- Research article
- Open Access
Elevated C1orf63 expression is correlated with CDK10 and predicts better outcome for advanced breast cancers: a retrospective study
BMC Cancer volume 15, Article number: 548 (2015)
Chromosome 1 open reading frame 63 (C1orf63) is located on the distal short arm of chromosome 1, whose allelic loss has been observed in several human cancers. C1orf63 has been reported to be up-regulated in IL-2-starved T lymphocytes, which suggests it might be involved in cell cycle control, a common mechanism for carcinogenesis. Here we investigated the expression and clinical implication of C1orf63 in breast cancer.
Paraffin-embedded specimens, clinicopathological features and follow-up data of the breast cancer patients were collected. Publicly available microarray and RNA-seq datasets used in this study were downloaded from ArrayExpress of EBI and GEO of NCBI. KM plotter tool was also adopted. The expression of C1orf63 and CDK10, one known cell cycle-dependent tumor suppressor in breast cancer, was assessed by immunohistochemistry. Western blotting was performed to detect C1orf63 protein in human breast cancer cell lines, purchased from the Culture Collection of the Chinese Academy of Sciences, Shanghai.
In a group of 12 human breast tumors and their matched adjacent non-cancerous tissues, C1orf63 expression was observed in 7 of the 12 breast tumors, but not in the 12 adjacent non-cancerous tissues (P < 0.001). Similar results were observed of C1orf63 mRNA expression both in breast cancer and several other cancers, including lung cancer, prostate cancer and hepatocellular carcinoma. In another group of 182 breast cancer patients, C1orf63 expression in tumors was not correlated with any clinicopathological features collected in this study. Survival analyses showed that there was no significant difference of overall survival (OS) rates between the C1orf63 (+) group and the C1orf63 (−) group (P = 0.145). However, the analyses of KM plotter displayed a valid relationship between C1orf63 and RFS (relapse free survival)/OS (P < 0.001; P = 0.007). Notablely, in breast cancers with advanced TNM stages (III ~ IV) among these 182 patients, C1orf63 expression was an independent prognostic factor predicting better clinical outcome (HR: 0.41; 95 % CI: 0.17 ~ 0.97; P = 0.042). Additionally, we found that CDK10 mRNA expression was positively correlated with C1orf63, which was consistent with the relationship of protein expression between C1orf63 and CDK10 (rs = 0.391; P < 0.001).
Compared to adjacent non-cancerous tissues, C1orf63 expression was elevated in tumor tissues. However, C1orf63 predicts better prognosis for breast cancers with advanced TNM stage, and the underlying mechanism is unknown. In addition, C1orf63 is correlated with the cell cycle related gene, CDK10.
The initiation and development of breast cancer is a multistep process encompassing progressive changes in genetic aberrations in normal tissue, resulting in hyperplasia with or without atypia, in situ carcinomas, invasive carcinomas, and finally metastatic carcinoma . Increasing evidence reveals that molecular subtyping of this malignancy is crucial to better understand the clinical behavior of these tumors and to identify the targets for better therapy [2, 3].
Chromosome 1 open reading frame 63 (C1orf63), also known as arginine/serine-rich protein 1 (RSRP1, NCBI Gene ID: 57035), is located at 1p36.13 - p35.1. Although the function of C1orf63 is still unclear, frequent allelic loss on the distal short arm of chromosome 1 has been reported in a broad range of solid human tumors, including breast, non-small cell lung and colorectal cancers . Especially, allelic loss at 1p31.1-36.3 was shown to be an early event in the carcinogenesis of breast cancer . The allelic loss at 1p34-36 was demonstrated to be an independent predictor of shorter disease-free survival for patients with node-negative breast cancer . Thus, these regions on 1p may harbor tumor suppressor genes . Furthermore, it was reported that the transcription of C1orf63 was upregulated in the interleukin (IL)-2-dependent human T cells, which were forced to exit cell cycle by IL-2 withdrawal, indicating that C1orf63 could be involved in cell cycle exit and acted as a cellular quiescence-controlling gene. Its expression might represent one early event for tumorigenesis . However, the involvement of C1or63 in the oncogenesis and progression of breast cancer has not been reported before.
In the current study, C1orf63 protein expression was detected in breast cancer tissues, and correlated to the clinicopathological features and prognosis of breast cancer. Then the relationship between C1orf63 and cyclin-dependent kinase 10 (CDK10), a known cell cycle-dependent tumor suppressor in breast cancer [9, 10] was investigated. Furthermore, the potential association between the expression of C1orf63 and known breast cancer biomarkers including estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER-2) were also examined.
Tumor samples and cell culture
Paraffin-embedded archival pathological specimens, complete clinicopathological features and follow-up data were retrieved for 182 breast cancer patients (women, median age: 51 years; range: 29–88 years). The patients had undergone curative surgery without preoperative therapy, at the Cancer Hospital of Shantou University Medical College, between October 2001 and November 2002. Clinical tumor stage (TNM stage) was grouped in accordance with the American Joint Committee on Cancer (AJCC) 6th Ed Cancer Staging Manual (2002). In this study, stages III and IV were designated as advanced stage, while stages I and II were early stage . The clinicopathologic features for these patients, including expression status of ER, PR and HER-2, were summarized in Table 1. The corresponding adjacent normal tissues of 12 patients were also obtained from surgical resections. The observation period ranged from 1 to 159 months (the median period was 42 months). Informed consent for the use of their samples was obtained from all the patients. This study was approved by the medical ethics committee of the Cancer Hospital of Shantou University Medical College.
Four breast cancer cell lines used in this study, namely MCF-7, MDA-MB-231, SK-BR-3 and BT549, were purchased from the Culture Collection of the Chinese Academy of Sciences, Shanghai, and maintained in DMEM (high glucose) containing 5 % fetal bovine serum.
Immunohistochemistry of breast tissues
Immunohistochemistry (IHC) for C1orf63 and CDK10 was carried out using a standard EnVision complex method . Briefly, sections (4-μm) were fixed in 10 % buffered formalin and embedded in paraffin. After deparaffinization and rehydration, endogenous peroxidase activity was blocked with 0.3 % hydrogen peroxide for 30 min. Then tissue sections were autoclaved at 121 °C in citrate buffer (pH 6.0) for 10 min, and incubated with rabbit anti-C1orf63 polyclonal antibody (1:100 dilution, Beijing Biosynthesis Biotechnology Co., Ltd., China) or CDK10 antibody (1:300 dilution, Abgent, San Diego, USA). IHC staining was carried out by an EnVision antibody complex (anti-mouse/rabbit) method using an Envision™ Detection kit (ZSGB-BIO, Beijing, China) and 3,3’-diaminobenzidine as the chromogen substrate. A negative control was obtained by replacing the primary antibody with normal rabbit IgG.
IHC staining for C1orf63 was scored, as described  by a combination of intensity (0, no staining; 1, weak staining; 2, moderate staining; 3, strong staining) and proportion (0, < 5 % of tumor cells stained; 1, 5 - 25 % positive cells; 2, 26-50 % positive cells; 3, 51 - 75 % positive cells; 4, more than 76 % positive cells). If the product of multiplication between staining intensity and the proportion of positive cells was > 4, expression was defined as positive. Two pathologists independently assessed the cellular location and intensity of immunostaining in each section.
Cells were lysed with a lysis buffer [50 mmol/L Tris–HCl (pH 8.0), 150 mmol/L NaCl, 1 % Triton X-100, and 100ug/ml PMSF] on ice for 30 min and centrifuged at 12000 rpm for 15 min at 4 °C. Cell lysates (20 ug) were electrophoresed on 10 % SDS-polyacrylamide gel and transferred onto a PVDF membrane. After blocking with Tris-buffered saline containing 0.05 % Tween 20 (TBST) and 5 % non-fat milk for 1 h at room temperature, the filters were washed 3 times/5 min with TBST and then incubated with antibodies against either anti rabbit C1orf63 (1:3000) or anti mouse actin (1:6000, Santa Cruz Biotechnology, Santa Cruz, USA) diluted in blocking buffer for 1 h, followed by incubation with horseradish peroxidase-labelled antirabbit (1:6000, Novus Biologicals, Littleton, USA) or antimouse (1:6000, Santa Cruz Biotechnology) IgG, and washed with TBST. The blots were visualized with chemiluminescence. Human β-actin was employed as an endogenous control.
Gene expression data
The microarray datasets employed in this study was publicly available from ArraryExpress (http://www.ebi.ac.uk/arrayexpress/) of EBI and GEO (http://www.ncbi.nlm.nih.gov/gds/) of NCBI, including 6 independent cohorts of breast cancer (accession numbers: GSE15852 , GSE42568 , GSE4922 , GSE5847 , GSE23988 , E-TABM-158 ), 2 of lung cancer (E-MEXP-231 , GSE19804 ), 2 of prostate cancer (GSE6956 , GSE6919 ) and 2 of hepatocellular carcinoma (GSE14323 , GSE6764 ). The CEL files containing the raw data from each experiment were directly downloaded from the websites with particular accession number. Since RNA-seq is another popular method for genome-wide transcriptome profiling , one normalized RNA-seq dataset (GSE60788) of breast cancer was downloaded from GEO. Details of these datasets were summarized in Table 2 and Table 3.
In this paper, KM Plotter (http://kmplot.com/analysis/), a tool for the meta-analysis based biomarker assessment , including gene expression and survival data of more than 4000 breast cancer patients, was used to perform Kaplan Meier survival analysis to further assess the relationship between C1orf63 mRNA expression and RFS (relapse free survival)/OS (overall survival). Breast cancer patients were split by the median expression of C1orf63 into two groups, namely patients with high or low expression of C1orf63.
Statistical analyses were performed using software SPSS (version 13.0) and R (version 3.0.2). The difference of C1orf63 protein expression between tumors and adjacent non-cancerous tissues were detected by Wilcoxon test, and the difference of online datasets retrieved C1orf63 mRNA expression between cases and controls of several cancer types included in this study were detected by Student t-test. Correlations between C1orf63 expression and clinicopathologic features were analyzed using chi-square test. Survival curves were calculated using the Kaplan–Meier method with log rank test. The Cox regression analysis was used to study the effects of C1orf63 expression on OS. OS (in months) was defined as the time from diagnosis to the date of last contact or of death from any cause. For gene expression microarray analyses, data were normalized using Robust Multi-array Analysis (RMA) with R-package “affy”. The normalized expression values (on a log-2 scale) of probes representing the same gene were averaged. Pearson’s correlation and Spearman’s rank correlation were applied for examining the relationship between C1orf63 and CDK10. P < 0.05 (two-tailed) was considered as statistically different.
C1orf63 expression in breast cancer tissues and cell lines
The tumor specimens and their matched adjacent non-cancerous tissues were collected from a group of 12 breast cancer patients to examine C1orf63 expression by IHC. As shown in Fig. 1A (i, ii, iii), C1orf63 protein was expressed primarily in the cytoplasm. We found 7 of the 12 primary tumors (58.3 %) expressed C1orf63 (Table 4), whereas 5 of the 12 tumors (41.7 %) had indistinctive expression of C1orf63. In contrast, all the adjacent normal tissues lacked elevated C1orf63 expression (Wilcoxon test: P < 0.001, Fig. 1A iv). Additionally, though analyzing the publicly available datasets, upregulation of C1orf63 mRNA expression was found in cases of breast cancer as well as other cancers, including lung cancer, prostate cancer and hepatocellular carcinoma (Table 3 and Fig. 1B), when compared to the relevant normal controls.
We also performed western blotting to detect whether C1orf63 was expressed in breast cancer cells. Four human breast cancer cell lines, including the ER+/PR+ cell line MCF-7, ER−/PR−/Her-2− cell lines BT549 and MDA-MB-231, and ER−/PR−/Her-2+ cell line SK-BR-3, were examined. As shown in Fig. 2, these cells have comparable levels of C1orf63 expression, regardless of receptor status.
Relationship of C1orf63 with clinicopathologic features in a cohort of 182 breast cancer patients
To evaluate the relationship of C1orf63 expression with clinicopathological features, tumor sections from 182 primary breast cancer patients were immunostained to detect the expression of C1orf63, and these patients were subsequently divided into two groups according to their IHC scores: 44 (24.2 %) tumors expressing C1orf63 [C1orf63 (+) group] and 138 (75.8 %) tumors lacking C1orf63 expression [C1orf63 (−) group]. As shown in Table 1, no significant correlations were found between the expression of C1orf63 and the clinicopathological features collected in this study, including age, depth of invasion, lymph node metastasis and TNM stage. C1orf63 IHC score were also not associated to the expression of known breast cancer biomarkers including ER, PR or HER-2.
Impact of C1orf63 expression on OS of breast cancer patients
To examine whether the expression status of C1orf63 has any prognostic value for breast cancer, univariate and multivariate analyses using the Kaplan-Meier method and Cox regression were carried out. As shown in Table 5, of the 182 patients breast cancer, the OS rate in the C1orf63 (+) group was higher than that in the C1orf63 (−) group (3-year OS rates: 83.3 % vs 76.9 %; 5-year OS rates: 73.5 % vs. 64.9 %), but no significant difference was seen between these two groups (Log Rank P = 0.145, Fig. 3a), consistent with the result of univariate Cox regression (Table 6 left). KM Plotter tool was used to further assess the relationship between the mRNA expression of C1orf63 and RFS/OS of breast cancer patients. As shown in Fig. 3c and Fig. 3d, high expression of C1orf63 predicted a longer RFS and OS in breast cancer patients (P = 0.007; P < 0.001). The discordance between these two analyses suggests that the sample size of current IHC study (182 patients) may not be powerful enough to predict the outcome of the whole cohort. Since breast cancer is a heterogeneous disease with defined subtypes, we correlated IHC score of C1orf63 to the OS in individual subgroups, namely luminal (Fig. 4A), HER-2 enriched (Fig. 4B), and triple negative breast cancer patients (Fig. 4C), and no significant correlation was found. For the 182 breast cancer patients, log rank test also demonstrated that, depth of invasion (P < 0.001), lymph node metastasis (P < 0.001), advanced TNM stage (P < 0.001) and negative PR (P = 0.036), positive HER-2 (P = 0.028) were poor prognostic factors for OS. Patients with elder age (P = 0.074) or negative ER status (P = 0.242) had a shorter overall survival, but didn’t reach statistical significance (Table 5), which was consistent with the result of univariate Cox regression (Table 6 left).
Next, multivariate analysis was performed to evaluate the implication of parameters including depth of invasion (T3 ~ T4), lymph node metastasis (N2 ~ N3), TNM stage (III ~ IV), PR negativity and HER-2 negativity on breast cancer prognosis (Table 6 right). We found that only TNM stage (HR: 5.75; 95 % CI: 2.76 ~ 12.00; P < 0.001) and PR (HR: 0.54; 95 % CI: 0.31 ~ 0.96; P =0.035) were independent prognostic indicators for breast cancer patients in our study.
Impact of C1orf63 expression on OS of breast cancer patients with TNM III ~ IV Stages
Given the result of multivariate analysis mentioned above (Table 6 right), patients were further divided according to either TNM stage or PR levels, in order to analyze the impact of Clorf63 expression on OS in patients with different TNM stages or PR status. As shown in Table 7, tumors from 27 of 107 patients (25.2 %) with TNM III ~ IV stages expressed C1orf63, whereas tumors from the remaining 80 patients (74.8 %) lacked C1orf63 expression. Kaplan-Meier analysis revealed that patients in TNM III ~ IV stages with C1orf63 (+) tended to have a better prognosis than those without C1orf63 expression (3-year OS: 80.0 % vs. 58.0 %; 5-year OS: 72.7 % vs. 46.2 %; P = 0.036, Fig. 3B). In contrast, C1orf63 could not predict OS in patients with TNM early stage (TNM I ~ II stages, P = 0.432), or patients with PR negativity (P = 0.906) or PR positivity (P = 0.106) expression.
The relationship of C1orf63 expression with clinicopathological factors in patients with TNM III ~ IV stages was further evaluated using Cox regression. As shown in Table 8 left, the univariate analysis revealed that the C1orf63 (+) group tended to have a better prognosis than the C1orf63 (−) group (HR = 0.41; 95 % CI: 0.18 ~ 0.98; P = 0.044). Positive PR was also shown as a good prognosis factor for patients in TNM III ~ IV stages (HR = 0.52; 95 % CI: 0.27 ~ 0.97; P = 0.039). However, no significant difference was observed regarding other clinicopathological features. To examine whether C1orf63 was an independent prognosis factor for patients with TNM III ~ IV stages, multivariate analysis was performed. It demonstrated that both C1orf63 expression (Table 8 right, HR: 0.41; 95 % CI: 0.17 ~ 0.97; P = 0.042) and PR (HR: 0.51; 95 % CI: 0.27 ~ 0.95; P = 0.035) were independent prognostic factors for patients in this subgroup.
Association between C1orf63 and CDK10 in breast cancers
CDK10 has been shown to play a role in cellular progression as well as a known prognostic factor predicting better outcome for breast cancers. Given the suggested role of C1orf63 on cell cycle exit , and its capability to predict better prognosis for breast cancers (Fig. 3B and Table 8), we thus examined the relationship between C1orf63 and CDK10. We firstly took advantage of four publicly available microarray datasets, each including a cohort of patients with breast cancer, to evaluate whether mRNA expression of C1orf63 could be related to that of CDK10. As shown in Fig. 5B, for mRNA expression, C1orf63 was positively correlated with CDK10, and the RNA-seq dataset also displayed a significant correlation between these two genes (r = 0.521, P < 0.001; Table 2). Further, CDK10 protein expression was examined by IHC. As shown in Fig. 5Ai, CDK10 primarily expressed in the nucleus and the relationship between the IHC scores of CDK 10 and C1orf63 was consistent with that of their mRNA expressions, which demonstrated that C1orf63 expression was positively correlated with CDK10 (rs = 0.391; P < 0.001).
Aberrations of chromosome 1 are one of the most frequently detected alterations in a variety of cancers [28–32]. There are numerous putative candidate oncogenes located on chromosome 1, e.g., NEGR1 (1p31.1), JTB (1q21), CKS1B (1q21.2), CHD1L (1q12), SHC1 (1q21) and KIF14 (1q32.1) [33–35]. Besides, 1p36 deletion has been reported to be associated with carcinogenesis, and contain genes such as CHD5 (1p36.31), CAMTA1 (1p36.31-p36.23), KIF1B (1p36.22), and CASZ1 (1p36.22). This specific location suggests C1orf63 might be related to initiation and development of cancer. However, the function of C1orf63 has been rarely described. It is demonstrated that C1orf63 protein is interacted with CLK3 (CDC-like kinase 3) and CLK2 (CDC-like kinase 2) protein , both of which are involved in protein phosphorylation and regulation of RNA splicing. It was stated that AKT activation controls cell survival to ionizing radiation by phosphorylating CLK2 . As a CLK2-interacting protein, C1orf63 might participate in these processes. Additionally, an association between a nonsynonymous SNP (rs1043879) in C1orf63 and ESR (erythrocyte sedimentation rate), which is a marker of several serious disease such as infection, autoimmune disorder, and malignancy , was revealed by a genome-wide association study with unclear biological significance. However, all the speculations about C1orf63 still need further study. Current study is the first to focus on the implication of C1orf63 in breast cancers.
The genes with abnormal expression hold important clinical implications as prognostic markers and/or targets for cancer therapy. According to our results, C1orf63 seems to have dual functions. The tumor-promoting function of C1orf63 in the initialization of breast cancer was suggested not only by the higher IHC score of C1orf63 in breast tumors when compared to adjacent non-cancerous tissues, also by the higher mRNA expression of C1orf63 in breast tumor vs. normal controls through analyzing several breast cancer gene expression datasets. More importantly, the tumor- promoting function of C1orf63 might not be limited to breast cancer, because gene expression dataset analysis showed that C1orf63 expression was also elevated in several other cancer types, including lung, prostate and hepatocellular carcinoma. Current study also indicated that the tumor-promoting function of C1orf63 might not involve ER, PR or HER-2, as no significant correlation was observed between the expression of C1orf63 and these biomarkers in either breast cancer tissues or cell lines. KM Plotter analysis of breast cancer patients showed that elevated mRNA expression of C1orf63 is significantly correlated with both longer RFS (P < 0.001) and betetr OS (P = 0.007), suggested a tumor suppression function of C1orf63. Most probably limited by the sample size of current IHC study, the C1orf63 IHC score failed to correlate with OS of all the breast cancer patients, but is capable of predicting a better prognosis for breast cancer patients in TNM III ~ IV stages, strongly indicating that C1orf63 could also act as a tumor suppressor, especially in the advanced stage of breast cancer. Until now, the relationship of C1orf63 with cancer remains largely unknown. Pils et al.  demonstrated that C1orf63 mRNA was differently expressed between epithelial ovarian cancer patients and controls, but the evidence is still limited. We provided the first evidence for the implication of C1orf63 in breast cancer tumorigenesis and progression, and demonstrated that the function of C1orf63 was complicated.
C1orf63 has been suggested to function in typical tumor initiation event as cell cycle exit and maintenance of quiescent state of cells . Many chemotherapeutical drugs such as Paclitaxel and 5-FU elicit their anti-tumor activities through forcing cancer cells staying quiescently [40, 41]. Whether C1orf63 could enhance the efficacy of therapeutical drugs via keeping cells in a quiescent state and thus predict a better outcome of cancer patients is unknown but a potential mechanism. Similar to C1orf63, the dual functions have been observed for many proteins, such as SRSF1 (serine/arginine-rich splicing factor 1). SRSF1 is a proto-oncogene that is overexpressed in many different cancers. However, increased SRSF1 expression in primary human fibroblasts could ultimately triggers oncogene-induced senescence via stabilizing p53 . Even so, the mechanism under the seemingly reversible action of C1orf63 still needs further study.
Recent studies have shown that CDK10 is a potential tumor suppressor in breast cancers, and CDK10/Ets2/c-RAF signaling has been demonstrated as an important determinant of breast cancer resistance to endocrine therapy . Since C1orf63 might be involved in cell cycle exit, we thus correlated the IHC score of CDK10 to that of C1orf63 in the same cohort, and detected that higher C1orf63 expression was positively associated with enhanced CDK10 expression, suggesting that C1orf63 probably function in a mechanism involving CDK10. Further research is needed to detect the underlying mechanism.
C1orf63 expression was supposed to be an early event of breast cancer oncogensis. It served as a favourable and independent prognostic marker for patients with breast cancer in TNM III ~ IV stages, suggesting C1orf63 might elicit two different functions involved in the oncogenesis and progression of breast cancer. Moreover, its positive correlation with CDK10 suggests that C1orf63 might be involved in cell cycle progression. Further work are warranted to better understand the potential function of C1orf63 in cancer pathogenesis.
Chromosome 1 open reading frame 63
Cyclin-dependent kinase 10
Human epidermal growth factor receptor 2
Relapse free survival
Russo J, Hu YF, Yang X, Russo IH. Developmental, cellular, and molecular basis of human breast cancer. J Natl Cancer Inst Monogr. 2000;27:17–37.
Perou CM, Sorlie T, Eisen MB, van de Rijn M, Jeffrey SS, Rees CA, et al. Molecular portraits of human breast tumours. Nature. 2000;406:747–52.
Peppercorn J, Perou CM, Carey LA. Molecular subtypes in breast cancer evaluation and management: divide and conquer. Cancer Invest. 2008;26:1–10.
Henrich KO, Schwab M, Westermann F. 1p36 tumor suppression--a matter of dosage? Cancer Res. 2012;72:6079–88.
Ragnarsson G, Eiriksdottir G, Johannsdottir JT, Jonasson JG, Egilsson V, Ingvarsson S. Loss of heterozygosity at chromosome 1p in different solid human tumours: association with survival. Br J Cancer. 1999;79:1468–74.
Utada Y, Emi M, Yoshimoto M, Kasumi F, Akiyama F, Sakamoto G, et al. Allelic loss at 1p34-36 predicts poor prognosis in node-negative breast cancer. Clin Cancer Res. 2000;6:3193–8.
Munn KE, Walker RA, Varley JM. Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast. Oncogene. 1995;10:1653–7.
Chechlinska M, Siwicki JK, Gos M, Oczko-Wojciechowska M, Jarzab M, Pfeifer A, et al. Molecular signature of cell cycle exit induced in human T lymphoblasts by IL-2 withdrawal. BMC Genomics. 2009;10:261.
Heller G, Ziegler B, Brandstetter A, Novak S, Rudas M, Hennig G, et al. CDK10 is not a target for aberrant DNA methylation in breast cancer. Anticancer Res. 2009;29:3939–44.
Yu JH, Zhong XY, Zhang WG, Wang ZD, Dong Q, Tai S, et al. CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells. Oncol Rep. 2012;27:1266–76.
Hwang SB, Bae JW, Lee HY, Kim HY. Circulating tumor cells detected by RT-PCR for CK-20 before surgery indicate worse prognostic impact in triple-negative and HER2 subtype breast cancer. J Breast Cancer. 2012;15:34–42.
Patel RM, Folpe AL. Immunohistochemistry for human telomerase reverse transcriptase catalytic subunit (hTERT): a study of 143 benign and malignant soft tissue and bone tumours. Pathology. 2009;41:527–32.
Han YP, Ma CK, Wang SQ, Enomoto A, Zhao Y, Takahashi M, et al. Evaluation of osteopontin as a potential biomarker for central nervous system embryonal tumors. J Neurooncol. 2014;119(2):343–51.
Pau Ni IB, Zakaria Z, Muhammad R, Abdullah N, Ibrahim N, Aina Emran N, et al. Gene expression patterns distinguish breast carcinomas from normal breast tissues: the Malaysian context. Pathol Res Pract. 2010;206:223–8.
Clarke C, Madden SF, Doolan P, Aherne ST, Joyce H, O’Driscoll L, et al. Correlating transcriptional networks to breast cancer survival: a large-scale coexpression analysis. Carcinogenesis. 2013;34:2300–8.
Ivshina AV, George J, Senko O, Mow B, Putti TC, Smeds J, et al. Genetic reclassification of histologic grade delineates new clinical subtypes of breast cancer. Cancer Res. 2006;66:10292–301.
Boersma BJ, Reimers M, Yi M, Ludwig JA, Luke BT, Stephens RM, et al. A stromal gene signature associated with inflammatory breast cancer. Int J Cancer. 2008;122:1324–32.
Iwamoto T, Bianchini G, Booser D, Qi Y, Coutant C, Shiang CY, et al. Gene pathways associated with prognosis and chemotherapy sensitivity in molecular subtypes of breast cancer. J Natl Cancer Inst. 2011;103:264–72.
Chin K, DeVries S, Fridlyand J, Spellman PT, Roydasgupta R, Kuo WL, et al. Genomic and transcriptional aberrations linked to breast cancer pathophysiologies. Cancer Cell. 2006;10:529–41.
Yap YL, Lam DC, Luc G, Zhang XW, Hernandez D, Gras R, et al. Conserved transcription factor binding sites of cancer markers derived from primary lung adenocarcinoma microarrays. Nucleic Acids Res. 2005;33:409–21.
Lu TP, Tsai MH, Lee JM, Hsu CP, Chen PC, Lin CW, et al. Identification of a novel biomarker, SEMA5A, for non-small cell lung carcinoma in nonsmoking women. Cancer Epidemiol Biomarkers Prev. 2010;19:2590–7.
Wallace TA, Prueitt RL, Yi M, Howe TM, Gillespie JW, Yfantis HG, et al. Tumor immunobiological differences in prostate cancer between African-American and European-American men. Cancer Res. 2008;68:927–36.
Yu YP, Landsittel D, Jing L, Nelson J, Ren B, Liu L, et al. Gene expression alterations in prostate cancer predicting tumor aggression and preceding development of malignancy. J Clin Oncol. 2004;22:2790–9.
Mas VR, Maluf DG, Archer KJ, Yanek K, Kong X, Kulik L, et al. Genes involved in viral carcinogenesis and tumor initiation in hepatitis C virus-induced hepatocellular carcinoma. Mol Med. 2009;15:85–94.
Wurmbach E, Chen YB, Khitrov G, Zhang W, Roayaie S, Schwartz M, et al. Genome-wide molecular profiles of HCV-induced dysplasia and hepatocellular carcinoma. Hepatology. 2007;45:938–47.
Sirbu A, Kerr G, Crane M, Ruskin HJ. RNA-Seq vs dual- and single-channel microarray data: sensitivity analysis for differential expression and clustering. PLoS One. 2012;7:e50986.
Gyorffy B, Surowiak P, Budczies J, Lanczky A. Online survival analysis software to assess the prognostic value of biomarkers using transcriptomic data in non-small-cell lung cancer. PLoS One. 2013;8:e82241.
Rao PH, Roberts D, Zhao YJ, Bell D, Harris CP, Weber RS, et al. Deletion of 1p32-p36 is the most frequent genetic change and poor prognostic marker in adenoid cystic carcinoma of the salivary glands. Clin Cancer Res. 2008;14:5181–7.
Puerto S, Marcos R, Ramirez MJ, Galofre P, Creus A, Surralles J. Equal induction and persistence of chromosome aberrations involving chromosomes 1, 4 and 10 in thyroid cancer patients treated with radioactive iodine. Mutat Res. 2000;469:147–58.
Egeli U, Ozkan L, Tunca B, Kahraman S, Cecener G, Ergul E, et al. The relationship between genetic susceptibility to head and neck cancer with the expression of common fragile sites. Head Neck. 2000;22:591–8.
Smedley D, Sidhar S, Birdsall S, Bennett D, Herlyn M, Cooper C, et al. Characterization of chromosome 1 abnormalities in malignant melanomas. Genes Chromosomes Cancer. 2000;28:121–5.
Okawa ER, Gotoh T, Manne J, Igarashi J, Fujita T, Silverman KA, et al. Expression and sequence analysis of candidates for the 1p36.31 tumor suppressor gene deleted in neuroblastomas. Oncogene. 2008;27:803–10.
Takita J, Chen Y, Okubo J, Sanada M, Adachi M, Ohki K, et al. Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma. Cancer Sci. 2011;102:1645–50.
Chen L, Chan TH, Guan XY. Chromosome 1q21 amplification and oncogenes in hepatocellular carcinoma. Acta Pharmacol Sin. 2010;31:1165–71.
Corson TW, Huang A, Tsao MS, Gallie BL. KIF14 is a candidate oncogene in the 1q minimal region of genomic gain in multiple cancers. Oncogene. 2005;24:4741–53.
Rolland T, Tasan M, Charloteaux B, Pevzner SJ, Zhong Q, Sahni N, et al. A proteome-scale map of the human interactome network. Cell. 2014;159:1212–26.
Nam SY, Seo HH, Park HS, An S, Kim JY, Yang KH, et al. Phosphorylation of CLK2 at serine 34 and threonine 127 by AKT controls cell survival after ionizing radiation. J Biol Chem. 2010;285:31157–63.
Kullo IJ, Ding K, Shameer K, McCarty CA, Jarvik GP, Denny JC, et al. Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. Am J Hum Genet. 2011;89:131–8.
Pils D, Tong D, Hager G, Obermayr E, Aust S, Heinze G, et al. A combined blood based gene expression and plasma protein abundance signature for diagnosis of epithelial ovarian cancer--a study of the OVCAD consortium. BMC Cancer. 2013;13:178.
Meng X, Zhang Q, Zheng G, Pang R, Hua T, Yang S, et al. Doxorubicin combined with celecoxib inhibits tumor growth of medullary thyroid carcinoma in xenografted mice. Oncol Lett. 2014;7:2053–8.
Deng L, Ren Z, Jia Q, Wu W, Shen H, Wang Y. Schedule-dependent antitumor effects of 5-fluorouracil combined with sorafenib in hepatocellular carcinoma. BMC Cancer. 2013;13:363.
Fregoso OI, Das S, Akerman M, Krainer AR. Splicing-factor oncoprotein SRSF1 stabilizes p53 via RPL5 and induces cellular senescence. Mol Cell. 2013;50:56–66.
Iorns E, Turner NC, Elliott R, Syed N, Garrone O, Gasco M, et al. Identification of CDK10 as an important determinant of resistance to endocrine therapy for breast cancer. Cancer Cell. 2008;13:91–104.
This research was supported by the grants of (1) the National Natural Science Fundation of China (No. 81272931); (2) Guangdong Provincial Sci-Tech Program (No. 2010B031600133, No. 2011B031800323); (3) the State Key Developmental Program for Basic Science and Technology (973 Program, No. 2011CB707705) to YKC. CQH was supported by (4) the Seed Grant of Guangdong Provincial Key Laboratory for Breast Cancer Diagnosis and Treatment; (5) the Natural Science Foundation of Guangdong (No. S2013010015969); (6) the Youth Research Grant from Shantou University Medical College Cancer Hospital (No. 2014/10), and (7) the Key Medical Project of Science and Technology Planning of Shantou (No. 2012/113). WLQ was supported by (8) Guangdong Provincial Sci-Tech Program (20120314); XJC and AEG were supported by (9) National Institutes of Health (CA151610); (10) the Avon Foundation (02-2014-063); (11) David Salomon Translational Breast Cancer Research Fund, and (12) the Fashion Footwear Charitable Foundation of New York, Inc. and (13) the Margie and Robert E. Petersen Foundation.
The authors declare that they have no competing interests.
CQH collected the clinical data. CQH and YJY designed and performed the experiments. FZ performed the statistical analysis. FZ and YJY drafted the manuscript. WLQ, AEG, XJC and GJZ helped to draft and revise the manuscript. YKC conceived of the study, participated in revise the manuscript and supervised the work. All authors read and approved the final manuscript.
Chao-Qun Hong and Fan Zhang contributed equally to this work.
About this article
Cite this article
Hong, CQ., Zhang, F., You, YJ. et al. Elevated C1orf63 expression is correlated with CDK10 and predicts better outcome for advanced breast cancers: a retrospective study. BMC Cancer 15, 548 (2015). https://doi.org/10.1186/s12885-015-1569-2
- Overall survival
- TNM stage