Prolonged particulate hexavalent chromium exposure suppresses homologous recombination repair in human lung cells

Cynthia L. Browning, Qin Qin, Deborah F. Kelly, Rohit Prakash, Fabio Vanoli, Maria Jasin, John Pierce Wise

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Genomic instability is one of the primary models of carcinogenesis and a feature of almost all cancers. Homologous recombination (HR) repair protects against genomic instability by maintaining high genomic fidelity during the repair of DNA double strand breaks. The defining step of HR repair is the formation of the Rad51 nucleofilament, which facilitates the search for a homologous sequence and invasion of the template DNA strand. Particulate hexavalent chromium (Cr(VI)), a human lung carcinogen, induces DNA double strand breaks and chromosome instability. Since the loss of HR repair increases Cr(VI)-induced chromosome instability, we investigated the effect of extended Cr(VI) exposure on HR repair. We show acute (24 h) Cr(VI) exposure induces a normal HR repair response. In contrast, prolonged (120 h) exposure to particulate Cr(VI) inhibited HR repair and Rad51 nucleofilament formation. Prolonged Cr(VI) exposure had a profound effect on Rad51, evidenced by reduced protein levels and Rad51 mislocalization to the cytoplasm. The response of proteins involved in Rad51 nuclear import and nucleofilament formation displayed varying responses to prolonged Cr(VI) exposure. BRCA2 formed nuclear foci after prolonged Cr(VI) exposure, while Rad51C foci formation was suppressed. These results suggest that particulate Cr(VI), a major chemical carcinogen, inhibits HR repair by targeting Rad51, causing DNA double strand breaks to be repaired by a low fidelity, Rad51-independent repair pathway. These results further enhance our understanding of the underlying mechanism of Cr(VI)-induced chromosome instability and thus, carcinogenesis.

Original languageEnglish (US)
Pages (from-to)70-78
Number of pages9
JournalToxicological Sciences
Volume153
Issue number1
DOIs
StatePublished - Sep 1 2016

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Recombinational DNA Repair
Repair
Lung
Chromosomal Instability
Double-Stranded DNA Breaks
Chromosomes
DNA
Genomic Instability
Carcinogens
chromium hexavalent ion
Carcinogenesis
Cell Nucleus Active Transport
Sequence Homology
Proteins
Cytoplasm

All Science Journal Classification (ASJC) codes

  • Toxicology

Cite this

Browning, Cynthia L. ; Qin, Qin ; Kelly, Deborah F. ; Prakash, Rohit ; Vanoli, Fabio ; Jasin, Maria ; Wise, John Pierce. / Prolonged particulate hexavalent chromium exposure suppresses homologous recombination repair in human lung cells. In: Toxicological Sciences. 2016 ; Vol. 153, No. 1. pp. 70-78.
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Prolonged particulate hexavalent chromium exposure suppresses homologous recombination repair in human lung cells. / Browning, Cynthia L.; Qin, Qin; Kelly, Deborah F.; Prakash, Rohit; Vanoli, Fabio; Jasin, Maria; Wise, John Pierce.

In: Toxicological Sciences, Vol. 153, No. 1, 01.09.2016, p. 70-78.

Research output: Contribution to journalArticle

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AU - Browning, Cynthia L.

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