The DOI matches its Crossref record; 48 of the 49 references it cites were found in a registry or an index.
Transcriptional control of autophagy-lysosome function drives pancreatic cancer metabolism
Open accessAbstract
Activation of cellular stress response pathways to maintain metabolic homeostasis is emerging as a critical growth and survival mechanism in many cancers. The pathogenesis of pancreatic ductal adenocarcinoma (PDA) requires high levels of autophagy, a conserved self-degradative process. However, the regulatory circuits that activate autophagy and reprogram PDA cell metabolism are unknown. Here we show that autophagy induction in PDA occurs as part of a broader transcriptional program that coordinates activation of lysosome biogenesis and function, and nutrient scavenging, mediated by the MiT/TFE family of transcription factors. In human PDA cells, the MiT/TFE proteins--MITF, TFE3 and TFEB--are decoupled from regulatory mechanisms that control their cytoplasmic retention. Increased nuclear import in turn drives the expression of a coherent network of genes that induce high levels of lysosomal catabolic function essential for PDA growth. Unbiased global metabolite profiling reveals that MiT/TFE-dependent autophagy-lysosome activation is specifically required to maintain intracellular amino acid pools. These results identify the MiT/TFE proteins as master regulators of metabolic reprogramming in pancreatic cancer and demonstrate that transcriptional activation of clearance pathways converging on the lysosome is a novel hallmark of aggressive malignancy.
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“recent studies have shown that the use of DON or analogs in murine PDAC models also appear to have immunomodulatory effects204,205”
From Pancreatic cancer: Advances and challenges (2023) · cites this paper as [205]
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“FOXO transcription factors, especially FOXO1 and FOXO3, also play critical roles in the regulation of autophagy gene expression [660, 913, 978].”
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1 retracted
Zehorai, E., & Seger, R. (2013) · Molecular and Cellular Biology · doi:10.1128/mcb.00799-13 · Cited by 34
RetractedSystematic and integrative analysis of large gene lists using DAVID bioinformatics resources
Huang, D. W., Sherman, B. T., & Lempicki, R. A. (2009) · Nature Protocols · doi:10.1038/nprot.2008.211 · Cited by 35,890
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
Eng, J. K., McCormack, A. L., & Yates, J. R. (1994) · Journal of the American Society for Mass Spectrometry · doi:10.1016/1044-0305(94)80016-2 · Cited by 6,484
Autophagy regulates lipid metabolism
Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975
Core Signaling Pathways in Human Pancreatic Cancers Revealed by Global Genomic Analyses
Jones, S., Zhang, X., Parsons, D. W., Lin, J. C.-H., Leary, R. J., Angenendt, P., Mankoo, P., Carter, H., Kamiyama, H., Jimeno, A., et al. (2008) · Science · doi:10.1126/science.1164368 · Cited by 3,969
mTOR: from growth signal integration to cancer, diabetes and ageing
Zoncu, R., Efeyan, A., & Sabatini, D. M. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3025 · Cited by 3,941
Self-citationElias, J. E., & Gygi, S. P. (2007) · Nature Methods · doi:10.1038/nmeth1019 · Cited by 3,925
Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila
Moy, R. H., & Cherry, S. R. (2013) · Journal of Innate Immunity · doi:10.1159/000350326 · Cited by 3,551
Autophagy and the Integrated Stress Response
Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506
Flagged first, then by citations
1 of the 49 references couldn’t be matched to a known paper.
Research works printed but not linked: 4
- Commisso, C. et al. Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells. Nature 497, 633–637 (2013) · DOI · Paper page
- Settembre, C. et al. TFEB links autophagy to lysosomal biogenesis. Science 332, 1429–1433 (2011) · DOI · Paper page
- Ballabio, A. & Gieselmann, V. Lysosomal disorders: from storage to cellular damage. Biochim. Biophys. Acta 1793, 684–696 (2009) · DOI · Paper page
- Ting, L., Rad, R., Gygi, S. P. & Haas, W. MS3 eliminates ratio distortion in isobaric multiplexed quantitative proteomics. Nature Methods 8, 937–940 (2011) · DOI · Paper page
Cited by
Sorted by citations
Items 301–400 of 801
Advances in measuring cancer cell metabolism with subcellular resolution
Ruiz‐Rodado, V., Lita, A., & Larion, M. (2022) · Nature Methods · doi:10.1038/s41592-022-01572-6 · Cited by 48
Targeting KRAS in Pancreatic Ductal Adenocarcinoma: The Long Road to Cure
de Jesus, V. H. F., Mathias-Machado, M. C., de Farias, J. P. F., Aruquipa, M. P. S., Jacome, A. A. D. A., & Peixoto, R. D. (2023) · Cancers · doi:10.3390/cancers15205015 · Cited by 51
Min, Y., Lee, S., Kim, M., Chun, E., & Lee, K. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01827 · Cited by 47
Macropinocytosis Renders a Subset of Pancreatic Tumor Cells Resistant to mTOR Inhibition
Michalopoulou, E., Auciello, F. R., Bulusu, V., Strachan, D., Campbell, A. D., Tait-Mulder, J., Karim, S. A., Morton, J. P., Sansom, O. J., & Kamphorst, J. J. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.080 · Cited by 50
Pik3ip1 Is a Negative Immune Regulator that Inhibits Antitumor T-Cell Immunity
Chen, Y., Wang, J., Wang, X., Li, X., Song, J., Fang, J., Liu, X., Liu, T., Wang, D., Li, Q., et al. (2019) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-18-4134 · Cited by 46
Autophagy-related Proteins as a Prognostic Factor of Patients With Colorectal Cancer
Koustas, E., Sarantis, P., Theoharis, S., Saetta, A. A., Chatziandreou, I., Kyriakopoulou, G., Giannopoulou, I., Michelli, M., Schizas, D., Papavassiliou, A. G., et al. (2019) · American Journal of Clinical Oncology · doi:10.1097/coc.0000000000000592 · Cited by 44
ESAT6 inhibits autophagy flux and promotes BCG proliferation through MTOR
Hu, D., Wu, J., Zhao, R., Xuewei, X., Mu, M., Ru, C., Xing, Y., Shengfa, N., & Rongbo, Z. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.06.042 · Cited by 45
Autophagic response to cellular exposure to titanium dioxide nanoparticles
Popp, L., Tran, V., Patel, R. K., & Segatori, L. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.08.021 · Cited by 45
Autophagy and cancer: Basic mechanisms and inhibitor development
Hama, Y., Ogasawara, Y., & Noda, N. N. (2023) · Cancer Science · doi:10.1111/cas.15803 · Cited by 47
Wu, M.-Y., Wang, S.-F., Cai, C.-Z., Tan, J., Li, M., Lu, J., Chen, X., Wang, Y., Zheng, W., & Lu, J. (2017) · Oncotarget · doi:10.18632/oncotarget.20767 · Cited by 44
Targeting Cancer Lysosomes with Good Old Cationic Amphiphilic Drugs
Ellegaard, A., Bach, P. B., & Jäättelä, M. (2020) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/112_2020_56 · Cited by 44
Lysosomes in Cancer—At the Crossroad of Good and Evil
Eriksson, I., & Öllinger, K. M. (2024) · Cells · doi:10.3390/cells13050459 · Cited by 48
Tan, C., Li, Y., Huang, X., Wei, M., Huang, Y., Tang, Z., Huang, H., Zhou, W., Wang, Y., & Hu, J. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-2144-6 · Cited by 43
The Role of Autophagy in Pancreatic Cancer: From Bench to the Dark Bedside
Görgülü, K., Diakopoulos, K. N., Kaya-Aksoy, E., Ciecielski, K. J., Ai, J., Lesina, M., & Algül, H. (2020) · Cells · doi:10.3390/cells9041063 · Cited by 43
MiT Family Transcriptional Factors in Immune Cell Functions
Kim, S., Song, H.-S., Yu, J., & Kim, Y. (2021) · Molecules and Cells · doi:10.14348/molcells.2021.0067 · Cited by 43
Bian, Y., Zeng, H., Tao, H., Huang, L., Du, Z., Wang, J., & Ding, K. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.06.054 · Cited by 42
Gupta, N., & Yelamanchi, R. (2021) · World Journal of Gastroenterology · doi:10.3748/wjg.v27.i23.3158 · Cited by 47
Asrani, K. V., Woo, J., Mendes, A. A. D. A., Schaffer, E. D., Vidotto, T., Villanueva, C. R., Feng, K., Oliveira, L., Murali, S., Liu, H. B., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34617-7 · Cited by 44
Autophagy in cancer immunotherapy: Perspective on immune evasion and cell death interactions
Yu, Q., Ding, J., Li, S., & Li, Y. (2024) · Cancer Letters · doi:10.1016/j.canlet.2024.216856 · Cited by 45
Deretic, V. P. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.4mr0216-079r · Cited by 43
Slade, L., Biswas, D., Ihionu, F., Hiani, Y. E., Kienesberger, P. C., & Pulinilkunnil, T. (2019) · Biochemical Journal · doi:10.1042/bcj20190596 · Cited by 40
Transcriptional and Post-Transcriptional Regulation of Autophagy
Ma, Q., Long, S., Gan, Z., Tettamanti, G., Li, K., & Tian, L. (2022) · Cells · doi:10.3390/cells11030441 · Cited by 42
MDH1 and MPP7 Regulate Autophagy in Pancreatic Ductal Adenocarcinoma
New, M. I., Acker, T. V., Sakamaki, J.-I., Jiang, M., Saunders, R. E., Long, J. S., Wang, V. M.-Y., Behrens, A., Cerveira, J., Sudhakar, P., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-2553 · Cited by 41
Mechanically stressed cancer microenvironment: Role in pancreatic cancer progression
Hadden, M. K., Mittal, A., Samra, J. S., Zreiqat, H., Sahni, S., & Ramaswamy, Y. (2020) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2020.188418 · Cited by 40
Exploring the Role of Autophagy Dysfunction in Neurodegenerative Disorders
Rana, T., Behl, T., Sehgal, A., Mehta, V., Singh, S., Bhatia, S., Al‐Harrasi, A., & BUNGAU, S. G. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02472-0 · Cited by 42
Therapeutic advances in metastatic pancreatic cancer: a focus on targeted therapies
Turpin, A., Neuzillet, C., Colle, E., Dusetti, N., Nicolle, R., Cros, J. F., de Mestier, L., Bachet, J., & Hammel, P. R. (2022) · Therapeutic Advances in Medical Oncology · doi:10.1177/17588359221118019 · Cited by 41
Ho, R., & Stroupe, C. (2016) · Traffic · doi:10.1111/tra.12421 · Cited by 35
Metabolic plasticity in heterogeneous pancreatic ductal adenocarcinoma
Liang, C., Qin, Y., Zhang, B., Ji, S., Shi, S., Xu, W., Liu, J., Xiang, J., Liang, D., Hu, Q., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.09.001 · Cited by 39
GNS561, a new lysosomotropic small molecule, for the treatment of intrahepatic cholangiocarcinoma
Brun, S., Bassissi, F., Serdjebi, C., Novello, M., Tracz, J., Autelitano, F., Guillemot, M., Fabre, P., Courcambeck, J., Ansaldi, C., et al. (2019) · Investigational New Drugs · doi:10.1007/s10637-019-00741-3 · Cited by 39
In Vivo Remodeling of Altered Autophagy-Lysosomal Pathway by a Phosphopeptide in Lupus
Wang, F., Tasset, I., Cuervo, A. M., & Muller, S. (2020) · Cells · doi:10.3390/cells9102328 · Cited by 39
The biological role of metabolic reprogramming in pancreatic cancer
Suzuki, T., Otsuka, M., Seimiya, T., Iwata, T., Kishikawa, T., & Koike, K. (2020) · MedComm · doi:10.1002/mco2.37 · Cited by 38
Andersen, H. B., Ialchina, R., Pedersen, S. F., & Czaplińska, D. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-10004-4 · Cited by 40
Autophagy-related proteins: Potential diagnostic and prognostic biomarkers of aging-related diseases
Miceli, C., Leri, M., Stefani, M., & Bucciantini, M. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101967 · Cited by 39
Baumann, J., Ignashkova, T. I., Chirasani, S. R., Ramírez‐Peinado, S., Alborzinia, H., Gendarme, M., Kuhnigk, K., Kramer, V., Lindemann, R. K., & Reiling, J. H. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-06-0418 · Cited by 39
Monitoring autophagy in cancer: From bench to bedside
Long, M., & McWilliams, T. G. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.05.016 · Cited by 30
Endoplasmic reticulum and Golgi stress in microcephaly
Passemard, S., Perez, F., Gressèns, P., & Ghouzzi, V. E. (2019) · Cell Stress · doi:10.15698/cst2019.12.206 · Cited by 38
O-GlcNAcylation of PFKFB3 is required for tumor cell proliferation under hypoxia
Lei, Y., Chen, T., Li, Y., Shang, M., Zhang, Y., Jin, Y., Yu, Q., Guo, F., & Wang, T. (2020) · Oncogenesis · doi:10.1038/s41389-020-0208-1 · Cited by 41
El-Houjeiri, L., Biondini, M., Paquette, M., Kuasne, H., Pacis, A., Park, M., Siegel, P. M., & Pause, A. (2021) · Journal of Clinical Investigation · doi:10.1172/jci144871 · Cited by 39
Xu, G., Zhang, Q., Cheng, R., Qu, J., & Li, W. (2025) · Autophagy · doi:10.1080/15548627.2025.2452149 · Cited by 41
Ping-Pong—Tumor and Host in Pancreatic Cancer Progression
Mu, W., Wang, Z., & Zöller, M. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2019.01359 · Cited by 37
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Cabrera-Rodríguez, R., Pérez-Yanes, S., Estévez‐Herrera, J., Márquez-Arce, D., Cabrera, C., Espert, L., Blanco, J., & Valenzuela-Fernández, A. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.661446 · Cited by 37
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Petruzzelli, R., Mariniello, M., Cegli, R. D., Catalano, F., Guida, F., Schiavi, E. D., & Polishchuk, R. (2022) · Cells · doi:10.3390/cells11020219 · Cited by 36
Cysteine Cathepsins in Breast Cancer: Promising Targets for Fluorescence-Guided Surgery
Linders, D. G. J., Bijlstra, O. D., Fallert, L. C., Hilling, D. E., Walker, E., Straight, B., March, T. L., Valentijn, A. R. P. M., Pool, M., Burggraaf, J., et al. (2022) · Molecular Imaging and Biology · doi:10.1007/s11307-022-01768-4 · Cited by 36
TMX2 potentiates cell viability of hepatocellular carcinoma by promoting autophagy and mitophagy
Zhang, W., Tang, Y., Yang, P., Chen, Y., Xu, Z., Qi, C., Huang, H., Liu, R., Qin, H., Ke, H., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2358732 · Cited by 38
Lysosomal acidification impairment in astrocyte-mediated neuroinflammation
Zeng, J., Indajang, J., Pitt, D., & Lo, C. H. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03410-w · Cited by 44
Chauhan, N., & Patro, B. S. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216599 · Cited by 35
High expression of TFEB is associated with aggressive clinical features in colorectal cancer
Liang, J., Jia, X., Wang, K., & Zhao, N. (2018) · OncoTargets and Therapy · doi:10.2147/ott.s180112 · Cited by 35
Chen, Y., Navarrete, M. S., Wang, Y., McClintock, N. C., Sakurai, R., Wang, F., Chen, K. T., Chou, T., Rehan, V. K., Lee, D. J., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-68615-w · Cited by 36
TFEB Supports Pancreatic Cancer Growth through the Transcriptional Regulation of Glutaminase
Kim, J. H., Lee, J., Cho, Y.-R., Lee, S., Sung, G., Shin, D., Choi, K., & Son, J. (2021) · Cancers · doi:10.3390/cancers13030483 · Cited by 38
The role of autophagy in pancreatic cancer progression
Wang, Y., Qin, C., Yang, G., Zhao, B., & Wang, W. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188592 · Cited by 35
Ying, C., Jin, C., Zeng, S., Chao, M., & Hu, X. (2022) · Oncogene · doi:10.1038/s41388-022-02396-6 · Cited by 35
Hu, P., Li, H., Sun, W., Wang, H.-Z., Yu, X.-X., Qing, Y.-J., Wang, Z., Zhu, M.-Y., Xu, J.-Y., Guo, Q.-L., et al. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.02.004 · Cited by 31
USP21 deubiquitinase elevates macropinocytosis to enable oncogenic KRAS bypass in pancreatic cancer
Hou, P., Ma, X., Yang, Z., Zhang, Q., Wu, C.-J., Li, J., Tan, L., Yao, W., Yan, L., Zhou, X., et al. (2021) · Genes & Development · doi:10.1101/gad.348787.121 · Cited by 35
The Role of Autophagy in Pancreatic Cancer—Recent Advances
New, M. I., & Tooze, S. A. (2019) · Biology · doi:10.3390/biology9010007 · Cited by 34
Li, J., Lou, J., Yu, G., Chen, Y., Chen, R., Chen, Z., Wu, C., Ding, J. H., Xu, Y. M., Jiang, J., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.643996 · Cited by 34
Autophagy Inhibition in BRAF-Driven Cancers
Foth, M., & McMahon, M. (2021) · Cancers · doi:10.3390/cancers13143498 · Cited by 33
Interplays of AMPK and TOR in Autophagy Regulation in Yeast
Alao, J. P., Legon, L., Dabrowska, A. F., Tricolici, A.-M., Kumar, J., & Rallis, C. (2023) · Cells · doi:10.3390/cells12040519 · Cited by 33
Emerging roles of the MiT/TFE factors in cancer
Zoncu, R., & Perera, R. M. (2023) · Trends in cancer · doi:10.1016/j.trecan.2023.06.005 · Cited by 33
Self-citationZhen, Y., Liu, K., Shi, L., Shah, S., Xu, Q., Ellis, H., Balasooriya, E. R., Kreuzer, J., Morris, R. T., Baldwin, A. S., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47514-y · Cited by 36
Self-citationLysosomal quality control Review
Henn, D., Yang, X., & Li, M. (2025) · Autophagy · doi:10.1080/15548627.2025.2469206 · Cited by 35
Jia, H., Wei, J., Zheng, W., & Li, Z. Y. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06595-z · Cited by 33
Role of TFEB-driven autophagy regulation in pancreatic cancer treatment
Klein, K., Werner, K., Teske, C., Schenk, M., Giese, T., Weitz, J., & Welsch, T. (2016) · International Journal of Oncology · doi:10.3892/ijo.2016.3505 · Cited by 34
Chang, V. H.-S., Tsai, Y., Tsai, Y.-L., Peng, S.-L., Chen, S., Chang, T. M., Yu, W., & Ch'ang, H.-J. (2017) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2017.01.001 · Cited by 32
Metabolic Reprogramming and Oncogenesis
Costa, A. S. H., & Frezza, C. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.01.001 · Cited by 32
ALDH1A1 and HLTF modulate the activity of lysosomal autophagy inhibitors in cancer cells
Piao, S., Ojha, R., Rebecca, V. W., Samanta, A., Ma, X.-H., Mcafee, Q. W., Nicastri, M. C., Buckley, M. E., Brown, E. J., Winkler, J. D., et al. (2017) · Autophagy · doi:10.1080/15548627.2017.1377377 · Cited by 33
Zeng, W., Xiao, T., Cai, A., Cai, W., Liu, H., Liu, J., Li, J., Tan, M., Xie, L., Liu, Y., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000481971 · Cited by 32
The role of metabolic adaptation to nutrient stress in pancreatic cancer
Derle, A., Santis, M. C. D., Gozzelino, L., Ratto, E., & Martini, M. (2018) · Cell Stress · doi:10.15698/cst2018.12.166 · Cited by 33
Endolysosomal TRPMLs in Cancer
Xu, M., & Dong, X. (2021) · Biomolecules · doi:10.3390/biom11010065 · Cited by 33
Sajidah, E. S., Lim, K., & Wong, R. W.-C. (2021) · Cells · doi:10.3390/cells10061424 · Cited by 33
Koehler, B. C., Jassowicz, A., Scherr, A., Lorenz, S., Radhakrishnan, P., Kautz, N., Elßner, C., Weiß, J., Jaeger, D., Schneider, M., et al. (2015) · BMC Cancer · doi:10.1186/s12885-015-1929-y · Cited by 32
Zhou, X., Lai, Y.-H., Zhang, J., Li, Y., Wu, X., Yang, Y., Zhang, X., Ma, L., Zheng, K.-M., Liu, Y., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06540-w · Cited by 32
Goren, L., Zhang, G., Kaushik, S., Breslin, P. A. S., Du, Y. N., & Foster, D. A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216024 · Cited by 31
Weng, N., Qin, S., Liu, J., Huang, X., Jiang, J., Zhou, L., Zhang, Z., Xie, N., Wang, K., Jin, P., et al. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.01.018 · Cited by 32
Growth or death? Control of cell destiny by mTOR and autophagy pathways
Khalil, M. I. M., Ali, M. M., Holail, J., & Houssein, M. (2023) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2023.10.002 · Cited by 32
Song, T., Lv, S., Ma, X., Zhao, X., Li, F., Zou, Q., Li, N., Yan, Y., Zhang, W., & Sun, L. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104621 · Cited by 30
TFE3 is a diagnostic marker for solid pseudopapillary neoplasms of the pancreas
Jiang, Y., Xie, J., Wang, B., Mu, Y., & Liu, P. (2018) · Human Pathology · doi:10.1016/j.humpath.2018.07.005 · Cited by 30
Yang, L., Ying, S., Hu, S., Zhao, X., Li, M., Chen, M., Zhu, Y., Song, P., Zhu, L., Jiang, T., et al. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0059-4 · Cited by 30
Autophagy in the Immunosuppressive Perivascular Microenvironment of Glioblastoma
Molina, M. L., García‐Bernal, D., Martı́nez, S., & Valdor, R. (2019) · Cancers · doi:10.3390/cancers12010102 · Cited by 30
Amrutkar, M., & Gladhaug, I. P. (2021) · Cancers · doi:10.3390/cancers13040601 · Cited by 31
Fang, R., Wang, X., Xia, Q., Zhao, M., Zhang, H., Wang, X., Ye, S., Cheng, K., Yan, L., Cheng, Y., et al. (2021) · Oncogene · doi:10.1038/s41388-021-01776-8 · Cited by 30
The role of TFEB in tumor cell autophagy: Diagnostic and therapeutic opportunities
Bahrami, A., Bianconi, V., Pirro, M., Orafai, H. M., & Sahebkar, A. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117341 · Cited by 29
Gemcitabine promotes autophagy and lysosomal function through ERK- and TFEB-dependent mechanisms
Marchand, B., Poulin, M.-A., Lawson, C., Tai, L., Jean, S., & Boucher, M. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01342-z · Cited by 32
Li, Q., Zhang, G.-L., Hao, C., Ma, Y., Sun, X., Zhang, Y., Cao, K., Li, B., Yang, G., & Wang, X. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113430 · Cited by 29
Kim, N., Kim, S., Lee, M.-W., Jeon, H. J., Ryu, H., Kim, J., & Lee, H. J. (2021) · Cancers · doi:10.3390/cancers13122920 · Cited by 29
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Metadata
- Authors
- Perera, R. M., Stoykova, S., Nicolay, B. N., Ross, K. N., Fitamant, J., Boukhali, M., Lengrand, J., Deshpande, V., Selig, M. K., Ferrone, C. R., Settleman, J., Stephanopoulos, G., Dyson, N. J., Zoncu, R., Ramaswamy, S., Haas, W., & Bardeesy, N.
- Affiliations
- Harvard University (US)
- Massachusetts General Hospital (US)
- Massachusetts Institute of Technology (US)
- University of California, Berkeley (US)
- Corresponding author
- Bardeesy, Nabeel
- ORCID
- Venue
- Nature
- Published
- 2015-07-13
- Volume
- 524
- Issue
- 7565
- Pages
- 361-365
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5086585
- OpenAlex
- W1678795445
- Cited by
- 799
- References
- 49
- Citations by year
- 2026: 42 · 2025: 59 · 2024: 64 · 2023: 62 · 2022: 84 · 2021: 107 · 2020: 85 · 2019: 76 · 2018: 77 · 2017: 65 · 2016: 63 · 2015: 13
- FWCI
- 57.07
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- PMC
- Funders
- Hirshberg Foundation for Pancreatic Cancer Research
- National Institutes of Health (P50CA1270003)
- National Cancer Institute (P50CA127003, P50CA1270003, R01CA133557, DP2CA195761, P01CA117969)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Keywords
- autophagy, lysosomal biogenesis, pancreatic ductal adenocarcinoma, cancer metabolism, metabolic reprogramming, TFEB, TFE3, MITF, nuclear import, amino acid metabolism, cellular stress response, lysosomal catabolism
- MeSH terms
- Amino Acids, Animals, Autophagy, Energy Metabolism, Female, Homeostasis, Humans, Lysosomes, Neoplasm Transplantation, Pancreatic Neoplasms, Transcription Factors, Transcription, Genetic, Gene Expression Regulation, Neoplastic, Carcinoma, Pancreatic Ductal, Active Transport, Cell Nucleus, Cell Line, Tumor, Mice, Microphthalmia-Associated Transcription Factor, Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, Heterografts
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