peptide . Although the antibodies to HoxA9, HoxB3, and HoxD3 are purified against corresponding peptides of the human protein regions, it is unclear whether or not these sequences corresponded to protein sequences in canines. To demonstrate the staining characteristics for those antibodies in angiogenic status, canine granulation tissue was immunohistochemically stained. HoxD3 was used at a dilution attained by adding Can Get Signal.® immunostain Solution A (Toyobo, Osaka, Japan). Ki-67 antigen, VEGF-A, flt-1, flk-1, bFGF, HoxA9, HoxB3, HoxB7, Pbx1, and Meis1 were diluted by adding 1% bovine albumin/phosphate-buffered saline (PBS). In brief, 3-μm sections were deparaffinized in Lemosol (Wako Pure Chemical Industries, Osaka, Japan) and rehydrated in graded ethanol. For the antigen retrieval of vWF, flk-1, flt-1, HoxA9, HoxB3, HoxB7, Pbx1, and Meis1, sections were immersed in Target Retrieval Solution (Dako Cytomation) and heated for 15 min at 121°C in an autoclave. For antigen retrieval of Ki-67, sections were immersed in Target Retrieval Solution and heated for 25 min at 121°C in an autoclave. For demasking CD31, sections were digested with 0.5% proteinase K (Takara, Ohtsu, Japan) in Tris-HCl buffer (pH 7.0) for 5 min at 37°C. For demasking VEGF-A and bFGF, sections were digested with 0.1% trypsin (GIBCO Life Technologies, NY, USA) in Tris-HCl buffer (pH 7.0) for 15 min at 37°C. Endogenous peroxidase was blocked by incubation in 0.3% H2O2 in methanol for 20 min at room temperature (RT). To prevent the binding of nonspecific proteins to the primary antibody, the sections were treated with Protein Block Serum-Free (Dako Cytomation) for 30 min at RT. Sections were incubated with the primary antibody overnight at 4°C; for the negative control, PBS was used in place of the primary antibody. The sections were then washed with PBS and incubated with the appropriate secondary antibodies (Histofine.® simple stain MAX PO; Nichirei, Tokyo, Japan) at RT for 30 min. After washing thrice with PBS, binding was detected using 3,3'-diaminobenzidinetetrahydrochloride (Liquid DAB + Substrate Chromogen System; Dako Cytomation). Finally, the sections were washed in distilled water and counterstained with Mayer's hematoxylin.
The percentage of Ki-67-positive cells in each tumor tissue was calculated as the number of reddish brown-positive nuclei in a total of 1000 neoplastic cells (from 10 high-power fields); this value is indicated as a Ki-67 positive index (PI).
Detection of mRNA Expression by RT-PCR
Total RNA was extracted from 6 xenograft tumors using TRIzol reagent (Gibco Life Technologies). In brief, a snap-frozen sample was homogenized in 1 ml TRIzol by a polytron-type homogenizer and mixed with 0.2 ml chloroform before centrifugation. The aqueous phase was collected for total RNA extraction, mixed with 2-propanol to salt out, and washed with chilled 75% ethanol. Total RNA was detected after treatment with amplification-grade DNase I (Invitrogen, Carlsbad, CA, USA) followed by RT-PCR assay with Qiagen One step RT-PCR Kit (Qiagen, Valencia, CA, USA), according to the manufacturer's instructions. RT-PCR was carried out in a Thermal Cycler Dice Gradient (Takara). Amplifications were performed under the following conditions: reverse-transcription reaction for 30 min at 50°C, an initial polymerase activation step for 15 min at 95°C, denaturation for 30 s at 95°C, annealing for 30 s, extension for 1 min at 72°C, and a final extension for 10 min at 72°C. To confirm the omission of genomic contamination, RT-PCR was carried out for DNase I-treated total RNA with One Step Enzyme Mix, which was deactivated for reverse transcription activity by heating at 95°C for 15 min.
The primer sequences, annealing temperatures, annealing cycle number, product sizes used, and the accession number for generating the primer sets are listed in Additional file 1. Each primer used in this study was generated from canine-specific sequences, by accession number (e.g., Genbank). The sequences that the primers recognize in the sandwich splicing area and the predicted sizes differed among VEGF variants. The primers amplifying HoxA9 mRNA distinguished between HoxA9 mRNA, which contains the region encoding the homeodomain, and the HoxA9 mRNA lacking this region. RNA integrity was confirmed by the sufficient amplification of β-actin. The specificity of all canine primer sets was definitive, because there was no band in the RT-PCR for normal mouse spleens. The products of the PCR amplifications were electrophoresed in 2% agarose gel or 7.5% polyacrylamide gel for VEGF stained with ethidium bromide and visualized under ultraviolet light.
Expression of CD31, vWF, VEGF-A, flt-1, flk-1, bFGF, FGFR-1, EphB4, and Angiogenic Homeobox Genes
In this study, 6 xenograft canine HSAs were established. As compared to the original tumors, xenograft tissues tended to form neither vascular-like clefts of channels nor higher nuclear atypia of xenograft tumors; however, the histopathological structures of xenograft tumors were similar to those in original canine HSA, and mRNA expressions and immunoreactivities of vWF and CD31 were also detected in the xenograft tumors. Thus, the xenograft tumors in the present study maintained the canine endothelial nature. In immunohistochemistry for Ki-67 antigen using antibody clone MIB-1, xenograft tumor cells were clearly positive in the nucleus but negative in the surrounding murine tissues such as the epidermal basal cells. The MIB-1 antibody did not react with murine homologous antigen but reacted with canine homologous antigen; thus, xenograft tumors were confirmed as being of canine origin . Some xenograft tumors indicated higher Ki-67 PI values than those of original tumors. Thus, given the atypia and the Ki-67 PI of the original and xenograft tumors, it is suggested that more malignant components may be selected by repeated xenotransplantation.
In spontaneous canine HSAs, the mRNA of VEGF-A and bFGF and their receptors were detected; however, they can be immunohistochemically detected not only in neoplastic cells but also in inflammatory cells . Actually, the results of RT-PCR in spontaneous canine HSA uncovered the presence of both neoplastic cells and infiltrating inflammatory cells . Thus, contaminated inflammatory cells could disrupt HSA analysis, especially the detection of gene expression; it is difficult to resolve this problem when using solely clinical samples. We attempted to establish xenograft models in the present study, as they are powerful tools in resolving this problem. Because the expression of VEGF-A, flt-1, flk-1, bFGF, and FGFR-1 mRNA was detected in xenograft tumors by the canine-specific primers, amplified products originated precisely from canine neoplastic ECs. These results suggest that accurate gene expression could be detected in the xenograft models established in the present study. In addition, xenograft HSA tumors showed positive immunolabeling for VEGF-A, bFGF, flt-1, and flk-1, similar to the original tumors; thus, those xenograft models maintain a proliferative mechanism similar to that found in spontaneous canine HSA.
There is increasing evidence that the dysregulation of molecular pathways governing angiogenesis may be important to HSA pathogenesis . Yonemaru et al. suggest that canine HSA might have an autocrine or a paracrine mechanism via VEGF-A and/or bFGF receptor(s) . VEGF-A, a strong angiogenic factor, is expressed at low levels in normal mammalian tissues; increased levels of VEGF-A were observed during ischemia or hypoxia, and in lesions characterized by angiogenesis. In a recent study , VEGF-A120, VEGF-A164, and VEGF-A188 were detected in normal canine tissues, and VEGF-A164, which corresponds to human VEGF-A165, is the dominant molecular species. Canine VEGF-A164 contains all the necessary information for the normal growth, remodeling, and patterning of blood vessels . Some reports investigate the expression of VEGF-A variants in various human neoplasms [33–39]. The increased expression of human VEGF-A165 and VEGF-A189 in osteosarcoma , renal cell carcinoma , non-small-cell lung cancer [35–37], and colon cancer  correlates with neovascularization, tumor progression, and poor prognosis. In human angiosarcoma, the expression of VEGF-A mRNA has been demonstrated, but the expression of VEGF-A variants has not been investigated . VEGF-A120 and VEGF-A164 have been detected as major bands in canine HSA, while VEGF-A144 and VEGF-A188 have been detected as minor bands; however, spontaneous HSA contains contaminating inflammatory cells that express VEGF-A mRNA . In the present study, primers for VEGF-A were expected to produce 3 splicing variants, namely, VEGF-A164, VEGF-A182, and VEGF-A188. VEGF-A164 and VEGF-A188 but not VEGF-A182 were detected in all xenograft tumors and normal canine spleens. VEGF-A164 has been demonstrated to have a higher expression as compared to the expression of VEGF-A182 and VEGF-A188 in both spontaneous and xenograft HSA tumors.
The expression of bFGF mRNA was different among the xenografts. In 3 of the xenografts--Si, Ud, and Sy--the expression levels of bFGF mRNA were found, by RT-PCR, to be higher than those of other xenografts. The intensity of specific bands for bFGF was similar to those of normal canine spleen samples, which were used as a positive control; however, spleens contain various cells--including leukocytes, ECs, and other stromal cells--and thus the actual expression of bFGF in splenic ECs might be low. Therefore, the expression levels of bFGF mRNA in Si, Ud, and Sy might be high and must be measured quantitatively. bFGF is one of the most effective angiogenic growth factors; therefore, it might play a role in malignant endothelial growth in HSA.
In recent studies, it has been demonstrated that several homeobox genes regulate the behavior of ECs during angiogenesis and it is suggested that the homeobox proteins of HoxA9, HoxD3, and Pbx1 are involved in the malignancy of canine HSA [13, 17, 27]. HoxA9, HoxB3, HoxB7, and HoxD3 proteins regulate the expression of downstream genes involved in angiogenesis; Pbx1 and Meis1 assist in the functioning of Hox protein, as cofactors [16, 41]. In the present study, immunostaining of xenograft HSA tumors was positive for HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1, which is similar to the proteins detected by immunostaining of the original tumors. The expression of HoxA9, HoxB3, HoxB7, HoxD3, Pbx1, and Meis1 mRNA was also detected in all xenograft tumors. HoxA9 mediates EC migration and proliferation during angiogenesis by regulating the expression of EphB4, a member of the Eph receptor tyrosine kinase family [13, 42]. HoxA9 binds the EphB4 promoter and induces the transcription of the EphB4 mRNA directory . Therefore, the expression of EphB4 mRNA in all xenograft tumors suggests that HoxA9 may induce the expression of EphB4 in HSA. Moreover, HoxA9 has been found to be a key regulator that induces acute myeloid leukemia in mice . Although coactivation of HoxA9 and Meis1 in mouse bone marrow cells has reportedly induced acute myeloid leukemia rapidly, this phenomenon was not observed in terms of an individual overexpression of each of the homeobox genes . The function of HoxA9 in HSA may have been enhanced by the presence of Meis1.
HoxD3 both induces an angiogenic phenotype and enhances the expression of both integrin αvβ3 and urokinase-type plasminogen activator--the latter of which, in turn, facilitates EC migration and adhesion during bFGF-induced angiogenesis [17, 44]. In human hemangioma, expression levels of HoxD3 mRNA in the proliferation phase are higher than those in the involution phase . Pbx1 is known to be necessary for angiogenesis mediated by HoxD3 ; therefore, one of the functions of HoxD3 is to induce ECs so that they are in an active phase--proliferative and migratory--and it is suggested that HoxD3 is involved in the tumorigenesis of canine HSA. Moreover, HoxB3 promotes capillary morphogenesis during angiogenesis, and HoxB7 directly upregulates the expression of bFGF in human melanoma cells; the activation of bFGF induces EC proliferation in vitro [14, 46]. Finally, in 2 recent studies, it was demonstrated that Pbx1 functions as a cofactor with HoxB3 and HoxB7 [47, 48]. The result--that HoxB7 and bFGF are expressed in HSA--may suggest that HoxB7 induces the proliferation of tumor cells mediated by bFGF.
The cytoplasmic localization of HoxA9, HoxB3, HoxD3, Pbx1, and Meis1 proteins in original tumors was maintained in all xenograft HSA tumors. Previous studies have shown the cytoplasmic localization of homeobox proteins, suggesting modifications in their localization during tumorigenesis [49–51]. The localization of homeobox proteins might be involved in tumorigenesis in HSA. Although xenograft models that demonstrate the expression of homeobox genes have been reported in human small-cell lung cancers, there is no model available to analyze homeobox expression in HSA . Recent studies have indicated the possibility of a novel tumor therapy that involves regulating aberrant expressions of homeobox genes [53–55]; Plowright et al., for example, suggest that the interaction between Hox and Pbx proteins is a potential therapeutic target . Therefore, the present xenograft HSA models may be useful in evaluating a novel molecularly targeted therapy involving homeobox protein.
In this study, no metastatic lesion was observed in any of the xenograft tumors. Although there might not have been sufficient time for the tumor to metastasize, the occurrence of metastasis depends on the mouse strains in the xenograft tumors and tumor cell lines [57–59]. Therefore, the metastasis model of xenografted canine HSAs may be established by the transplanting the present xenograft tumors into SCID or NOD-SCID mice. In general, orthotopic transplanted tumors have a greater tendency than heterotopic transplanted tumors to metastasize to any organ [60–62]. Therefore, orthotopic canine HSA transplantation may lead to the development of metastatic lesions in nude mice. It may be possible that the xenograft tumors lost the expression of the factors required to develop metastasis. Alternatively, metastasis-promoting factors produced by xenograft canine tumors might not react with mice. However, the relationship between metastasis and the factors could not be elucidated in this study.
Since the chemotherapy and radiotherapy was not carried out in this study, the effects of these therapies for the xenografted models are unclear. In medicine, surgical resection and radiotherapy for HSA has been reported to result in long-term survival in many cases [3, 4]. On the other hand, no standard chemotherapy for HSA has been established; nevertheless, several approaches in chemotherapy have been attempted, such as liposomal doxorubicin, interleukin-2, and interferon-α [63–65]. In recent years, anti-angiogenic therapy has attracted considerable attention as a possible therapy for HSA [66–68]. Given the inferred mechanism of proliferation via VEGF-A or bFGF in HSA, anti-angiogenic therapy would be the logical strategy for the treatment of HSA [9, 10]. Therefore, it is hoped that the xenografted models, which are HSA tumors producing VEGF-A, bFGF, and their receptors, will be useful to evaluate the efficacy of the novel drug that inhibits VEGF- or bFGF-mediated neoplastic proliferation in HSA.
In the present study, 6 murine xenograft canine HSA tumors were established. All xenograft tumors expressed CD31, vWF, VEGF-A, bFGF, and their receptors; thus, these tissues maintained endothelial characteristics, especially active ECs. Moreover, angiogenic homeobox genes were expressed in the xenograft tissues. Together, these xenograft canine HSA tumors constitute the first model to demonstrate the expression of homeobox genes in HSA and canine tumors. Since the tumors from the frozen xenografts replicated the characteristics of original tumors, the models are capable of reproducing xenografted HSA tumors at any time. They may contribute to elucidating the mechanism of HSA proliferation and aid in the development of novel HSA therapy for dogs and humans alike.
- Pawlik TM, Paulino AF, McGinn CJ, Baker LH, Cohen DS, Morris JS, Rees R, Sondak VK: Cutaneous angiosarcoma of the scalp: a multidisciplinary approach. Cancer. 2003, 98: 1716-1726. 10.1002/cncr.11667.View ArticlePubMedGoogle Scholar
- Mark RJ, Tran LM, Sercarz J, Fu YS, Calcaterra TC, Juillard GF: Angiosarcoma of the head and neck. The UCLA experience 1955 through 1990. Arch Otolaryngol Head Neck Surg. 1993, 119: 973-978.View ArticlePubMedGoogle Scholar
- Mark RJ, Poen JC, Tran LM, Fu YS, Juillard GF: Angiosarcoma. A report of 67 patients and a review of the literature. Cancer. 1996, 77: 2400-2406. 10.1002/(SICI)1097-0142(19960601)77:11<2400::AID-CNCR32>3.0.CO;2-Z.View ArticlePubMedGoogle Scholar
- Abraham JA, Hornicek FJ, Kaufman AM, Harmon DC, Springfield DS, Raskin KA, Mankin HJ, Kirsch DG, Rosenberg AE, Nielsen GP, et al: Treatment and outcome of 82 patients with angiosarcoma. Ann Surg Oncol. 2007, 14: 1953-1967. 10.1245/s10434-006-9335-y.View ArticlePubMedGoogle Scholar
- Thamm DH: Miscellaneous Tumors. Withrow and Macewen's Small Animal Clinical Oncology. Edited by: Withrow SJ, Vail DM. 2007, St. Louis: Saunders, 785-794. FourthGoogle Scholar
- Murakami M, Sakai H, Kodama A, Mori T, Maruo K, Yanai T, Masegi T: Expression of the anti-apoptotic factors Bcl-2 and survivin in canine vascular tumours. J Comp Pathol. 2008, 139: 1-7. 10.1016/j.jcpa.2008.02.001.View ArticlePubMedGoogle Scholar
- Murakami M, Sakai H, Kodama A, Yanai T, Mori T, Maruo K, Masegi T: Activation of matrix metalloproteinase (MMP)-2 by membrane type 1-MMP and abnormal immunolocalization of the basement membrane components laminin and type IV collagen in canine spontaneous hemangiosarcomas. Histol Histopathol. 2009, 24: 437-446.PubMedGoogle Scholar
- Yonemaru K, Sakai H, Murakami M, Kodama A, Mori T, Yanai T, Maruo K, Masegi T: The significance of p53 and retinoblastoma pathways in canine hemangiosarcoma. J Vet Med Sci. 2007, 69: 271-278. 10.1292/jvms.69.271.View ArticlePubMedGoogle Scholar
- Itakura E, Yamamoto H, Oda Y, Tsuneyoshi M: Detection and characterization of vascular endothelial growth factors and their receptors in a series of angiosarcomas. J Surg Oncol. 2008, 97: 74-81. 10.1002/jso.20766.View ArticlePubMedGoogle Scholar
- Yonemaru K, Sakai H, Murakami M, Yanai T, Masegi T: Expression of vascular endothelial growth factor, basic fibroblast growth factor, and their receptors (flt-1, flk-1, and flg-1) in canine vascular tumors. Vet Pathol. 2006, 43: 971-980. 10.1354/vp.43-6-971.View ArticlePubMedGoogle Scholar
- Deschamps J, Meijlink F: Mammalian homeobox genes in normal development and neoplasia. Crit Rev Oncog. 1992, 3: 117-173.PubMedGoogle Scholar
- Mavilio F: Regulation of vertebrate homeobox-containing genes by morphogens. Eur J Biochem. 1993, 212: 273-288. 10.1111/j.1432-1033.1993.tb17660.x.View ArticlePubMedGoogle Scholar
- Bruhl T, Urbich C, Aicher D, Acker-Palmer A, Zeiher AM, Dimmeler S: Homeobox A9 transcriptionally regulates the EphB4 receptor to modulate endothelial cell migration and tube formation. Circ Res. 2004, 94: 743-751. 10.1161/01.RES.0000120861.27064.09.View ArticlePubMedGoogle Scholar
- Myers C, Charboneau A, Boudreau N: Homeobox B3 promotes capillary morphogenesis and angiogenesis. J Cell Biol. 2000, 148: 343-351. 10.1083/jcb.148.2.343.View ArticlePubMedPubMed CentralGoogle Scholar
- Ohta H, Hamada J, Tada M, Aoyama T, Furuuchi K, Takahashi Y, Totsuka Y, Moriuchi T: HOXD3-overexpression increases integrin alpha v beta 3 expression and deprives E-cadherin while it enhances cell motility in A549 cells. Clin Exp Metastasis. 2006, 23: 381-390. 10.1007/s10585-006-9047-5.View ArticlePubMedGoogle Scholar
- Charboneau A, East L, Mulholland N, Rohde M, Boudreau N: Pbx1 is required for Hox D3-mediated angiogenesis. Angiogenesis. 2005, 8: 289-296. 10.1007/s10456-005-9016-7.View ArticlePubMedGoogle Scholar
- Boudreau N, Andrews C, Srebrow A, Ravanpay A, Cheresh DA: Induction of the angiogenic phenotype by Hox D3. J Cell Biol. 1997, 139: 257-264. 10.1083/jcb.139.1.257.View ArticlePubMedPubMed CentralGoogle Scholar
- Gehring WJ, Hiromi Y: Homeotic genes and the homeobox. Annu Rev Genet. 1986, 20: 147-173. 10.1146/annurev.ge.20.120186.001051.View ArticlePubMedGoogle Scholar
- Thamm DH, Dickerson EB, Akhtar N, Lewis R, Auerbach R, Helfand SC, MacEwen EG: Biological and molecular characterization of a canine hemangiosarcoma-derived cell line. Res Vet Sci. 2006, 81: 76-86. 10.1016/j.rvsc.2005.09.005.View ArticlePubMedGoogle Scholar
- Fosmire SP, Dickerson EB, Scott AM, Bianco SR, Pettengill MJ, Meylemans H, Padilla M, Frazer-Abel AA, Akhtar N, Getzy DM, et al: Canine malignant hemangiosarcoma as a model of primitive angiogenic endothelium. Lab Invest. 2004, 84: 562-572. 10.1038/labinvest.3700080.View ArticlePubMedGoogle Scholar
- Kobie K, Kawabata M, Hioki K, Tanaka A, Matsuda H, Mori T, Maruo K: The tyrosine kinase inhibitor imatinib [STI571] induces regression of xenografted canine mast cell tumors in SCID mice. Res Vet Sci. 2007, 82: 239-241. 10.1016/j.rvsc.2006.06.006.View ArticlePubMedGoogle Scholar
- Akhtar N, Padilla ML, Dickerson EB, Steinberg H, Breen M, Auerbach R, Helfand SC: Interleukin-12 inhibits tumor growth in a novel angiogenesis canine hemangiosarcoma xenograft model. Neoplasia. 2004, 6: 106-116. 10.1593/neo.03334.View ArticlePubMedPubMed CentralGoogle Scholar
- Jin I, Yuji M, Yoshinori N, Makoto K, Mikio M: Anti-tumor effect of PDT using Photofrin in a mouse angiosarcoma model. Arch Dermatol Res. 2008, 300: 161-166. 10.1007/s00403-007-0820-3.View ArticlePubMedGoogle Scholar
- Ferrer L, Fondevila D, Rabanal RM, Vilafranca M: Immunohistochemical detection of CD31 antigen in normal and neoplastic canine endothelial cells. J Comp Pathol. 1995, 112: 319-326. 10.1016/S0021-9975(05)80013-1.View ArticlePubMedGoogle Scholar
- von Beust BR, Suter MM, Summers BA: Factor VIII-related antigen in canine endothelial neoplasms: an immunohistochemical study. Vet Pathol. 1988, 25: 251-255. 10.1177/030098588802500401.View ArticlePubMedGoogle Scholar
- Kodama A, Sakai H, Kobayashi K, Mori T, Maruo K, Kudo T, Yanai T, Masegi T: B-cell intestinal lymphoma with Mott cell differentiation in a 1-year-old miniature Dachshund. Vet Clin Pathol. 2008, 37: 409-415. 10.1111/j.1939-165X.2008.00067.x.View ArticlePubMedGoogle Scholar
- Kodama A, Sakai H, Murakami M, Murai A, Mori T, Maruo K, Yanai T, Masegi T: Immunohistochemical Demonstration of Angiogenesis-Associated Homeobox Proteins in Canine Vascular Tumours. J Comp Pathol. 2009, 141: 199-203. 10.1016/j.jcpa.2009.04.004.View ArticlePubMedGoogle Scholar
- Azcoitia V, Aracil M, Martinez AC, Torres M: The homeodomain protein Meis1 is essential for definitive hematopoiesis and vascular patterning in the mouse embryo. Dev Biol. 2005, 280: 307-320. 10.1016/j.ydbio.2005.01.004.View ArticlePubMedGoogle Scholar
- Birner P, Ritzi M, Musahl C, Knippers R, Gerdes J, Voigtlander T, Budka H, Hainfellner JA: Immunohistochemical detection of cell growth fraction in formalin-fixed and paraffin-embedded murine tissue. Am J Pathol. 2001, 158: 1991-1996.View ArticlePubMedPubMed CentralGoogle Scholar
- Stephen J, Withrow DMV, (ed): Withrow and Macewen's Small Animal Clinical Oncology. 2007, St. Louis, Missouri: Saunders, an imprint of Elsevier Inc, Fourth
- Uchida N, Nagai K, Sakurada Y, Shirota K: The expression of VEGF and flt-1 in the Normal Dog tissues. J Vet Med Sci. 2008, 70: 1273-1276. 10.1292/jvms.70.1273.View ArticlePubMedGoogle Scholar
- Stalmans I: Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome. Verh K Acad Geneeskd Belg. 2005, 67: 229-276.PubMedGoogle Scholar
- Lee YH, Tokunaga T, Oshika Y, Suto R, Yanagisawa K, Tomisawa M, Fukuda H, Nakano H, Abe S, Tateishi A, et al: Cell-retained isoforms of vascular endothelial growth factor (VEGF) are correlated with poor prognosis in osteosarcoma. Eur J Cancer. 1999, 35: 1089-1093. 10.1016/S0959-8049(99)00073-8.View ArticlePubMedGoogle Scholar
- Tomisawa M, Tokunaga T, Oshika Y, Tsuchida T, Fukushima Y, Sato H, Kijima H, Yamazaki H, Ueyama Y, Tamaoki N, et al: Expression pattern of vascular endothelial growth factor isoform is closely correlated with tumour stage and vascularisation in renal cell carcinoma. Eur J Cancer. 1999, 35: 133-137. 10.1016/S0959-8049(98)00278-0.View ArticlePubMedGoogle Scholar
- Oshika Y, Nakamura M, Tokunaga T, Ozeki Y, Fukushima Y, Hatanaka H, Abe Y, Yamazaki H, Kijima H, Tamaoki N, et al: Expression of cell-associated isoform of vascular endothelial growth factor 189 and its prognostic relevance in non-small cell lung cancer. Int J Oncol. 1998, 12: 541-544.PubMedGoogle Scholar
- Yuan A, Yu CJ, Chen WJ, Lin FY, Kuo SH, Luh KT, Yang PC: Correlation of total VEGF mRNA and protein expression with histologic type, tumor angiogenesis, patient survival and timing of relapse in non-small-cell lung cancer. Int J Cancer. 2000, 89: 475-483. 10.1002/1097-0215(20001120)89:6<475::AID-IJC2>3.0.CO;2-T.View ArticlePubMedGoogle Scholar
- Yuan A, Yu CJ, Kuo SH, Chen WJ, Lin FY, Luh KT, Yang PC, Lee YC: Vascular endothelial growth factor 189 mRNA isoform expression specifically correlates with tumor angiogenesis, patient survival, and postoperative relapse in non-small-cell lung cancer. J Clin Oncol. 2001, 19: 432-441.PubMedGoogle Scholar
- Tokunaga T, Oshika Y, Abe Y, Ozeki Y, Sadahiro S, Kijima H, Tsuchida T, Yamazaki H, Ueyama Y, Tamaoki N, et al: Vascular endothelial growth factor (VEGF) mRNA isoform expression pattern is correlated with liver metastasis and poor prognosis in colon cancer. Br J Cancer. 1998, 77: 998-1002.View ArticlePubMedPubMed CentralGoogle Scholar
- Gasparini G: Prognostic value of vascular endothelial growth factor in breast cancer. Oncologist. 2000, 5 (Suppl 1): 37-44. 10.1634/theoncologist.5-suppl_1-37.View ArticlePubMedGoogle Scholar
- Hashimoto M, Ohsawa M, Ohnishi A, Naka N, Hirota S, Kitamura Y, Aozasa K: Expression of vascular endothelial growth factor and its receptor mRNA in angiosarcoma. Lab Invest. 1995, 73: 859-863.PubMedGoogle Scholar
- Kroon E, Krosl J, Thorsteinsdottir U, Baban S, Buchberg AM, Sauvageau G: Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b. Embo J. 1998, 17: 3714-3725. 10.1093/emboj/17.13.3714.View ArticlePubMedPubMed CentralGoogle Scholar
- Steinle JJ, Meininger CJ, Forough R, Wu G, Wu MH, Granger HJ: Eph B4 receptor signaling mediates endothelial cell migration and proliferation via the phosphatidylinositol 3-kinase pathway. J Biol Chem. 2002, 277: 43830-43835. 10.1074/jbc.M207221200.View ArticlePubMedGoogle Scholar
- Thorsteinsdottir U, Mamo A, Kroon E, Jerome L, Bijl J, Lawrence HJ, Humphries K, Sauvageau G: Overexpression of the myeloid leukemia-associated Hoxa9 gene in bone marrow cells induces stem cell expansion. Blood. 2002, 99: 121-129. 10.1182/blood.V99.1.121.View ArticlePubMedGoogle Scholar
- Boudreau NJ, Varner JA: The homeobox transcription factor Hox D3 promotes integrin alpha5beta1 expression and function during angiogenesis. J Biol Chem. 2004, 279: 4862-4868. 10.1074/jbc.M305190200.View ArticlePubMedGoogle Scholar
- Hansen SL, Dosanjh A, Young DM, Boudreau N, Hoffman WY: Hemangiomas and homeobox gene expression. J Craniofac Surg. 2006, 17: 767-771. 10.1097/00001665-200607000-00031.View ArticlePubMedGoogle Scholar
- Care A, Felicetti F, Meccia E, Bottero L, Parenza M, Stoppacciaro A, Peschle C, Colombo MP: HOXB7: a key factor for tumor-associated angiogenic switch. Cancer Res. 2001, 61: 6532-6539.PubMedGoogle Scholar
- Krosl J, Baban S, Krosl G, Rozenfeld S, Largman C, Sauvageau G: Cellular proliferation and transformation induced by HOXB4 and HOXB3 proteins involves cooperation with PBX1. Oncogene. 1998, 16: 3403-3412. 10.1038/sj.onc.1201883.View ArticlePubMedGoogle Scholar
- Shiraishi K, Yamasaki K, Nanba D, Inoue H, Hanakawa Y, Shirakata Y, Hashimoto K, Higashiyama S: Pre-B-cell leukemia transcription factor 1 is a major target of promyelocytic leukemia zinc-finger-mediated melanoma cell growth suppression. Oncogene. 2007, 26: 339-348. 10.1038/sj.onc.1209800.View ArticlePubMedGoogle Scholar
- Crijns AP, de Graeff P, Geerts D, Ten Hoor KA, Hollema H, Sluis van der T, Hofstra RM, de Bock GH, de Jong S, Zee van der AG, et al: MEIS and PBX homeobox proteins in ovarian cancer. Eur J Cancer. 2007, 43: 2495-2505. 10.1016/j.ejca.2007.08.025.View ArticlePubMedGoogle Scholar
- Puppin C, Puglisi F, Pellizzari L, Manfioletti G, Pestrin M, Pandolfi M, Piga A, Di Loreto C, Damante G: HEX expression and localization in normal mammary gland and breast carcinoma. BMC Cancer. 2006, 6: 192-10.1186/1471-2407-6-192.View ArticlePubMedPubMed CentralGoogle Scholar
- D'Elia AV, Tell G, Russo D, Arturi F, Puglisi F, Manfioletti G, Gattei V, Mack DL, Cataldi P, Filetti S, et al: Expression and localization of the homeodomain-containing protein HEX in human thyroid tumors. J Clin Endocrinol Metab. 2002, 87: 1376-1383. 10.1210/jc.87.3.1376.View ArticlePubMedGoogle Scholar
- Tiberio C, Barba P, Magli MC, Arvelo F, Le Chevalier T, Poupon MF, Cillo C: HOX gene expression in human small-cell lung cancers xenografted into nude mice. Int J Cancer. 1994, 58: 608-615. 10.1002/ijc.2910580426.View ArticlePubMedGoogle Scholar
- Buzzai M, Licht JD: New molecular concepts and targets in acute myeloid leukemia. Curr Opin Hematol. 2008, 15: 82-87. 10.1097/MOH.0b013e3282f3ded0.View ArticlePubMedGoogle Scholar
- Reddy SD, Ohshiro K, Rayala SK, Kumar R: MicroRNA-7, a homeobox D10 target, inhibits p21-activated kinase 1 and regulates its functions. Cancer Res. 2008, 68: 8195-8200. 10.1158/0008-5472.CAN-08-2103.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhang X, Zhu T, Chen Y, Mertani HC, Lee KO, Lobie PE: Human growth hormone-regulated HOXA1 is a human mammary epithelial oncogene. J Biol Chem. 2003, 278: 7580-7590. 10.1074/jbc.M212050200.View ArticlePubMedGoogle Scholar
- Plowright L, Harrington KJ, Pandha HS, Morgan R: HOX transcription factors are potential therapeutic targets in non-small-cell lung cancer (targeting HOX genes in lung cancer). Br J Cancer. 2009, 100: 470-475. 10.1038/sj.bjc.6604857.View ArticlePubMedPubMed CentralGoogle Scholar
- Furukawa T, Kubota T, Watanabe M, Nishibori H, Kuo TH, Saikawa Y, Kase S, Tanino H, Teramoto T, Ishibiki K, et al: A suitable model for experimental liver metastasis of human colon cancer xenografts using mice with severe combined immunodeficiency. J Surg Oncol. 1993, 52: 64-67. 10.1002/jso.2930520117.View ArticlePubMedGoogle Scholar
- Nomura T, Takahama Y, Hongyo T, Inohara H, Takatera H, Fukushima H, Ishii Y, Hamaoka T: SCID (severe combined immunodeficiency) mice as a new system to investigate metastasis of human tumors. J Radiat Res (Tokyo). 1990, 31: 288-292. 10.1269/jrr.31.288.View ArticleGoogle Scholar
- Garofalo A, Chirivi RG, Scanziani E, Mayo JG, Vecchi A, Giavazzi R: Comparative study on the metastatic behavior of human tumors in nude, beige/nude/xid and severe combined immunodeficient mice. Invasion Metastasis. 1993, 13: 82-91.PubMedGoogle Scholar
- Fidler IJ: Orthotopic implantation of human colon carcinomas into nude mice provides a valuable model for the biology and therapy of metastasis. Cancer Metastasis Rev. 1991, 10: 229-243. 10.1007/BF00050794.View ArticlePubMedGoogle Scholar
- Morikawa K, Walker SM, Nakajima M, Pathak S, Jessup JM, Fidler IJ: Influence of organ environment on the growth, selection, and metastasis of human colon carcinoma cells in nude mice. Cancer Res. 1988, 48: 6863-6871.PubMedGoogle Scholar
- Naito S, von Eschenbach AC, Fidler IJ: Different growth pattern and biologic behavior of human renal cell carcinoma implanted into different organs of nude mice. J Natl Cancer Inst. 1987, 78: 377-385.PubMedGoogle Scholar
- Ohguri T, Imada H, Nomoto S, Yahara K, Hisaoka M, Hashimoto H, Tokura Y, Nakamura K, Shioyama Y, Honda H, et al: Angiosarcoma of the scalp treated with curative radiotherapy plus recombinant interleukin-2 immunotherapy. Int J Radiat Oncol Biol Phys. 2005, 61: 1446-1453. 10.1016/j.ijrobp.2004.08.008.View ArticlePubMedGoogle Scholar
- Wollina U, Fuller J, Graefe T, Kaatz M, Lopatta E: Angiosarcoma of the scalp: treatment with liposomal doxorubicin and radiotherapy. J Cancer Res Clin Oncol. 2001, 127: 396-399. 10.1007/s004320000221.View ArticlePubMedGoogle Scholar
- Ulrich L, Krause M, Brachmann A, Franke I, Gollnick H: Successful treatment of angiosarcoma of the scalp by intralesional cytokine therapy and surface irradiation. J Eur Acad Dermatol Venereol. 2000, 14: 412-415. 10.1046/j.1468-3083.2000.00111.x.View ArticlePubMedGoogle Scholar
- Taylor KL, Oates RK, Grane R, Leaman DW, Borden EC, Lindner DJ: IFN-alpha1,8 inhibits tumor-induced angiogenesis in murine angiosarcomas. J Interferon Cytokine Res. 2006, 26: 353-361. 10.1089/jir.2006.26.353.View ArticlePubMedGoogle Scholar
- Ma G, Masuzawa M, Hamada Y, Haraguchi F, Tamauchi H, Sakurai Y, Fujimura T, Katsuoka K: Treatment of murine angiosarcoma with etoposide, TNP-470 and prednisolone. J Dermatol Sci. 2000, 24: 126-133. 10.1016/S0923-1811(00)00089-X.View ArticlePubMedGoogle Scholar
- Vogt T, Hafner C, Bross K, Bataille F, Jauch KW, Berand A, Landthaler M, Andreesen R, Reichle A: Antiangiogenetic therapy with pioglitazone, rofecoxib, and metronomic trofosfamide in patients with advanced malignant vascular tumors. Cancer. 2003, 98: 2251-2256. 10.1002/cncr.11775.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/9/363/prepub
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