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MiR223-3p promotes synthetic lethality in BRCA1-deficient cancers.
Srinivasan, Gayathri; Williamson, Elizabeth A; Kong, Kimi; Jaiswal, Aruna S; Huang, Guangcun; Kim, Hyun-Suk; Schärer, Orlando; Zhao, Weixing; Burma, Sandeep; Sung, Patrick; Hromas, Robert.
Afiliação
  • Srinivasan G; Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Williamson EA; Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Kong K; Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Jaiswal AS; Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Huang G; Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Kim HS; Center for Genomic Integrity, Institute for Basic Science, Ulsan 689-798, Republic of Korea.
  • Schärer O; Center for Genomic Integrity, Institute for Basic Science, Ulsan 689-798, Republic of Korea.
  • Zhao W; Department of Biological Sciences, School of Life Sciences, Ulsan National Institute of Science and Technology, Ulsan 44919, Republic of Korea.
  • Burma S; Department of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Sung P; Department of Biochemistry and Structural Biology, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
  • Hromas R; Department of Neurosurgery, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229.
Proc Natl Acad Sci U S A ; 116(35): 17438-17443, 2019 08 27.
Article em En | MEDLINE | ID: mdl-31395736
Defects in DNA repair give rise to genomic instability, leading to neoplasia. Cancer cells defective in one DNA repair pathway can become reliant on remaining repair pathways for survival and proliferation. This attribute of cancer cells can be exploited therapeutically, by inhibiting the remaining repair pathway, a process termed synthetic lethality. This process underlies the mechanism of the Poly-ADP ribose polymerase-1 (PARP1) inhibitors in clinical use, which target BRCA1 deficient cancers, which is indispensable for homologous recombination (HR) DNA repair. HR is the major repair pathway for stressed replication forks, but when BRCA1 is deficient, stressed forks are repaired by back-up pathways such as alternative nonhomologous end-joining (aNHEJ). Unlike HR, aNHEJ is nonconservative, and can mediate chromosomal translocations. In this study we have found that miR223-3p decreases expression of PARP1, CtIP, and Pso4, each of which are aNHEJ components. In most cells, high levels of microRNA (miR) 223-3p repress aNHEJ, decreasing the risk of chromosomal translocations. Deletion of the miR223 locus in mice increases PARP1 levels in hematopoietic cells and enhances their risk of unprovoked chromosomal translocations. We also discovered that cancer cells deficient in BRCA1 or its obligate partner BRCA1-Associated Protein-1 (BAP1) routinely repress miR223-3p to permit repair of stressed replication forks via aNHEJ. Reconstituting the expression of miR223-3p in BRCA1- and BAP1-deficient cancer cells results in reduced repair of stressed replication forks and synthetic lethality. Thus, miR223-3p is a negative regulator of the aNHEJ DNA repair and represents a therapeutic pathway for BRCA1- or BAP1-deficient cancers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína BRCA1 / Predisposição Genética para Doença / MicroRNAs / Mutações Sintéticas Letais / Neoplasias Limite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína BRCA1 / Predisposição Genética para Doença / MicroRNAs / Mutações Sintéticas Letais / Neoplasias Limite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2019 Tipo de documento: Article País de publicação: Estados Unidos