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Relationship between DNA Mismatch Repair Deficiency and Endometrial Cancer

Some cases of endometrial cancer are associated with a familial tumor and are referred to as hereditary nonpolyposis colorectal cancer (HNPCC or Lynch syndrome). Lynch syndrome is thought to be induced by germline mutation of the DNA mismatch repair (MMR) gene. An aberration in the MMR gene prevents...

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Detalles Bibliográficos
Autores principales: Masuda, Kenta, Banno, Kouji, Yanokura, Megumi, Kobayashi, Yusuke, Kisu, Iori, Ueki, Arisa, Ono, Asuka, Asahara, Nana, Nomura, Hiroyuki, Hirasawa, Akira, Susumu, Nobuyuki, Aoki, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235885/
https://www.ncbi.nlm.nih.gov/pubmed/22175017
http://dx.doi.org/10.4061/2011/256063
Descripción
Sumario:Some cases of endometrial cancer are associated with a familial tumor and are referred to as hereditary nonpolyposis colorectal cancer (HNPCC or Lynch syndrome). Lynch syndrome is thought to be induced by germline mutation of the DNA mismatch repair (MMR) gene. An aberration in the MMR gene prevents accurate repair of base mismatches produced during DNA replication. This phenomenon can lead to an increased frequency of errors in target genes involved in carcinogenesis, resulting in cancerization of the cell. On the other hand, aberrant DNA methylation is thought to play a key role in sporadic endometrial carcinogenesis. Hypermethylation of unmethylated CpG islands in the promoter regions of cancer-related genes associated with DNA repair leads to the cell becoming cancerous. Thus, both genetic and epigenetic changes are intricately involved in the process through which cells become cancerous. In this review, we introduce the latest findings on the DNA mismatch repair pathway in endometrial cancer.