School of Biomedical Sciences, The University of Hong Kong, Hong Kong.
Department of Clinical Oncology, The University of Hong Kong, Hong Kong.
Cancer Res. 2017 Sep 1;77(17):4602-4612. doi: 10.1158/0008-5472.CAN-16-3456. Epub 2017 Jul 3.
Identifying critical factors involved in the metastatic progression of hepatocellular carcinoma (HCC) may offer important therapeutic opportunities. Here, we report that the proapoptotic stress response factor TP53INP1 is often selectively downregulated in advanced stage IV and metastatic human HCC tumors. Mechanistic investigations revealed that TP53INP1 downregulation in early-stage HCC cells promoted metastasis via DUSP10 phosphatase-mediated activation of the ERK pathway. The DUSP10 promoter included putative binding sites for p73 directly implicated in modulation by TP53INP1. Overall, our findings show how TP53INP1 plays a critical role in limiting the progression of early-stage HCC, with implications for developing new therapeutic strategies to attack metastatic HCC. .
确定与肝细胞癌(HCC)转移进展相关的关键因素可能提供重要的治疗机会。在这里,我们报告促凋亡应激反应因子 TP53INP1 在晚期 IV 期和转移性人 HCC 肿瘤中经常被选择性地下调。机制研究表明,早期 HCC 细胞中 TP53INP1 的下调通过 DUSP10 磷酸酶介导的 ERK 途径的激活促进了转移。DUSP10 启动子包含直接涉及 TP53INP1 调节的 p73 的假定结合位点。总的来说,我们的研究结果表明 TP53INP1 如何在限制早期 HCC 的进展中发挥关键作用,这对开发新的治疗策略来攻击转移性 HCC 具有重要意义。