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丝氨酸羟甲基转移酶2(SHMT2)表达增加与口腔鳞状细胞癌的不良预后和高级别病理分级相关。

Increased Expression of SHMT2 Is Associated With Poor Prognosis and Advanced Pathological Grade in Oral Squamous Cell Carcinoma.

作者信息

Wu Zhi-Zhong, Wang Shuo, Yang Qi-Chao, Wang Xiao-Long, Yang Lei-Lei, Liu Bing, Sun Zhi-Jun

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST), Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, China.

Department of Oral Maxillofacial Head and Neck Oncology, School and Hospital of Stomatology, Wuhan University, Wuhan, China.

出版信息

Front Oncol. 2020 Oct 9;10:588530. doi: 10.3389/fonc.2020.588530. eCollection 2020.

Abstract

This study focused on the expression of mitochondrial serine hydroxymethyltransferase (SHMT2) in oral squamous cell carcinoma (OSCC) and its correlation with clinical traits and the prognosis of OSCC patients. Immunochemical staining and Western blotting were used to quantify the expression of SHMT2 and related immune markers in OSCC. Using OSCC microarrays and The Cancer Genome Atlas (TCGA) database, we evaluated the association between SHMT2 and various clinical traits. We found that increased expression of SHMT2 was detected in OSCC and correlated with advanced pathological grade and recurrence of OSCC. By a multivariate Cox proportional hazard model, high expression of SHMT2 was shown to indicate a negative prognosis. In addition, in the OSCC microenvironment, increasing the expression of SHMT2 was associated with high expression levels of programmed cell death-ligand 1 (PD-L1), CKLF-like MARVEL transmembrane domain containing 6 (CMTM6), V-type immunoglobulin domain-containing suppressor (VISTA), B7-H4, Slug, and CD317. In the future, more effort will be required to investigate the role of SHMT2 in the OSCC microenvironment.

摘要

本研究聚焦于线粒体丝氨酸羟甲基转移酶(SHMT2)在口腔鳞状细胞癌(OSCC)中的表达及其与OSCC患者临床特征和预后的相关性。采用免疫化学染色和蛋白质印迹法对OSCC中SHMT2及相关免疫标志物的表达进行定量分析。利用OSCC基因芯片和癌症基因组图谱(TCGA)数据库,我们评估了SHMT2与各种临床特征之间的关联。我们发现,在OSCC中检测到SHMT2表达增加,且与OSCC的高级别病理分级和复发相关。通过多变量Cox比例风险模型显示,SHMT2高表达提示预后不良。此外,在OSCC微环境中,SHMT2表达增加与程序性细胞死亡配体1(PD-L1)、含CKLF样MARVEL跨膜结构域6(CMTM6)、含V型免疫球蛋白结构域的抑制因子(VISTA)、B7-H4、锌指蛋白Slug和CD317的高表达水平相关。未来,需要更多的研究来探究SHMT2在OSCC微环境中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23fd/7581701/c75eef00bdf8/fonc-10-588530-g001.jpg

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