Xia Hongwei, Chen Qingjuan, Chen Ying, Ge Xiaojun, Leng Weibing, Tang Qiulin, Ren Ming, Chen Liang, Yuan Dandan, Zhang Yucheng, Liu Ming, Gong Qiyong, Bi Feng
Laboratory of Signal Transduction & Molecular Targeted Therapy, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu, Sichuan Province, China.
Department of Medical Oncology, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Oncotarget. 2016 Aug 30;7(35):56209-56218. doi: 10.18632/oncotarget.10941.
The metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is frequently over-expressed and serves as a prognostic marker in human cancers. However, little is known about the role of MALAT1 in gastric cancer. Here, we reported that the tissue and plasma MALAT1 levels were significantly higher in gastric cancer patients with distant metastasis (P<0.01) than patients without distant metastasis and the healthy controls. In addition, high levels of plasma MALAT1 independently correlated to a poor prognosis for gastric cancer patients (hazard ratio, 0.242; 95% CI, 0.154-0.836; P=0.036; Cox regression analysis). Functional studies revealed that knockdown of MALAT1 could inhibit cell proliferation, cell cycle progression, migration and invasion, and promote apoptosis in gastric cancer cells. Furthermore, the miR-122-IGF-1R signaling correlated with the dysregulated MALAT1 expression in gastric cancer. These data suggest that MALAT1 could function as an oncogene in gastric cancer, and high MALAT1 level could serve as a potential biomarker for the distant metastasis of gastric cancer.
转移相关的肺腺癌转录本1(MALAT1)在人类癌症中经常过度表达,并作为一种预后标志物。然而,关于MALAT1在胃癌中的作用知之甚少。在此,我们报道,远处转移的胃癌患者的组织和血浆MALAT1水平显著高于无远处转移的患者和健康对照(P<0.01)。此外,血浆MALAT1水平高与胃癌患者预后不良独立相关(风险比,0.242;95%置信区间,0.154 - 0.836;P = 0.036;Cox回归分析)。功能研究表明,敲低MALAT1可抑制胃癌细胞的增殖、细胞周期进程、迁移和侵袭,并促进其凋亡。此外,miR - 122 - IGF - 1R信号通路与胃癌中MALAT1表达失调相关。这些数据表明,MALAT1可能在胃癌中作为癌基因发挥作用,且高MALAT1水平可作为胃癌远处转移的潜在生物标志物。