The CpG Island Methylator Phenotype Status in Synchronous and Solitary Primary Colorectal Cancers: Prognosis and Effective Therapeutic Drug Prediction

被引:2
作者
Weng, Yun-Yun [1 ]
Huang, Ming-Yii [1 ,2 ]
机构
[1] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Radiat Oncol, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Coll Med, Sch Med, Dept Radiat Oncol, Kaohsiung 807, Taiwan
关键词
CpG island methylator phenotype; synchronous colorectal cancers; therapeutic drug; MICROSATELLITE INSTABILITY; DNA METHYLATION; CLINICOPATHOLOGICAL FEATURES; MOLECULAR CLASSIFICATION; BRAF MUTATION; COLON; CARCINOMA; SUBSETS; ADENOCARCINOMAS; HETEROGENEITY;
D O I
10.3390/ijms25105243
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synchronous colorectal cancer (sCRC) is characterized by the occurrence of more than one tumor within six months of detecting the first tumor. Evidence suggests that sCRC might be more common in the serrated neoplasia pathway, marked by the CpG island methylator phenotype (CIMP), than in the chromosomal instability pathway (CIN). An increasing number of studies propose that CIMP could serve as a potential epigenetic predictor or prognostic biomarker of sCRC. Therapeutic drugs already used for treating CIMP-positive colorectal cancers (CRCs) are reviewed and drug selections for sCRC patients are discussed.
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页数:14
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