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Autophagic activity dictates the cellular response to oncogenic RAS
Open accessAbstract
RAS is frequently mutated in human cancers and has opposing effects on autophagy and tumorigenesis. Identifying determinants of the cellular responses to RAS is therefore vital in cancer research. Here, we show that autophagic activity dictates the cellular response to oncogenic RAS. N-terminal Apoptosis-stimulating of p53 protein 2 (ASPP2) mediates RAS-induced senescence and inhibits autophagy. Oncogenic RAS-expressing ASPP2 (Δ3/Δ3) mouse embryonic fibroblasts that escape senescence express a high level of ATG5/ATG12. Consistent with the notion that autophagy levels control the cellular response to oncogenic RAS, overexpressing ATG5, but not autophagy-deficient ATG5 mutant K130R, bypasses RAS-induced senescence, whereas ATG5 or ATG3 deficiency predisposes to it. Mechanistically, ASPP2 inhibits RAS-induced autophagy by competing with ATG16 to bind ATG5/ATG12 and preventing ATG16/ATG5/ATG12 formation. Hence, ASPP2 modulates oncogenic RAS-induced autophagic activity to dictate the cellular response to RAS: to proliferate or senesce.
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“Indeed, some studies have shown that inhibition of autophagy facilitates senescence (Kang et al. 2011a; Wang et al. 2012), but this might be due in part to the loss of cell-protective roles of autophagy, which facilitates senescence effectors under some stressful conditions, where cells are not prone to apoptosis.”
From Cellular senescence and its effector programs (2014) · cites this paper as Wang et al. 2012
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Cites
Autophagy fights disease through cellular self-digestion
Mizushima, N., Levine, B., Cuervo, A. M., & Klionsky, D. J. (2008) · Nature · doi:10.1038/nature06639 · Cited by 6,452
Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a
Serrano, M., Lin, A. W., McCurrach, M. E., Beach, D., & Lowe, S. W. (1997) · Cell · doi:10.1016/s0092-8674(00)81902-9 · Cited by 5,218 · cited 3×
“ASPP2( 3/ 3) + RAS Tu m or W ei gh t ( g) vector (1-1128)(1-360) (123-1128) 0 20 40 60 ASPP2( 3/ 3) + RAS”
BackgroundTargeting RAS signalling pathways in cancer therapy
Downward, J. (2003) · Nature reviews. Cancer · doi:10.1038/nrc969 · Cited by 3,354
Pancreatic cancers require autophagy for tumor growth
Yang, S., Wang, X., Contino, G., Liesa, M., Sahin, E., Ying, H., Bause, A., Li, Y., Stommel, J. M., Dell'Antonio, G., et al. (2011) · Genes & Development · doi:10.1101/gad.2016111 · Cited by 1,498
Self-citationActivated Ras requires autophagy to maintain oxidative metabolism and tumorigenesis
Guo, J. Y., Chen, H.-Y., Mathew, R., Fan, J., Strohecker, A. M., Karsli-Uzunbas, G., Kamphorst, J. J., Chen, G., Lemons, J. M. S., Karantza, V., et al. (2011) · Genes & Development · doi:10.1101/gad.2016311 · Cited by 1,323
Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma
Amaravadi, R. K., Yu, D., Lum, J. J., Bui, T., Christophorou, M. A., Evan, G. I., Thomas‐Tikhonenko, A., & Thompson, C. B. (2007) · Journal of Clinical Investigation · doi:10.1172/jci28833 · Cited by 1,158
Autophagy mediates the mitotic senescence transition
Young, A. R. J., Narita, M., Ferreira, M., Kirschner, K., Sadaie, M., Darot, J. F. J., Tavaré, S., Arakawa, S., Shimizu, S., Watt, F. M., et al. (2009) · Genes & Development · doi:10.1101/gad.519709 · Cited by 1,078
ASPP Proteins Specifically Stimulate the Apoptotic Function of p53
Samuels-Lev, Y., O'Connor, D. J., Bergamaschi, D., Trigiante, G., Hsieh, J.-K., Zhong, S., Campargue, I., Naumovski, L., Crook, T., & Lu, X. (2001) · Molecular Cell · doi:10.1016/s1097-2765(01)00367-7 · Cited by 664
Self-citationAltered Growth of Human Colon Cancer Cell Lines Disrupted at Activated Ki- ras
Shirasawa, S., Furuse, M., Yokoyama, N., & Sasazuki, T. (1993) · Science · doi:10.1126/science.8465203 · Cited by 615
Autophagy: Basic Principles and Relevance to Disease
Kundu, M., & Thompson, C. B. (2008) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev.pathmechdis.2.010506.091842 · Cited by 523
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Mariño, G., Niso-Santano, M., Baehrecke, E. H., & Kroemer, G. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3735 · Cited by 2,172
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Herranz, N., & Gil, J. (2018) · Journal of Clinical Investigation · doi:10.1172/jci95148 · Cited by 1,232
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Galluzzi, L., Pietrocola, F., Bravo‐San Pedro, J. M., Amaravadi, R. K., Baehrecke, E. H., Cecconi, F., Codogno, P., Debnath, J., Gewirtz, D. A., Karantza, V., et al. (2015) · The EMBO Journal · doi:10.15252/embj.201490784 · Cited by 1,182
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Salama, R., Sadaie, M., Hoare, M., & Narita, M. (2014) · Genes & Development · doi:10.1101/gad.235184.113 · Cited by 855
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Gu, Y., Han, J., Jiang, C., & Zhang, Y. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101036 · Cited by 797
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Bryant, K. L., Mancias, J. D., Kimmelman, A. C., & Der, C. J. (2014) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2013.12.004 · Cited by 693
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Pérez-Mancera, P. A., Young, A. R. J., & Narita, M. (2014) · Nature Reviews Cancer · doi:10.1038/nrc3773 · Cited by 462
A dual role for autophagy in a murine model of lung cancer
Rao, S., Tortola, L., Perlot, T., Wirnsberger, G., Novatchkova, M., Nitsch, R., Sykacek, P., Frank, L., Schramek, D., Komnenovic, V., et al. (2014) · Nature Communications · doi:10.1038/ncomms4056 · Cited by 453
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Wiley, C. D., & Campisi, J. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.010 · Cited by 440
Mitochondria in Cell Senescence: Is Mitophagy the Weakest Link?
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“In contrast to the earlier reports suggesting an OIS-promoting role of autophagy (Narita et al., 2011; Young et al., 2009) more recent reports have shown that autophagy can act as a mechanism to bypass RAS-induced senescence and facilitate tumour growth (Wang et al., 2012).”
BackgroundResultMesenchymal Stem/Stromal Cell Senescence: Hallmarks, Mechanisms, and Combating Strategies
Weng, Z., Wang, Y., Ouchi, T., Liu, H., Qiao, X., Wu, C., Zhao, Z., Li, L., & Li, B. (2022) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szac004 · Cited by 303
Self-citationBoone, B. A., Bahary, N., Zureikat, A. H., Moser, A. J., Normolle, D. P., Wu, W.-C., Singhi, A. D., Bao, P., Bartlett, D. L., Liotta, L. A., et al. (2015) · Annals of Surgical Oncology · doi:10.1245/s10434-015-4566-4 · Cited by 234
Chloroquine and hydroxychloroquine for cancer therapy
Manic, G., Obrist, F., Kroemer, G., Vitale, I., & Galluzzi, L. (2014) · Molecular & Cellular Oncology · doi:10.4161/mco.29911 · Cited by 231
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Salminen, A., Kaarniranta, K., & Kauppinen, A. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2012.11.004 · Cited by 173
Autophagy and senescence: A partnership in search of definition
Gewirtz, D. A. (2013) · Autophagy · doi:10.4161/auto.23922 · Cited by 166
Wang, Y., Bu, F., Royer, C., Serres, S., Larkin, J. R., Soto, M. S., Sibson, N. R., Salter, V., Fritzsche, F. R., Turnquist, C., et al. (2014) · Nature Cell Biology · doi:10.1038/ncb3050 · Cited by 145
Self-citationHigh Glucose Induces Bone Marrow-Derived Mesenchymal Stem Cell Senescence by Upregulating Autophagy
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Wang, Y., Xiong, H., Liu, D., Hill, C. N., Ertay, A., Li, J., Zou, Y., Miller, P., White, E., Downward, J., et al. (2019) · Autophagy · doi:10.1080/15548627.2019.1569912 · Cited by 134
Self-citationAutophagy and senescence: A new insight in selected human diseases
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Ferreira, A. I., Pereira, F. D. S., Reis, C. A., Oliveira, M. J., Sousa, M. J., & Preto, A. (2022) · Cells · doi:10.3390/cells11142183 · Cited by 111
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Liu, K., Shi, Y., Guo, X., Wang, S., Ouyang, Y., Hao, M., Liu, D., Qiao, L., Li, N., Zheng, J., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.276 · Cited by 99
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Wang, H., Wang, R., Carrera, I., Xu, S., & Lakshmana, M. K. (2016) · eNeuro · doi:10.1523/eneuro.0042-16.2016 · Cited by 76
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Gong, W., Luo, C., Peng, F., Xiao, J., Zeng, Y., Yin, B., Chen, X., Li, S., He, X., Liu, Y., et al. (2021) · Clinical Science · doi:10.1042/cs20210447 · Cited by 75
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Song, B., Bian, Q., Zhang, Y., Shao, C., Li, G., Liu, A., Jing, W., Liu, R., Zhou, Y., Jin, G., et al. (2015) · Molecular Cancer · doi:10.1186/s12943-015-0447-5 · Cited by 50
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Self-citationHashemi, M., Nadafzadeh, N., Imani, M. H., Rajabi, R., Ziaolhagh, S., Bayanzadeh, S. D., Norouzi, R., Rafiei, R., Koohpar, Z. K., Raei, B., et al. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-023-01053-z · Cited by 52
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Self-citationChen, Z., Bao, N., Chen, S., & Zhao, J. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7206 · Cited by 16
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Shi, H., Zhang, Y., Ji, J., Xu, P., Shi, H., Yue, X., Ren, F., Chen, D., Duan, Z., & Chen, D. (2018) · Scientific Reports · doi:10.1038/s41598-018-36208-3 · Cited by 10
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Metadata
- Authors
- Wang, Y., Wang, X. D., Lapi, E., Sullivan, A., Jia, W., He, Y.-W., Ratnayaka, I., Zhong, S., Goldin, R. D., Goemans, C. G., Tolkovsky, A. M., & Lu, X.
- Affiliations
- University of Oxford (GB)
- Duke Medical Center (US)
- Imperial College London (GB)
- University of Cambridge (GB)
- Ludwig Institute for Cancer Research Ltd., Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7DQ, United Kingdom;
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-07-30
- Volume
- 109
- Issue
- 33
- Pages
- 13325-13330
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3421174
- OpenAlex
- W2074957956
- Cited by
- 117
- References
- 31
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 3 · 2023: 6 · 2022: 13 · 2021: 9 · 2020: 4 · 2019: 7 · 2018: 12 · 2017: 11 · 2016: 9 · 2015: 9 · 2014: 18 · 2013: 8 · 2012: 3
- FWCI
- 9.10
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Wellcome Trust
- National Institute of Allergy and Infectious Diseases (R01AI074944)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- oncogenic Ras, autophagy, cellular senescence, ASPP2, ATG5, ATG12, Atg16, ATG3, mouse embryonic fibroblasts, Ras-induced senescence, carcinogenesis, p53
- MeSH terms
- Autophagy-Related Protein 5, Autophagy-Related Protein 12, Animals, Autophagy, Embryo, Nonmammalian, Fibroblasts, Humans, Microtubule-Associated Proteins, Oncogenes, Protein Binding, Proteins, Proto-Oncogene Proteins p21(ras), Cellular Senescence, Tumor Suppressor Proteins, Multiprotein Complexes, Mice, Protein Stability
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