| Literature DB >> 30292352 |
Andrea E Murmann1, Jindan Yu2, Puneet Opal3, Marcus E Peter4.
Abstract
Many neurodegenerative diseases are caused by unstable trinucleotide repeat (TNR) expansions located in disease-associated genes. siRNAs based on CAG repeat expansions effectively kill cancer cell lines in vitro through RNAi. They also cause significant reduction in tumor growth in a human ovarian cancer mouse model with no toxicity to the treated mice. This suggests that cancer cells are particularly sensitive to CAG TNR-derived siRNAs, and explains a reported inverse correlation between the length of CAG TNRs and reduced global cancer incidences in some CAG TNR diseases. This review discusses both mutant proteins and mutant RNAs as a cause of TNR diseases, with a focus on RNAi and its role in contributing to disease pathology and in suppressing cancer.Entities:
Keywords: AR; Huntington’s disease; RNA; SBMA; TNR; cancer
Mesh:
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Year: 2018 PMID: 30292352 PMCID: PMC6613933 DOI: 10.1016/j.trecan.2018.08.004
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025