The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Tuberous sclerosis complex-1 and -2 gene products function together to inhibit mammalian target of rapamycin (mTOR)-mediated downstream signaling
Open accessAbstract
Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder that occurs upon mutation of either the TSC1 or TSC2 genes, which encode the protein products hamartin and tuberin, respectively. Here, we show that hamartin and tuberin function together to inhibit mammalian target of rapamycin (mTOR)-mediated signaling to eukaryotic initiation factor 4E-binding protein 1 (4E-BP1) and ribosomal protein S6 kinase 1 (S6K1). First, coexpression of hamartin and tuberin repressed phosphorylation of 4E-BP1, resulting in increased association of 4E-BP1 with eIF4E; importantly, a mutant of TSC2 derived from TSC patients was defective in repressing phosphorylation of 4E-BP1. Second, the activity of S6K1 was repressed by coexpression of hamartin and tuberin, but the activity of rapamycin-resistant mutants of S6K1 were not affected, implicating mTOR in the TSC-mediated inhibitory effect on S6K1. Third, hamartin and tuberin blocked the ability of amino acids to activate S6K1 within nutrient-deprived cells, a process that is dependent on mTOR. These findings strongly implicate the tuberin-hamartin tumor suppressor complex as an inhibitor of mTOR and suggest that the formation of tumors within TSC patients may result from aberrantly high levels of mTOR-mediated signaling to downstream targets.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Loss of the TSC1–TSC2 protein complex leads to hyperactivation of mTOR complex 1 (mTORC1)18, a key signalling node that regulates cellular anabolic and catabolic processes19.”
From mTORC1 drives cell-autonomous astrocyte reactivity in tuberous sclerosis (2026) · cites this paper as [18]
In the citing paper
“The integration of the majority of external and survival signals feeding into the (m)TORC1 pathway occurs through the TSC complex (TSCC), composed of tuberous sclerosis complex protein 1 (TSC1) and TSC2, also known as hamartin and tuberin, and TBC1D7, which is the key signal integrator and negative regulator upstream of Rheb.”
From Signal integration in the (m)TORC1 growth pathway (2018) · cites this paper as Tee et al., 2002
In the citing paper
“This identification of this regulatory mechanism, shown using the human proteins, unequivocally identified TSC1-TSC2 as inhibitors of the mTORC1 signaling pathway (Inoki et al., 2002; Tee et al., 2002), specifically by virtue of TSC2 GAP activity toward the small GTPase Rheb (Castro et al., 2003; Garami et al., 2003; Inoki et al., 2003; Saucedo et al., 2003;”
From Signal integration in the (m)TORC1 growth pathway (2018) · cites this paper as Tee et al., 2002
Citations
Cites
TOR, a Central Controller of Cell Growth
Schmelzle, T., & Hall, M. N. (2000) · Cell · doi:10.1016/s0092-8674(00)00117-3 · Cited by 1,914
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
Self-citationRegulation of translation initiation by FRAP/mTOR
Gingras, A.-C., Raught, B., & Sonenberg, N. (2001) · Genes & Development · doi:10.1101/gad.887201 · Cited by 1,545
Hara, K., Yonezawa, K., Weng, Q.-P., Kozlowski, M. T., BELHAM, C. M., & Avruch, J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.23.14484 · Cited by 1,370
Chung, J., Kuo, C. J., Crabtree, G. R., & Blenis, J. (1992) · Cell · doi:10.1016/0092-8674(92)90643-q · Cited by 1,151
Self-citationMammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E
Fingar, D. C., Salama, S., Tsou, C., Harlow, E., & Blenis, J. (2002) · Genes & Development · doi:10.1101/gad.995802 · Cited by 1,093
Self-citationMalignant transformation by a eukaryotic initiation factor subunit that binds to mRNA 5' cap
Lazaris-Karatzas, A., Montine, K. S., & Sonenberg, N. (1990) · Nature · doi:10.1038/345544a0 · Cited by 971
Mammalian TOR: a homeostatic ATP sensor
Dennis, P. B., Jaeschke, A., Saitoh, M., Fowler, B., Kozma, S. C., & Thomas, G. (2001) · Science · doi:10.1126/science.1063518 · Cited by 962
Kwiatkowski, D. J. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.5.525 · Cited by 674
Self-citationThe mRNA 5′ cap-binding protein eIF4E and control of cell growth
Sonenberg, N., & Gingras, A. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80150-6 · Cited by 673
Research works printed but not linked: 4
- E R Gomez, J R Sampson, V H Whittemore Developmental Perspectives in Psychiatry (Oxford Univ. Press, Oxford, 1999).
- T L Plank, R S Yeung, E P Henske Cancer Res 58, 4766–4770 (1998).
- Martin K. A. & Blenis J. (2002) Adv. Cancer Res. 86 in press.
- D Rousseau, A C Gingras, A Pause, N Sonenberg Oncogene 13, 2415–2420 (1996).
Cited by
Sorted by citations
Items 501–600 of 828
Pradhan, S. A., Rather, M. I., Tiwari, A., Bhat, V. K., & Kumar, A. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku278 · Cited by 22
From tuberous sclerosis complex to end stage renal disease: who are these patients?
Vabret, E., Couchoud, C., Lassalle, M., & Vigneau, C. M. (2020) · Journal of Nephrology · doi:10.1007/s40620-020-00714-3 · Cited by 21
Left‐right asymmetry in the light of TOR: An update on what we know so far
Tena, T. C., Burkhalter, M. D., & Philipp, M. (2015) · Biology of the Cell · doi:10.1111/boc.201400094 · Cited by 20
Kladney, R. D., Cardiff, R. D., Kwiatkowski, D. J., Chiang, G. G., Weber, J. D., Arbeit, J. M., & Lu, Z. H. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-1646 · Cited by 21
Self-citationmTORC1 and mTORC2 expression in inner retinal neurons and glial cells
Losiewicz, M. K., Elghazi, L., Fingar, D. C., Rajala, R. V. S., Lentz, S. I., Fort, P. E., Abcouwer, S. F., & Gardner, T. W. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108131 · Cited by 20
Self-citationDeciphering the physiopathology of neurodevelopmental disorders using brain organoids
Dionne, O., Sabatié, S., & Laurent, B. (2024) · Brain · doi:10.1093/brain/awae281 · Cited by 22
Sadowski, K., Sijko, K., Domańska‐Pakieła, D., Borkowska, J., Chmielewski, D., Ulatowska, A., Jóźwiak, S., & Kotulska, K. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.704978 · Cited by 20
Exonic Variants Associated with Development of Aspirin Exacerbated Respiratory Diseases
Shin, S., Park, B. L., Chang, H. S., Park, J., Bae, D.-J., Song, H., Choi, I. S., Kim, M.-K., Park, H.-S., Kim, L. H., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0111887 · Cited by 20
Yi, P., Liang, Y., Yuan, D. M. K., Jie, Z., Kwota, Z., Chen, Y., Cong, Y., Fan, X., & Sun, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-04260-0 · Cited by 21
Increasing our understanding of human cognition through the study of fragile X syndrome
Cook, D., Nuro, E., & Murai, K. K. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22096 · Cited by 22
Mechanisms of translational control in dendrites
Glanzer, J. G. (2003) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.04.006 · Cited by 20
Sirolimus Ointment for Facial Angiofibromas in Individuals with Tuberous Sclerosis Complex
Amin, S., Lux, A. L., Khan, M. A., & O'Callaghan, F. J. (2017) · International Scholarly Research Notices · doi:10.1155/2017/8404378 · Cited by 19
Yefidoff‐Freedman, R., Chen, T., Sahoo, R., Chen, L., Wagner, G., Halperin, J. A., Aktas, B. H., & Chorev, M. (2014) · ChemBioChem · doi:10.1002/cbic.201300723 · Cited by 19
Wang, P., Drackley, J. K., Lanier, J. S., Keisler, D. H., & Loor, J. J. (2013) · Journal of Dairy Science · doi:10.3168/jds.2013-7042 · Cited by 20
Mammalian target of rapamycin: A new target in prostate cancer
Rai, J. S., Henley, M., & Ratan, H. L. (2009) · Urologic Oncology Seminars and Original Investigations · doi:10.1016/j.urolonc.2009.03.023 · Cited by 19
Fujita, A., Ando, K., Kobayashi, E., Mitani, K., Okudera, K., Nakashima, M., Miyatake, S., Tsurusaki, Y., Saitsu, H., Seyama, K., et al. (2015) · Human Genetics · doi:10.1007/s00439-015-1611-0 · Cited by 19
Potential of Capric Acid in Neurological Disorders: An Overview
Shekhar, N., Tyagi, S., Rani, S., & Thakur, A. K. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03809-4 · Cited by 20
Lesma, E. A., Chiaramonte, E., Ancona, S., Orpianesi, E., Giulio, A. M. D., & Gorio, A. (2015) · BioMed Research International · doi:10.1155/2015/315240 · Cited by 18
Mitchell, R. A., Barton, S., Harvey, A. S., Ure, A. M., & Williams, K. J. (2021) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.14787 · Cited by 18
Involvement of Lymphatics in Lymphangioleiomyomatosis
Glasgow, C. G., Taveira‐DaSilva, A. M., Pacheco–Rodriguez, G., Steagall, W. K., Tsukada, K., Cai, X., El‐Chemaly, S., & Moss, J. (2009) · Lymphatic Research and Biology · doi:10.1089/lrb.2009.0017 · Cited by 18
Jiang, X., Sinnett‐Smith, J. W., & Rozengurt, E. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.07.060 · Cited by 18
Carbonell-Roig, J., Aaltonen, A., Wilson, K., Molinari, M., Cartocci, V., McGuirt, A. F., Mosharov, E. V., Kehr, J., Lieberman, O. J., Sulzer, D., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114997 · Cited by 17
Mitchell, R. A., Mitchell, M. J., & Williams, K. J. (2022) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.15307 · Cited by 18
Cerebral organoids as an in vitro model to study autism spectrum disorders
Rabeling, A., & Goolam, M. (2022) · Gene Therapy · doi:10.1038/s41434-022-00356-z · Cited by 17
Analysis of TSC1 mutation spectrum in mucosal melanoma
Ma, M., Dai, J., Xu, T., Yu, S., Yu, H., Tang, H., Yan, J., Wu, X., Yu, J., Chi, Z., et al. (2017) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-017-2550-z · Cited by 17
Sporadic renal angiomyolipoma in a patient with Birt-Hogg-Dubé: chaperones in pathogenesis
Sager, R., Woodford, M. R., Shapiro, O., Mollapour, M., & Bratslavsky, G. (2018) · Oncotarget · doi:10.18632/oncotarget.25164 · Cited by 17
mTOR-regulated U2af1 tandem exon splicing specifies transcriptome features for translational control
Chang, J.-W., Yeh, H.-S., Park, M., Erber, L. N., Sun, J., Cheng, S. L. A., Bui, A. M., Fahmi, N. A., Nasti, R. A., Kuang, R., et al. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz761 · Cited by 18
Suppressed Expression of Autophagosomal Protein LC3 in Cortical Tubers of Tuberous Sclerosis Complex
Miyahara, H., Natsumeda, M., Shiga, A., Aoki, H., Toyoshima, Y., Zheng, Y., Takeuchi, R., Murakami, H., Masuda, H., Kameyama, S., et al. (2012) · Brain Pathology · doi:10.1111/j.1750-3639.2012.00634.x · Cited by 17
Oral and neurocutaneous phenotypes of familial tuberous sclerosis
Araujo, L. D. J., Lima, L. S., Alvarenga, T. M. M., Martelli‐Júnior, H., Coletta, R. D., de Aquino, S. N., & Bonan, P. R. F. (2010) · Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology · doi:10.1016/j.tripleo.2010.07.002 · Cited by 17
Inherited disorders as a risk factor and predictor of neurodevelopmental outcome in pediatric cancer
Ullrich, N. J. (2008) · Developmental Disabilities Research Reviews · doi:10.1002/ddrr.30 · Cited by 17
IGF-I activates the eIF4F system in cardiac muscle in vivo
Vary, T. C., & Lang, C. H. (2005) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-005-7551-6 · Cited by 17
Yoon, H., Ramachandiran, S., Chacko, M. S., Monks, T. J., & Lau, S. S. (2004) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00234.2003 · Cited by 17
Correlation between epilepsy and genotype: A large retrospective tuberous sclerosis complex cohort
Ding, Y., Zhou, Y., Yu, L., Zhang, L., Zhou, S., Wang, Y., & Wang, J. (2021) · Seizure · doi:10.1016/j.seizure.2021.06.036 · Cited by 16
Capuano, I., Buonanno, P., Riccio, E., Crocetto, F., & Pisani, A. (2022) · Journal of Nephrology · doi:10.1007/s40620-022-01375-0 · Cited by 16
Kútna, V., Uttl, L., Waltereit, R., Krištofiková, Z., Kaping, D., Petrásek, T., Höschl, C., & Ovsepian, S. V. (2019) · Neurotherapeutics · doi:10.1007/s13311-019-00812-6 · Cited by 16
Experimental Approaches in Delineating mTOR Signaling
Qian, J., Su, S., & Liu, P. (2020) · Genes · doi:10.3390/genes11070738 · Cited by 17
Kramer, K., Yang, J., Swanson, W. B., Hayano, S., Toda, M., Pan, H., Kim, J. K., Krebsbach, P. H., & Mishina, Y. M. (2018) · genesis · doi:10.1002/dvg.23220 · Cited by 17
Current Status of Mammalian Target of Rapamycin Inhibitors in Lung Cancer
Gómez-Martín, C., Rubio‐Viqueira, B., & Hidalgo, M. M. (2005) · Clinical Lung Cancer · doi:10.3816/clc.2005.s.003 · Cited by 16
Akt negatively regulates translation of the ternary complex factor Elk-1
Figueroa‐Romero, C., & Vojtek, A. B. (2003) · Oncogene · doi:10.1038/sj.onc.1206496 · Cited by 16
Heterozygous inactivation of tsc2 enhances tumorigenesis in p53 mutant zebrafish
Kim, S., Kowalski, M. L., Carson, R. P., Bridges, L. R., & Ess, K. C. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.011494 · Cited by 16
Ohsawa, M., Kobayashi, T., Okura, H., Igarashi, T., Mizuguchi, M., & Hino, O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054503 · Cited by 15
Liu, F., Lunsford, E. P., Tong, J., Ashitate, Y., Gibbs, S. L., Yu, J. J., Choi, H. S., Henske, E. P., & Frangioni, J. V. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038589 · Cited by 15
Chien, K.-Y., Blackburn, K., Liu, H., & Goshe, M. B. (2012) · Journal of Proteome Research · doi:10.1021/pr300471y · Cited by 15
Hemimegalencephaly and tuberous sclerosis complex: A rare yet challenging association
Sidira, C., Vargiami, E., Dragoumi, P., & Zafeiriou, D. (2020) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2020.12.007 · Cited by 16
TSC2 Mutations Were Associated with the Early Recurrence of Patients with HCC Underwent Hepatectomy
Song, K., He, F., Xin, Y., Guan, G., Huo, J., Zhu, Q., Fan, N., Guo, Y., Zang, Y.-J., & Wu, L.-Q. (2021) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s294307 · Cited by 15
Oncogenic role of MiR-130a in oral squamous cell carcinoma
Mallela, K., Swamy, S. S., Gopinath, K. S., & Kumar, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-87388-4 · Cited by 15
Modulo is a target of Myc selectively required for growth of proliferative cells in Drosophila
Perrin, L., Benassayag, C., Morello, D., Pradel, J., & Montagne, J. (2003) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00049-2 · Cited by 15
Targeting NRF2 and FSP1 to Overcome Ferroptosis Resistance in TSC2-Deficient and Cancer Cells
Tahsin, T., McPhail, D. K., Champion, J. D., Alzahrani, M. A. M., Hilditch, M. L., Faris-Orr, A., Calver, B. L., Sexton, D. W., Cronin, J., Rivas, J. C. M., et al. (2025) · Cancers · doi:10.3390/cancers17162714 · Cited by 19
Self-citationChange and Regulation of Nutritional Metabolism in Silver Pomfret During Compensatory Growth
Hu, J., Zhang, Y., Yan, K., Zhang, M., Li, Y., Li, Y., Gu, W., Xu, S., Wang, Y., & Yan, X. (2023) · Marine Biotechnology · doi:10.1007/s10126-023-10261-0 · Cited by 14
Synaptic Plasticity as a Therapeutic Target in the Treatment of Autism-related Single-gene Disorders
Pignatelli, M., Feligioni, M., Piccinin, S., Molinaro, G., Nicoletti, F., & Nisticò, R. (2013) · Current Pharmaceutical Design · doi:10.2174/1381612811319360008 · Cited by 14
Manne, B. K., Bhatlekar, S., Middleton, E. A., Weyrich, A. S., Borst, O., & Rondina, M. T. (2020) · Journal of Thrombosis and Haemostasis · doi:10.1111/jth.14748 · Cited by 14
Wang, X., Xing, Z., Xu, H., Yang, H., & Xing, T. (2021) · Aging · doi:10.18632/aging.202976 · Cited by 14
Predisposition to tetraploidy in pulmonary vascular smooth muscle cells derived from the Eker rats
Gui, Y., He, G. H., Walsh, M. P., & Zheng, X. (2007) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00016.2007 · Cited by 14
Modulating Autophagy in Osteoarthritis: Exploring Emerging Therapeutic Drug Targets
Andrei, C., Mihai, D. P., Nițulescu, G. M., Nițulescu, G., & Zanfirescu, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413695 · Cited by 15
Bonnevier, J. L., Yarke, C. A., & Mueller, D. L. (2006) · European Journal of Immunology · doi:10.1002/eji.200535626 · Cited by 13
O'Callaghan, F. J. (2008) · Paediatrics and Child Health · doi:10.1016/j.paed.2007.10.013 · Cited by 13
Role of mTOR Signaling for Tubular Function and Disease
Grahammer, F., Huber, T. B., & Artunç, F. (2021) · Physiology · doi:10.1152/physiol.00021.2021 · Cited by 13
Morales, C., Balanta‐Melo, J., Arias‐Calderón, M., Hernández, N., Gómez‐Valenzuela, F., Escobar, A. F., Jaimovich, E., & Buvinic, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23169444 · Cited by 13
Ishii, R., Wataya‐Kaneda, M., Canuet, L., Nonomura, N., Nakai, Y., & Takeda, M. (2015) · Neuropsychiatric Electrophysiology · doi:10.1186/s40810-015-0004-x · Cited by 13
Genetic Syndromes Affecting Kidney Development
Pal, A., & Reidy, K. J. (2017) · Results and problems in cell differentiation · doi:10.1007/978-3-319-51436-9_10 · Cited by 13
The Mechanisms of Insulin Action
White, M. F., & Copps, K. D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00033-0 · Cited by 12
Hosseini-Farahabadi, S., Baradaran‐Heravi, A., Zimmerman, C., Choi, K., Flibotte, S., & Roberge, M. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001221 · Cited by 13
Indinavir alters regulators of protein anabolism and catabolism in skeletal muscle
Hong‐Brown, L. Q., Pruznak, A. M., Frost, R. A., Vary, T. C., & Lang, C. H. (2005) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00591.2004 · Cited by 13
Signal integration in the (m)TORC1 growth pathway
Ramlaul, K., & Aylett, C. H. S. (2018) · Frontiers in Biology · doi:10.1007/s11515-018-1501-7 · Cited by 12
An mTORC1 to HRI signaling axis promotes cytotoxicity of proteasome inhibitors in multiple myeloma
Darawshi, O., Muz, B., Gershon-Naamat, S., Praveen, B., Mahameed, M., Goldberg, K., Dipta, P., Shmuel, M., Forno, F., Boukeileh, S., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05421-4 · Cited by 12
Fallone, L., Walzer, T., & Marçais, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612736 · Cited by 13
Liu, M., Ye, J., & You, X. (2023) · Child s Nervous System · doi:10.1007/s00381-023-06200-y · Cited by 12
Unraveling the function of TSC1-TSC2 complex: implications for stem cell fate
Wang, S., Ma, R., Gao, C., Tian, Y.-N., Hu, R., Zhang, H., Li, L., & Li, Y. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04170-3 · Cited by 15
Congenital lymphedema as a rare and first symptom of tuberous sclerosis complex
Klinner, J., Krüger, M., Brunet, T., Makowski, C. C., Riedhammer, K. M., Mollweide, A., Wagner, M., & Hoefele, J. (2020) · Gene · doi:10.1016/j.gene.2020.144815 · Cited by 12
Becker, B., & Strowd, R. E., III (2019) · Dermatologic Clinics · doi:10.1016/j.det.2019.05.015 · Cited by 12
Kútna, V., O’Leary, V. B., Newman, E. L., Höschl, C., & Ovsepian, S. V. (2021) · Neurotherapeutics · doi:10.1007/s13311-020-01000-7 · Cited by 13
White, M. F., & White, M. F. (2011) · Springer eBooks · doi:10.1007/978-1-4614-1028-7_2 · Cited by 12
Retracted Tuberous sclerosis complex: molecular pathogenesis and animal models
Piedimonte, L. R., Wailes, I. K., & Weiner, H. L. (2006) · Neurosurgical FOCUS · doi:10.3171/foc.2006.20.1.5 · Cited by 12
RetractedSmall-molecule correctors divert CFTR-F508del from ERAD by stabilizing sequential folding states
Riepe, C., Wąchalska, M., Deol, K. K., Amaya, A. K., Porteus, M. H., Olzmann, J. A., & Kopito, R. R. (2023) · Molecular Biology of the Cell · doi:10.1091/mbc.e23-08-0336 · Cited by 12
Neuropsychological Problems in Neuro-oncology
Armstrong, C. L., Schmus, C. J., & Belasco, J. B. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1364-7_3 · Cited by 11
Mitchell, R. A., Barton, S., Harvey, A. S., & Williams, K. J. (2017) · Systematic Reviews · doi:10.1186/s13643-017-0448-0 · Cited by 11
Phosphoproteomics of cAMP signaling of Bordetella adenylate cyclase toxin in mouse dendritic cells
Novák, J., Fabrik, I., Linhartová, I., Link, M., Černý, O., Stulík, J., & Šebo, P. (2017) · Scientific Reports · doi:10.1038/s41598-017-14501-x · Cited by 11
Tian, X., Xu, W., Anwaier, A., Wang, H., Wan, F., Cao, D., Luo, W., Shi, G., Qu, Y., Zhang, H., et al. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16323 · Cited by 11
Li, F., Bondra, K. M., Ghilu, S., Studebaker, A. W., Liu, Q., Michalek, J. E., Kogiso, M., Li, X., Kalapurakal, J. A., James, C. D., et al. (2022) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-22-1052 · Cited by 12
Fox, T. E., Young, M. M., Pedersen, M. M., Han, X., Gardner, T. W., & KESTER, M. A. (2012) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.11-7626 · Cited by 11
Emerging treatments and personalised medicine for ciliopathies associated with cystic kidney disease
Molinari, E., & Sayer, J. A. (2017) · Expert Opinion on Orphan Drugs · doi:10.1080/21678707.2017.1372282 · Cited by 11
Melnik, B. C. (2012) · Humana Press eBooks · doi:10.1007/978-1-62703-167-7_37 · Cited by 11
Dunlop, E. A., Dodd, K. M., Land, S. C., Davies, P. A., Martins, N., Stuart, H., McKee, S. A., Kingswood, J. C., Saggar, A., Corderio, I., et al. (2011) · European Journal of Human Genetics · doi:10.1038/ejhg.2011.38 · Cited by 11
Self-citationInvestigational agents for treatment of AIDS-related Kaposi’s sarcoma
Konstantinopoulos, P. A., Sullivan, R. J., Karamouzis, M. V., & Dezube, B. J. (2007) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.16.4.495 · Cited by 11
Ras mediates cell survival by regulating tuberin
Freilinger, A., Rosner, M. R., Hanneder, M., & Hengstschläger, M. (2008) · Oncogene · doi:10.1038/sj.onc.1210844 · Cited by 14
Regulation of PCNA and CAF-1 expression by the two tuberous sclerosis gene products
Hengstschläger, M., Rosner, M., Fountoulakis, M., & Lübec, G. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)01238-5 · Cited by 11
Shahabi, F., Abdoli, S., Bazi, Z., Shamsabadi, F. T., Yamchi, A., & Shahbazi, M. (2023) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2023.1268048 · Cited by 10
Li, K., Cao, J., Gong, Y., Li, X., Wu, M., Qi, Y., Ying, X., Liu, D., Ma, X., & Zhang, X. (2024) · Neurochemistry International · doi:10.1016/j.neuint.2024.105746 · Cited by 10
Moavero, R., Folgiero, V., Carai, A., Miele, E., Ferretti, E., Pò, A., Diomedi‐Camassei, F., Lepri, F. R., Vigevano, F., Curatolo, P., et al. (2015) · Pediatric Blood & Cancer · doi:10.1002/pbc.25851 · Cited by 10
The Molecular Landscape Influencing Prognoses of Epithelial Ovarian Cancer
Liu, C.-L., Yuan, R., & Mao, T. (2021) · Biomolecules · doi:10.3390/biom11070998 · Cited by 10
Tuber Brain Proportion Determines Epilepsy Onset in Children With Tuberous Sclerosis Complex
Zhang, F., Xie, L., He, X., Song, X., Zheng, H., Wang, L., & Jiang, L. (2021) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2021.12.012 · Cited by 10
Rare and Unusual Endocrine Cancer Syndromes With Mutated Genes
Lodish, M. B., & Stratakis, C. A. (2010) · Seminars in Oncology · doi:10.1053/j.seminoncol.2010.10.019 · Cited by 10
Tsc2 Expression Increases the Susceptibility of Renal Tumor Cells to Apoptosis
Kolb, T. M., Duan, L., & Davis, M. A. (2005) · Toxicological Sciences · doi:10.1093/toxsci/kfi310 · Cited by 10
Phosphoinositide signalling in type 2 diabetes: a β-cell perspective
Rameh, L. E., & Deeney, J. T. (2016) · Biochemical Society Transactions · doi:10.1042/bst20150229 · Cited by 9
He, L., Zhang, X., Huang, Y., Yang, H., Wang, Y., & Zhang, Z. (2017) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2017.06.001 · Cited by 9
Emerging Link between Tsc1 and FNIP Co-Chaperones of Hsp90 and Cancer
Backe, S. J., Sager, R., Meluni, K. A., Woodford, M. R., Bourboulia, D., & Mollapour, M. (2022) · Biomolecules · doi:10.3390/biom12070928 · Cited by 9
Wittenstein, A., Caspi, M., Rippin, I., Elroy‐Stein, O., Eldar-Finkelman, H., Thoms, S., & Rosin‐Arbesfeld, R. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002355 · Cited by 11
Pulmonary Cystic Disease and Its Mimics
Jones, K. D. (2020) · Surgical pathology clinics · doi:10.1016/j.path.2019.11.007 · Cited by 9
Benign Brain Tumors and Tumors Associated With Phakomatoses
Daras, M., & Kaley, T. J. (2015) · CONTINUUM Lifelong Learning in Neurology · doi:10.1212/01.con.0000464177.73440.44 · Cited by 8
Fujii, H., Sato, N., Kimura, Y., Mizutani, M., Kusama, M., Sumitomo, N., Chiba, E., Shigemoto, Y., Takao, M., Takayama, Y., et al. (2022) · American Journal of Neuroradiology · doi:10.3174/ajnr.a7573 · Cited by 8
Metadata
- Authors
- Tee, A. R., Fingar, D. C., Manning, B. D., Kwiatkowski, D. J., Cantley, L. C., & Blenis, J.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Blenis, John
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2002-09-23
- Volume
- 99
- Issue
- 21
- Pages
- 13571-13576
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC129715
- OpenAlex
- W2087812126
- Cited by
- 827
- References
- 31
- Citations by year
- 2026: 9 · 2025: 13 · 2024: 17 · 2023: 27 · 2022: 29 · 2021: 35 · 2020: 40 · 2019: 22 · 2018: 37 · 2017: 35 · 2016: 31 · 2015: 45 · 2014: 28 · 2013: 43 · 2012: 42
- FWCI
- 17.27
- Type
- journal article
- Language
- en
- Update notices
- correction (2021-08-09)
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (GM 41890, GM51405, R01GM056203, GM 56203, R01GM051405, R01GM041890, R37GM041890)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Health Sciences › Medicine › Genetics (clinical) › Tuberous Sclerosis Complex Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- tuberous sclerosis complex, TSC1, TSC2, hamartin, tuberin, mTOR signaling, 4E-BP1, S6K1, amino acid signaling, nutrient deprivation, rapamycin resistance, protein phosphorylation, eIF4E, tumor formation
- MeSH terms
- Tuberous Sclerosis Complex 1 Protein, Tuberous Sclerosis Complex 2 Protein, Amino Acids, Carrier Proteins, Cell Line, Humans, Insulin, Models, Biological, Phosphoproteins, Phosphorylation, Protein Kinases, Proteins, Repressor Proteins, Tuberous Sclerosis, Signal Transduction, Point Mutation, Cell Cycle Proteins, Phosphatidylinositol 3-Kinases, Ribosomal Protein S6 Kinases, Tumor Suppressor Proteins, Adaptor Proteins, Signal Transducing, TOR Serine-Threonine Kinases, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review