Abstract

BackgroundAmphiregulin (AREG) and Epiregulin (EREG), ligands of EGFR, are reported to be predictive biomarkers of colorectal cancer patients treated with Cetuximab, an anti-EGFR antibody. The purpose of this study is to determine the correlation of AREG and EREG expression between primary colorectal cancer and corresponding liver metastases.MethodsOne hundred twenty colorectal cancer patients with liver metastases (100 with synchronous metastases, 20 with metachronous) were evaluated. No patients had ever received anti-EGFR antibody agents. AREG and EREG mRNA expression from both the primary tumor and liver metastases were measured using real-time RT-PCR. KRAS codon 12, 13 mutation status was analyzed by direct sequencing.ResultsModest, but significant, correlations were observed between primary tumor and corresponding liver metastases in both AREG mRNA expression (Rs = 0.54, p < 0.0001) and EREG mRNA expression (Rs = 0.58, p < 0.0001). AREG and EREG mRNA expression was strongly correlated in both the primary tumor (Rs = 0.81, p < 0.0001) and the liver metastases (Rs = 0.87, p < 0.0001). No significant survival difference was observed between low and high AREG or EREG patients when all 120 patients were analyzed. However, when divided by KRAS status, KRAS wild-type patients with low EREG mRNA levels in the primary site showed significantly better overall survival rates than those with high levels (p = 0.018). In multivariate analysis, low EREG expression was significantly associated with better overall survival (p = 0.006).ConclusionsAREG and EREG expression showed a modest correlation between primary tumor and liver metastases. As EREG mRNA expression was associated with decreased survival, it is appeared to be a useful prognostic marker in KRAS wild-type patients who never received anti-EGFR therapy.

Highlights

  • Amphiregulin (AREG) and Epiregulin (EREG), ligands of Epidermal growth factor receptor (EGFR), are reported to be predictive biomarkers of colorectal cancer patients treated with Cetuximab, an anti-EGFR antibody

  • Analyzed the gene expression profile of 110 patients with colorectal cancer treated with Cetuximab to identify genes that were expressed differentially between the disease control group and the non-responders, demonstrated that AREG and EREG expression was associated with progression-free survival [10]

  • AREG and EREG relative mRNA expression levels in primary colorectal cancer and liver metastases There were no significant differences of median AREG and EREG relative mRNA levels between primary tumor and liver metastases (AREG: primary vs. liver = 0.16 vs. 0.21, p = 0.34, EREG: 0.030 vs. 0.034, p = 0.057) (Table 2)

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Summary

Introduction

Amphiregulin (AREG) and Epiregulin (EREG), ligands of EGFR, are reported to be predictive biomarkers of colorectal cancer patients treated with Cetuximab, an anti-EGFR antibody. The purpose of this study is to determine the correlation of AREG and EREG expression between primary colorectal cancer and corresponding liver metastases. Two large studies on AREG and EREG expression in patients with colorectal cancer who received Cetuximab were published. Analyzed the gene expression profile of 110 patients with colorectal cancer treated with Cetuximab to identify genes that were expressed differentially between the disease control group and the non-responders, demonstrated that AREG and EREG expression was associated with progression-free survival [10]. Jacobs et al examined 220 colorectal cancer patients treated with Cetuximab, and reported that there was a significant association between EREG and AREG expression and the response to Cetuximab in KRAS wild-type patients, but not in KRAS mutant patients [11]. Formalin-fixed paraffin-embedded (FFPE) samples from primary colorectal cancer were used in this study

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