Zheng Hua-Chuan, Liu Li-Li
Department of Experimental Oncology and Animal Center, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Department of Pathology, Harbin Medical University-Daqing, Daqing 163319, China.
Oncotarget. 2017 Nov 3;8(64):108261-108273. doi: 10.18632/oncotarget.22369. eCollection 2017 Dec 8.
FHIT (fragile histine triad) acts as diadenosine P1, P3-bis (5'-adenosyl)-triphosphate adenylohydrolase involved in purine metabolism, and induces apoptosis as a tumor suppressor. We performed a systematic meta- and bioinformatics analysis through multiple online databases up to March 14, 2017. The down-regulated FHIT expression was found in gastric cancer, compared with normal mucosa and dysplasia ( < 0.05). FHIT expression was negatively with depth of invasion, lymph node metastasis, distant metastasis, TNM staging and dedifferentiation of gastric cancer ( < 0.05). A positive association between FHIT expression and favorable overall survival was found in patients with gastric cancer ( < 0.05). According to Kaplan-Meier plotter, we found that a higher FHIT expression was negatively correlated with overall and progression-free survival rates of all cancer patients, even stratified by aggressive parameters ( < 0.05). These findings indicated that FHIT expression might be employed as a potential marker to indicate gastric carcinogenesis and subsequent progression, even prognosis.
脆性组氨酸三联体(FHIT)作为一种参与嘌呤代谢的二腺苷P1,P3 - 双(5'-腺苷)-三磷酸腺苷水解酶,并作为肿瘤抑制因子诱导细胞凋亡。我们通过多个在线数据库进行了一项截至2017年3月14日的系统的荟萃分析和生物信息学分析。与正常黏膜和发育异常相比,在胃癌中发现FHIT表达下调(<0.05)。FHIT表达与胃癌的浸润深度、淋巴结转移、远处转移、TNM分期和去分化呈负相关(<0.05)。在胃癌患者中发现FHIT表达与良好的总生存率呈正相关(<0.05)。根据Kaplan-Meier绘图仪,我们发现较高的FHIT表达与所有癌症患者的总生存率和无进展生存率呈负相关,即使按侵袭性参数分层也是如此(<0.05)。这些发现表明,FHIT表达可能被用作一种潜在的标志物来指示胃癌的发生、后续进展甚至预后。