Ontology highlight
ABSTRACT: Objectives
Approximately 35% of colorectal cancer (CRC) risk is attributable to heritable factors known hereditary syndromes, accounting for 6%. The remainder may be due to lower penetrance polymorphisms particularly of DNA repair genes. DNA repair pathways, including base excision repair (BER), nucleotide excision repair (NER), mismatch repair (MMR), direct reversal repair (DRR), and double-strand break repair are complex, evolutionarily conserved, and critical in carcinogenesis. Germline mutations in these genes are associated with high-penetrance CRC syndromes such as Lynch syndrome. However, the association of low-penetrance polymorphisms of DNA repair genes with CRC risk remains unclear.Methods
A systematic literature review of PubMed, Embase, and HuGENet databases was
SUBMITTER: Aggarwal N
PROVIDER: S-EPMC5539343 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature