综合分析和鉴定m6A RNA甲基化调节因子对前列腺癌进展及预后的影响
张乐1, 宁静华1, 张鑫1, 王振1, 刘虹汝1, 张钰哲1,2,31. 大理大学基础医学院病理学与病理生理学教研室, 云南 大理 671000;
2. 云南抗病原药用植物筛选重点实验室, 云南 大理 671000;
3. 云南省昆虫生物医药重点实验室, 云南 大理 671000
收稿日期:
2022-12-31出版日期:
2023-11-30发布日期:
2023-11-07通讯作者:
张钰哲E-mail:lzuzyz1568@hotmail.com作者简介:
张乐(1996-),女,硕士研究生.基金资助:
云南省地方本科高校(部分)基础研究联合专项面上项目(202001BA070001-064,202101BA070001-102);云南省昆虫生物医药研发重点实验室开放课题立项项目(AP2022016);大理大学博士科研启动费立项项目(KYBS2018012)关键词: m6A, 前列腺癌, 癌症基因组图谱, 甲基化修饰, ROMO1
Abstract: Objective To analyze N6-methyladenosine (m6A) RNA methylation regulators using data from The Cancer Genome Atlas (TCGA) and explore the molecular characteristics and clinical significance of m6A regulators in prostate cancer progression. Methods Prostate cancer data were analyzed with respect to 13 m6A regulators to identify different subgroups and perform differential expression analyses. The LASSO Cox regression model was constructed based on the differentially expressed genes. Kaplan-Meier survival curves and receiver operator characteristic curves were drawn. The area under the curve was calculated to determine the predictive performance of the model. Key factors were analyzed based on immune infiltration. Results Based on the 13 m6A regulators, subgroups closely associated with prostate cancer development were identified, and a risk model was constructed using six m6A regulatorys (OAS3, MYOF, SMIM22, SNORD60, ROMO1, and MRPL41). ROMO1 is highly expressed in prostate cancer and is strongly correlated with the immune infiltration of CD8+T cells. Conclusion The results of this study show that the expression of m6A regulators is highly correlated with the clinicopathological features of prostate cancer. ROMO1 may serve as an independent biomarker to predict the prognosis of prostate cancer. The high expression of ROMO1 in prostate cancer provides clues for understanding and exploring the early diagnosis and clinical treatment of prostate cancer from the perspective of epigenetic modification of mRNA.
Key words: m6A, prostate cancer, The Cancer Genome Atlas, methylation modification, ROMO1
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