Skip to main content
Download PDF

Exploratory biomarker analysis for treatment response in KRAS wild type metastatic colorectal cancer patients who received cetuximab plus irinotecan

BMC Cancer volume 15, Article number: 747 (2015) Cite this article

Abstract

Background

More than half of the patients selected based on KRAS mutation status fail to respond to the treatment with cetuximab in metastatic colorectal cancer (mCRC). We designed a study to identify additional biomarkers that could act as indicators for cetuximab treatment in mCRC.

Methods

We investigated 58 tumor samples from wild type KRAS CRC patients treated with cetuximab plus irinotecan (CI). We conducted the genotyping for mutations in either BRAF or PIK3CA and profiled comprehensively the expression of 522 kinase genes.

Results

BRAF mutation was detected in 5.1 % (3/58) of patients. All 50 patients showed wild type PIK3CA. Gene expression patterns that categorized patients with or without the disease control to CI were compared by supervised classification analysis. PSKH1, TLK2 and PHKG2 were overexpressed significantly in patients with the disease control to IC. The higher expression value of PSKH1 (r = 0.462, p < 0.001) and TLK2 (r = 0.361, p = 0.005) had the significant correlation to prolonged PFS.

Conclusion

The result of this work demonstrated that expression nature of kinase genes such as PSKH1, TLK2 and PHKG2 may be informative to predict the efficacy of CI in wild type KRAS CRC. Mutations in either BRAF or PIK3CA were rare subsets in wild type KRAS CRC.

Peer Review reports

Background

Colorectal cancer (CRC) has been a significant cause of morbidity and mortality throughout the world [1]. Metastatic CRC (mCRC) is associated with a particularly poor prognosis. Despite progress in cytotoxic chemotherapy during past decade, the five year survival rate for mCRC remains below 10 % [2]. There have been recent and rapid advances in the development of agents targeted against components of receptor tyrosine kinase signaling cascades for use in cancer-therapy. A monoclonal antibody (mAb) against epidermal growth factor receptor (EGFR), referred to as cetuximab, is a product of this movement, and has been implemented to treat selected mCRC patients.

However, only 10–20 % of the selected mCRC patients benefit from anti-EGFR therapy [3–6], highlighting a distinct need for individualized treatment. Following the discovery that mutations in KRAS are associated with resistance to anti-EGFR treatment, determination of KRAS status is now recommended in mCRC patients before starting anti-EGFR therapies. Despite the application of these selective strategies, less than half of the chosen wild type KRAS patient population benefits from anti-EGFR treatment [7–9]. More recently, other oncogenic alterations such as mutations in BRAF and PIK3CA were identified as candidates associated with resistance to anti-EGFR therapies in wild type KRAS patients [8, 10–13]. However, there is still a need to identify and confirm additional biomarkers that can be used to more accurately select wild type mCRC patients that will respond to anti-EGFR therapy.

Protein kinases control many cellular processes including metabolism, transcription, cell cycle progression, cytoskeletal rearrangement, cell movement, apoptosis, and differentiation [14, 15]. Therefore, protein kinases are essential targets for molecular therapy. Indeed, various protein kinase inhibitors have been shown to be effective against cancer cells. Cancers often result from the interconnectivity of complex pathways, some of which are not well understood. For this reason, we surmise that the anti-tumor activity of cetuximab may be affected by various kinase genes involved different pathways.

In order to identify additional selective biomarkers for CI indication, we genotyped wild type KRAS colorectal tumor samples from patients that received CI treatment for mutations in either BRAF or PIK3CA, and profiled comprehensively the expression of 522 kinase genes involved different pathways.

Methods

Patients and samples

Fifty-eight mCRC patients with CI, for whom collection of tumor samples was part of their routine care and treatment, were enrolled for this analysis. Patients were treated by CI after confirming KRAS mutational status (wild type). The tumor samples were sufficient to study additional biomarkers, such as genotyping for BRAF and PIK3CA and targeted gene expression profiling. In all cases, we reviewed patient age at diagnosis, gender, Eastern Cooperative Oncology Group (ECOG) performance status, the number of involved organs, metastatic site, and chemotherapy data. All hematoxylin and eosin stained slides were reviewed, and representative paraffin blocks were selected for further studies.

DNA extraction and mutation analysis for BRAF and PIK3CA

DNA was extracted from five 10-μm thick formalin fixed paraffin embedded (FFPE) sections containing a representative portion of each tumor block, using the QIAamp DNA Mini kit (Qiagen, Hilden, Germany). A pathologist reviewed each slide and verified the presence of adequate tumor tissue with greater than 50 % representative malignant cells.

Peptide nucleic acid-locked nucleic acid (PNA–LNA) PCR clamp reactions were carried out using the PNA-Clamp™ BRAF, and PNA-Clamp™ PIK3CA Mutation Detection Kits (Panagene, Inc., Daejeon, Korea), as described previously. Briefly, this reaction consists of the following; all reactions were done in 20 μl volumes using 10–25 ng template DNA, primer and PNA probe set, and SYBR Green PCR master mix. All necessary reagents are included with the kit. Real-time PCR reactions of PNA-mediated clamping PCR were performed using a CFX 96 system (Bio-Rad, USA). PCR conditions started with a 5 min hold at 94 °C, followed by 40 cycles of 94 °C for 30 s, 70 °C for 20 s, 63 °C for 30 s, and 72 °C for 30 s. Detection of each of mutation in BRAF exon 15, and 3 mutations in PIK3CA exons 2 & 9 was possible using one-step PNA-mediated real-time PCR clamping.

Targeted gene expression profiling

The Nanostring-based multigene assay was performed in tissue samples of 58 patients who received cetuximab-based therapy for mCRC. Total RNA was extracted from one or two sections of 4-μm thick FFPE tumor sections using the High Pure RNA Paraffin kit (Roche Diagnostic, Mannheim, Germany) after removing non-tumor elements by manual macrodissection guided by hematoxylin and eosin stained slides. nCounter® GX Human Kinase Kit (NanoString Technologies, Seattle, WA, USA) was used for gene expression analyses. One hundred nanogram of total RNA was hybridized with the pre-built code set of 522 genes for 18 h at 65 °C and processed according to manufacturer’s instruction [16].

Ethics statement

The institutional review board of the Samsung Medical Center (SMC) approved the process of acquiring tissue samples in mCRC patients with cetuximab-based therapy. All study participants provided a written informed consent form, which was approved by the institutional review board. The methods in this study were carried out in accordance with the approved guidelines by SMC and all experimental protocols were approved by the ethics committees of SMC.

Statistical analysis

To discover differential expression of 522 kinase genes between two groups (partial response plus stable disease vs. progressive disease), t-test is applied after the data is normalized by quantile method. Response definitions that differentiated two groups were according to Response Evaluation Criteria in Solid Tumors (RECIST) 1.1. To identify gene set that is associated with disease control, t-test statistics of 522 genes were further assessed by Pathway Activity inference using Condition-responsive genes (PAC). Spearman’s test was used to assess the correlation between progression free survival (PFS) and expression vales of selected kinase genes that related to the disease control for cetuximab. Results were considered statistically significant when p-values were < 0.05. Gene expression difference analysis and pathway analysis were performed using R (version 2.15 and package 2.10) (http://www.R-project.org), and other statistical analyses were performed using SPSS software (SPSS Inc., Chicago, IL, USA).

Pathway association analysis

To identify gene set that associated with disease control (partial response plus stable disease vs. progressive disease), we conducted Efron-Tibshirani’s gene set analysis (GSA) maxmean test embedded in the BRB Array Tool. We examined 92 gene sets in Biocarta Pathway database and the threshold of determining significant gene sets is 0.01.

Results

Clinicopathological features

As summarized in Table 1, 58 wild type KRAS mCRC patients of a median age of 59 years (range, 39–91) received CI treatment. The study included 33 (56.9 %) male and 25 (43.1 %) female patients. Most of the patients (96.6 %) had a good performance status (ECOG 1) and over half of the patients (75.9 %) had metastatic disease at diagnosis. More than half of patients (51.7 %) had three or more metastatic lesions and 91.4 % received CI as third or more line treatment. Only 18 patients (31 %) had prior anti-VEGF therapy before CI.

Table 1 Baseline characteristics of the patients enrolled in this study
Full size table

Frequency of BRAF and PIK3CA mutations

BRAF mutation status was assessed in 54 of 58 (93.1 %) patients. Three of these (5.6 %) patients harbored BRAF mutations (V600E). PIK3CA mutation status was evaluated in 50 of 58 (86.2 %) patients, and all 50 patients showed wild type PIK3CA (Table 1). CI did not reveal the anti-tumor effect in all 3 patients with BRAF mutation.

Expression of kinase genes and cetuximab treatment outcome

Among the 58 patients receiving cetuximab-based therapy, 21 achieved a confirmed partial response and nine had stable disease, resulting in an overall response rate (ORR) of 36.2 % (21/58) and disease control rate (DCR) 51.7 % (30/58) (Table 2). There were 522 kinase genes analyzed by nCounter assay and a supervised method was used to find statistically significant differentially expressed genes between patients with and without the disease control for CI. A hierarchical clustering analysis was then performed on the samples based on expression value of 522 genes in 58 patients (Fig. 1). We found three kinase genes such as PSKH1, TLK2 and PHKG2 that were presented significantly higher expression levels in patients with the disease control to CI (Fig. 2).

Table 2 Treatment outcomes of cetuximab therapy and the corresponding number of patients
Full size table
Fig. 1
figure 1

Supervised clustering of 522 kinase genes that are differentially expressed between patients with and without tumor response to CI and between patients with and without the disease control to CI. RR; complete response plus partial response: DCR; RR plus stable disease

Full size image
Fig. 2
figure 2

Kinase genes (PSKH1, TLK2 and PHKG2) that were differentially expressed between patients with and without the disease control to CI

Full size image

Progression free survival and expression of PSKH1, TLK2 and PHKG2

All 58 patients with cetuximab-based therapy were analyzed for progression free survival (PFS) and exhibited a median PFS of 2.4 months (95 % CI, 0.0–7.2) (Fig. 3). The correlation was analyzed between PFS and the expression values of PSKH1, TLK2 and PHKG2. The higher expression value of PSKH1 (r = 0.462, p < 0.001) (Fig. 4a) and TLK2 (r = 0.361, p = 0.005) (Fig. 4b) had the significant correlation to prolonged PFS. However, the statistically significant correlation was not observed between PHK2G2 and PFS (r = 0.236, p = 0.075) (Fig. 4c).

Fig. 3
figure 3

Kaplan-Meier estimate of progression free survival (PFS)

Full size image
Fig. 4
figure 4

The correlation between PFS and the expression value of (a) PSKH1, (b) TLK2 and (c) PHKG2

Full size image

Signaling pathways related to the anti-tumor activity of CI

We performed pathway analysis using gene set enrichment analysis for expression of 522 kinase genes. For the disease-controlled cohort, 3 out of 92 investigated Biocarta pathway gene sets passed the 0.01 significance threshold as verified by Efron-Tibshirani’s GSA maxmean test. These included the CCR3 signaling pathway, the cdMac signaling pathway, and the integrin signaling pathway (Table 3).

Table 3 Results of the gene-set enrichment analysis of the Biocarta pathway for disease control
Full size table

Discussion

Despite exclusion of 30–40 % of patients with KRAS mutant tumors, cetuximab-based therapy fail in more than half of CRC patients harboring wild type KRAS [4, 9, 17–19]. Recently, mutations in other downstream effectors of the EGFR pathway, such as BRAF, NRAS, and PIK3CA have also been implicated as possible predictors for anti-EGFR response [12, 18, 20, 21]. Overall, the benefit of analyzing these candidates has been difficult to determine due to low mutation frequencies for individual markers. In an attempt to identify additional biomarkers for the efficacy of cetuximab-based therapy in CRC patients with wild type KRAS, we performed targeted gene expression profiling for 522 kinase genes in addition to genotyping for BRAF and PIK3CA. Our analysis suggested that the overexpression of PSKH1, TLK2 and PHKG2 may be a considered a potential biomarker to predict the efficacy of CI in wild type KRAS CRC. Moreover, the higher expression value of PSKH1 (r = 0.462, p < 0.001) and TLK2 (r = 0.361, p = 0.005) had the significant correlation to prolonged PFS. However, among 522 kinase genes, any gene didn’t have significant prognostic value for overall survival (OS). We also conducted the multivariate analysis (Cox proportional hazard modeling) for PFS with clinical variable and expression nature of kinase genes such as PSKH1, TLK2 and PHKG2. Univariate analysis showed that prolonged PFS was significantly associated with metastatic sites of ≤ 2, and expressed of PSKH1, TLK2 and PHKG2. In multivariate analysis, only expressed of PSKH1 (hazard ratio [HR], 2.219; 95 % confidence interval [CI], 1.085 TO 4.541; p = 0.029) was significantly with prolonged PFS.

We used an nCounter assay to analyze the expression of kinase genes. The nCounter assay can profile 522 human kinase genes in one reaction tube with only 100 ng of total RNA. Previously, we compared the results of an nCounter assay with immunohistochemistry results using three biomarkers (EGFR, HER2 and MET) in a gastric cancer (GC) model [22]. Relative to immunohistochemistry findings, the NanoString-based assay sensitivities and specificities were 85.7 % and 82.8 % for EGFR, 100 % and 97.2 % for HER2, and 100 % and 100 % for MET, respectively. Hence, nCounter assays may be feasible as a relatively reliable option in the clinic, where only small amount of RNA (~100 ng) can be rendered from paraffin-embedded tissues. Based on our previous study, NanoString-based kinase assay has been used as a feasible screening tool for initially identifying patients who have GC with overexpressed drug targets in our institution. This study suggested that nCounter assays could be used efficiently as a platform for implementing personalized medicine of CRC.

PSKH1 is a 424 amino acids long ubiquitously expressed autophosphorylating humane protein serine kinase [23, 24]. PSKH1 has been known to have a useful structural and regulatory role in the maintenance of the Golgi apparatus [25]. TLK2 is a nuclear serine/threonine kinase which is a cell cycle check point regulating chromatin assembly and is inactivated in response to DNA damage [26]. Although the higher expression value for PSKH1 and TLK2 is likely to be related to prolonged PFS as well as antitumor effect for CI in CRC patients in this analysis, the molecular determinants for overexpression for PSKH1 and TLK2 are unknown for the effect of cetuximab. Further functional analysis of these kinase genes is needed to apply these markers in clinical practice.

Assessment of some mutations could improve the objective response rate; objective response rates were 24.4 % in unselected population, 36.3 % in population harboring the wild type KRAS, and 41.2 % in the KRAS, BRAF, NRAS, and PIK3CA exon 20 wild type populations [18]. However, cetuximab still fails to meet expectations in more than half of patients who were selected via genotyping of multiple genes. There are some limitations in our study. A small sample size, heterogeneous patient population, retrospective nature, and limited validated data didn’t allow us to draw any significant conclusions. Especially, our study included only 3 patients with BRAF mutation. Thus, the role of BRAF mutation as predictive marker for cetuximab needs to be validated and studied. Tissue availability was also a potential limitation of the current retrospective biomarker-analysis. It is better to verify the PSKH1, TLK2, and PHKG2 expression identified by nCounter assay in tissues using independent methods such as in situ hybridization, immune histochemistry or RT-qPCR. However, patients analyzed in this study had refractory cancer. Among these patients, it was difficult to get the tumor tissue for biomarker-analysis. Nevertheless, our attempts to whether expression of kinase genes could serve as biomarkers for the efficacy of cetuximab therapy in wild type KRAS CRC patients is worth noting.

Many crucial signaling pathways become dysregulated during cancer initiation and progression. Identifying the pathways involved and quantifying their deregulation is an important step toward understanding carcinogenesis [27–30]. Because advanced therapies target specific pathways, pathway-level understanding is also a necessity in the development of personalized cancer treatments. Previously, we found that KRAS mutant CRC patients with low RAS signature scores were likely to benefit from treatment with cetuximab, irinotecan plus simvastatin [31]. This finding suggested that differential RAS signaling in KRAS mutant CRC patients is a useful biomarker for choosing the proper treatment regimen. Based on our analysis, CCR3, cdMac, and integrin pathways are significantly associated with the activity of cetuximab as the down-regulation of these pathways correlated with an observed increase in cetuximab efficacy, though these results must be validated. Additional, work will also need to be done to evaluate whether the CCR3, cdMac, and integrin pathways are interconnected with the EGFR signaling that was known as the key pathway for the effect of cetuximab. Many new investigational agents, such as inhibitors of MAP2K, PI3K, mTOR, EGFR, and BRAF will be extremely useful for elucidating these networks [32]. These pathway-based approaches will be used as novel algorithms for precision medicine.

In conclusion, our study suggested that expression nature of kinase genes such as PSKH1, TLK2 and PHKG2 may be informative to predict the efficacy of CI in wild type KRAS CRC. In addition to known EGFR pathway, the CCR3, cdMac, and integrin pathways may also be useful in predicting cetuximab response in these patients. Our findings warrant further independent validation. In the future, multiple-biomarker assessment will be needed in mCRC patients in order to optimize identification of patients that will benefit from cetuximab.

Conclusion

The result of this work demonstrated that CI did not have anti-tumor activity in BRAF mutant CRC. Additionally, expression nature of kinase genes such as PSKH1, TLK2 and PHKG2 may be informative to predict the efficacy of CI in wild type KRAS CRC.

Ethics statement

The Ethics Committee at Samsung Medical Center approved the study in accordance with the Declaration of Helsinki. All individuals gave written informed consent for participation in the study.

References

  1. Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002. CA Cancer J Clin. 2005;55:74–108.

    Article  PubMed  Google Scholar 

  2. Sargent DJ, Wieand HS, Haller DG, Gray R, Benedetti JK, Buyse M, et al. Disease-free survival versus overall survival as a primary end point for adjuvant colon cancer studies: individual patient data from 20,898 patients on 18 randomized trials. J Clin Oncol. 2005;23:8664–70.

    Article  PubMed  Google Scholar 

  3. Bokemeyer C, Bondarenko I, Makhson A, Hartmann JT, Aparicio J, de Braud F, et al. Fluorouracil, leucovorin, and oxaliplatin with and without cetuximab in the first-line treatment of metastatic colorectal cancer. J Clin Oncol. 2009;27:663–71.

    CAS  Article  PubMed  Google Scholar 

  4. 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.

    Article  PubMed  Google Scholar 

  5. Douillard JY, Siena S, Cassidy J, Tabernero J, Burkes R, Barugel M, et al. Randomized, phase III trial of panitumumab with infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX4) versus FOLFOX4 alone as first-line treatment in patients with previously untreated metastatic colorectal cancer: the PRIME study. J Clin Oncol. 2010;28:4697–705.

    CAS  Article  PubMed  Google Scholar 

  6. Sobrero AF, Maurel J, Fehrenbacher L, Scheithauer W, Abubakr YA, Lutz MP, et al. EPIC: phase III trial of cetuximab plus irinotecan after fluoropyrimidine and oxaliplatin failure in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26:2311–9.

    CAS  Article  PubMed  Google Scholar 

  7. Benvenuti S, Sartore-Bianchi A, Di Nicolantonio F, Zanon C, Moroni M, Veronese S, et al. Oncogenic activation of the RAS/RAF signaling pathway impairs the response of metastatic colorectal cancers to anti-epidermal growth factor receptor antibody therapies. Cancer Res. 2007;67:2643–8.

    CAS  Article  PubMed  Google Scholar 

  8. Sartore-Bianchi A, Di Nicolantonio F, Nichelatti M, Molinari F, De Dosso S, Saletti P, et al. Multi-determinants analysis of molecular alterations for predicting clinical benefit to EGFR-targeted monoclonal antibodies in colorectal cancer. PLoS One. 2009;4:e7287.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Van Cutsem E, Kohne CH, Lang I, Folprecht G, Nowacki MP, Cascinu S, et al. Cetuximab plus irinotecan, fluorouracil, and leucovorin as first-line treatment for metastatic colorectal cancer: updated analysis of overall survival according to tumor KRAS and BRAF mutation status. J Clin Oncol. 2011;29:2011–9.

    Article  PubMed  Google Scholar 

  10. Bardelli A, Siena S. Molecular mechanisms of resistance to cetuximab and panitumumab in colorectal cancer. J Clin Oncol. 2010;28:1254–61.

    CAS  Article  PubMed  Google Scholar 

  11. Rajagopalan H, Bardelli A, Lengauer C, Kinzler KW, Vogelstein B, Velculescu VE. Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status. Nature. 2002;418:934.

    CAS  Article  PubMed  Google Scholar 

  12. Laurent-Puig P, Cayre A, Manceau G, Buc E, Bachet JB, Lecomte T, et al. Analysis of PTEN, BRAF, and EGFR status in determining benefit from cetuximab therapy in wild-type KRAS metastatic colon cancer. J Clin Oncol. 2009;27:5924–30.

    CAS  Article  PubMed  Google Scholar 

  13. De Roock W, Lambrechts D, Tejpar S. K-ras mutations and cetuximab in colorectal cancer. N Engl J Med. 2009;360:834. author reply 835–6.

    PubMed  Google Scholar 

  14. Manning G, Whyte DB, Martinez R, Hunter T, Sudarsanam S. The protein kinase complement of the human genome. Science. 2002;298:1912–34.

    CAS  Article  PubMed  Google Scholar 

  15. Blume-Jensen P, Hunter T. Oncogenic kinase signalling. Nature. 2001;411:355–65.

    CAS  Article  PubMed  Google Scholar 

  16. Geiss GK, Bumgarner RE, Birditt B, Dahl T, Dowidar N, Dunaway DL, et al. Direct multiplexed measurement of gene expression with color-coded probe pairs. Nat Biotechnol. 2008;26:317–25.

    CAS  Article  PubMed  Google Scholar 

  17. Amado RG, Wolf M, Peeters M, Van Cutsem E, Siena S, Freeman DJ, et al. Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer. J Clin Oncol. 2008;26:1626–34.

    CAS  Article  PubMed  Google Scholar 

  18. De Roock W, Claes B, Bernasconi D, De Schutter J, Biesmans B, Fountzilas G, et al. Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis. Lancet Oncol. 2010;11:753–62.

    Article  PubMed  Google Scholar 

  19. De Roock W, Piessevaux H, De Schutter J, Janssens M, De Hertogh G, Personeni N, et al. KRAS wild-type state predicts survival and is associated to early radiological response in metastatic colorectal cancer treated with cetuximab. Ann Oncol. 2008;19:508–15.

    Article  PubMed  Google Scholar 

  20. Sartore-Bianchi A, Martini M, Molinari F, Veronese S, Nichelatti M, Artale S, et al. PIK3CA mutations in colorectal cancer are associated with clinical resistance to EGFR-targeted monoclonal antibodies. Cancer Res. 2009;69:1851–7.

    CAS  Article  PubMed  Google Scholar 

  21. 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.

    Article  PubMed  Google Scholar 

  22. Kim ST, Do IG, Lee J, Sohn I, Kim KM, Kang WK. The NanoString-based multigene assay as a novel platform to screen EGFR, HER2, and MET in patients with advanced gastric cancer. Clin Transl Oncol. 2014 (In Press).

  23. Brede G, Solheim J, Prydz H. PSKH1, a novel splice factor compartment-associated serine kinase. Nucleic Acids Res. 2002;30:5301–9.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  24. Brede G, Solheim J, Troen G, Prydz H. Characterization of PSKH1, a novel human protein serine kinase with centrosomal, golgi, and nuclear localization. Genomics. 2000;70:82–92.

    CAS  Article  PubMed  Google Scholar 

  25. Brede G, Solheim J, Stang E, Prydz H. Mutants of the protein serine kinase PSKH1 disassemble the Golgi apparatus. Exp Cell Res. 2003;291:299–312.

    CAS  Article  PubMed  Google Scholar 

  26. Li Z, Gourguechon S, Wang CC. Tousled-like kinase in a microbial eukaryote regulates spindle assembly and S-phase progression by interacting with Aurora kinase and chromatin assembly factors. J Cell Sci. 2007;120:3883–94.

    CAS  Article  PubMed  Google Scholar 

  27. Markert EK, Mizuno H, Vazquez A, Levine AJ. Molecular classification of prostate cancer using curated expression signatures. Proc Natl Acad Sci U S A. 2011;108:21276–81.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  28. Thomas DC, Baurley JW, Brown EE, Figueiredo JC, Goldstein A, Hazra A, et al. Approaches to complex pathways in molecular epidemiology: summary of a special conference of the American Association for Cancer Research. Cancer Res. 2008;68:10028–30.

    CAS  Article  PubMed  Google Scholar 

  29. Segal E, Friedman N, Koller D, Regev A. A module map showing conditional activity of expression modules in cancer. Nat Genet. 2004;36:1090–8.

    CAS  Article  PubMed  Google Scholar 

  30. Chin L, Hahn WC, Getz G, Meyerson M. Making sense of cancer genomic data. Genes Dev. 2011;25:534–55.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  31. Lee J, Hong YS, Hong JY, Han SW, Kim TW, Kang HJ, et al. Effect of simvastatin plus cetuximab/irinotecan for KRAS mutant colorectal cancer and predictive value of the RAS signature for treatment response to cetuximab. Invest New Drugs. 2014;32:535–41.

    CAS  Article  PubMed  Google Scholar 

  32. De Roock W, De Vriendt V, Normanno N, Ciardiello F, Tejpar SKRAS, BRAF. PIK3CA, and PTEN mutations: implications for targeted therapies in metastatic colorectal cancer. Lancet Oncol. 2011;12:594–603.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

1. This work was supported by grants from the Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea (HI13C1951).

2. This study was supported by Samsung Biomedical Research Institute (#CB11093).

3. This work was supported by grants from 20 by 20 project of Samsung Medical center (GF01140111). This study was supported by a grant from the Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea (HI14C3418) .

Author information

Author notes

    Authors and Affiliations

    1. Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

      Seung Tae Kim, Su Jin Lee, Se Hoon Park, Joon Oh Park, Young Suk Park, Ho Yeong Lim, Won Ki Kang & Jeeyun Lee

    2. Department of Pathology & Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

      Tae Jin Ahn, Eunjin Lee, In-Gu Do & Suk Hyeong Kim

    3. Samsung Genome Institute, Samsung Biological Research Institute, Seoul, Korea

      Tae Jin Ahn & Eunjin Lee

    4. Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

      Hee Cheol Kim

    5. Colorectal Cancer Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

      Seung Tae Kim, Su Jin Lee, Se Hoon Park, Joon Oh Park, Young Suk Park, Ho Yeong Lim, Won Ki Kang, Suk Hyeong Kim, Jeeyun Lee & Hee Cheol Kim

    6. Innovative Cancer Medicine Institute, Samsung Medical Center, Seoul, Korea

      Joon Oh Park

    Authors
    1. Seung Tae Kim
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Tae Jin Ahn
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Eunjin Lee
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. In-Gu Do
      View author publications

      You can also search for this author in PubMed Google Scholar

    5. Su Jin Lee
      View author publications

      You can also search for this author in PubMed Google Scholar

    6. Se Hoon Park
      View author publications

      You can also search for this author in PubMed Google Scholar

    7. Joon Oh Park
      View author publications

      You can also search for this author in PubMed Google Scholar

    8. Young Suk Park
      View author publications

      You can also search for this author in PubMed Google Scholar

    9. Ho Yeong Lim
      View author publications

      You can also search for this author in PubMed Google Scholar

    10. Won Ki Kang
      View author publications

      You can also search for this author in PubMed Google Scholar

    11. Suk Hyeong Kim
      View author publications

      You can also search for this author in PubMed Google Scholar

    12. Jeeyun Lee
      View author publications

      You can also search for this author in PubMed Google Scholar

    13. Hee Cheol Kim
      View author publications

      You can also search for this author in PubMed Google Scholar

    Corresponding authors

    Correspondence to Jeeyun Lee or Hee Cheol Kim.

    Additional information

    Competing interests

    The authors declare that they have no competing interests.

    Author contributions

    S.T.K., T.J.A., J.L., and H.C.K. undertook analysis of data and wrote the manuscript; S.T.K., T.J.A., E.L., I-G. D., S.H.K., and J.L complied patient information and helped to analyze the genomic data; T.J.A., E.L., S.H.K., and J.L. developed the software and bioinformatics tool and pipelines; J.L., S.T.K., S.J.L., J.O.P., S.H.P., Y.S.P, H.Y.L., W.K.K, and H.C.K. supported and conducted this study and edited the manuscript; J.L., S.T.K., S.H.K., and I-G.D. performed functional studies and helped to write the manuscript; J.L., and H.C.K. designed and led this study.

    Seung Tae Kim and Tae Jin Ahn contributed equally to this work.

    Rights and permissions

    Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

    Reprints and Permissions

    About this article

    Verify currency and authenticity via CrossMark

    Cite this article

    Kim, S.T., Ahn, T.J., Lee, E. et al. Exploratory biomarker analysis for treatment response in KRAS wild type metastatic colorectal cancer patients who received cetuximab plus irinotecan. BMC Cancer 15, 747 (2015). https://doi.org/10.1186/s12885-015-1759-y

    Download citation

    • Received:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/s12885-015-1759-y

    Keywords

    • KRAS
    • Cetuximab
    • Colorectal cancer

    BMC Cancer

    ISSN: 1471-2407

    Contact us