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BRCA1-No Matter How You Splice It. | LitMetric

AI Article Synopsis

  • The breast cancer 1 (BRCA1) gene is known for its role in breast cancer susceptibility and is highly subjected to alternative splicing, which may regulate its activity in both hereditary and sporadic cases of breast cancer.
  • Alternative splicing produces different transcripts that can have similar, unique, or even opposing functions compared to the full-length BRCA1 transcript.
  • This review focuses on summarizing these alternative transcripts and discusses advanced next-generation sequencing methods to detect alternative splicing patterns, which could aid in cancer diagnosis, prognosis, and treatment.

Article Abstract

(breast cancer 1, early onset), a well-known breast cancer susceptibility gene, is a highly alternatively spliced gene. alternative splicing may serve as an alternative regulatory mechanism for the inactivation of the gene in both hereditary and sporadic breast cancers, and other -associated cancers. The alternative transcripts of can mimic known functions, possess unique functions compared with the full-length transcript, and in some cases, appear to function in opposition to full-length In this review, we will summarize the functional "naturally occurring" alternative splicing transcripts of and then discuss the latest next-generation sequencing-based detection methods and techniques to detect alternative splicing patterns and their potential use in cancer diagnosis, prognosis, and therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497576PMC
http://dx.doi.org/10.1158/0008-5472.CAN-18-3190DOI Listing

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