Fudan University Shanghai Cancer Center and Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, China.
Liver Cancer Institute, Zhongshan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Hepatology. 2018 Jan;67(1):171-187. doi: 10.1002/hep.29405. Epub 2017 Nov 15.
Long noncoding RNAs can serve as oncogenes or tumor suppressors in human cancer; however, their biological functions and underlying mechanism in hepatocarcinogenesis are largely unknown. Here, we report a novel tumor suppressor long noncoding RNA on chromosome 8p12 (termed TSLNC8) that is frequently deleted and down-regulated in hepatocellular carcinoma (HCC) tissues. The loss of TSLNC8 is highly associated with the malignant features of HCC and serves as a prognostic indicator for HCC patients. TSLNC8 significantly suppresses the proliferation and metastasis of HCC cells in vitro and in vivo. TSLNC8 exerts its tumor suppressive activity by competitively interacting with transketolase and signal transducer and activator of transcription 3 (STAT3) and modulating the STAT3-Tyr705 and STAT3-Ser727 phosphorylation levels and STAT3 transcriptional activity, thus resulting in inactivation of the interleukin-6-STAT3 signaling pathway in HCC cells.
TSLNC8 is a promising prognostic predictor for patients with HCC, and the TSLNC8-transketolase-STAT3 axis is a potential therapeutic target for HCC treatment. (Hepatology 2018;67:171-187).
长非编码 RNA 可作为人类癌症中的癌基因或肿瘤抑制因子;然而,它们在肝癌发生中的生物学功能和潜在机制在很大程度上尚不清楚。在这里,我们报告了一种新型的肿瘤抑制性长非编码 RNA,位于 8p12 染色体上(称为 TSLNC8),在肝癌组织中经常缺失和下调。TSLNC8 的丢失与 HCC 的恶性特征高度相关,并且是 HCC 患者的预后指标。TSLNC8 显著抑制 HCC 细胞的体外和体内增殖和转移。TSLNC8 通过与转酮醇酶和信号转导子和转录激活子 3(STAT3)竞争性相互作用,以及调节 STAT3-Tyr705 和 STAT3-Ser727 磷酸化水平和 STAT3 转录活性,从而使 HCC 细胞中的白细胞介素-6-STAT3 信号通路失活,发挥其肿瘤抑制活性。
TSLNC8 是 HCC 患者有前途的预后预测因子,TSLNC8-转酮醇酶-STAT3 轴是 HCC 治疗的潜在治疗靶点。(《肝脏病学》2018 年;67:171-187)。