The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Hypoxia regulates TSC1/2–mTOR signaling and tumor suppression through REDD1-mediated 14–3–3 shuttling
Open accessAbstract
Hypoxia induces rapid and dramatic changes in cellular metabolism, in part through inhibition of target of rapamycin (TOR) kinase complex 1 (TORC1) activity. Genetic studies have shown the tuberous sclerosis tumor suppressors TSC1/2 and the REDD1 protein to be essential for hypoxia regulation of TORC1 activity in Drosophila and in mammalian cells. The molecular mechanism and physiologic significance of this effect of hypoxia remain unknown. Here, we demonstrate that hypoxia and REDD1 suppress mammalian TORC1 (mTORC1) activity by releasing TSC2 from its growth factor-induced association with inhibitory 14–3–3 proteins. Endogenous REDD1 is required for both dissociation of endogenous TSC2/14–3–3 and inhibition of mTORC1 in response to hypoxia. REDD1 mutants that fail to bind 14–3–3 are defective in eliciting TSC2/14–3–3 dissociation and mTORC1 inhibition, while TSC2 mutants that do not bind 14-3-3 are inactive in hypoxia signaling to mTORC1. In vitro, loss of REDD1 signaling promotes proliferation and anchorage-independent growth under hypoxia through mTORC1 dysregulation. In vivo, REDD1 loss elicits tumorigenesis in a mouse model, and down-regulation of REDD1 is observed in a subset of human cancers. Together, these findings define a molecular mechanism of signal integration by TSC1/2 that provides insight into the ability of REDD1 to function in a hypoxia-dependent tumor suppressor pathway.
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“A recent study showed that endogenous Redd1 is required for both dissociation of endogenous TSC2/14–3-3 proteins and inhibition of mTOR in response to hypoxia [127].”
From PKR, the double stranded RNA‐dependent protein kinase as a critical target in Alzheimer's disease (2009) · cites this paper as [127]
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“Another example of this localization dependency includes hypoxia-dependent regulation through REDD1 (Brugarolas et al., 2004), which disrupts cytosolic 14-3-3-bound TSC2 and enables subsequent TSC2 localization to the lysosome where it can inhibit Rheb (DeYoung et al., 2008).”
From Signal integration in the (m)TORC1 growth pathway (2018) · cites this paper as DeYoung et al., 2008
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Upstream and downstream of mTOR
Hay, N., & Sonenberg, N. (2004) · Genes & Development · doi:10.1101/gad.1212704 · Cited by 4,181
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Inoki, K., Li, Y., Zhu, T., Wu, J., & Guan, K.-L. (2002) · Nature Cell Biology · doi:10.1038/ncb839 · Cited by 3,083
Defining the role of mTOR in cancer
Guertin, D. A., & Sabatini, D. M. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.05.008 · Cited by 2,833
Rheb GTPase is a direct target of TSC2 GAP activity and regulates mTOR signaling
Inoki, K., Li, Y., Xu, T., & Guan, K.-L. (2003) · Genes & Development · doi:10.1101/gad.1110003 · Cited by 1,911
Shaw, R. J., Kosmatka, M., Bardeesy, N., Hurley, R. L., Witters, L. A., DePinho, R. A., & Cantley, L. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308061100 · Cited by 1,797
The Tuberous Sclerosis Complex
Crino, P. B., Nathanson, K. L., & Henske, E. P. (2006) · New England Journal of Medicine · doi:10.1056/nejmra055323 · Cited by 1,793
Growing roles for the mTOR pathway
Sarbassov, D. D., Ali, S. M., & Sabatini, D. M. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.09.009 · Cited by 1,590
Manning, B. D., Tee, A. R., Logsdon, M. N., Blenis, J., & Cantley, L. C. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00568-3 · Cited by 1,555
Brugarolas, J., Lei, K., Hurley, R. L., Manning, B. D., Reiling, J. H., Hafen, E., Witters, L. A., Ellisen, L. W., & Kaelin, W. G. (2004) · Genes & Development · doi:10.1101/gad.1256804 · Cited by 1,384
Self-citationGene expression profiling identifies clinically relevant subtypes of prostate cancer
Lapointe, J., Li, C., Higgins, J., van de Rijn, M., Bair, E., Montgomery, K. D., Ferrari, M. K., Egevad, L., Rayford, W., Bergerheim, U. S. R., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0304146101 · Cited by 1,282
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Inhibition of mTOR Signalling: A Potential Anti-aging Drug Strategy
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Dera, H. S. A., Eleawa, S. M., Al-Hashem, F. H., Mahzari, M. M., Hoja, I. M., & Alkhateeb, M. A. (2017) · Archives of Physiology and Biochemistry · doi:10.1080/13813455.2016.1275701 · Cited by 2
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Yao, Y., Parnell, N., & Inoki, K. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-394447-4.30035-9 · Cited by 3
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Manning, B. D. (2010) · Wiley eBooks · doi:10.1002/9783527630073.ch6 · Cited by 2
In vitro analysis of potential anticancer effects associated with watercress
Cavell, B. E. (2012) · ePrints Soton (University of Southampton) · Cited by 2
Goz, R. U., Silas, A., Buzel, S., & LoTurco, J. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/544973 · Cited by 1
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Manshadi, M. D., Tajik, F., Zanjani, L. S., Hashemi, F., Rahimi, M., Fattahi, F., Safaei, S., Madjd, Z., & Ghods, R. (2025) · Discover Oncology · doi:10.1007/s12672-025-02065-6 · Cited by 1
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Wang, T., Zhang, W., Gong, S., Zeng, L., Tao, Y., Chang, L., Wei, Q., Yang, Y., Zining, M., & Liu, X. L. (2026) · Aquaculture Reports · doi:10.1016/j.aqrep.2026.103459 · Cited by 1
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Murakami, T. (2012) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.1.163
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Georgievich, R. V., & Константинович, П. В. (2013)
Swerdlow, S. (2010) · OhioLink ETD Center (Ohio Library and Information Network)
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Nogueira, D. A. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2017.tde-09122016-154805
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Soliman, M. A. (2014) · TSpace (University of Toronto)
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Thème 2. Nutrition et contrôle de la masse musculaire dans les sports à challenge métabolique
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Bigard, X. A., & Malgoyre, A. (2015) · INSEP-Éditions eBooks · doi:10.4000/books.insep.1874
Heberle, A. M. (2019) · University of Groningen research database (University of Groningen / Centre for Information Technology)
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Koltai, T., Reshkin, S. J., Baltazar, F., & Fliegel, L. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90528-2.00006-0
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Huang, J., & Li, J. (2018) · Ibrain · doi:10.1002/j.2769-2795.2018.tb00027.x
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Theye, C. C. D. (2016) · Research Publications (Maastricht University) · doi:10.26481/dis.20160122cd
Faculty Opinions recommendation of mTOR at the nexus of nutrition, growth, ageing and disease.
Ferguson, S. M. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.737205281.793574661
Wu, Y., Ko, B., & Liou, J. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_101693-1
mTORC1: Upstream and Downstream
Yao, Y., & Inoki, K. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00182-6
Shin, U., You, H., Lee, G. Y., Son, Y., & Han, S. N. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4163419
Translation initiation and dysregulation of initiation factors in rare diseases
Kamble, V. S., Pachpor, T. A., Khandagale, S. B., Wagh, V. V., & Khare, S. (2022) · Gene Reports · doi:10.1016/j.genrep.2022.101738
mTOR signaling and autophagy regulation
Singh, A., & Bhutia, S. K. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-90142-0.00001-3
Salmonella Enteritidis RfbD interferes with autophagy through REDD1 to promote bacterial survivalPreprint
Zhou, Y., Xiong, D., Kang, X., Song, H., Huang, J., Meng, C., Gu, D., Jiao, X., & Pan, Z. (2024) · Research Square · doi:10.21203/rs.3.rs-4006770/v1
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Tsakiridis, E. E., Ahmadi, E., Gautam, J., She, Y. R. H., Fayyazi, R., Lally, J., Wang, S. J. H., Pastena, F. D., Valvano, C. M., Rosso, D. D., et al. (2025) · JHEP Reports · doi:10.1016/j.jhepr.2025.101354
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Li, L., Rong, J., Liao, F., Shangguan, J., Xie, C., Zhu, Y., & Shu, X. (2025) · Cell Biology International · doi:10.1002/cbin.70092
Kondratieva, S. A., Skvortsova, Y. V., Vishnyakova, P., Grigorov, A., Bychenko, O. S., & Azhikina, T. L. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11259-8
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Kainz, S. (2013) · University of Regensburg Publication Server (University of Regensburg) · doi:10.5283/epub.24569
Insulin-Like Growth Factor Signaling during Myogenesis.
Ren, H. (2009) · Deep Blue (University of Michigan)
Zhang, Y., Liu, X., Wang, Y., Lai, S., Wang, Z., Yang, Y., Liu, W., Wang, H., & Tang, B. (2022) · Figshare · doi:10.6084/m9.figshare.20861197
Zhang, Y., Liu, X., Wang, Y., Lai, S., Wang, Z., Yang, Y., Liu, W., Wang, H., & Tang, B. (2022) · Figshare · doi:10.6084/m9.figshare.20861194
Zhang, Y., Liu, X., Wang, Y., Lai, S., Wang, Z., Yang, Y., Liu, W., Wang, H., & Tang, B. (2022) · Figshare · doi:10.6084/m9.figshare.20861209
Zhang, Y., Liu, X., Wang, Y., Lai, S., Wang, Z., Yang, Y., Liu, W., Wang, H., & Tang, B. (2022) · Figshare · doi:10.6084/m9.figshare.20861203
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You, P., Qi, Z.-X., Luo, H., Cai, B., Hu, X., Pan, J., Gan, P., Zeng, X.-Y., Liao, R.-J., Tang, Q., et al. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102121 · Cited by 1
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Guan, W., Meng, Y.-T., & Miao, Y. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.117878 · Cited by 1
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Larichaudy, J. D. (2012) · theses.fr (ABES) · doi:10.70675/b97ff403z6fa7z464fzb67czaa56e3753d9e
Cormerais, Y. (2016) · theses.fr (ABES) · doi:10.70675/94cc6971z3a1dz454fzb65dzf153dc0a3a05
Han, M., Hu, Y., Chiou, J., Chung, H., Ko, Y.-C., Tsai, C., Chen, J., Kuo, C., Huang, C., Tzou, W., et al. (2026) · FEBS Journal · doi:10.1111/febs.70521
Rôle de l'autophagie dans l'émergence des cellules souches cancéreuses : implication du métabolisme
El-Hout, M. (2019) · theses.fr (ABES) · doi:10.70675/881cf980z01caz4a56z8a81zdcebe1247536
Heydt, Q. (2017) · theses.fr (ABES) · doi:10.70675/dc051486z8261z4fd2z9854z7fb85667ce95
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Rerra, A. (2019) · theses.fr (ABES) · doi:10.70675/d10332bfzd22cz480cz8f5czc0114d6c93c5
Muselli, F. (2020) · theses.fr (ABES) · doi:10.70675/96bf921az71baz4a4dz8d53z2717fadd83a6
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Yolba, R. L. (2021) · theses.fr (ABES) · doi:10.70675/9cadea77z03ccz4a54zb381zf34a432615a5
Functional characterization of the GATOR1 complex in cisplatin resistance
Pan, Z. (2024) · theses.fr (ABES) · doi:10.70675/2ddcf286zc553z40fdzb34ez875b3288c76b
Apoptosis-related gene model predicts the prognosis in patients with acute myeloid leukemia
Pei, X., Liu, W., Li, Y., Wei, H., Wang, M., & Wang, J. (2026) · Blood Science · doi:10.1097/bs9.0000000000000292
REDD1 deficiency alleviates podocyte PANoptosis and restores autophagy in diabetic kidney disease
Li, Y., Yuan, C., Li, Y., Song, S., Mu, L., Bian, Y., Li, X., Yu, X., Li, G., & Shi, Y. (2026) · Molecular Medicine · doi:10.1186/s10020-026-01510-8
Ando, Y., & Murakami, T. (2026) · Journal of Nutrition · doi:10.1016/j.tjnut.2026.101629
Mechanistic target of rapamycin in neurodegenerative disorders
Roy, T., Chatterjee, A., & Swarnakar, S. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-44173-8.00010-3
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Metadata
- Authors
- DeYoung, M. P., Horak, P., Sofer, A., Sgroi, D., & Ellisen, L. W.
- Affiliations
- Harvard University (US)
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2008-01-15
- Volume
- 22
- Issue
- 2
- Pages
- 239-251
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC2192757
- OpenAlex
- W2130396048
- Cited by
- 710
- References
- 41
- Citations by year
- 2026: 24 · 2025: 26 · 2024: 17 · 2023: 32 · 2022: 37 · 2021: 43 · 2020: 34 · 2019: 38 · 2018: 41 · 2017: 42 · 2016: 44 · 2015: 42 · 2014: 48 · 2013: 45 · 2012: 47
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Cancer Institute (R01CA122589)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Health Sciences › Medicine › Genetics (clinical) › Tuberous Sclerosis Complex Research
- Keywords
- hypoxia, TSC1/2, mTORC1, REDD1, 14-3-3 proteins, TORC1 inhibition, tumor suppression, anchorage-independent growth, carcinogenesis, cellular metabolism, signal integration
- MeSH terms
- Tuberous Sclerosis Complex 1 Protein, Tuberous Sclerosis Complex 2 Protein, Animals, Breast Neoplasms, Cells, Cultured, Humans, Mice, Nude, Models, Biological, Neoplasm Transplantation, Protein Kinases, Transcription Factors, Signal Transduction, Cell Hypoxia, Tumor Suppressor Proteins, Mice, TOR Serine-Threonine Kinases
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