- Research article
- Open Access
- Open Peer Review
Cancerous inhibitor of protein phosphatase 2A (CIP2A) is an independent prognostic marker in wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy
BMC Cancervolume 15, Article number: 301 (2015)
The impact of KRAS signaling on cancerous inhibitor of protein phosphatase 2A (CIP2A) expression has not yet been explored. We investigated the impact of KRAS on CIP2A expression in colorectal cancer patients after colorectal liver metastasectomy.
We examined CIP2A expression by immunohistochemistry (IHC) and used direct sequencing to identify the mutational status of KRAS exon 2 (codon 12 and 13). The association between CIP2A expression, KRAS genotype, clinicopathological parameters and survival were examined by the Kaplan–Meier method and the Cox proportional hazards model. A combination of immunoblotting and proliferation assays were employed to elucidate the role of CIP2A in signal transduction pathways in wild-type KRAS Caco-2 cells.
A total of 220 colorectal cancer patients who had undergone colorectal liver metastasectomy were included in the study. The mutant KRAS genotype was associated with CIP2A overexpression. CIP2A expression was an independent prognostic marker in patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy (relative risk = 1.873, P = 0.019). Targeted silencing of CIP2A in Caco-2 cells (wild-type KRAS) led to decreased expression of pERK/ERK and decreased cell proliferation. Overexpression of mutant KRAS G12D in Caco-2 cells led to an increase in CIP2A expression and cell proliferation. In Caco-2 cells with the KRAS G12D, KRAS overexpression preserved the regulation effect of CIP2A in KRAS and abrogated the impact of CIP2A regulation on pERK/ERK and cell proliferation. CIP2A inhibition also increased the efficacy of cetuximab in Caco-2 cells.
CIP2A is an independent prognostic marker in patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy.
Approximately one-third of patients with colorectal cancer develop metastatic disease, with metastases commonly occurring in the liver [1,2]. The standard treatment for patients with colorectal liver metastasis is colorectal liver metastasectomy ; however, the rate of recurrence is high (~70%) for first-time colorectal liver metastasectomy patients [3-5]. Thus, the identification of novel oncogenes or targets as biomarkers for colorectal liver cancer recurrence is necessary.
Cancerous inhibitor of protein phosphatase 2A (CIP2A) is a recently identified oncoprotein that is overexpressed in several malignancies, including leukemia, breast, gastric, prostate, lung, ovarian, head and neck carcinoma, and colorectal cancer [6-21]. CIP2A plays an important role in cell proliferation, transformation, drug resistance and maintenance of a malignant cellular phenotype . Notably, CIP2A is associated with the epidermal growth factor receptor (EGFR) signaling pathway (Figure 1). CIP2A expression is positively correlated with EGFR expression and amplification in serous ovarian cancer . Furthermore, in hepatoma cells, CIP2A expression is also associated with resistance to the anti-EGFR bio-agent, erlotinib (Tarceva), in vitro . It is well documented that EGFR signaling is the most important pathway in treating metastatic colorectal cancer [25,26]. Therefore, the interplay between EGFR signaling and CIP2A in metastatic colorectal cancer warrants further investigation.
V-Ki-Ras2 Kirsten Rat Sarcoma Viral Oncogene (KRAS) is the most important downstream effector in the EGFR pathway. Approximately 40% of patients with metastatic colorectal cancer carry KRAS mutations affecting codons 12 and 13 in exon 2 . Indeed, mutation of KRAS is a predictive marker of cetuximab efficacy in metastatic colorectal cancer patients [26,27]. However, to date, the prognostic value of KRAS mutations in metastatic colorectal cancer remains inconclusive [5,28-33]. Our previous study in colorectal cancer cell lines revealed that the KRAS G12D mutation decreased the impact of CIP2A on downstream effectors of the EGFR signaling pathway, when cells were treated with temsirolimus . To the best of our knowledge, the interaction between KRAS mutant status and CIP2A has not been previously explored following colorectal liver metastasectomy.
In this study, we therefore investigated the association of CIP2A expression and KRAS genotype in the context of colorectal liver metastasectomy. We found that CIP2A only acts as an independent prognostic marker in patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy.
Patients and tissue blocks
A total of 220 patients undergoing colorectal liver metastasectomy at Taipei Veterans General Hospital in Taiwan, were enrolled in our study between January 2000 and January 2010. Disease stage was assessed based on the American Joint Committee on Cancer staging system, 6th edition. Clinicopathological staging and clinical course were determined by searching a computer database containing detailed information. The medical residual samples of patients came from residual sample bank of Taipei Veterans General Hospital and this study was approved by the Institutional Review Board of Taipei Veterans General Hospital (VGHIRB No 2012-03-027BC). Thus, The VGHIRB waive the requirement of inform consent form. The decision to perform hepatic resection was made by a multidisciplinary specialist committee. After hepatic resection, decisions regarding adjuvant chemotherapy were made on an individual patient basis at the discretion of the attending physicians. Patients were followed until the end of assessment (March 2012) or death, whichever occurred earlier. Patient follow-ups occurred at least every 3 months from the time of hepatic resection for the first 2 years, then every 6 months for the next 5 years, and subsequently annually until the patient’s death. Overall survival (OS) was defined as the period from liver surgery to death due to cancer.
CIP2A expression was assessed by IHC using monoclonal antibodies to CIP2A (NB100-74663, 1:1200; Novus Biologicals, Littleton, CO, USA). IHC staining was performed as previously described . Negative (no primary antibody) and positive tissue controls (colon carcinoma) were stained in parallel with each set of tumor specimens studied.
IHC staining was evaluated by two pathologists who were unaware of the patients’ clinical information. The intensity of stained cells was scored as 0, 1, 2 or 3. Percentages of stained cells were counted, and a final immunohistochemical score (H-score) was calculated by summing the products of the staining intensities (0–3) and distributions (0–100%). H-scores ranged from 0–300. For CIP2A staining, an H-score of ≥ 150 points was defined as strongly positive, whereas an H-score of < 150 points was defined as weakly positive.
DNA extraction and KRAS mutation analyses
Tumor regions were macrodissected and examined to confirm that at least 80% of the cells in the tissue were cancer cells. DNA extraction was performed using a Nucleon HT DNA extraction kit (Piscataway, NJ, USA), according to the manufacturer’s instructions. Exon 2 of KRAS was separately amplified as previously described . Purified PCR products were sequenced using the BigDyeR Terminator v3.1 cycle sequencing kit (Applied Biosystems, Foster City, CA, USA) and analyzed using a 3730 ABI capillary electrophoresis system (Applied Biosystems).
Cell culture and transfection
The Caco-2 human colon cancer cell line, harboring wild-type KRAS (American Type Culture Collection; ATCC) was maintained in Dulbecco’s Modified Eagle Medium (Gibco, Grand Island, USA). Cells were maintained at 37°C in a humidified atmosphere of air and 5% CO2. Transfections were performed using Lipofectamine 2000 in accordance with the manufacturer’s protocol (Invitrogen, Massachusetts, USA). The KRAS wild type genotype in Caco-2 cells was confirmed by analysis of KRAS codon 12 and 13 mutations.
Cell viability assay
Caco-2 cells were seeded in 96-well plates (10,000 cells/well) and after incubation for 12 h, cells were treated with cetuximab (Merck, Taiwan). Cell viability was then assessed using the TACS MTT cell proliferation assay kit (TREVIGEN, Gaithersburg, MD, USA), according to the manufacturer’s instructions. The dose–response or time-response curves were analyzed using GraphPad Software (Institute for Scientific Information, Philadelphia, PA, USA).
Immunoblot analysis was performed as previously described . The following proteins were evaluated by immunoblot: CIP2A (1:500; Novus Biologicals, CO, USA), pERK (1:1000; Cell Signaling Technology, Boston, MA, USA), ERK (1:5000; Zymed, Grand Island, NY, USA) and β-actin (1:500; Santa Cruz Biotechnology, Santa Cruz, CA, USA). β-actin was used as a loading control. Immunoblot quantification was performed using Image J software (http://rsb.info.nih.gov/ij/index.html).
Knockdown of CIP2A and KRAS in colon cancer cells
The siRNA construct targeting CIP2A (pLKO.1-shCIP2A, TRCN0000135532, target sequence: (5′-CCACAGTTTAAGTGGTGGAAA-3′) and non-targeting siRNA control (pLKO.1-shLuc) were obtained from the National RNAi Core Facility, Taiwan (http://rnai.genmed.sinica.edu.tw/index). Lentivirus production and infection were performed as previously described . The KRAS G12D mutant construct (pCMV6-Entry-KRAS G12D, RC400104) and control vector (pCMV6-AC-GFP, PS100010) were purchased from Origene (Rockville, Maryland, USA).
Statistical and survival analyses
The correlations between clinicopathological variables and genomic alterations were analyzed by χ2 test or Fisher’s exact test. Survival was estimated using the Kaplan–Meier method, and the log-rank test was used for comparison of survival curves as well as for univariate analysis. The Cox proportional hazards model was applied for multivariate analyses. Variables with P-values ≤ 0.010 in the log-rank test were entered in multivariate analyses. The t-test was used to compare data from the proliferation studies. A two-sided P-value of < 0.05 was considered statistically significant. SPSS software (version 16.00, SPSS, Chicago, IL, USA) was used for all statistical analyses.
Patient characteristics and association of clinical parameters with CIP2A expression
A total of 220 patients who had undergone colorectal liver metastasectomy were enrolled in our study (Table 1). The median age at diagnosis was 62.0 years (range: 30–87 years). The median OS after colorectal liver metastasectomy was 51.0 months, and the 5-year survival rate was 52.7%. To investigate the association between CIP2A expression and patient clinical parameters, CIP2A expression was examined in colorectal liver metastases sections by IHC staining (representative images are shown in Figure 2a and b). Ninety-one patients (41.4%) exhibited strong CIP2A expression. CIP2A expression was not significantly correlated with sex, age, initial stage at diagnosis, location of primary tumor, pathology, grade, margin, distribution of liver metastasis, number of liver metastases, size of liver metastasis or extrahepatic metastasis. However, CIP2A overexpression was associated with KRAS mutation status (P < 0.001). Among patients with KRAS codon 12 mutations, 57.6% exhibited strong CIP2A expression. Among patients with KRAS codon 13 mutations, 54.5% exhibited strong CIP2A expression. Only 30.5% of patients with the wild-type KRAS genotype exhibited strong CIP2A expression.
The intensity of CIP2A staining in paired colon cancer and colorectal liver metastasis samples was also compared in 24 patients (representative images are shown in Figure 2c and d). CIP2A expression was similar between paired colon cancer and colorectal liver metastasis samples, with no significant difference in H-score between primary and metastatic tumors (Figure 2e).
Prognostic factors for OS according to univariate and multivariate analyses in patients after colorectal liver metastasectomy
To clarify the role of CIP2A in patients following colorectal liver metastasectomy, the Cox proportional hazards model was applied (Table 2). In the univariate model, initial stage at diagnosis, number of colorectal liver metastases, margin and CIP2A expression (hazard ratio [HR] = 1.447, P = 0.049) were prognostic factors. However, in the multivariate model, CIP2A expression was not an independent prognostic factor after controlling for other risk factors (HR = 1.373, P = 0.096).
Impact of CIP2A levels on OS in patients after colorectal liver metastasectomy according to KRAS genotype
OS after colorectal liver metastasectomy was significantly worse in patients with strong CIP2A expression compared with those with weak CIP2A expression, in patients with wild-type KRAS (Figure 3a, P = 0.035). In contrast, we observed no difference in OS between strong and weak CIP2A expression in patients with mutant KRAS (Figure 3b, P = 0.759).
Prognostic factors for OS according to univariate and multivariate analyses in patients with wild-type KRAS after colorectal liver metastasectomy
To clarify the role of CIP2A in patients exhibiting the wild-type KRAS genotype, the Cox proportional hazards model was applied (Table 3). In the univariate model, the number of colorectal liver metastases, grade, margin and CIP2A expression were prognostic factors, whereas age, initial stage at diagnosis, distribution, size of colorectal metastases and extrahepatic metastasis were not. Significant factors in the univariate model were subsequently used in the multivariate model. After controlling for other risk factors, CIP2A expression was still an independent prognostic factor in patients with wild-type KRAS genotype (HR = 2.109, P = 0.006).
Association of CIP2A expression, KRAS genotype, cetuximab and proliferation in wild-type KRAS Caco-2 colon cancer cells
To explain our clinical findings, we conducted additional studies in Caco-2 colon cancer cells, which express wild-type KRAS. Targeted silencing of CIP2A using shCIP2A led to decreased expression of CIP2A, KRAS, and pERK (Figure 4a), and a concomitant decrease in cell proliferation (Figure 4b, P = 0.013). Overexpression of mutant KRAS (pCMV6-KRAS G12D, Figure 4a) led to increased expression of KRAS, CIP2A, and pERK, and increased cell proliferation (Figure 4b, P = 0.043). While targeted silencing of CIP2A also led to decreased CIP2A expression in cells transfected with pCMV6-KRAS G12D (Figure 4a), we did not observe a decrease in the expression of pERK/ERK or a significant decrease in proliferation. Last, the efficacy of cetuximab in Caco-2 cells increased after CIP2A knockdown compared with control (Figure 5).
To the best of our knowledge, this is the first study to report an association between CIP2A expression and KRAS genotype in patients with metastatic colorectal cancer after colorectal liver metastasectomy. After adjusting for other confounding factors, we found that CIP2A acts as an independent prognostic marker in patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy.
Overexpression of CIP2A is associated with tumor aggressiveness, lymph node and lymphovascular involvement, and advanced stage colon cancer, which may partially explain why CIP2A functions as a prognostic marker in patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy [10,36]. CIP2A overexpression is also associated with colon cancer cell proliferation, tumorigenesis in vitro, and resistance to cetuximab, 5-fluorouracil, oxaliplatin and SN38 (an active metabolite of irinotecan) [10,34]. Cetuximab, 5-fluorouracil, oxaliplatin and irinotecan are commonly used for post-operative chemotherapy after colorectal liver metastasectomy or for salvage chemotherapy in the treatment of metastatic colorectal cancer .
In our analysis, the value of CIP2A as a prognostic marker was limited to patients with wild-type KRAS metastatic colorectal cancer after colorectal liver metastasectomy. This observation may be explained by multiple previous reports. First, Zhao et al. investigated Helicobacter pylori infection-induced CIP2A expression, and determined that it was dependent on RAS/mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) pathways, indicating that EGFR pathway activation increased CIP2A expression . Khanna et al.  further concluded that CIP2A overexpression was dependent on the EGFR-ERK-ETS1 signaling pathway. Both studies illustrate that the EGFR pathway interacts with CIP2A in vitro and that the interaction is bi-directional. Furthermore, studies by Bockelman et al. demonstrated that EGFR protein expression and amplification were associated with CIP2A overexpression in vivo . Similarly, we observed that a mutant KRAS genotype was associated with CIP2A overexpression. Finally, in colorectal cancer, the EGFR/RAS pathway is an important signaling pathway. KRAS is well established as an important downstream effector of the EGFR signaling pathway, and mutational activation of KRAS by further active downstream effectors like ERK induces drug resistance to EGFR antagonists (for example, cetuximab) . The results of our cellular experiments support this finding. Indeed, we observed that targeted silencing of CIP2A in Caco-2 cells expressing mutant KRAS G12D led to decreased expression of CIP2A expression but not pERK/ERK. Overexpression of mutant KRAS G12D impaired the suppression of pERK/ERK and effects on cell proliferation mediated by CIP2A silencing. Based on the above results, CIP2A acts as a prognostic marker in patients with wild-type KRAS metastatic colorectal cancer following colorectal liver metastasectomy, because the mutational activation of KRAS weakens CIP2A regulation on cell survival.
One constraint of our study is that a limited number of patients received cetuximab (EGFR antagonist) as a bio-chemotherapy throughout the entire course of treatment. Thus, we could not demonstrate that CIP2A expression is a predictive marker of response to cetuximab in metastatic colorectal cancer patients with wild-type KRAS. Further studies are therefore required to investigate this relationship.
Mutant KRAS is associated with CIP2A overexpression. CIP2A is an independent prognostic marker in patients with metastatic colorectal cancer exhibiting wild-type KRAS after colorectal liver metastasectomy.
Cancerous inhibitor of protein phosphatase 2A
Epidermal growth factor receptor
v-ets avian erythroblastosis virus E26 oncogene homolog 1
v-Ki-Ras2 Kirsten Rat Sarcoma Viral Oncogene
Mitogen-activated protein kinase
Extracellular signal-regulated kinase
Khatri VP, Petrelli NJ, Belghiti J. Extending the frontiers of surgical therapy for hepatic colorectal metastases: is there a limit? J Clin Oncol. 2005;23:8490–9.
Primrose JN. Surgery for colorectal liver metastases. Br J Cancer. 2010;102:1313–8.
Poston GJ, Adam R, Alberts S, Curley S, Figueras J, Haller D, et al. OncoSurge: a strategy for improving resectability with curative intent in metastatic colorectal cancer. J Clin Oncol. 2005;23:7125–34.
Cummings LC, Payes JD, Cooper GS. Survival after hepatic resection in metastatic colorectal cancer: a population-based study. Cancer. 2007;109:718–26.
Teng HW, Huang YC, Lin JK, Chen WS, Lin TC, Jiang JK, et al. BRAF mutation is a prognostic biomarker for colorectal liver metastasectomy. J Surg Oncol. 2012;106:123–9.
Katz J, Jakymiw A, Ducksworth MK, Stewart CM, Bhattacharyya I, Cha S, et al. CIP2A expression and localization in oral carcinoma and dysplasia. Cancer Biol Ther. 2010;10:694–9.
Huang LP, Adelson ME, Mordechai E, Trama JP. CIP2A expression is elevated in cervical cancer. Cancer Biomark. 2010;8:309–17.
Vaarala MH, Vaisanen MR, Ristimaki A. CIP2A expression is increased in prostate cancer. J Exp Clin Cancer Res. 2010;29:136.
Kerosuo L, Fox H, Perala N, Ahlqvist K, Suomalainen A, Westermarck J, et al. CIP2A increases self-renewal and is linked to Myc in neural progenitor cells. Differentiation. 2010;80:68–77.
Teng HW, Yang SH, Lin JK, Chen WS, Lin TC, Jiang JK, et al. CIP2A is a predictor of poor prognosis in colon cancer. J Gastrointest Surg. 2012;16:1037–47.
Xue Y, Wu G, Wang X, Zou X, Zhang G, Xiao R, et al. CIP2A is a predictor of survival and a novel therapeutic target in bladder urothelial cell carcinoma. Med Oncol. 2013;30:406.
Tseng LM, Liu CY, Chang KC, Chu PY, Shiau CW, Chen KF. CIP2A is a target of bortezomib in human triple negative breast cancer cells. Breast Cancer Res. 2012;14:R68.
Come C, Laine A, Chanrion M, Edgren H, Mattila E, Liu X, et al. CIP2A is associated with human breast cancer aggressivity. Clin Cancer Res. 2009;15:5092–100.
He H, Wu G, Li W, Cao Y, Liu Y. CIP2A is highly expressed in hepatocellular carcinoma and predicts poor prognosis. Diagn Mol Pathol. 2012;21:143–9.
Wang J, Li W, Li L, Yu X, Jia J, Chen C. CIP2A is over-expressed in acute myeloid leukaemia and associated with HL60 cells proliferation and differentiation. Int J Lab Hematol. 2011;33:290–8.
Qu W, Li W, Wei L, Xing L, Wang X, Yu J. CIP2A is overexpressed in esophageal squamous cell carcinoma. Med Oncol. 2012;29:113–8.
Li W, Ge Z, Liu C, Liu Z, Bjorkholm M, Jia J, et al. CIP2A is overexpressed in gastric cancer and its depletion leads to impaired clonogenicity, senescence, or differentiation of tumor cells. Clin Cancer Res. 2008;14:3722–8.
Fang Y, Li Z, Wang X, Zhang S. CIP2A is overexpressed in human ovarian cancer and regulates cell proliferation and apoptosis. Tumour Biol. 2012;33:2299–306.
Dong QZ, Wang Y, Dong XJ, Li ZX, Tang ZP, Cui QZ, et al. CIP2A is Overexpressed in Non-Small Cell Lung Cancer and Correlates with Poor Prognosis. Ann Surg Oncol. 2010;18:857–65.
Lin YC, Chen KC, Chen CC, Cheng AL, Chen KF. CIP2A-mediated Akt activation plays a role in bortezomib-induced apoptosis in head and neck squamous cell carcinoma cells. Oral Oncol. 2012;48:585–93.
Yu G, Liu G, Dong J, Jin Y. Clinical implications of CIP2A protein expression in breast cancer. Med Oncol. 2013;30:524.
Junttila MR, Puustinen P, Niemela M, Ahola R, Arnold H, Bottzauw T, et al. CIP2A inhibits PP2A in human malignancies. Cell. 2007;130:51–62.
Bockelman C, Lassus H, Hemmes A, Leminen A, Westermarck J, Haglund C, et al. Prognostic role of CIP2A expression in serous ovarian cancer. Br J Cancer. 2011;105:989–95.
Chen KF, Pao KC, Su JC, Chou YC, Liu CY, Chen HJ, et al. Development of erlotinib derivatives as CIP2A-ablating agents independent of EGFR activity. Bioorg Med Chem. 2012;20:6144–53.
Park JH, Han SW, Oh DY, Im SA, Jeong SY, Park KJ, et al. Analysis of KRAS, BRAF, PTEN, IGF1R, EGFR intron 1 CA status in both primary tumors and paired metastases in determining benefit from cetuximab therapy in colon cancer. Cancer Chemother Pharmacol. 2011;68:1045–55.
Van Cutsem E, Kohne CH, Hitre E, Zaluski J, Chang Chien CR, Makhson A, et al. Cetuximab and chemotherapy as initial treatment for metastatic colorectal cancer. N Engl J Med. 2009;360:1408–17.
Bokemeyer C, Bondarenko I, Hartmann JT, de Braud F, Schuch G, Zubel A, et al. Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study. Ann Oncol. 2011;22:1535–46.
Andreyev HJ, Norman AR, Cunningham D, Oates JR, Clarke PA. Kirsten ras mutations in patients with colorectal cancer: the multicenter “RASCAL” study. J Natl Cancer Inst. 1998;90:675–84.
French AJ, Sargent DJ, Burgart LJ, Foster NR, Kabat BF, Goldberg R, et al. Prognostic significance of defective mismatch repair and BRAF V600E in patients with colon cancer. Clin Cancer Res. 2008;14:3408–15.
Kakar S, Deng G, Sahai V, Matsuzaki K, Tanaka H, Miura S, et al. Clinicopathologic characteristics, CpG island methylator phenotype, and BRAF mutations in microsatellite-stable colorectal cancers without chromosomal instability. Arch Pathol Lab Med. 2008;132:958–64.
Ogino S, Nosho K, Kirkner GJ, Kawasaki T, Meyerhardt JA, Loda M, et al. CpG island methylator phenotype, microsatellite instability, BRAF mutation and clinical outcome in colon cancer. Gut. 2009;58:90–6.
Roth AD, Tejpar S, Delorenzi M, Yan P, Fiocca R, Klingbiel D, et al. Prognostic role of KRAS and BRAF in stage II and III resected colon cancer: results of the translational study on the PETACC-3, EORTC 40993, SAKK 60–00 trial. J Clin Oncol. 2010;28:466–74.
Yokota T, Ura T, Shibata N, Takahari D, Shitara K, Nomura M, et al. BRAF mutation is a powerful prognostic factor in advanced and recurrent colorectal cancer. Br J Cancer. 2011;104:856–62.
Wang HW, Yang SH, Huang GD, Lin JK, Chen WS, Jiang JK, et al. Temsirolimus enhances the efficacy of cetuximab in colon cancer through a CIP2A-dependent mechanism. J Can Res Clin Oncol. 2014;140:561–71.
Tol J, Nagtegaal ID, Punt CJ. BRAF mutation in metastatic colorectal cancer. N Engl J Med. 2009;361:98–9.
Peng XY, Chen W, Zhou K, Fu JP, Fu P. Zeng QL: [Expression of cancerous inhibitor of protein phosphatase 2A in tissue microarray of colorectal cancer and its clinical significance]. Zhonghua Wei Chang Wai Ke Za Zhi. 2013;16:1102–6.
Zhao D, Liu Z, Ding J, Li W, Sun Y, Yu H, et al. Helicobacter pylori CagA upregulation of CIP2A is dependent on the Src and MEK/ERK pathways. J Med Microbiol. 2010;59:259–65.
Khanna A, Okkeri J, Bilgen T, Tiirikka T, Vihinen M, Visakorpi T, et al. ETS1 mediates MEK1/2-dependent overexpression of cancerous inhibitor of protein phosphatase 2A (CIP2A) in human cancer cells. PLoS One. 2011;6:e17979.
Di Nicolantonio F, Martini M, Molinari F, Sartore-Bianchi A, Arena S, Saletti P, et al. Wild-type BRAF is required for response to panitumumab or cetuximab in metastatic colorectal cancer. J Clin Oncol. 2008;26:5705–12.
This work was supported by the Division of Experimental Surgery of the Department of Surgery, Taipei Veterans General Hospital (102DHA0100184 V101E2-006) and by the Taiwan Clinical Oncology Research Foundation.
The authors declare that they have no competing interests.
KFC, CCY and HWT analyzed the data and wrote the manuscript. JKL, WSC, JKJ and SHY provided clinical information. WLL, YTL, CCL, HCY and HMH prepared the samples for exome sequencing. HWT and CCY designed and managed the study. All authors read and approved the final manuscript.