Deng Fang, Li Ming, Shan Wu-Lin, Qian Li-Ting, Meng Shui-Ping, Zhang Xiao-Lei, Wang Bao-Long
Department of Clinical Laboratory, Affiliated Provincial Hospital of Anhui Medical University, Hefei, Anhui 230022, P.R. China.
Department of Clinical Laboratory, Anhui Provincial Cancer Hospital, Hefei, Anhui 230031, P.R. China.
Oncol Lett. 2017 Apr;13(4):2359-2365. doi: 10.3892/ol.2017.5711. Epub 2017 Feb 10.
Epidermal growth factor receptor (EGFR) mutations are more common in non-small cell lung cancer (NSCLC) and in female patients of East Asian origin. Therefore, the present study investigated the presence of EGFR mutations in advanced NSCLC, and assessed its correlation with clinicopathologic factors, including the expression of estrogen receptor-β (ER-β) and patient prognosis. The present study performed a retrospective analysis of 83 patients with stage IIIB-IV NSCLC. The expression of ER-β and p53 were examined using immunohistochemical methods. EGFR mutations were evaluated using the amplification refractory mutation system. The expression of ER-β and p53 were detected in 37 (45.6%) and 48 (57.8%) of the patient tumors, respectively. EGFR mutations were identified in 36 (45.4%) cases. EGFR mutations were more frequently observed in ER-β-negative tumors (26/46; 56.5%), compared with ER-β-positive tumors (10/37; 27%). The expression of ER-β was significantly associated with EGFR mutations with an odds ratio (OR) of 0.241 (P=0.029). However, no significant correlation was observed between the expression of p53 and mutations in EGFR (OR=1.792; P=0.340). In addition, the expression of ER-β and lymph node metastasis were associated with poor prognosis, whereas EGFR mutations were significantly associated with favorable prognosis in terms of progression-free survival rates. However, there was no prognostic significance associated with the expression of p53. In conclusion, the expression of ER-β was significantly correlated with the presence of EGFR mutations. The expression of ER-β and mutations of EGFR were found to be prognostic factors for survival rates in patients with advanced NSCLC.
表皮生长因子受体(EGFR)突变在非小细胞肺癌(NSCLC)及东亚裔女性患者中更为常见。因此,本研究调查了晚期NSCLC中EGFR突变的存在情况,并评估了其与临床病理因素的相关性,包括雌激素受体-β(ER-β)的表达及患者预后。本研究对83例IIIB-IV期NSCLC患者进行了回顾性分析。采用免疫组织化学方法检测ER-β和p53的表达。使用扩增阻滞突变系统评估EGFR突变。分别在37例(45.6%)和48例(57.8%)患者肿瘤中检测到ER-β和p53的表达。在36例(45.4%)病例中鉴定出EGFR突变。与ER-β阳性肿瘤(10/37;27%)相比,ER-β阴性肿瘤(26/46;56.5%)中更频繁观察到EGFR突变。ER-β的表达与EGFR突变显著相关,优势比(OR)为0.241(P=0.029)。然而,未观察到p53表达与EGFR突变之间存在显著相关性(OR=1.792;P=0.340)。此外,ER-β的表达和淋巴结转移与预后不良相关,而就无进展生存率而言,EGFR突变与良好预后显著相关。然而,p53的表达无预后意义。总之,ER-β的表达与EGFR突变的存在显著相关。发现ER-β的表达和EGFR的突变是晚期NSCLC患者生存率的预后因素。