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- W4309767539 endingPage "105626" @default.
- W4309767539 startingPage "105626" @default.
- W4309767539 abstract "Tumors with BRCA1 mutations have poor prognoses due to genomic instability. Yet this genomic instability has risks and BRCA1-deficient (def) cancer cells must develop pathways to mitigate these risks. One such risk is the accumulation of unfolded proteins in BRCA1-def cancers from increased mutations due to their loss of genomic integrity. Little is known about how BRCA1-def cancers survive their genomic instability. Here we show that BRCA1 is an E3 ligase in the endoplasmic reticulum (ER) that targets the unfolded protein response (UPR) stress sensors, Eukaryotic Translation Initiation Factor 2-alpha Kinase 3 (PERK) and Serine/Threonine-Protein Kinase/Endoribonuclease Inositol-Requiring Enzyme 1 (IRE1) for ubiquitination and subsequent proteasome-mediated degradation. When BRCA1 is mutated or depleted, both PERK and IRE1 protein levels are increased, resulting in a constitutively activated UPR. Furthermore, the inhibition of protein folding or UPR signaling markedly decreases the overall survival of BRCA1-def cancer cells. Our findings define a mechanism used by the BRCA1-def cancer cells to survive their increased unfolded protein burden which can be used to develop new therapeutic strategies to treat these cancers." @default.
- W4309767539 created "2022-11-29" @default.
- W4309767539 creator A5008820047 @default.
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- W4309767539 creator A5086940969 @default.
- W4309767539 date "2022-12-01" @default.
- W4309767539 modified "2023-09-30" @default.
- W4309767539 title "BRCA1 mediates protein homeostasis through the ubiquitination of PERK and IRE1" @default.
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