癌症
DNA甲基化
甲基化
生物
癌症研究
计算生物学
分子生物学
基因
基因表达
遗传学
作者
Jianbiao Xu,Jianlin Song,Tong‐Min Wang,Wenchuan Zhu,Liangyu Zuo,Jinzhi Wu,Jianhui Guo,Xiaochun Yang
出处
期刊:Epigenomics
[Future Medicine]
日期:2021-10-01
卷期号:13 (19): 1557-1570
被引量:16
标识
DOI:10.2217/epi-2021-0080
摘要
Aim: This study aimed to validate a combination of mSEPT9, mRNF180 and CA724 for gastric cancer (GC) detection. Patients & methods: The performance of mSEPT9, mRNF180 and CA724 was examined in a prospective cohort study with 518 participants (151 with GC, 56 with atrophic gastritis, 87 with other gastrointestinal diseases and 224 with no evidence of disease). Results: mSEPT9, mRNF180 or CA724 alone detected 48.3, 37.1 and 43.1% of GC, respectively. The combination of mSEPT9 and mRNF180 detected 60.3% of GC, and the combination of all three markers detected 68.6% of GC. The detection sensitivity of mSEPT9 and mRNF180 was significantly higher for gastric body and in elder subjects. mSEPT9 was correlated with poorer GC survival. Conclusion: The combination of mSEPT9, mRNF180 and CA724 was adequately sensitive for GC detection. The blood mSEPT9 was predictive for GC prognosis.
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