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糖苷转移酶 B4GALNT2 作为结肠癌预后良好的预测因子:来自数据库的经验。

Glycosyltransferase B4GALNT2 as a Predictor of Good Prognosis in Colon Cancer: Lessons from Databases.

机构信息

Department of Experimental, Diagnostic and Specialty Medicine (DIMES), General Pathology Building, University of Bologna, Via San Giacomo 14, 40126 Bologna, Italy.

出版信息

Int J Mol Sci. 2021 Apr 21;22(9):4331. doi: 10.3390/ijms22094331.

Abstract

BACKGROUND

glycosyltransferase B4GALNT2 and its cognate carbohydrate antigen Sd are highly expressed in normal colon but strongly downregulated in colorectal carcinoma (CRC). We previously showed that CRC patients expressing higher mRNA levels displayed longer survival. Forced expression reduced the malignancy and stemness of colon cancer cells.

METHODS

Kaplan-Meier survival curves were determined in "The Cancer Genome Atlas" (TCGA) COAD cohort for several glycosyltransferases, oncogenes, and tumor suppressor genes. Whole expression data of coding genes as well as miRNA and methylation data for were downloaded from TCGA.

RESULTS

the prognostic potential of was the best among the glycosyltransferases tested and better than that of many oncogenes and tumor suppressor genes; high expression was associated with a lower malignancy gene expression profile; differential methylation of an intronic gene position and miR-204-5p expression play major roles in regulation.

CONCLUSIONS

high expression is a strong predictor of good prognosis in CRC as a part of a wider molecular signature that includes , , , and . Differential DNA methylation and miRNA expression contribute to regulating expression during colorectal carcinogenesis.

摘要

背景

糖基转移酶 B4GALNT2 及其同源碳水化合物抗原 Sd 在正常结肠中高度表达,但在结直肠癌(CRC)中强烈下调。我们之前表明,表达更高水平 mRNA 的 CRC 患者具有更长的生存时间。强制表达降低了结肠癌细胞的恶性程度和干性。

方法

在“癌症基因组图谱”(TCGA)COAD 队列中确定了几种糖基转移酶、癌基因和肿瘤抑制基因的 Kaplan-Meier 生存曲线。从 TCGA 下载了编码基因的全表达数据以及 miRNA 和 甲基化数据。

结果

在所测试的糖基转移酶中, 的预后潜力是最好的,优于许多癌基因和肿瘤抑制基因;高表达与较低的恶性基因表达谱相关;内含子 基因位置的差异甲基化和 miR-204-5p 的表达在 调控中起主要作用。

结论

高表达是 CRC 预后良好的强烈预测因子,是一个更广泛的分子特征的一部分,包括 、 、 、和 。结直肠发生过程中差异 DNA 甲基化和 miRNA 表达有助于调节 表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8d9/8122605/6136db35b8f6/ijms-22-04331-g001.jpg

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