Sun Ping-Li, Kim Ji Eun, Yoo Seol Bong, Kim Hyojin, Jin Yan, Jheon Sanghoon, Kim Kwhanmien, Lee Choon Taek, Chung Jin-Haeng
Department of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Republic of Korea.
Ann Surg Oncol. 2014 Dec;21 Suppl 4:S610-8. doi: 10.1245/s10434-014-3715-5. Epub 2014 Apr 26.
Yes-associated protein (YAP) has been reported to be associated with the prognosis of various cancers and also to affect epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) activity in ovarian cancer cell lines. However, few studies have evaluated YAP protein expression in lung cancer, and the results have lacked consistency.
YAP expression was evaluated in a total of 205 curatively resected lung adenocarcinomas and 36 cases of EGFR-mutated TKI-treated patients. Correlations between the expression of YAP and clinicopathologic features, response to EGFR-TKI treatment, and prognostic significance were analyzed.
High cytoplasmic YAP expression was positively correlated with the clinicopathologic parameters that have been associated with favorable prognosis. Multivariate analysis revealed that high cytoplasmic YAP expression was an independent prognostic factor in lung adenocarcinomas (progression-free survival: hazard ratio [HR] 0.659; 95 % confidence interval [CI] 0.431-1.010; p = 0.050; overall survival: HR, 0.474; 95 % CI 0.263-0.854; p = 0.013) and EGFR-TKI-treated patients with EGFR mutation (progression-free survival: HR, 0.346; 95 % CI 0.146-0.818; p = 0.016; overall survival: HR, 0.291; 95 % CI 0.125-0.676; p = 0.004).
High cytoplasmic YAP expression predicted a good clinical outcome for patients with lung adenocarcinoma and in EGFR-TKI-treated patients. Therefore, YAP may play a role in EGFR-TKI-treated lung cancer, and YAP targeting may enhance therapeutic effects in combination with other cancer drugs.
有报道称Yes相关蛋白(YAP)与多种癌症的预后相关,并且在卵巢癌细胞系中影响表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKI)的活性。然而,很少有研究评估YAP蛋白在肺癌中的表达,且结果缺乏一致性。
对总共205例接受根治性切除的肺腺癌患者以及36例接受EGFR突变TKI治疗的患者的YAP表达进行评估。分析YAP表达与临床病理特征、对EGFR-TKI治疗的反应以及预后意义之间的相关性。
高细胞质YAP表达与已被证实与良好预后相关的临床病理参数呈正相关。多变量分析显示,高细胞质YAP表达是肺腺癌患者(无进展生存期:风险比[HR] 0.659;95%置信区间[CI] 0.431 - 1.010;p = 0.050;总生存期:HR,0.474;95% CI 0.263 - 0.854;p = 0.013)以及接受EGFR-TKI治疗的EGFR突变患者(无进展生存期:HR,0.346;95% CI 0.146 - 0.818;p = 0.016;总生存期:HR,0.291;95% CI 0.125 - 0.676;p = 0.004)的独立预后因素。
高细胞质YAP表达预示着肺腺癌患者以及接受EGFR-TKI治疗患者的良好临床结局。因此,YAP可能在接受EGFR-TKI治疗的肺癌中发挥作用,靶向YAP可能与其他抗癌药物联合增强治疗效果。