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Autophagy mitigates metabolic stress and genome damage in mammary tumorigenesis
Vassiliki Karantza‐Wadsworth, Shyam A. Patel, Olga Kravchuk, Guanghua Chen, Robin Mathew, Shengkan Jin, Eileen White
Genes & Development · 2007 · ▲ 833 citations
Abstract
Autophagy(definition) is a catabolic process involving self-digestion of cellular organelles during starvation as a means of cell survival; however, if it proceeds to completion, autophagy can lead to cell death. Autophagy is also a haploinsufficient tumor suppressor mechanism for mammary tumorigenesis, as the essential autophagy regulator beclin1 is monoallelically deleted in breast carcinomas. However, the mechanism by which autophagy suppresses breast cancer remains elusive. Here we show that allelic loss of beclin1 and defective autophagy sensitized mammary epithelial cells to metabolic stress and accelerated lumen formation in mammary acini. Autophagy defects also activated the DNA damage response in vitro and in mammary tumors in vivo, promoted gene amplification, and synergized with defective apoptosis to promote mammary tumorigenesis. Therefore, we propose that autophagy limits metabolic stress to protect the genome, and that defective autophagy increases DNA damage and genomic instability that ultimately facilitate breast cancer progression.
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- 10.1101/gad.1565707
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- 2026-06-05 MST
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APA
Karantza‐Wadsworth, V., Patel, S.A., Kravchuk, O., Chen, G., Mathew, R., Jin, S., & White, E. (2007). Autophagy mitigates metabolic stress and genome damage in mammary tumorigenesis. <em>Genes & Development</em>. https://doi.org/10.1101/gad.1565707
Vancouver
Karantza‐Wadsworth V, Patel SA, Kravchuk O, Chen G, Mathew R, Jin S, et al. Autophagy mitigates metabolic stress and genome damage in mammary tumorigenesis. Genes & Development. 2007. doi:10.1101/gad.1565707.
BibTeX
@article{vassiliki2007Autoph,
title = {Autophagy mitigates metabolic stress and genome damage in mammary tumorigenesis},
author = {Vassiliki Karantza‐Wadsworth and Shyam A. Patel and Olga Kravchuk and Guanghua Chen and Robin Mathew and Shengkan Jin and Eileen White},
journal = {Genes & Development},
year = {2007},
doi = {10.1101/gad.1565707},
}
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