Oka Soichi, Uramoto Hidetaka, Shimokawa Hidehiko, Yamada Sohsuke, Tanaka Fumihiro
Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Oncology. 2014;86(5-6):263-70. doi: 10.1159/000360089. Epub 2014 Jun 4.
The overexpression of Arf6 and GEP100 is responsible for the invasive activity that is crucial for the activation of the epidermal growth factor receptor (EGFR) signaling pathways in human cancer. However, whether or not the expression of the EGFR-GEP100-Arf6 axis can be used as a biomarker for the prognosis of lung cancer has yet to be fully determined. Tumor specimens were collected from 182 patients who underwent a complete resection for lung adenocarcinoma. We analyzed phospho-EGFR (p-EGFR), GEP100, and Arf6 expression levels in the primary tumor by immunohistochemical analysis. The expression of p-EGFR, GEP100, and Arf6 was observed in 65 (35.7%), 95 (52.2%), and 20 (11.0%) patients, respectively. Significant associations between p-EGFR and GEP100 expression and vessel invasion were identified. The expression of these individual molecules was not associated with any statistically significant differences in survival. However, triple positive expression of p-EGFR, GEP100, and Arf6 was significantly associated with an increased risk of death based on the multivariate analysis. The EGFR-GEP100-Arf6 axis affected the prognosis of patients with primary lung adenocarcinoma. The combination of p-EGFR, GEP100, and Arf6 staining can predict the prognosis of patients after surgery.
Arf6和GEP100的过表达导致了侵袭活性,这对人类癌症中表皮生长因子受体(EGFR)信号通路的激活至关重要。然而,EGFR-GEP100-Arf6轴的表达是否可作为肺癌预后的生物标志物尚未完全确定。从182例行肺腺癌根治性切除术的患者中收集肿瘤标本。我们通过免疫组织化学分析来检测原发性肿瘤中磷酸化EGFR(p-EGFR)、GEP100和Arf6的表达水平。分别在65例(35.7%)、95例(52.2%)和20例(11.0%)患者中观察到p-EGFR、GEP100和Arf6的表达。p-EGFR和GEP100的表达与血管侵犯之间存在显著关联。这些单个分子的表达与生存方面的任何统计学显著差异均无关联。然而,基于多变量分析,p-EGFR、GEP100和Arf6的三联阳性表达与死亡风险增加显著相关。EGFR-GEP100-Arf6轴影响原发性肺腺癌患者的预后。p-EGFR、GEP100和Arf6染色的联合可预测患者术后的预后。