高表达的线粒体裂变调节因子2与食管鳞状细胞癌患者生存不良的关系

IF 2.5 Q3 ONCOLOGY
Hongwei Li, Xingzhuang Zhu, Wei Zhang, Wenjie Lu, Chuan Liu, Jinbo Ma, Rukun Zang, Yipeng Song
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引用次数: 0

摘要

线粒体裂变调节因子2 (MTFR2)与线粒体分裂有关,但很少有研究评估MTFR2表达与食管鳞状细胞癌(ESCC)临床特征或预后之间的关系。本研究采用免疫组化(IHC)方法比较了6例ESCC肿瘤和相对正常组织中MTFR2的表达。为了评估MTFR2表达对临床病理特征和生存的影响,我们对115例石蜡包埋的ESCC组织样本进行了免疫组化染色。此外,我们还研究了ESCC患者的临床病理特性与MTFR2表达之间的关系。生存率分析采用Cox回归模型。我们发现,与正常食管上皮细胞相比,MTFR2在ESCC肿瘤中的表达显著增加。对115例患者石蜡包埋的ESCC肿瘤标本进行免疫组化分析发现,MTFR2的表达与临床分期(P < 0.001)、肿瘤分型(P < 0.001)、组织学分级(P < 0.001)等临床病理特征有显著相关性。单因素和多因素分析均显示,MTFR2表达与ESCC患者的生存率呈负相关。综上所述,MTFR2的表达与ESCC的临床病理特征及预后显著相关。因此,MTFR2表达可作为ESCC患者潜在的重要预后生物标志物和临床靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association of High Expression of Mitochondrial Fission Regulator 2 with Poor Survival of Patients with Esophageal Squamous Cell Carcinoma.

Association of High Expression of Mitochondrial Fission Regulator 2 with Poor Survival of Patients with Esophageal Squamous Cell Carcinoma.

Association of High Expression of Mitochondrial Fission Regulator 2 with Poor Survival of Patients with Esophageal Squamous Cell Carcinoma.

Association of High Expression of Mitochondrial Fission Regulator 2 with Poor Survival of Patients with Esophageal Squamous Cell Carcinoma.

Mitochondrial fission regulator 2 (MTFR2) is associated with mitochondrial fission, while few studies have assessed the associations between MTFR2 expression and clinical characteristics or prognosis of esophageal squamous cell carcinoma (ESCC). In this study, we compared the expression of MTFR2 in 6 ESCC tumors and relative normal tissues by immunohistochemistry (IHC). To assess the effect of MTFR2 expression on clinicopathologic characteristics and survival, 115 paraffin embedded ESCC tissue samples were assessed by IHC staining. Furthermore, the association between clinicopathological properties and MTFR2 expression in patients with ESCC was examined. The survival analysis was performed using the Cox regression models. We found that MTFR2 expression was significantly increased in ESCC tumors compared with normal esophageal epithelial cells. IHC analysis of 115 paraffin embedded ESCC tumor specimens of the patients showed that the expression of MTFR2 was significantly associated with clinical stage (P < 0.001), tumor classification (P < 0.001), histological grade (P < 0.001), and other clinicopathological characteristics. Both univariate and multivariate analyses showed that MTFR2 expression was inversely correlated with the survival of ESCC patients. In conclusion, the expression of MTFR2 is significantly associated with clinicopathologic characteristics and prognosis of ESCC. Thus, MTFR2 expression could serve as a potentially important prognostic biomarker and clinical target for patients with ESCC.

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