Luo Chen-Hui, Zhao Min, Chen Xiao-Yan, Shahabi Shohreh, Qiang Wenan, Zeng Liang, Wang Jing, Zhou Hong-Hao
Laboratory Animal Research Center, Hunan Cancer Hospital, the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, People's Republic of China.
Department of Clinical Pharmacology, Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
J Cancer. 2018 Jun 14;9(14):2472-2479. doi: 10.7150/jca.25184. eCollection 2018.
For recurrent ovarian cancer (ROC), secondary cytoreductive surgery (SCS) is recommended as one optional treatment. However, little is known about the expression and clinical significance of biomarkers during SCS. Human epididymis protein 4 (HE4) is a clinical biomarker for ovarian cancer. Eukaryotic translation initiation factor 3a (eIF3a) is investigated extensively as a potential biomarker for malignancy. The purpose of this study was to investigate the expressions of HE4 and eIF3a at SCS, as well as their associations with surgical outcome and survival in ROC patients. Immunohistochemistry was performed to determine the expressions of HE4 and eIF3a in ovarian tumors taken from both initial and secondary cytoreductive surgery of 35 ROC patients. eIF3a levels were significantly increased at SCS, compared to those at initial cytoreductive surgery (ICS), while HE4 levels were similar. Both HE4 and eIF3a expressions were associated with surgical outcome, in terms of residual tumor. For ICS, patients with high HE4 expression achieved a higher incidence of optimal cytoreduction than those with low HE4 expression (81.0% 33.3%, P = 0.015). A similar result happened in SCS, indicated by higher incidence of no residual tumor in patients with high HE4 expression (76.4% 44.4%, P = 0.046). And high HE4 expression at SCS was more likely to enhance surgical outcome of SCS (77.8% 29.4%, P = 0.038). Therefore, high HE4 expression at either surgery is a predictor of better overall survival (OS) (P = 0.011 and 0.002). Furthermore, patients with an elevated total score (TS) of HE4 between the two surgeries tended to have prolonged OS, compared to those with a non-elevated TS of HE4 (P = 0.076). For eIF3a, initial eIF3a expression was associated with secondary residual tumor (P = 0.035), and the difference in eIF3a expression between the two surgeries correlated with OS (P = 0.052). The expressions of HE4 and eIF3a in tumor specimens correlated with surgical outcome and predicted OS in ROC patients with SCS, thus meriting further investigation.
对于复发性卵巢癌(ROC),推荐二次肿瘤细胞减灭术(SCS)作为一种可选治疗方法。然而,关于生物标志物在SCS期间的表达及临床意义却知之甚少。人附睾蛋白4(HE4)是卵巢癌的一种临床生物标志物。真核翻译起始因子3a(eIF3a)作为一种潜在的恶性肿瘤生物标志物受到广泛研究。本研究的目的是调查SCS时HE4和eIF3a的表达情况,以及它们与ROC患者手术结果和生存的相关性。采用免疫组织化学方法测定35例ROC患者初次和二次肿瘤细胞减灭术中获取的卵巢肿瘤组织中HE4和eIF3a的表达。与初次肿瘤细胞减灭术(ICS)相比,SCS时eIF3a水平显著升高,而HE4水平相似。就残留肿瘤而言,HE4和eIF3a的表达均与手术结果相关。对于ICS,HE4高表达患者实现最佳肿瘤细胞减灭的发生率高于HE4低表达患者(81.0%对33.3%,P = 0.015)。SCS时也出现了类似结果,HE4高表达患者无残留肿瘤的发生率更高(76.4%对44.4%,P = 0.046)。并且SCS时HE4高表达更有可能改善SCS的手术结果(77.8%对29.4%,P = 0.038)。因此,任何一次手术时HE4高表达都是更好总生存期(OS)的一个预测指标(P = 0.011和0.002)。此外,与HE4总分(TS)未升高的患者相比,两次手术之间HE4的TS升高的患者往往有更长的OS(P = 0.076)。对于eIF3a,初次eIF3a表达与二次残留肿瘤相关(P = 0.035),两次手术之间eIF3a表达的差异与OS相关(P = 0.052)。肿瘤标本中HE4和eIF3a的表达与SCS的ROC患者的手术结果相关并可预测OS,因此值得进一步研究。