This article has Open Peer Review reports available.
Prognostic relevance of Centromere protein H expression in esophageal carcinoma
- Xian-Zhi Guo†1, 2, 6,
- Ge Zhang†5,
- Jun-Ye Wang3,
- Wan-Li Liu1, 2,
- Fang Wang4,
- Ju-Qin Dong1, 2,
- Li-Hua Xu1, 2,
- Jing-Yan Cao1, 2,
- Li-Bing Song1, 2 and
- Mu-Sheng Zeng1, 2Email author
© Guo et al; licensee BioMed Central Ltd. 2008
Received: 15 May 2008
Accepted: 13 August 2008
Published: 13 August 2008
Many kinetochore proteins have been shown to be associated with human cancers. The aim of the present study was to clarify the expression of Centromere protein H (CENP-H), one of the fundamental components of the human active kinetochore, in esophageal carcinoma and its correlation with clinicopathological features.
We examined the expression of CENP-H in immortalized esophageal epithelial cells as well as in esophageal carcinoma cells, and in 12 cases of esophageal carcinoma tissues and the paired normal esophageal tissues by RT-PCR and Western blot analysis. In addition, we analyzed CENP-H protein expression in 177 clinicopathologically characterized esophageal carcinoma cases by immunohistochemistry. Statistical analyses were applied to test for prognostic and diagnostic associations.
The level of CENP-H mRNA and protein were higher in the immortalized cells, cancer cell lines and most cancer tissues than in normal control tissues. Immunohistochemistry showed that CENP-H was expressed in 127 of 171 ESCC cases (74.3%) and in 3 of 6 esophageal adenocarcinoma cases (50%). Statistical analysis of ESCC cases showed that there was a significant difference of CENP-H expression in patients categorized according to gender (P = 0.013), stage (P = 0.023) and T classification (P = 0.019). Patients with lower CENP-H expression had longer overall survival time than those with higher CENP-H expression. Multivariate analysis suggested that CENP-H expression was an independent prognostic marker for esophageal carcinoma patients. A prognostic value of CENP-H was also found in the subgroup of T3~T4 and N0 tumor classification.
Our results suggest that CENP-H protein is a valuable marker of esophageal carcinoma progression. CENP-H might be used as a valuable prognostic marker for esophageal carcinoma patients.
During the proliferation of normal cells, the centrosome ensures the equal segregation of chromosomes to the postmitotic daughter cells by organizing the bipolar mitotic spindle. In contrast, in cancer cells multipolar mitotic spindles and various centrosomal anomalies, such as supernumerary centrosomes, centrosomes of abnormal size and shape, and prematurely split centrosomes are frequently observed [1–3] It is conceivable that such abnormalities disrupt normal chromosomal segregation, producing aneuploid cells and causing chromosomal instability (CIN).
CIN has been recognized as a hallmark of human cancer and is caused by continuous chromosome missegregation during mitosis. Proper chromosome segregation requires a physical connection between spindle microtubules and centromeric DNA and this attachment occurs at proteinaceous structures called kinetochore . Several kinetochore proteins have been identified in humans, and the list of kinetochore associated proteins continues to grow, including centromere protein (CENP)-A, CENP-B, CENP-C, CENP-E, CENP-F, CENP-H, CENP-I, and INCENP [6, 7]. Studies have shown that kinetochore malfunction is a major cause of aneuploidy and is closely associated with CIN [8, 9]. Normal expression of core kinetochore components is essential to prevent chromosome instability . CENP-H was initially identified as a component of the mouse centromere . Human CENP-H protein was recently isolated and shown to localize in the inner plate together with CENP-A and CENP-C and is a fundamental component of the active centromere complex [12, 13]. Studies using budding yeast have shown that a molecular core consisting of CENP-A, CENP-C, CENP-H, and Ndc80/HEC plays a central role in linking centromeres to the spindle microtubule .
Recent research has shown that CENP-H is up-regulated in most colorectal cancers, and ectopic expression of CENP-H induces chromosome missegregation and aneuploidy in diploid cell lines . Another study found significant association between the level of CENP-H mRNA expression and clinical stage in oral squamous cell carcinomas and indicated that human CENP-H was closely linked to the increased or abnormal cell proliferation in malignant conditions . Previously, we have demonstrated a correlation between expression of CENP-H and both tumor progression and poor prognosis of the patients in the human nasopharyngeal carcinoma. Although CENP-H may play an important role in chromosome instability and carcinogenesis, there are no reports on its role in tumorigenesis and progression of esophageal carcinoma. In this study, we thus investigated the CENP-H expression and its clinical significance in human esophageal carcinoma.
The NE-3 and 108CA cell lines were obtained from Dr. Jin (the University of Hong Kong, P. R. China) and were cultured in Keratinocyte-SFM (Invitrogen, Carlsbad, CA) supplemented with antibiotics (100 μg/μL streptomycin and 100 μg/μL penicillin). The NE-3 is an immortalized esophageal epithelial cell lines and the latter is an ESCC cell line[18, 19]. The ESCC cell lines Eca-109, TE-1, and Kyse140 (Cell Bank of Type Culture Collection of Chinese Academy of Sciences, Shanghai, China) were grown in RPMI 1640 (Invitrogen) supplemented with 10% fetal bovine serum, 100 μg/μL streptomycin, and 100 μg/μL penicillin in a humidified incubator containing 5% CO2 at 37°C.
Patients and tissue specimens
Clinicopathologic characteristics of patient samples and expression of CENP-H in esophageal carcinoma.
(n = 171)
Squamous cell carcinoma
≥ 40 mm
Depth of invasion
Vital status(at follow-up)
Death because of esophageal carcinoma
Death because of unknown cancer or other than esophageal carcinoma
Expression of CENP-H
RNA extraction and reverse transcription-PCR
Total RNAs from cells, tumor tissue and nontumorous tissues was extracted using Trizol reagent (Invitrogen) according to the manufacturer's instructions. The RNA was pretreated with DNase and used for cDNA synthesis with random hexamers. The full-length open reading frame of CENP-H was PCR amplified from cDNA samples of normal tissue and ESCC cell lines. The following primers were used for amplification of CENP-H: sense primer, 5'-TGCAAGAAAAGCAAATCGAA-3'; antisense primer, 5'-ATCCCAAGATTCCTGCTGTG-3'. Glyceraldehyde-3-phosphate dehydrogenase was amplified as an internal control using sense primer, 5'-AATCCCATCACCATCTTCCA-3' and antisense primer, 5'-CCTGCTTCACCACCTTCTTG-3'. The appropriate size of PCR products was confirmed by agarose gel electrophoresis.
Protein extraction and immunoblotting
Frozen tissue samples were solubilized in lysis buffer [7 mol/L urea, 2 mol/L thiourea, 2% CHAPS, 0.1 mol/L DTT, 0.1% NP40, 40 mmol/L Tris-HCl] using a Polytron homogenizer following centrifugation (100,000 g) for 1 h at 4°C. Cultured cells were harvested in 1× SDS sample buffer [62.5 mmol/L Tris-HCl (pH 6.8), 2% SDS, 10% glycerol, and 5% 2-mercaptoethanol] and were heated for 5 min at 100°C. Protein concentration was determined by the Bradford assay (Bio-Rad Laboratories, Hercules, CA). Equal amounts of proteins were separated electrophoretically on 12% SDS polyacrylamide gels and transferred onto polyvinylidene difluoride membranes (Amersham Pharmacia Biotech, Piscataway, NJ). The membrane was probed with an anti-CENP-H rabbit polyclonal antibody (1:1,000; Bethyl Laboratories, Montgomery, TX). Expression of CENP-H was determined with horseradish peroxidase-conjugated anti-rabbit immunoglobulin G (1:3,000; Amersham Pharmacia Biotech) and enhanced chemiluminescence (Amersham Pharmacia Biotech) according to the manufacturer's suggested protocols. An anti-α-tubulin mouse monoclonal antibody (1:1,000; Santa Cruz Biotechnology, Santa Cruz, CA) was used to confirm equal loading.
Immunohistochemistry was done to study altered protein expression in 177 human esophageal cancer tissues. In brief, paraffin-embedded specimens were cut into 4-μm sections and baked at 65°C for 30 min. The sections were deparaffinized with xylenes and rehydrated. Sections were submerged into EDTA antigenic retrieval buffer and microwaved for antigenic retrieval. The sections were treated with 3% hydrogen peroxide in methanol to quench the endogenous peroxidase activity, followed by incubation with 3% bovine serum albumin to block the nonspecific binding. Rabbit polyclonal anti-CENP-H (1:500; Bethyl Laboratories) was incubated with the sections overnight at 4°C. For negative controls, the primary antibody was replaced by normal rabbit serum. After washing, the tissue sections were treated with biotinylated anti-rabbit secondary antibody (Zymed, San Francisco, CA), followed by further incubation with streptavidin horseradish peroxidase complex (Zymed). The tissue sections were immersed in 3-amino-9-ethyl carbazole and counterstained with 10% Mayer's hematoxylin, dehydrated, and mounted in Crystal Mount. The degree of immunostaining of formalin-fixed, paraffin-embedded sections was reviewed and scored by two independent observers. The proportion of the stained cells and the extent of the staining were used as criteria of evaluation. For each case, at least 1,000 tumor cells were analyzed and the percentage of positively nuclear stained tumor cells was recorded. For each sample, the proportion of CENP-H-expressing cells varied from 0% to 100%, and the intensity of nuclear staining varied from weak to strong. One score was given according to the percent of positive cells as: < 5% of the cells:1 point; 6–35% of the cells:2 point; 36–70% of the cells:3 point; >71% of the cells: 4 point. Another score was given according to the intensity of staining as negative staining: 1 point; weak staining (light yellow): 2 point; moderate staining(yellowish brown): 3 point; and strong staining(brown): 4 point. A final score was then calculated by multiple the above two scores. If the final score was equal or bigger than four, the tumor was considered high expression; otherwise, the tumor was considered low expression .
Since the number of esophageal adenocarcinoma is small, all statistical analyses were carried out in 171 ESCC cases using the SPSS 13.0 statistical software package. Mann-Whitney U test was used to analyze the relationship between CENP-H expression and clinicopathologic characteristics. Survival curves were plotted by the Kaplan-Meier method and compared by the log-rank test. The significance of various variables for survival was analyzed by the Cox proportional hazards model in the multivariate analysis. P < 0.05 in all cases was considered statistically significant.
Expression of CENP-H in esophageal carcinoma cell lines
Expression of CENP-H in paired esophageal cancer and nontumorous tissues
Expression of CENP-H in archival esophageal cancer tissues
Correlation between CENP-H protein expression and clinicopathological features
Correlation between the clinicopathologic features and expression of CENP-H protein
≥ 40 mm
Depth of invasion
Univariate and multivariate analysis of different prognostic parameters in patients with esophageal carcinoma by Cox-regression analysis
95% confidence interval
In this report, we presented the first evidence that a kinetochore protein, CENP-H, was overexpressed at both mRNA and protein levels in immortalized cells, ESCC cell lines and most esophageal carcinoma tissues. Overexpression of CENP-H protein was also frequently observed in ESCC specimens and correlated with several aspects of tumor progression summarized in the tumor-node-metastasis classification.
The expression of CENP-H in various kinds of malignant tumors has been reported . However, only a few reports, including our previous article, showed the prognostic relevance of CENP-H expression in neoplasms. Tomonaga et al.  first reported that up-regulation of CENP-H was occurred in primary human colorectal cancer tissues as well as in CIN tumor cells. Shigeishi et al.  reported that the expression level of CENP-H mRNA was significantly higher in oral squamous cell carcinomas than normal gingivae and found a significant association between the level of expression of CENP-H mRNA and clinical stage in oral squamous cell carcinomas. Our previous study  showed that the expression level of CENP-H was higher in nasopharyngeal carcinoma cell lines and in immortalized nasopharyngeal epithelial cells than in the normal nasopharyngeal epithelial cell line at both transcriptional and translational levels. Importantly, patients with higher CENP-H expression had shorter overall survival time, whereas patients with lower CENP-H expression had better survival, and CENP-H expression was an independent prognostic factor. These results indicated an important role for CENP-H in the development and progression of ESCC.
More and more kinetochore proteins have been shown to be associated with carcinogenesis. CENP-F and INCENP are upregulated in human cancer cells [28, 29]. CENP-A has been shown to be overexpressed in colorectal cancer cells and is mistargeted to noncentromeric regions. CENP-F has been implicated in malignancy [31, 32], and its expression is correlated with tumor size in node-negative breast cancer . The CENP-F gene is amplified and overexpressed in head and neck squamous cell carcinoma . A recent study has shown that increased CENP-F protein levels influence tumorigenesis at early stages of tumor development . These findings suggest that kinetochore proteins up-regulation is a common abnormality in tumors.
Being consistent with our previous study, we found that CENP-H was overexpressed in immortalized and ESCC cell lines as well as in ESCC tissues both at transcriptional and translational levels. We further analyzed the relationship between the expression of CENP-H and clinical characteristics of the patients. There was no significant correlation between the expression of CENP-H and age, histologic classification, histological differentiation, tumor diameter, depth of invasion, pN classification or distant metastasis of esophageal cancer patients. However, there was a significant relationship of CENP-H expression in patients categorized according to stage (P = 0.023) and T classification (P = 0.019), strongly suggesting that CENP-H can be used as a marker to identify subsets of ESCC cancer patients with more aggressive disease. In addition, our study suggested that the expression of CENP-H protein in male patients was higher than in female patients. Generally, The female patients had better survival, whereas the male patients had shorter survival . Our analysis showed the same result (data not shown), in accordance with the relation analysis between the expression of CENP-H protein and the overall survival (Fig. 4). With regard to the correlation between immunohistochemical CENP-H staining and the prognosis of esophageal carcinoma, we have shown in univariate and multivariate analyses that high expression of CENP-H is an independent prognosticator for patient survival of esophageal cancer. We also analyzed higher CENP-H expression had significantly shorter overall survival during the T3~T4 patients subgroups. The pathological TNM classification indicated that T classification was based on the depth of invasion for carcinogenesis. At the same time, more and more kinetochore proteins have been shown to be associated with carcinogenesis, including CENP-A, CENP-F and INCENP. Shigeishi et al. [16, 31] reported CENP-H and CENP-F was closely linked to the increased or abnormal cell proliferation in malignant conditions. It suggests that overexpression of CENP-H might be correlated with abnormal cell proliferation in ESCC. In addition, we found that CENP-H might function as a new prognostic marker in ESCC for the N0 patient subgroups, because in these subgroups there is also a trend toward shorter overall survival times of patients with high expression of CENP-H. The combination of pTNM classification and CENP-H expression level in tumor cells is useful for predicting the prognosis of patients with ESCC. Further studies are clearly needed to verify these findings to establish CENP-H as a prognostic marker in ESCC and to clarify its role in carcinogenesis by functional analysis.
These observations highlight the important role of CENP-H in the development and progression of ESCC. As study in colorectal cancer cell lines showed that overexpression of CENP-H remarkably induced aneupoidy. Moreover, CENP-H stable transfectant of mouse embryonic fibrolast/3T3 cell lines showed aberrant interphase micronuclei, characteristic of chromosomes missegregation . Other reports show that deletion of CENP-H results in an accumulation of cells in metaphase and subsequent cell death as a result of chromosome aberrations and missegregation . CENP-H is a component of active centromere-kinetochore complexes in mammals, colocalizing with both CENP-A and CENP-C, which are found in the inner kinetochore plate throughout the cell cycle [13, 36, 37]. Inappropriate expression of CENP-H might deplete other centromere-kinetochore components and disrupt the kinetochore complex, or prevent normal kinetochore assembly and consequently cause aneuploidy and induce the development of cancer . These results suggest that CENP-H may be crucial for the appropriate localization and the proper function of the kinetochore. Chromosomal abnormalities, including abnormal chromosome numbers, chromosome deletion, and amplification, are commonly found in ESCC [23–25]. It was reported that defects in mitotic checkpoints occur frequently (~40%) in ESCC cells . Evidence has shown that chromosomal instability plays an important role in the development and progression of ESCC because aneuploidy is frequently found in the earliest stages of tumorigenesis . Up-regulation of CENP-H in esophageal cancer cells may contribute to chromosomal instability and thus play a role in the progression of ESCC.
The development and progression of ESCC stages, including single hyperplasia and single squamous metaplasia, atypical hyperplasia and allotype squamous metaplasia, in situ carcinoma, infiltrating carcinoma, and metastatic carcinoma, may involve the accumulation of multiple genetic alterations over a long period of time . Cell immortalization is the ability of normal cells to grow through an in definite number of divisions in culture. Because immortalized cells are capable of unlimited proliferation and represent the early stage of transformation before malignant transformation, we examined CENP-H expression in immortalized esophageal epithelial cell line NE3 and found that CENP-H protein was up-regulated in NE3 cells (Fig. 1). These results suggest that CENP-H may be an early transformation factor of esophageal epithelial cells.
This is the first study showing the expression of CENP-H in esophageal cancer cell lines as well as tumor tissues, highlighting the clinical significance of CENP-H in esophageal carcinoma. An examination of CENP-H expression is a useful molecular marker for esophageal carcinoma and an indicator for determining malignant properties, including clinical outcome in patients with esophageal carcinoma. However, further studies are needed to clarify the mechanism by which CENP-H is involved in the development and progression of esophageal carcinoma and its exact role in the regulation of chromosome instability in esophageal carcinoma.
This study was supported partially by grants from the National Natural Science Foundation of China 30630068 and 30570701, grants from the Ministry of Science and Technology of China 2007AA02Z477 and 2006CB910104, and grants from the National Natural Science Foundation of Guangdong Province, China 04300288. MZ is supported by Program for New Century Excellent Talents in University.
- Fukasawa K: Oncogenes and tumour suppressors take on centrosomes. Nat Rev Cancer. 2007, 7: 911-924. 10.1038/nrc2249.View ArticlePubMedGoogle Scholar
- Haase SB, Winey M, Reed SI: Multi-step control of spindle pole body duplication by cyclin-dependent kinase. Nat Cell Biol. 2001, 3: 38-42. 10.1038/35050543.View ArticlePubMedGoogle Scholar
- Pihan GA, Purohit A, Wallace J, Knecht H, Woda B, Quesenberry P, Doxsey SJ: Centrosome defects and genetic instability in malignant tumors. Cancer Res. 1998, 58: 3974-3985.PubMedGoogle Scholar
- Krämer A, Neben K, Ho AD: Centrosome replication, genomic instability and cancer. Leukemia. 2002, 16: 767-775. 10.1038/sj.leu.2402454.View ArticlePubMedGoogle Scholar
- Yuen KW, Montpetit B, Hieter P: The kinetochore and cancer: what's the connection?. Curr Opin Cell Biol. 2005, 17: 576-582. 10.1016/j.ceb.2005.09.012.View ArticlePubMedGoogle Scholar
- Dalal Y, Furuyama T, Vermaak D, Henikoff S: Structure, dynamics, and evolution of centromeric nucleosomes. Proc Natl Acad Sci USA. 2007, 104: 15974-15981. 10.1073/pnas.0707648104.View ArticlePubMedPubMed CentralGoogle Scholar
- Morris CA, Moazed D: Centromere assembly and propagation. Cell. 2007, 128: 647-650. 10.1016/j.cell.2007.02.002.View ArticlePubMedGoogle Scholar
- Schafer-Hales K, Iaconelli J, Snyder JP, Prussia A, Nettles JH, El-Naggar A, Khuri FR, Giannakakou P, Marcus AI: Farnesyl transferase inhibitors impair chromosomal maintenance in cell lines and human tumors by compromising CENP-E and CENP-F function. Mol Cancer Ther. 2007, 6: 1317-1328. 10.1158/1535-7163.MCT-06-0703.View ArticlePubMedGoogle Scholar
- Bharadwaj R, Yu H: The spindle checkpoint, aneuploidy, and cancer. Oncogene. 2004, 23: 2016-2027. 10.1038/sj.onc.1207374.View ArticlePubMedGoogle Scholar
- Musacchio A, Salmon ED: The spindle-assembly checkpoint in space and time. Nat Rev Mol Cell Biol. 2007, 8: 379-393. 10.1038/nrm2163.View ArticlePubMedGoogle Scholar
- Sugata N, Munekata E, Todokoro K: Characterization of a novel kinetochore protein, CENP-H. J Biol Chem. 1999, 274: 27343-27346. 10.1074/jbc.274.39.27343.View ArticlePubMedGoogle Scholar
- Okada M, Cheeseman IM, Hori T, Okawa K, McLeod IX, Yates JR, Desai A, Fukagawa T: The CENP-H-I complex is required for the efficient incorporation of newly synthesized CENP-A into centromeres. Nat Cell Biol. 2006, 8: 446-457. 10.1038/ncb1396.View ArticlePubMedGoogle Scholar
- Sugata N, Li S, Earnshaw WC, Yen TJ, Yoda K, Masumoto H, Munekata E, Warburton PE, Todokoro K: Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere – kinetochore complexes. Hum Mol Genet. 2000, 9: 2919-2926. 10.1093/hmg/9.19.2919.View ArticlePubMedGoogle Scholar
- Westermann S, Cheeseman IM, Anderson S, Yates JR, Drubin DG, Barnes G: Architecture of the budding yeast kinetochore reveals a conserved molecular core. J Cell Biol. 2003, 163: 215-222. 10.1083/jcb.200305100.View ArticlePubMedPubMed CentralGoogle Scholar
- Tomonaga T, Matsushita K, Ishibashi M, Nezu M, Shimada H, Ochiai T, Yoda K, Nomura F: Centromere protein H is up-regulated in primary human colorectal cancer and its overexpression induces aneuploidy. Cancer Res. 2005, 65: 4683-4689. 10.1158/0008-5472.CAN-04-3613.View ArticlePubMedGoogle Scholar
- Shigeishi H, Higashikawa K, Ono S, Mizuta K, Ninomiya Y, Yoneda S, Taki M, Kamata N: Increased expression of CENP-H gene in human oral squamous cell carcinomas harboring high-proliferative activity. Oncol Rep. 2006, 16: 1071-1075.PubMedGoogle Scholar
- Liao WT, Song LB, Zhang HZ, Zhang X, Zhang L, Liu WL, Feng Y, Guo BH, Mai HQ, Cao SM, Li MZ, Qin HD, Zeng YX, Zeng MS: Centromere protein H is a novel prognostic marker for nasopharyngeal carcinoma progression and overall patient survival. Clin Cancer Res. 2007, 13: 508-514. 10.1158/1078-0432.CCR-06-1512.View ArticlePubMedGoogle Scholar
- Zhang H, Jin Y, Chen X, Jin C, Law S, Tsao S, Kwong Y: Cytogenetic aberrations in immortalization of esophageal epithelial cells. Cancer Genetics and Cy. 2003, 165: 25-35. 10.1016/j.cancergencyto.2005.07.016.View ArticleGoogle Scholar
- Seng TJ, Low JSW, Li H, Cui Y, Goh HK, Wong MLY, Srivastava G, Sidransky D, Califano J, Steenbergen RDM, Rha SY, Tan J, Hsieh W-S, Ambinder RF, Lin X, Chan ATC, Tao Q: The major 8p22 tumor suppressor DLC1 is frequently silenced by methylation in both endemic and sporadic nasopharyngeal, esophageal, and cervical carcinomas, and inhibits tumor cell colony formation. Oncogene. 2007, 26: 934-944. 10.1038/sj.onc.1209839.View ArticlePubMedGoogle Scholar
- Sobin LH, Fleming ID: TNM classification of malignant tumors, 5th edition. Cancer. 1997, 80: 1803-1804. 10.1002/(SICI)1097-0142(19971101)80:9<1803::AID-CNCR16>3.0.CO;2-9.View ArticlePubMedGoogle Scholar
- Ciocca DR, Clark GM, Tandon AK, Fuqua SA, Welch WJ, McGuire WL: Heat shock protein hsp70 in patients with axillary lymph node-negative breast cancer: prognostic implications. J Natl Cancer Inst. 1993, 85: 570-574. 10.1093/jnci/85.7.570.View ArticlePubMedGoogle Scholar
- Izuta H, Ikeno M, Suzuki N, Tomonaga T, Nozaki N, Obuse C, Kisu Y, Goshima N, Nomura F, Nomura N, Yoda K: Comprehensive analysis of the ICEN (Interphase Centromere Complex) components enriched in the CENP-A chromatin of human cells. Genes Cells. 2006, 11: 673-684. 10.1111/j.1365-2443.2006.00969.x.View ArticlePubMedGoogle Scholar
- Kwong D, Lam A, Guan X, Chujo M, Uchida Y, Mueller W, Gabbert HE: Chromosomal aberrations in esophageal squamous cell carcinoma among Chinese: gain of 12p predicts poor prognosis after surgery. Hum Patho. 2004, 35: 309-316. 10.1016/j.humpath.2003.10.020.View ArticleGoogle Scholar
- Noguchi T, Kimura Y, Takeno S, Chujo M, Uchida Y, Mueller W, Gabbert HE: Chromosomal imbalance in esophageal squamous cell carcinoma: 3q gain correlates with tumor progression but not prognostic significance. Oncol Rep. 2003, 10: 1393-1400.PubMedGoogle Scholar
- Tada K, Oka M, Tangoku A, Hayashi H, Oga A, Sasaki K: Gains of 8q23-qter and 20q and loss of 11q22-qter in esophageal squamous cell carcinoma associated with lymph node metastasis. Cancer. 2000, 88: 268-273. 10.1002/(SICI)1097-0142(20000115)88:2<268::AID-CNCR4>3.0.CO;2-B.View ArticlePubMedGoogle Scholar
- Yen CC, Chen YJ, Chen JT, Hsia JY, Chen PM, Liu JH, Fan FS, Chiou TJ, Wang WS, Lin CH: Comparative genomic hybridization of esophageal squamous cell carcinoma: correlations between chromosomal aberrations and disease progression/prognosis. Cancer. 2001, 92: 2769-2777. 10.1002/1097-0142(20011201)92:11<2769::AID-CNCR10118>3.0.CO;2-M.View ArticlePubMedGoogle Scholar
- Kops GJ, Weaver BA, Cleveland DW: On the road to cancer: aneuploidy and the mitotic checkpoint. Nat Rev Cancer. 2005, 5 (10): 773-785. 10.1038/nrc1714.View ArticlePubMedGoogle Scholar
- O'Brien SL, Fagan A, Fox EJ, Millikan RC, Culhane AC, Brennan DJ, McCann AH, Hegarty S, Moyna S, Duffy MJ, Higgins DG, Jirström K, Landberg G, Gallagher WM: CENP-F expression is associated with poor prognosis and chromosomal instability in patients with primary breast cancer. Int J Cancer. 2007, 120: 1434-1443. 10.1002/ijc.22413.View ArticlePubMedGoogle Scholar
- Adams RR, Eckley DM, Vagnarelli P, Wheatley SP, Gerloff DL, Mackay AM, Svingen PA, Kaufmann SH, Earnshaw WC: Human INCENP colocalizes with the Aurora-B/AIRK2 kinase on chromosomes and is overexpressed in tumour cells. Chromosoma. 2001, 110: 65-74. 10.1007/s004120100130.View ArticlePubMedGoogle Scholar
- Tomonaga T, Matsushita K, Yamaguchi S, Oohashi T, Shimada H, Ochiai T, Yoda K, Nomura F: Overexpression and mistargeting of centromere protein-A in human primary colorectal cancer. Cancer Res. 2003, 63: 3511-3516.PubMedGoogle Scholar
- Shigeishi H, Mizuta K, Higashikawa K, Yoneda S, Ono S, Kamata N: Correlation of CENP-F gene expression with tumor-proliferating activity in human salivary gland tumors. Oral Oncol. 2005, 41: 716-722. 10.1016/j.oraloncology.2005.03.008.View ArticlePubMedGoogle Scholar
- Erlanson M, Casiano CA, Tan EM, Lindh J, Roos G, Landberg G: Immunohistochemical analysis of the proliferation associated nuclear antigen CENP-F in non-Hodgkin's lymphoma. Mod Pathol. 1999, 12: 69-74.PubMedGoogle Scholar
- Clark GM, Allred DC, Hilsenbeck SG, Chamness GC, Osborne CK, Jones D, Lee WH: Mitosin (a new proliferation marker) correlates with clinical outcome in node-negative breast cancer. Cancer Res. 1997, 57: 5505-5508.PubMedGoogle Scholar
- de la Guardia C, Casiano CA, Trinidad-Pinedo J, Báez A: CENP-F gene amplification and overexpression in head and neck squamous cell carcinomas. Head Neck. 2001, 23: 104-112. 10.1002/1097-0347(200102)23:2<104::AID-HED1005>3.0.CO;2-0.View ArticlePubMedGoogle Scholar
- Varis A, Salmela AL, Kallio MJ: Cenp-F (mitosin) is more than a mitotic marker. Chromosoma. 2006, 115: 288-295. 10.1007/s00412-005-0046-0.View ArticlePubMedGoogle Scholar
- Fukagawa T, Mikami Y, Nishihashi A, Regnier V, Haraguchi T, Hiraoka Y, Sugata N, Todokoro K, Brown W, Ikemura T: CENP-H, a constitutive centromere component, is required for centromere targeting of CENP-C in vertebrate cells. EMBO J. 2001, 20: 4603-4617. 10.1093/emboj/20.16.4603.View ArticlePubMedPubMed CentralGoogle Scholar
- Alonso A, Fritz B, Hasson D, Abrusan G, Cheung F, Yoda K, Radlwimmer B, Ladurner AG, Warburton PE: Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres. Genome Biol. 2007, 8: R148-10.1186/gb-2007-8-7-r148.View ArticlePubMedPubMed CentralGoogle Scholar
- Orthaus S, Ohndorf S, Diekmann S: RNAi knockdown of human kinetochore protein CENP-H. Biochem Biophys Res Commun. 2006, 348: 36-46. 10.1016/j.bbrc.2006.06.187.View ArticlePubMedGoogle Scholar
- Mikami Y, Hori T, Kimura H, Fukagawa T: The functional region of CENP-H interacts with the Nuf2 complex that localizes to centromere during mitosis. Mol Cell Biol. 2005, 25: 1958-1970. 10.1128/MCB.25.5.1958-1970.2005.View ArticlePubMedPubMed CentralGoogle Scholar
- Mandard AM, Hainaut P, Hollstein M: Genetic steps in the development of squamous cell carcinoma of the esophagus. Mutat Res. 2000, 462: 335-342. 10.1016/S1383-5742(00)00019-3.View ArticlePubMedGoogle Scholar
- Shay JW, Wright WE: Senescence and immortalization: role of telomeres and telomerase. Carcinogenesis. 2005, 26: 867-874. 10.1093/carcin/bgh296.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/8/233/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.