The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Autophagy mediates the mitotic senescence transition
Open accessAbstract
As a stress response, senescence is a dynamic process involving multiple effector mechanisms whose combination determines the phenotypic quality. Here we identify autophagy as a new effector mechanism of senescence. Autophagy is activated during senescence and its activation is correlated with negative feedback in the PI3K–mammalian target of rapamycin (mTOR) pathway. A subset of autophagy-related genes are up-regulated during senescence: Overexpression of one of those genes, ULK3, induces autophagy and senescence. Furthermore, inhibition of autophagy delays the senescence phenotype, including senescence-associated secretion. Our data suggest that autophagy, and its consequent protein turnover, mediate the acquisition of the senescence phenotype.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Some studies have touched on the functional relevance of autophagy in senescence, where its role appears to vary depending on cell type and senescence triggers (Patschan et al. 2007; Young et al. 2009; Leidal et al. 2012; Mosieniak et al. 2012; Singh et al. 2012; Dörr et al. 2013).”
From Cellular senescence and its effector programs (2014) · cites this paper as Young et al. 2009
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In preclinical models, proteotoxic stress not only drives entry into a senescent state, but also activates autophagy, which consequently buffers toxicity from misfolded SASP factors 44,45 .”
From Senescence and cancer — role and therapeutic opportunities (2022) · cites this paper as [44]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“they may have both similar and distinct functions that are tissue-or cell-type specific [637-641]”
From Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1 (2021) · cites this paper as [638]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The kinetics of these gene expression changes were similar to that of SASP components, implying some level of correlation between autophagy and the SASP.”
From Cellular senescence and its effector programs (2014) · cites this paper as Young et al. 2009
The cited source says what the claim attributes to it.
In the citing paper
“We recently showed that autophagy is activated during the dynamic phase of OIS in HDFs, which was accompanied by a concerted up-regulation of genes involved in both autophagy and lysosomal biogenesis (Young et al. 2009).”
From Cellular senescence and its effector programs (2014) · cites this paper as Young et al. 2009
The cited source says what the claim attributes to it.
In the citing paper
“Indeed, inhibition of autophagy suppressed the production of both IL6 and IL8 and delayed the establishment of senescence.”
From Cellular senescence and its effector programs (2014) · cites this paper as Young et al. 2009
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“ULK2 has a higher degree of identity with ULK1 than any of the other homologs”
From Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1 (2021) · cites this paper as [638]
Experimental — accuracy not yet measuredIn the citing paper
“macro-autophagy (hereafter referred to as autophagy)—a tightly regulated major lysosomal degradation pathway (27–30)—has been implicated in establishing the SASP through the target of rapamycin (TOR) autophagy spatial coupling compartment (TASCC).”
From The DNA damage response induces inflammation and senescence by inhibiting autophagy of GATA4. (2015) · cites this paper as [31]
In the citing paper
“Our results indicate that autophagy is both a negative and a positive regulator of senescence, resolving apparently contradictory reports in the literature (31–33, 44).”
From The DNA damage response induces inflammation and senescence by inhibiting autophagy of GATA4. (2015) · cites this paper as [31]
In the citing paper
“These cells use autophagy for their maintenance”
From p21 maintains senescent cell viability under persistent DNA damage response by restraining JNK and caspase signaling (2017) · cites this paper as Young et al, 2009
In the citing paper
“Autophagy is activated during senescence”
From Inside and out: the activities of senescence in cancer (2014) · cites this paper as [59]
In the citing paper
“Autophagy is dynamically activated during OIS and facilitates the synthesis of interleukin 6 (IL-6) and IL-8, major components of the SASP 58,59 .”
From Inside and out: the activities of senescence in cancer (2014) · cites this paper as [59]
In the citing paper
“and that the inhibition of autophagy delays of onset of senescence and SASP.”
From Inside and out: the activities of senescence in cancer (2014) · cites this paper as [59]
In the citing paper
“Autophagy is also required for the execution of the senescence program because its inhibition delays the senescence-related cell cycle arrest and SASP factor accumulation, at least in OIS [244].”
From Mechanisms and Regulation of Cellular Senescence (2021) · cites this paper as [244]
In the citing paper
“In senescence induced by oncogenic Ras, protein synthesis and autophagic degradation are simultaneous activated, and the same cell displays high autophagic activity and activated mTOR, the autophagy inhibitor [244].”
From Mechanisms and Regulation of Cellular Senescence (2021) · cites this paper as [244]
In the citing paper
“Moreover, autophagy is required for some instances of cell-autonomous tumor suppression by senescence (e.g., in oncogene-induced senescence caused by HRAS V12 and BRAF V600E ) 156,157 and cell death (e.g., in the context of ferroptosis) 158 (Figure 3A).”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [156]
In the citing paper
“Of note, proficient autophagy is required for the successful establishment of OIS.156”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [156]
In the citing paper
“Although BNIP3L is typically thought of as pro-apoptotic [181], anti-apoptotic roles have been recently discovered, particularly in reactive astrocytes during ALS disease progression [35]. Similarly, BNIP3L has been shown to increase in senescent cells to direct mitochondria to autophagosomes for degradation [174].”
From Early onset senescence and cognitive impairment in a murine model of repeated mTBI (2021) · cites this paper as [174]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Mariño, G., Salvador-Montoliu, N., Fueyo, A., Knecht, E., Mizushima, N., & López-Otı́n, C. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m701194200 · Cited by 427
RetractedAutophagy 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
The role of autophagy during the early neonatal starvation period
Kuma, A., Hatano, M., Matsui, M., Yamamoto, A., Nakaya, H., Yoshimori, T., Ohsumi, Y., Tokuhisa, T., & Mizushima, N. (2004) · Nature · doi:10.1038/nature03029 · Cited by 2,865
Impairment of starvation-induced and constitutive autophagy in Atg7 -deficient mice
Komatsu, M., Waguri, S., Ueno, T., Iwata, J., Murata, S., Tanida, I., Ezaki, J., Mizushima, N., Ohsumi, Y., Uchiyama, Y., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412022 · Cited by 2,331
Promotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene
Qu, X., Yu, J., Bhagat, G., Furuya, N., Hibshoosh, H., Troxel, A., Rosen, J., Eskelinen, E.-L., Mizushima, N., Ohsumi, Y., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20039 · Cited by 2,311
BRAFE600-associated senescence-like cell cycle arrest of human naevi
Michaloglou, C., Vredeveld, L. C. W., Soengas, M. S., Denoyelle, C., Kuilman, T., van der Horst, C. M. A. M., Majoor, D. M., Shay, J. W., Mooi, W. J., & Peeper, D. S. (2005) · Nature · doi:10.1038/nature03890 · Cited by 2,160
Yue, Z., Jin, S., Yang, C., Levine, A. J., & Heintz, N. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2436255100 · Cited by 2,116
Oncogene-Induced Senescence Relayed by an Interleukin-Dependent Inflammatory Network
Kuilman, T., Michaloglou, C., Vredeveld, L. C. W., Douma, S., van Doorn, R., Desmet, C. J., Aarden, L. A., Mooi, W. J., & Peeper, D. S. (2008) · Cell · doi:10.1016/j.cell.2008.03.039 · Cited by 2,086
Autophagy promotes tumor cell survival and restricts necrosis, inflammation, and tumorigenesis
Degenhardt, K., Mathew, R., Beaudoin, B., Bray, K., Anderson, D., Chen, G., Mukherjee, C., Shi, Y., Gélinas, C., Fan, Y., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.06.001 · Cited by 2,069
Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis
Chen, Z., Trotman, L. C., Shaffer, D., Lin, H.-K., Dotan, Z. A., Niki, M., Koutcher, J. A., Scher, H. I., Ludwig, T., Gerald, W., et al. (2005) · Nature · doi:10.1038/nature03918 · Cited by 1,993
Cited by
Sorted by citations
Items 701–800 of 1,000
Genes and pathways involved in senescence bypass identified by functional genetic screens
Roupakia, E., Markopoulos, G. S., & Kolettas, E. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111432 · Cited by 18
Raee, P., Tan, S. C., Najafi, S., Zandsalimi, F., Low, T. Y., Aghamiri, S., Fazeli, E., Aghapour, M., Mofarahe, Z. S., Heidari, M. H., et al. (2023) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-023-01134-1 · Cited by 18
Licence to kill senescent cells in idiopathic pulmonary fibrosis?
Mailleux, A., & Crestani, B. (2017) · European Respiratory Journal · doi:10.1183/13993003.01360-2017 · Cited by 18
Manea, A. J., & Ray, S. K. (2023) · Cells · doi:10.3390/cells12060897 · Cited by 17
Skrzeszewski, M., Maciejewska, M., Kobza, D., Gawrylak, A., Kiéda, C., & Waś, H. (2024) · Biochemical Pharmacology · doi:10.1016/j.bcp.2024.116277 · Cited by 17
Feng, Z., Ou, Y., Deng, X., Deng, M., Yan, X., Chen, L., Zhou, F., & Hao, L. (2024) · Cell & Bioscience · doi:10.1186/s13578-024-01291-9 · Cited by 18
Khalid, Z., & Almaghrabi, O. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-68696-7 · Cited by 17
Nano delivery of natural substances as prospective autophagy modulators in glioblastoma
Agarwal, S., & Maekawa, T. (2020) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2020.102270 · Cited by 17
Di, C., Du, Y., Zhang, R., Zhang, L., & Wang, S. (2023) · Journal of Thoracic Disease · doi:10.21037/jtd-23-312 · Cited by 17
Autophagic responses to hypoxia and anticancer therapy in head and neck cancer
Wu, H., Huang, S., & Zhang, D. (2014) · Pathology - Research and Practice · doi:10.1016/j.prp.2014.11.010 · Cited by 17
Anti-tumor immunity, autophagy and chemotherapy
Műzes, G. (2012) · World Journal of Gastroenterology · doi:10.3748/wjg.v18.i45.6537 · Cited by 17
Divergent mechanisms of metabolic dysfunction drive fibroblast and T-cell senescence
Callender, L. A., Carroll, E. C., Bober, E. A., & Henson, S. M. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.06.001 · Cited by 17
Quality and quantity control of proteins in senescence
Narita, M. (2010) · Aging · doi:10.18632/aging.100145 · Cited by 17
Self-citationThe Menace of Melanoma: A Photodynamic Approach to Adjunctive Cancer Therapy
Davids, L. M., & Kleem, B. (2013) · InTech eBooks · doi:10.5772/53676 · Cited by 17
A new insight into cell biological and biochemical changes through aging
Sahabi, S., Jafari-Gharabaghlou, D., & Zarghami, N. (2022) · Acta Histochemica · doi:10.1016/j.acthis.2021.151841 · Cited by 16
Autophagy: a necessary evil in cancer and inflammation
Mathur, A., Ritu, R., Chandra, P., & Das, A. (2024) · 3 Biotech · doi:10.1007/s13205-023-03864-w · Cited by 16
Jin, Y., Zhao, L., Zhang, Y., Chen, T., Shi, H., Sun, H., Ding, S., Chen, S., Cao, H., Zhang, G., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2393932 · Cited by 16
Madhu, B., Narita, M., Jauhiainen, A., Menon, S., Stubbs, M., Tavaré, S., Narita, M., & Griffiths, J. R. (2015) · Metabolomics · doi:10.1007/s11306-015-0838-z · Cited by 16
Self-citationQiu, L., Chang, G., Li, Z., Bi, Y., Liu, X., & Chen, G. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00996 · Cited by 16
Lee, J. S., Jang, E.-H., Woo, H. A., & Lee, K. (2020) · Cells · doi:10.3390/cells9010257 · Cited by 16
Bajbouj, K., Shafarin, J., Taneera, J., & Hamad, M. A. (2020) · Biology · doi:10.3390/biology9040068 · Cited by 16
Han, Y., Micklem, G., & Kim, S. Y. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101849 · Cited by 16
c-Cbl targets active Src for autophagy
Cecconi, F. (2011) · Nature Cell Biology · doi:10.1038/ncb2413 · Cited by 16
Drullion, C., Lagarde, V., Gioia, R., Legembre, P., Priault, M., Cardinaud, B., Lippert, É., Mahon, F., & Pasquet, J. (2012) · Leukemia Research and Treatment · doi:10.1155/2012/861301 · Cited by 16
Biliary Epithelial Apoptosis, Autophagy, and Senescence in Primary Biliary Cirrhosis
Sasaki, M., & Nakanuma, Y. (2010) · Hepatitis Research and Treatment · doi:10.1155/2010/205128 · Cited by 16
Profiling Celiac Disease-Related Transcriptional Changes
Castellanos–Rubio, A., & Bilbao, J. R. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.003 · Cited by 16
Fusobacterium nucleatum triggers senescence phenotype in gingival epithelial cells
Albuquerque‐Souza, E., Shelling, B., Jiang, M., Xia, X., Rattanaprukskul, K., & Sahingur, S. E. (2023) · Molecular Oral Microbiology · doi:10.1111/omi.12432 · Cited by 15
Trehalose attenuates testicular aging by activating autophagy and improving mitochondrial quality
Xi, H., Shan, W., Li, M., Wang, Z., & Li, Y. (2024) · Andrology · doi:10.1111/andr.13746 · Cited by 15
Song, J., & Yang, H. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1449668 · Cited by 15
Marmisolle, I., Chacón, E., Mansilla, S., Ruiz, S., Bresque, M., Martínez, J., Martínez‐Zamudio, R. I., Herbig, U., Liu, J., Finkel, T., et al. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103606 · Cited by 15
Montero, J. A., Lorda-Diez, C. I., & Hurlé, J. M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.593761 · Cited by 15
Fujita, Y., Iketani, M., Ito, M., & Ohsawa, I. (2022) · Experimental Gerontology · doi:10.1016/j.exger.2022.111866 · Cited by 15
Sun, J., Liu, C., Xu, J., An, Y., Xu, M., Zhong, X., Zeng, N., Ma, S.-Y., He, H., Zhang, Z.-B., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.908068 · Cited by 15
MicroRNAs-associated with FOXO3 in cellular senescence and other stress responses
Khor, Y.-S., & Wong, P. (2023) · Biogerontology · doi:10.1007/s10522-023-10059-6 · Cited by 15
Efavirenz induces autophagy and aberrant differentiation in normal human keratinocytes
Dong, Q., Oh, J.-E., Yi, J. K., Kim, R. H., SHIN, K.-H., Mitsuyasu, R. T., Park, N., & Kang, M. (2013) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2013.1327 · Cited by 15
Rheb may complex with RASSF1A to coordinate Hippo and TOR signaling
Nelson, N. C., & Clark, G. J. (2016) · Oncotarget · doi:10.18632/oncotarget.8447 · Cited by 15
Stress-induced cellular responses and cell death mechanisms during inflammatory cholangiopathies
Sasaki, M., & Nakanuma, Y. (2016) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2016.08.002 · Cited by 15
Chan, J. N. E., Humphry, M., Kitt, L., Krzyzanska, D., Filbey, K. J., Bennett, M. R., & Clarke, M. C. H. (2020) · European Journal of Immunology · doi:10.1002/eji.201948521 · Cited by 15
Jin, B., Ren, J. F., Chen, J., Dong, Z., Chen, G., & Liu, D. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03591-3 · Cited by 14
Xrp1 governs the stress response program to spliceosome dysfunction
Stanković, D., Tain, L. S., & Uhlířová, M. (2024) · Nucleic Acids Research · doi:10.1093/nar/gkae055 · Cited by 14
Precise immunofluorescence canceling for highly multiplexed imaging to capture specific cell states
Tomimatsu, K., Fujii, T., Bise, R., Hosoda, K., Taniguchi, Y., Ochiai, H., Ohishi, H., Ando, K., Minami, R., Tanaka, K. Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47989-9 · Cited by 14
Self-citationLiu, X., Chen, B., Liu, X., Zhang, X., & Wu, J. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1625357 · Cited by 14
Conformational plasticity of the ULK3 kinase domain
Mathea, S., Salah, E., Tallant, C., Chatterjee, D., Berger, B., Konietzny, R., Müller, S., Kessler, B. M., & Knapp, S. (2021) · Biochemical Journal · doi:10.1042/bcj20210257 · Cited by 14
Signs of Similarities and Differences in Cellular Models of Aging: A Scoping Review
Васильевна, М. Г., & Khokhlov, A. N. (2022) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392522030087 · Cited by 14
The establishment of mitotic errors-driven senescence depends on autophagy
Goutas, A., Outskouni, Z., Papathanasiou, I. V., Georgakopoulou, A., Karpetas, G. E., Gonos, E. S., & Trachana, V. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102701 · Cited by 14
Oncogene-mediated tumor transformation sensitizes cells to autophagy induction
Gargini, R., García‐Escudero, V., Izquierdo, M., & Wandosell, F. G. (2016) · Oncology Reports · doi:10.3892/or.2016.4699 · Cited by 14
Some remarks on the relationship between autophagy, cell aging, and cell proliferation restriction
Васильевна, М. Г., Клебанов, А. А., & Khokhlov, A. N. (2016) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392516040088 · Cited by 14
New concept: cellular senescence in pathophysiology of cholangiocarcinoma
Sasaki, M., & Nakanuma, Y. (2015) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/17474124.2016.1133291 · Cited by 14
Rags connect mTOR and autophagy
Narita, M., & Inoki, K. (2012) · Small GTPases · doi:10.4161/sgtp.19422 · Cited by 14
Self-citationCassidy, L. D., & Narita, M. (2015) · Science · doi:10.1126/science.aad2501 · Cited by 14
Self-citationChevalley, T., Dübi, M., Fumeaux, L., Merli, M. S., Sarre, A., Schaer, N., Siméoni, U., & Yzydorczyk, C. (2025) · Cells · doi:10.3390/cells14060467 · Cited by 13
Zhao, Y., Tan, F., Zhao, J., Zhou, S., Luo, Y., & Chen, G. (2025) · MedComm · doi:10.1002/mco2.70202 · Cited by 13
Jeong, D., Park, S. H., Kim, J., Kim, H., Jang, Y., Koh, J., Jeon, Y. K., Tasaki, T., Kwon, Y. T., Han, D., et al. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2425015122 · Cited by 13
Evasion of oncogene-induced senescence by gammaherpesviruses
Leidal, A. M., Pringle, E. S., & McCormick, C. (2012) · Current Opinion in Virology · doi:10.1016/j.coviro.2012.09.009 · Cited by 13
Autophagy : Moving Benchside Promises to Patient Bedsides
Belaïd, A., Ndiaye, P. D., Filippakis, H., Roux, J., Röttinger, É., Graba, Y., Brest, P., Hofman, P. M., & Mograbi, B. (2015) · Current Cancer Drug Targets · doi:10.2174/156800961508151001102452 · Cited by 13
Wu, N., Yang, D., Wu, Z., Yan, M., Zhang, P., & Liu, Y. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.12.130 · Cited by 13
Logli, E., Marzuolo, E., D'Agostino, M., Conti, L. A., Lena, A. M., Diociaiuti, A., Dellambra, E., Has, C., Cianfanelli, V., Zambruno, G., et al. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab318 · Cited by 13
Liu, H., HUANG, Z., Jiang, H., Su, K., Si, Z.-L., Wenhui, W. U., Hanyu, W. A. N. G., Dongxue, L. I., Ninghua, T. A. N., & Zhang, Z. (2023) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(23)60398-x · Cited by 13
Cooperative pro-tumorigenic adaptation to oncogenic RAS through epithelial-to-mesenchymal plasticity
Blander, H. D., Tonon, L., Fauvet, F., Pommier, R. M., Lamblot, C., Benhassoun, R., Angileri, F., Gibert, B., Rodriguez, R., Ouzounova, M., et al. (2024) · Science Advances · doi:10.1126/sciadv.adi1736 · Cited by 13
Macroautophagy and the Oncogene-Induced Senescence
Grasso, D., & Vaccaro, M. I. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00157 · Cited by 13
Hernández‐Breijo, B., Monserrat, J., Román, I. D., González‐Rodríguez, Á., Fernández-Moreno, D., Lobo, M. V. T., Valverde, Á. M., Gisbert, J. P., & Guijarro, L. G. (2013) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2013.07.024 · Cited by 13
Age-related dysfunction of the autophago-lysosomal pathway in human endothelial cells
Mai, S., Brehm, N., Auburger, G. W. J., Bereiter‐Hahn, J., & Jendrach, M. (2019) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-019-02288-x · Cited by 13
Yokouchi, H., Nishihara, H., Harada, T., Yamazaki, S., Kikuchi, H., Oizumi, S., Uramoto, H., Tanaka, F., Harada, M., Akie, K., et al. (2020) · Heliyon · doi:10.1016/j.heliyon.2020.e04439 · Cited by 13
Autophagy based cellular physiological strategies target oncogenic progression
Kumar, P., Jagtap, Y. A., Patwa, S. M., Kinger, S., Dubey, A. R., Prajapati, V. K., Dhiman, R., Poluri, K. M., & Mishra, A. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30567 · Cited by 13
Connecting Ras and CTP synthase in Drosophila
Zhou, Y., Liu, J., & Liu, J. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113155 · Cited by 13
Recent Anti-KRASG12D Therapies: A “Possible Impossibility” for Pancreatic Ductal Adenocarcinoma
Sobhani, N., Pittacolo, M., D’Angelo, A., & Marchegiani, G. (2025) · Cancers · doi:10.3390/cancers17040704 · Cited by 12
The paracrine effects of fibroblasts on Doxorubicin-treated breast cancer cells
Fourie, C., Davis, T., Kriel, J., & Engelbrecht, A. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.05.020 · Cited by 12
Zhao, G., Zhang, T., Liu, W. C., Edderkaoui, M., Hu, R., Li, J., Pandol, S. J., Fu, X., & Han, Y. (2022) · Cancers · doi:10.3390/cancers14061407 · Cited by 12
Wang, Q., Chen, J., Zhang, M., Wang, H., Zeng, Y., Huang, Y., & Xu, C. (2022) · Journal of Oncology · doi:10.1155/2022/6523195 · Cited by 12
Mitochondrial Metabolism in X-Irradiated Cells Undergoing Irreversible Cell-Cycle Arrest
Hirose, E., Noguchi, M., Ihara, T., & Yokoya, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24031833 · Cited by 12
Senescent Cells: Dual Implications on the Retinal Vascular System
Habibi-Kavashkohie, M. R., Scorza, T., & Oubaha, M. (2023) · Cells · doi:10.3390/cells12192341 · Cited by 12
How Human Tumor Viruses Make Use of Autophagy
Pratt, Z. L., & Sugden, B. (2012) · Cells · doi:10.3390/cells1030617 · Cited by 12
Schüller, H. E. K., & Gözüaçık, D. (2014) · TURKISH JOURNAL OF BIOLOGY · doi:10.3906/biy-1408-16 · Cited by 13
Activation of DNA Damage Response Induced by the Kaposi’s Sarcoma-Associated Herpes Virus
Domenico, E. G. D., Toma, L., Bordignon, V., Trento, E., D’Agosto, G., Cordiali‐Fei, P., & Ensoli, F. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17060854 · Cited by 12
Seno-suppressive molecules as new therapeutic perspectives in rheumatic diseases
Tachikart, Y., Malaise, O., Mumme, M., Jørgensen, C., & Brondello, J. (2019) · Biochemical Pharmacology · doi:10.1016/j.bcp.2019.03.017 · Cited by 12
Du, H., Wang, Y., Liu, X., Wang, S., Wu, S., Yuan, Z., & Zhu, X. (2020) · Cytokine · doi:10.1016/j.cyto.2020.155314 · Cited by 12
Cellular senescence and tumor promotion: Role of the Unfolded Protein Response
Pluquet, O., & Abbadie, C. (2021) · Advances in cancer research · doi:10.1016/bs.acr.2021.01.001 · Cited by 12
Zhang, M., Damba, T., Wu, Z., Salas, S. S., Buist‐Homan, M., Faber, K. N., & Moshage, H. J. (2022) · Food Bioscience · doi:10.1016/j.fbio.2022.102164 · Cited by 12
Senescence and Senescence-Related Disorders
Wang, Z. P., & Inuzuka, H. (2013) · InTech eBooks · doi:10.5772/56158 · Cited by 12
Kaul, Z., & Chakrabarti, O. (2018) · Traffic · doi:10.1111/tra.12569 · Cited by 12
Autophagy and senescence: Insights from normal and cancer stem cells
Talukdar, S., Das, S. K., Emdad, L., & Fisher, P. B. (2021) · Advances in cancer research · doi:10.1016/bs.acr.2021.01.005 · Cited by 12
Autophagy modulation in cancer
Guilbaud, E., Ryan, K. M., Green, D. R., & Galluzzi, L. (2026) · Nature Reviews Drug Discovery · doi:10.1038/s41573-026-01449-9 · Cited by 11
Schepers, A. G., Jochems, F., Lieftink, C., Wang, L., Pogacar, Z., de Oliveira, R. L., Conti, G. D., Beijersbergen, R. L., & Bernards, R. (2021) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-21-0146 · Cited by 11
Palbociclib-Induced Cellular Senescence Is Modulated by the mTOR Complex 1 and Autophagy
Cayo, Á., Venturini, W., Rebolledo-Mira, D., Moore‐Carrasco, R., Herrada, A. A., Nova‐Lamperti, E., Valenzuela, C. A., & Brown, N. E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119284 · Cited by 11
Modelling the dynamics of senescence spread
Martin, L., Schumacher, L. J., & Chandra, T. (2023) · Aging Cell · doi:10.1111/acel.13892 · Cited by 11
Systematic transcriptomic analysis and temporal modelling of human fibroblast senescence
Scanlan, R.-L., Pease, L., O’Keefe, H., Guimera, A. M., Rasmussen, L. J., Wordsworth, J., & Shanley, D. P. (2024) · Frontiers in Aging · doi:10.3389/fragi.2024.1448543 · Cited by 11
Kasak, L., Näks, M., Eek, P., Piirsoo, A., Bhadoria, R., Starkov, P., Saarma, M., Kasvandik, S., & Piirsoo, M. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b00356 · Cited by 11
Chan, K. T., Paavolainen, L., Hannan, K. M., George, A. J., Hannan, R. D., Simpson, K. J., Horváth, P., & Pearson, R. B. (2016) · Assay and Drug Development Technologies · doi:10.1089/adt.2016.739 · Cited by 11
Autophagy Induced during Pancreatitis Promotes KRAS-Dependent Transformation in the Pancreas
Iovanna, J. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00226 · Cited by 11
L’autophagie contribue à l’initiation du cancer pancréatique
Iovanna, J. (2017) · médecine/sciences · doi:10.1051/medsci/20173303022 · Cited by 11
Nam, H. Y., Park, S., Lee, G., Kim, E., Lee, S., Chang, H. W., Chang, E., Choi, K., & Kim, S. W. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01362-4 · Cited by 10
Nanomaterials intervene in cell senescence to reinforce cancer therapy
Sun, S., Yang, N., Nie, J., Yang, Z., Pei, Z., Ding, R., & Cheng, L. (2025) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2025.217012 · Cited by 10
Unveiling the Paradoxical Nature of Autophagy in Cancer Cell Fate
Shifa, J., Amin, T., Fakruddin, M., Rahman, K. A., & Islam, S. M. B. U. (2025) · Cancer Control · doi:10.1177/10732748251384365 · Cited by 10
Hellani, F., Leleu, I., Saïdi, N., Martin, N., Lecœur, C., Werkmeister, E., Koffi, D., Trottein, F., Etté, H. Y., Das, B. K., et al. (2023) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2023.12.030 · Cited by 10
Autophagy Determines Distinct Cell Fates in Human Amnion and Chorion Cells
Severino, M. E. L., Richardson, L., Kammala, A. K., Radnaa, E., Khanipov, K., Dalmacio, L. M. M., Mysorekar, I. U., Kacerovský, M., & Menon, R. (2024) · Autophagy Reports · doi:10.1080/27694127.2024.2306086 · Cited by 10
Hai, G., Bai, J., Liu, Y., Li, J., Liu, A., Wang, J., Liu, Q., Liu, W., Wan, P., & Fu, X. (2024) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2024.1376205 · Cited by 10
Lee, S. S., Halawani, A. A., Teo, J. D., Weiss, A. S., & Yeo, G. C. (2024) · Advanced Science · doi:10.1002/advs.202402168 · Cited by 10
Mir, K. B., Faheem, M. M., Ahmad, S. M., Rasool, J. U., Amin, T., Chakraborty, S., Bhagat, M., Ahmed, Z., Ali, A., & Goswami, A. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.1013500 · Cited by 10
Autophagy-dependent regulation of tumor metastasis by myeloid cells
Jinushi, M., Morita, T., Xu, Z., Kinoshita, I., Dosaka‐Akita, H., Yagita∥, H., & Kawakami, Y. (2017) · PLoS ONE · doi:10.1371/journal.pone.0179357 · Cited by 10
Hayat, M. A. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-812146-7.00001-9 · Cited by 10
Metadata
- Authors
- 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., & Narita, M.
- Affiliations
- Cancer Research UK (GB)
- European Bioinformatics Institute (GB)
- Tokyo Medical and Dental University (JP)
- ORCID
- Venue
- Genes & Development
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2009-03-11
- Volume
- 23
- Issue
- 7
- Pages
- 798-803
- ISSN
- 0890-9369 (ISSN-L)
- 1549-5477
- PMC
- PMC2666340
- OpenAlex
- W2113995129
- Cited by
- 1,078
- References
- 39
- Citations by year
- 2026: 19 · 2025: 36 · 2024: 53 · 2023: 56 · 2022: 62 · 2021: 90 · 2020: 64 · 2019: 52 · 2018: 70 · 2017: 64 · 2016: 78 · 2015: 60 · 2014: 78 · 2013: 86 · 2012: 72
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genes & Development (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Research Portal (King's College London) (submittedVersion)
- Funders
- Cancer Research UK (19556)
- University of Cambridge
- 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 › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- autophagy, cellular senescence, PI3K/mTOR pathway, ULK3, protein turnover, negative feedback regulation, autophagy-related genes
- MeSH terms
- Aging, Autophagy, Gene Expression Regulation, Humans, Immunohistochemistry, Microtubule-Associated Proteins, Mitosis, Neoplasms, Protein Kinases, Protein Serine-Threonine Kinases, Feedback, Physiological, TOR Serine-Threonine Kinases
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