Zhang Ju-Bo, Zhang Bo, Guo Lei, Lin Zhen-Hai, Li Xiao-Qiang, Guo Kun, Sun Hui-Chuan, Ye Qing-Hai
Liver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai, China.
Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shangai, China.
Oncotarget. 2015 Nov 24;6(37):40223-34. doi: 10.18632/oncotarget.5540.
Growing evidences support the concept that peritumoral microenvironment gene expression is an important element for physicians to make an accurate prognosis. Nonetheless, the correlation between peritumoral ubiquitin ligases and the hepatocellular carcinoma (HCC) survival remains unclear till this present. The expression of intratumoral and peritumoral Casitas B-lineage Lymphoma (Cbl) and epidermal growth factor receptor (EGFR) in hepatocellular carcinomas (HCCs) followed by curative resection was assessed by tissue microarray-based immune-histochemistry in two independent cohorts (n = 352). Their respective prognostic values and other clinicopathologic factors were then evaluated. The peritumoral Cbl density, much higher than that in intratumoral tissue, was an independent prognostic factor for overall survival (P < 0.001) and time to recurrence (P < 0.001) of HCCs after curative resection. The hazard ratio were 1.587 and 1.689, respectively. However, there was no correlation between intratumoral Cbl and prognosis. The peritumoral Cbl was also associated with prognosis even in HCC subgroups with small tumor size, negative AFP, without microvascular invasion and negative HBeAg. After a thorough analysis pertaining to the key role of Cbl on ubiquitination and degradation of activated receptor tyrosine kinases, we eventually discovered the negative correlation between peritumoral Cbl and EGFR (P = 0.015). Furthermore, the combination of peritumoral Cbl and EGFR serves as a much stronger indicator to make an accurate prognosis, especially during early recurrence (P < 0.001). These findings suggest that low expression of peritumoral Cbl and EGFR were positively associated with tumor size, microvascular invasion and patients survival after hepatectomy, highlighting the key role of peritumoral liver milieu in HCC progression.
越来越多的证据支持这样一种观念,即瘤周微环境基因表达是医生做出准确预后判断的重要因素。尽管如此,直到目前,瘤周泛素连接酶与肝细胞癌(HCC)生存率之间的相关性仍不清楚。通过基于组织芯片的免疫组织化学方法,在两个独立队列(n = 352)中评估了根治性切除术后肝细胞癌(HCC)肿瘤内和瘤周的Casitas B系淋巴瘤(Cbl)及表皮生长因子受体(EGFR)的表达。然后评估了它们各自的预后价值及其他临床病理因素。瘤周Cbl密度远高于肿瘤内组织,是HCC根治性切除术后总生存期(P < 0.001)和复发时间(P < 0.001)的独立预后因素。风险比分别为1.587和1.689。然而,肿瘤内Cbl与预后无相关性。即使在肿瘤体积小、甲胎蛋白阴性、无微血管侵犯及乙肝e抗原阴性的HCC亚组中,瘤周Cbl也与预后相关。在全面分析了Cbl对活化受体酪氨酸激酶泛素化和降解的关键作用后,我们最终发现瘤周Cbl与EGFR之间存在负相关(P = 0.015)。此外,瘤周Cbl和EGFR的联合是做出准确预后判断的更强指标,尤其是在早期复发时(P < 0.001)。这些发现表明,瘤周Cbl和EGFR的低表达与肿瘤大小、微血管侵犯及肝切除术后患者生存率呈正相关,突出了瘤周肝微环境在HCC进展中的关键作用。