The role of a new CD44st in increasing the invasion capability of the human breast cancer cell line MCF-7
© Fang et al; licensee BioMed Central Ltd. 2011
Received: 17 December 2009
Accepted: 12 July 2011
Published: 12 July 2011
CD44, a hyaluronan (HA) receptor, is a multistructural and multifunctional cell surface molecule involved in cell proliferation, cell differentiation, cell migration, angiogenesis, presentation of cytokines, chemokines and growth factors to the corresponding receptors, and docking of proteases at the cell membrane, as well as in signaling for cell survival. The CD44 gene contains 20 exons that are alternatively spliced, giving rise to many CD44 isoforms, perhaps including tumor-specific sequences.
Reverse transcriptase polymerase chain reaction (RT-PCR) and Western blotting were used to detect CD44st mRNA and CD44 protein in sensitive MCF-7, Lovo, K562 and HL-60 cell lines as well as their parental counterparts, respectively. The full length cDNA encoding CD44st was obtained from the total RNA isolated from MCF-7/Adr cells by RT-PCR, and subcloned into the pMD19-T vector. The CD44st gene sequence and open reading frame were confirmed by restriction enzyme analysis and nucleotide sequencing, and then inserted into the eukaryotic expression vector pcDNA3.1. The pcDNA3.1-CD44st was transfected into MCF-7 cells using Lipofectamine. After transfection, the positive clones were obtained by G418 screening. The changes of the MMP-2 and MMP-9 genes and protein levels were detected by RT-PCR and gelatin zymography, respectively. The number of the cells penetrating through the artificial matrix membrane in each group (MCF-7, MCF-7+HA, MCF-7/neo, MCF-7/neo+HA, MCF-7/CD44st, MCF-7/CD44st+HA and MCF-7/CD44st+Anti-CD44+HA) was counted to compare the change of the invasion capability regulated by the CD44st. Erk and P-Erk were investigated by Western blotting to approach the molecular mechanisms of MMP-2 and MMP-9 expression regulated by the CD44st.
Sensitive MCF-7, Lovo, K562 and HL-60 cells did not contain CD44st mRNA and CD44 protein. In contrast, the multidrug resistance MCF-7/Adr, Lovo/Adr, K562/Adr and HL-60/Adr cells expressed CD44st mRNA and CD44 protein. The CD44st mRNA gene sequence was successfully cloned into the recombinant vector pcDNA3.1 and identified by the two restriction enzymes. It was confirmed that the reconstructed plasmid contained the gene sequence of CD44st that was composed of exons 1 to 4, 16 to 17, and 1 to 205 bases of exons 18. The new gene sequence was sent to NCBI for publication, and obtained the registration number FJ216964. The up-regulated level of the mRNA of the CD44 gene and the CD44 protein were detected, respectively, by RT-PCR and flow cytometry in MCF-7 cells transfected with pcDNA3.1-CD44st. The invasiveness of the cells and the activity of MMP-2 and MMP-9 were clearly activated by HA treatment, and blocked by CD44 neutralizing antibody. MCF-7/CD44st cells pretreated with the neutralizing antibody against CD44, and the inhibitor of MAPKs signaling pathway, could strongly block the expression of P-Erk.
A new CD44st was expressed in multidrug resistant MCF-7/Adr, Lovo/Adr, K562/Adr and HL-60/Adr cells. The expression vector pcDNA3.1-CD44st was cloned and constructed successfully, and stably transfected into MCF-7 cells. HA could interact with the new CD44st and regulate the expression of MMP-2 and MMP-9, which could increase the invasion capability of MCF-7 cells through the Ras/MAPK signaling pathway.
Tumor invasion is one of the major factors contributing to patient mortality during disease progression. When a tumor cell metastasizes, it initially penetrates the surroundings of the extracellular matrix (ECM), invades the vascular system, and transports to distant sites of the body .
Currently, dozens of CD44 isoforms have been discovered. The standard CD44 (CD44s) is the most common form, in which exon 5 is directly connected to exon 16, and lacks the entire variant exon region . In our study, we used MCF-7/Adr cells to clone the novel CD44st, which contains exons 1 to 4, exons 16 to 17, and 1 to 205 bp of 18 exons (Figure 1). We found that HA-CD44st signaling leads to activation of MMP-2 and MMP-9 secretion in the MCF-7/CD44st cells, and subsequently increases a tumors' invasion capability [5, 6].
The type I transmembrane glycoprotein receptor CD44 is a cell membrane receptor that links hyaluronate to the cytoskeleton ankyrin to mediate signal transduction . CD44 also plays a role in cell migration, differentiation, and survival signaling, which is important both to normal cells and cancer cells. An animal model experiment has demonstrated that blocking CD44 with antibodies and antisense oligonucleotides decreases the malignant activities of the tumor . The intracellular region of short tail CD44 (CD44st) contains exons 18 and 20, which is potentially linked to the ability of cytoskeleton protein (ankyrin and actin) to mediate signal transduction [9, 10]. However, whether short tail CD44 (CD44st) is involved in signal transduction is currently unclear. Jiang H found that CD44st was not able to mediate the endocytosis process of the HA based on the fact that CD44st does not help HA integrate on the cell membrane .
HA, which has a high molecular weight, is widely distributed in the extracellular matrix (ECM), and could potentially combine with CD44 and participate in cell migration and cancer progression . HA plays a role in anti-angiogenesis, but the degradation products of HA stimulate the generation of endothelial cells, angiogenesis and migration, resulting in CD44 receptor activation . It has been previously demonstrated that HA synthase-1 may facilitate bladder cancer metastasis and therefore could potentially serve as a diagnostic marker .
Matrix metalloproteinases (MMPS) are zinc-required matrix-degrading enzymes that play an important role in tumor cell metastasis . Recent studies have shown that hyalurinan strongly activates MMP-2 secretion; the principal reason is due to CD44 expression . It has been demonstrated that MMP-9-CD44-EGFR interaction and the dimerization of the MMP-9 hemopexin domain are critical to the migration of fibrosarcoma cells . Thus, it appears that HA, CD44, and MMPS are all involved in the initiation of tumor invasion and are attractive targets for tumor therapy.
Reagents and Cell Culture
Fetal bovine serum was purchased from Hangzhou Sijiqing Biological Engineering Materials Co, Ltd. The following reagents used in this study were purchased from Invitrogen: 1640 medium, 2.5% trypsase with EDTA, Trizol, opti-MEM-I Reduced Serum Medium (OPTI-MEM), Lipofectamine 2000 and G418. The RT-PCR kit was purchased from Fermentas. Hyaluronan was purchased from Sigma. Matrigel was purchased from Becton Dickinson and Company. Transwell was purchased from Corning, and the FITC labeled CD44 antibody used for detection of flow cytometry was purchased from eBioscience. The CD44 antibody used for western blot detection was purchased from Abcam. The CD44 blocking antibody was obtained from Neromarker. Manumycin A, PD98059, Phospho-p44/42 MAPK (Thr202/Tyr204) Mouse mAb, and p42 MAP Kinase (Erk) Antibody were purchased from Cells singnal technology. The recombinant vector pcDNA3.1 was generously supplied by Dr. XU Wen-rong in the medical college of Jiangsu University. Human breast cancer cell lines (MCF-7 and MDR derivative MCF-7/Adr) and human colorectal cancer cell lines (Lovo and MDR derivative Lovo/Adr), human promyelocytic leukemia cell lines (HL-60 and MDR derivative HL-60/Adr), and human chronic myeloid leukemic cell lines (K562 and MDR derivative K562/Adr) were all obtained from the Shang-hai cell repository of Academia Sinica and the cells were maintained in 1640 medium with 10% heat-inactivated FBS at 37°C in a humidified atmosphere containing 5% CO2.
Construction and expression of eukaryotic expression vector pcDNA3.1-CD44st, RNA extraction, and reverse transcription-PCR
The total RNA of the cultured cells was extracted using Trizol reagent according to the manufacturer's directions. The RT-PCR kit was used to carry out RT-PCR of each RNA template according to the manufacturer's instructions. In brief, reverse transcription of each mRNA transcript occurred during incubation for 5 minute at 70°C, followed by incubation for 1 hour at 42°C and finally at 70°C for 10 minute. The primers of the CD44 (GenBank.NO.AJ251595) are as follows: forward primer, 5'-GGATGGACAAGTTTTGGTGGCACG-3'; reverse primer, 5'-GGTTACACCCCAATCTTCATGTCC-3'. PCR amplification for CD44st occurred as follows: incubation at 94°Cfor 5 minute, 30 cycles at 94°C for 30 seconds, incubation at 66°Cfor 30 seconds, and at 72°C for 2 minute, followed by incubation at 72°C for 10 minute, and storage at 4°C. The β-actin gene primers which were used as a control are as follows: forward primer, 5'-CTCGCGCTACTCTCTCTTTC-3', reverse primer, 5'-CATGTCTCGATCCCACTTAAC-3'. Reverse transcription occurred as above, and PCR amplification as follows: incubation at 94°C for 5 minute, 30 cycles at 94°C for 30 seconds, incubation at 58°C for 30 seconds, and at 72°C for 30 seconds, then at 72°C for 10 minutes, followed by storage at 4°C. PCR amplification for MMP-2 (GeneBank accession no. NM 004530) (forward primer, 5'-CGGTGCCCAAGAATAGATG-3; reverse primer, 5'-AAAGGAGAAGAGCCTGAAGTG-3') occurred as follows: incubation at 94°C for 5 minute, followed by 30 cycles at 94°C for 30 seconds, then incubation at 59.1°C for 30 seconds, and incubation at 72°C for 30 seconds, followed by incubation at 72°C for 10 minutes, and storage at 4°C. MMP-9 (GeneBank accession no. NM 004994) (forward primer, 5'-CGGAGCACGGAGACGGGTAT-3'; reverse primer 5'-GCCGCCACGAGGAAAACT-3') PCR amplification occurred as follows: incubation at 94°C for 5 minute, followed by 30 cycles at 94°C for 30 seconds, incubation at 62.7°C for 30 seconds, and at 72°C for 45 seconds, followed by incubation at 72°C for 10 minute, and storage at -20°C.
Gene clone and Plasmid construction
Transfection and obtaining the positive clone
The pcDNA3.1 and the pcDNA3.1-CD44st vectors were transferred to MCF-7 cells according to the manufacturers' protocol. After incubation for 48 hours, the transfected cells were replanted and exposed to G418 containing medium (800 μg/ml) for 1 week. When a large number of the cells appeared to be dying, the concentration of G418 was reduced to 200 μg/ml and the cells were incubated for 2 weeks. The positive clones were identified and selected for further development, and then cultured with a 200 μg/ml G418 solution to maintain resistance. The expression of CD44st was confirmed by RT-PCR, DNA sequencing, and flow cytometric analysis.
Flow cytometric analysis
Cells in the logarithmic phase were harvested via the cell scraper technique. After being washed three times with a PBS solution, the harvested cells were blown uniformly into PBS buffer to prepare a single-cell suspension. 5 × 105 cells/ml were incubated with the FITC conjugated rabbit antimouse antibody for 1 hour at 4°C, centrifuged at 1000 rpm for 5 min, and then the supernatant was discarded and cells were resuspended with 500 μL PBS. The relative fluorescence intensity was detected using the flow cytometer (Becton Dickinson). The data were analysed with Cell Quest software. The experiment was repeated three times.
The effects of CD44st on the invasion ability of MCF-7 cells
Treatment of Cells
The cells were digested by 0.25% trypsin in combination with 0.02% EDTA, and then 1.5 × 106 cells were seeded into a new culture flask and diluted with 1.5 ml 1640 medium without heat-inactivated 10% FBS. The cells pretreated with CD44 blocking antibody were incubated for 3 hours with serum-free medium containing CD44 blocking antibody (20 μg/ml). HA (100 μg/ml) was added to the HA treatment groups and the cells were then incubated for 24 hours. In order to eliminate potential contamination by growth factor, the HA solution was boiled at 100°C for 5 minutes before use .
Invasion assays by Matrigel
The transwell method (Corning) was used to perform invasion assays. The pretreatment filters (8 μm pore-size, Matrigel 100 μg/cm2) were rehydrated with 100 μl of medium. 1 × 105 cells in the volume of 100 μl medium were seeded onto the upper part of each well. The volume of 1 ml serum-free 1640 medium containing 0.1% BSA was added to the lower compartment of the transwell. After incubation for 24 h at 37°C, the cells located upon the membranes were wiped with the cotton buds. The cells that had invaded the lower part of the transwell were stained with the gentian and counted using light microscopy (×200, 5 random fields). The invasion capability of the tumor cells was determined by averaging the number of positively stained cells in each of the microscopic fields.
Gelatin zymography analysis was performed on 20 μl culture medium per sample according to the manufacturers' protocol. The positive control was a 1:1 ratio of whole human blood and 2 × non-denaturing loading buffer.
Western Blot Analysis
3 × 105 MCF-7/CD44st cells were seeded in wells of a 6-well plate, grown under routine conditions, and harvested at 80-90% confluence. Each sample was resuspended in 60 μl of boiling 2 × loading buffer. The activation of ERK was detected with a specific antibody to the phosphorylated form of ERK. After cells were lysed by sonication, the cell lysate was subjected to centrifugation at 12,000 × g for 15 min at 4°C. The gels were electro-transferred using an electrophoresis apparatus (Bio-Rad). The total protein of 20 μl/lane was isolated using 10% SDS-PAGE and transferred to a nitrocellulose transfer membrane (0.2 μm). A 5% non-fat milk solution with TBST was used to block the membrane for 1 hour at room temperature. The membrane was incubated with primal mouse anti-human monoclonal antibody (1:500) at 4°C overnight, washed with eluant three times within 30 minutes, incubated with secondary goat anti-rat monoclonal antibody (1:2000) for 1 h at room temperature, and finally washed as above. Immunoblots were visualized using a DAB coloring reagent kit according to the manufacturers' protocol. Gelatin zymography was performed to determine the activity level of MMPs in the culture medium.
Data were all presented as mean ± standard deviation (SD). To test for statistical significance, experimental data were analysed by One-Way ANOVA and SNK-q test. A p value less than 0.05 was considered to indicate a statistically significant result. All of the experiments were repeated in triplicate.
CD44st is expressed in multidrug resistant cells, but not in parental, sensitive cell lines
Expression of CD44st gene and protein in MCF-7/CD44st cells
MMP-2 and MMP-9 gene expression in MCF-7/CD44st cells pretreated with HA
CD44st and hyaluronan interaction causes increase of invasion in MCF-7/CD44st cells
Ras-MAPK signaling pathway plays a role in HA-induced MMP-2 and MMP-9 secretion in MCF-7/CD44st cells
In this study, we determined that CD44st mRNA transcripts and CD44 protein were highly expressed in the multidrug resistant cell line cells, but not in the parental sensitive cell lines. It appears that there must exist a functional link between CD44st and multidrug resistance. Additionally, we studied the function of the new CD44 isoforms (GeneBank NO. FJ216964) regarding tumor invasion using gelatin zymography and transwell experiments. Our findings indicated that the invasiveness of MCF-7/CD44st cells was clearly activated upon treatment with HA. Moreover, the invasiveness of MCF-7/CD44st cells was significantly suppressed by pretreatment with CD44 blocking antibody. Furthermore, statistically significant differences in the number of cells located in the lower compartment of the transwell experiment did not occur between the group of MCF-7 and the group of MCF-7 pretreated with HA. These results suggest that the activation of the tumor invasiveness is dependent upon HA linkage to CD44st. Finally, we approached the role of Ras-MAPK signaling pathways in HA-induced MMP-2 and MMP-9 secretion in MCF-7/CD44st cells. These results indicated that MMP-2 and MMP-9 secretion in MCF-7/CD44st cells is potentially regulated by the HA-CD44st signaling pathway. In addition, we demonstrated that CD44 blocking antibody could block MMP-2 and MMP-9 secretion as well as tumor invasion in MCF-7/CD44st cells.
The major causes of treatment failure in cancer are the development of metastases and drug resistance. Currently, there is some evidence indicating that metastases and multidrug resistance may have a functional link. The extracellular matrix metalloproteinase inducer (EMMPRIN) that is abundantly expressed on the surface of tumor cells potentially stimulates the production of matrix MMPs. MDR cells over-expressed EMMPRIN compared to the parental sensitive cell lines, and were capable of producing higher levels of MMP-1, MMP-2, and MMP-9 . In mammary cancer cells, the interaction among HA, CD44, and EMMPRIN potentially regulates the localization and function of the plasma membrane transporter, as well as the tumor MDR . CD44 and P-glycoprotein encoded by the MDR-1 gene have a functional link, and collectively regulate malignant biological phenotypes, tumor invasion, and MDR . Similarly, some recent studies also indicate that both HA and CD44 are involved in chemotherapeutic drug resistance in many cancers [23–27].
During tumor progression, blockage of the HA-CD44 signaling pathway may provide a new target that overcomes multidrug resistance in breast and ovarian carcinomas . The mitogen-activated protein kinase (MAPK) signaling pathway is important to normal cells as well as cancer cells. Inhibition of MAPK signaling pathways could suppress renal cell carcinoma growth by harming the tumor blood vessels . HA-CD44 potentially mediates the activation of ankyrin and Rho GTPase as the tumor progresses, and thus are also important markers for early diagnosis and evaluation of disease prognosis .
The role of the expression of CD44 isoforms in tumor progression has been widely studied in the last decade. When CD44, HA, and heparanase are highly expressed in breast cancer cells, they generate a microenvironment that facilitates tumor progression and invasion . The phenotype of CD44+/CD24- in breast cancer cells exhibits a higher potential compared to other phenotypes of breast cancer cell lines, however, this is not sufficient evidence to elucidate the relationship with pulmonary metastasis . However, it has been previously reported that the expression of CD44 potentially prevents breast cancer cells from metastasizing. In an experiment, the authors found that HA containing material could inhibit the invasion of the CD44 positive tumor cells. During cancer progression, HA-CD44 epithelial-stromal interaction potentially restrains tumor metastasis . As a result, some arguments remain regarding the relationship between CD44 expression and tumor progression and metastasis.
In summary, the results we present in this study suggest that the novel CD44st gene, cloned from MCF7-/Adr cells, plays an important role in the HA-dependent activation of MMP-2 and MMP-9, as well as the invasiveness of MCF-7/CD44st cells. Furthermore, it appears that the new CD44st gene and MDR-1 gene have some functional links which influence the tumor's multidrug resistance, invasion, and metastasis all together. This lay a ground work for further study. Our results potentially provide a new therapeutic target for tumor invasion through the regulation of the CD44st signal pathway. Finally, expression of CD44st could potentially be used as a dominant selectable marker for the detection of the phenotype of multidrug resistance and tumor cell invasion capabilities.
hyaluronan. RT-PCR: reverse transcript polymerase chain reaction
extracellular matrix metalloproteinase inducer
opti-MEM-Reduced Serum Medium.
This work was supported by school of medical science and laboratory medicine, Jiangsu University, Jiangsu Province, The People's Republic of China. The authors would like to thank Jiangsu University and the study staff in the laboratory.
- Hanahan D, Weinberg RA: The hallmarks of cancer. Cell. 2000, 100: 57-70. 10.1016/S0092-8674(00)81683-9.View ArticlePubMedGoogle Scholar
- Screaton GR, Bell MV, Jackson DG, Cornelis FB, Gerth U, Bell JI: Genomic structure of DNA encoding the lymphocyte homing receptor CD44 reveals at least 12 alternatively spliced exons. Proc Natl Acad Sci USA. 1992, 89: 12160-12164. 10.1073/pnas.89.24.12160.View ArticlePubMedPubMed CentralGoogle Scholar
- Screaton GR, Bell MV, Bell JI, Jackson DG: The identification of a new alternative exon with highly restricted tissue expression in transcripts encoding the mouse Pgp-1 (CD44) homing receptor. J Biol Chem. 1993, 268: 12235-12238.PubMedGoogle Scholar
- Naor D, Nedvetzki S: CD44 in rheumatoid arthritis. Arthritis Res Ther. 2003, 5: 105-115.View ArticlePubMedPubMed CentralGoogle Scholar
- Xin-Jian Fang, Wen-L-in Xu, Xu Zhang, Hui Qian, Chen Chen, LI-Li Fang, Qiao-Yun Chen: Construction of human CD44 eukaryotic expression vector and its expression in mammary carcinoma cells. Jian Su university medical journal. 2009, 19: 102-106.Google Scholar
- Fang XJ, Xu WL, Gong JL, Chen C, Fang LL, Chen QY: CD44 variant increases the invasive ability of human breast cancer cell line MCF-7 cells. Zhonghua Zhong Liu Za Zhi. 2010, 32 (1): 22-28.PubMedGoogle Scholar
- Ponta H, Sherman L, Herrlich PA: CD44: from adhesion molecules to signalling regulators. Nat Rev Mol Cell Biol. 2003, 4: 33-45. 10.1038/nrm1004.View ArticlePubMedGoogle Scholar
- Naor D, Nedvetzki S, Golan I, Melnik L, Faitelson Y: CD44 in cancer. Crit Rev Clin Lab Sci. 2002, 39: 527-579. 10.1080/10408360290795574.View ArticlePubMedGoogle Scholar
- Underhill C: CD44: the hyaluronan receptor. J Cell Sci. 1992, 103: 293-298.PubMedGoogle Scholar
- Rail Christopher, Rustgi Anil: CD44 isoform expression in primary and metastatic pancreatic adenocarcinoma. Cancer Res. 1995, 55: 1831-1835.Google Scholar
- Jiang H, Peterson RS, Wang W, Bartnik E, Knudson CB, Knudson W: A requirement for the CD44 cytoplasmic domain for hyaluronan binding, pericellular matrix assembly, and receptor-mediated endocytosis in COS-7 cells. J Biol Chem. 2002, 277: 10531-10538. 10.1074/jbc.M108654200.View ArticlePubMedGoogle Scholar
- Knudson W: tumor-associated hyaluronan providing an extracellular matrix that facilitates invasion. Am J Pathol. 1996, 148: 1721-1726.PubMedPubMed CentralGoogle Scholar
- Slevin M, Krupinski J, Gaffney J, Matou S, West D, Delisser H, Savani RC, Kumar S: Hyaluronan-mediated angiogenesis in vascular disease:Uncovering RHAMM and CD44 receptor signaling pathways. Matrix Biol. 2007, 26: 58-68. 10.1016/j.matbio.2006.08.261.View ArticlePubMedGoogle Scholar
- Golshani R, Lopez L, Estrella V, Kramer M, Iida N, Lokeshwar VB: Hyaluronic acid synthase-1 expression regulates bladder cancer growth, invasion, and angiogenesis through CD44. Cancer Res. 2008, 68: 483-491. 10.1158/0008-5472.CAN-07-2140.View ArticlePubMedGoogle Scholar
- Kleiner DE, Stetler-Stevenson WG: Matrix metalloproteinases and metastasis. Cancer Chemother Pharmacol. 1999, 43 (Suppl): S42-51.View ArticlePubMedGoogle Scholar
- Zhang Y, Thant AA, Machida K, Ichigotani Y, Naito Y, Hiraiwa Y, Senga T, Sohara Y, Matsuda S, Hamaguchi M: Hyaluronan-CD44s signaling regulates matrix metalloproteinase-2 secretion in a human lung carcinoma cell line QG90. Cancer Res. 2002, 62: 3962-3965.PubMedGoogle Scholar
- Dufour Antoine, Nicole S, Kuscu Cem, Zucker Stanley, Cao Jian: Abstract 533: Critical role of MMP-9 dimers in cell migration: design of inhibitory peptides. Cancer Research. 2010, 70 (8): Supplement 1Google Scholar
- Sohara Y, Ishiguro N, Machida K, Kurata H, Thant AA, Senga T, Matsuda S, Kimata K, Iwata H, and Hamaguchi M: Hyaluronan activates cell motility of v-Src-Transformed cells via Ras-mitogen-activated protein kinase and phosphoinositide3-kinase-Akt in a tumor-specific manner. Mol Biol Cell. 2001, 12: 1859-1868.View ArticlePubMedPubMed CentralGoogle Scholar
- Thorne RF, Legg JW, Isacke CM: The role of the CD44 transmembrane and cytoplasmic domains in co-ordinating adhesive and signalling events. J Cell Sci. 2004, 117: 373-380.View ArticlePubMedGoogle Scholar
- Yang JM, Xu Z, Wu H, Zhu H, Wu X, Hait WN: Overexpression of extracellular matrix metalloproteinase inducer in multidrug resistant cancer cells. Mol Cancer Res. 2003, 1: 420-427.PubMedGoogle Scholar
- Misra S, Ghatak S, Zoltan-Jones A, Toole BP: Regulation of multi-drug resistance in cancer cells by hyaluronan. J Biol Chem. 2003, 278: 25285-25288. 10.1074/jbc.C300173200.View ArticlePubMedGoogle Scholar
- Miletti-González KE, Chen S, Muthukumaran N, Saglimbeni GN, Wu X, Yang J, Apolito K, Shih WJ, Hait WN, Rodríguez-Rodríguez L: The CD44 receptor interacts with P-Glycoprotein to promote cell migration and invasion in cancer. Cancer Res. 2005, 65: 6660-6667. 10.1158/0008-5472.CAN-04-3478.View ArticlePubMedGoogle Scholar
- Slomiany MG, Grass GD, Robertson AD, Yang XY, Maria BL, Beeson C, Toole BP: Hyaluronan, CD44, and emmprin regulate lactate efflux and membrane localization of monocarboxylate transporters in human breast carcinoma cells. Cancer Res. 2009, 69: 1293-1301. 10.1158/0008-5472.CAN-08-2491.View ArticlePubMedPubMed CentralGoogle Scholar
- Slomiany MG, Dai L, Bomar PA, Knackstedt TJ, Kranc DA, Tolliver L, Maria BL, Toole BP: Abrogating drug resistance in malignant peripheral nerve sheath tumors by disrupting hyaluronan-CD44 interactions with small hyaluronan oligosaccharides. Cancer Res. 2009, 69: 4992-4998. 10.1158/0008-5472.CAN-09-0143.View ArticlePubMedPubMed CentralGoogle Scholar
- Cordo Russo, Garcia MG, Alaniz L, Blanco G, Alvarez E, Hajos SE: Hyaluronan oligosaccharides sensitize lymphoma resistant cell lines to vincristine by modulating P-glycoprotein activity and PI3K/Akt pathway. Int J Cancer. 2008, 122: 1012-1018.View ArticleGoogle Scholar
- Ohashi R, Takahashi F, Cui R, Yoshioka M, Gu T, Sasaki S, Tominaga S, Nishio K, and Takahashi K: Interaction between CD44 and hyaluronate induces chemoresistance in non-small cell lung cancer cell. Cancer Lett. 2007, 252: 225-234. 10.1016/j.canlet.2006.12.025.View ArticlePubMedGoogle Scholar
- Wang SJ, Peyrollier K, and Bourguignon LY: The influence of hyaluronan-CD44 interaction on topoisomerase II activity and etoposide cytotoxicity in head and neck cancer. Arch Otolaryngol Head Neck Surg. 2007, 133: 281-288. 10.1001/archotol.133.3.281.View ArticlePubMedGoogle Scholar
- Bourguignon LY, Peyrollier K, Xia W, Gilad E: Hyaluronan-CD44 interaction activates stem cell marker nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells. J Biol Chem. 2008, 283: 17635-17651. 10.1074/jbc.M800109200.View ArticlePubMedPubMed CentralGoogle Scholar
- Huang D, Ding Y, Luo WM, Bender S, Qian CN, Kort E, Zhang ZF, VandenBeldt K, Duesbery NS, Resau JH, Teh BT: Inhibition of MAPK kinase signaling pathways suppressed renal cell carcinoma growth and angiogenesis in vivo. Cancer Res. 2008, 68: 81-88. 10.1158/0008-5472.CAN-07-5311.View ArticlePubMedGoogle Scholar
- Bourguignon LY: Hyaluronan-mediated CD44 activation of Rho GTPase signaling and cytoskeleton function promotes tumor progression. Semin Cancer Biol. 2008, 18: 251-259. 10.1016/j.semcancer.2008.03.007.View ArticlePubMedPubMed CentralGoogle Scholar
- Götte M, Yip GW: Heparanase, hyaluronan, and CD44 in Cancers: a breast carcinoma perspective. Cancer Res. 2006, 66: 10233-10237. 10.1158/0008-5472.CAN-06-1464.View ArticlePubMedGoogle Scholar
- Sheridan C, Kishimoto H, Fuchs RK, Mehrotra S, Bhat-Nakshatri P, Turner CH, Goulet R, Badve S, Nakshatri H: CD44+/CD24-breast cancer cells exhibit enhanced invasive properties, an early step necessary for metastasis. Breast Cancer Res. 2006, 8: R59-10.1186/bcr1610.View ArticlePubMedPubMed CentralGoogle Scholar
- Lopez JI, Camenisch TD, Stevens MV, Sands BJ, McDonald J, Schroeder JA: CD44 attenuates metastatic invasion during breast cancer progression. Cancer Res. 2005, 65: 6755-6763. 10.1158/0008-5472.CAN-05-0863.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/11/290/prepub
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