The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
The role for autophagy in cancer
Open accessAbstract
Autophagy is a survival-promoting pathway that captures, degrades, and recycles intracellular proteins and organelles in lysosomes. Autophagy preserves organelle function, prevents the toxic buildup of cellular waste products, and provides substrates to sustain metabolism in starvation. Although in some contexts autophagy suppresses tumorigenesis, in most contexts autophagy facilitates tumorigenesis. Cancers can upregulate autophagy to survive microenvironmental stress and to increase growth and aggressiveness. Mechanisms by which autophagy promotes cancer include suppressing induction of the p53 tumor suppressor protein and maintaining metabolic function of mitochondria. Efforts to inhibit autophagy to improve cancer therapy have thereby attracted great interest.
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 cited source says what the claim attributes to it.
In the citing paper
“Of note, since autophagy activity has been linked to development and progression of a plethora of pathologies [9–11], it becomes increasingly fundamental to develop new strategies for the prediction of a specific autophagy status and/or step [8].”
From A gene toolbox for monitoring autophagy transcription (2021) · cites this paper as [11]
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
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
Vogelstein, B., Papadopoulos, N., Velculescu, V. E., Zhou, S., Diaz, L. A., & Kinzler, K. W. (2013) · Science · doi:10.1126/science.1235122 · Cited by 7,863
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
Autophagy: Renovation of Cells and Tissues
Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615
Control of inositol 1,4,5-trisphosphate-induced Ca2+ release by cytosolic Ca2+
Bootman, M. D., Missiaen, L., Parys, J. B., SMEDT, H. D., & Casteels, R. (1995) · Biochemical Journal · doi:10.1042/bj3060445 · Cited by 5,131
Autophagy and Viruses: Adversaries or Allies?
Dong, X., & Levine, B. (2013) · Journal of Innate Immunity · doi:10.1159/000346388 · Cited by 4,444
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
Induction of autophagy and inhibition of tumorigenesis by beclin 1
Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347
Discovery and saturation analysis of cancer genes across 21 tumour types
Lawrence, M. S., Stojanov, P., Mermel, C. H., Robinson, J. T., Garraway, L. A., Golub, T. R., Meyerson, M., Gabriel, S. B., Lander, E. S., & Getz, G. (2014) · Nature · doi:10.1038/nature12912 · Cited by 3,096 · cited 1×
“Note that large-scale genomic analysis of human cancers to date has failed to identify recurrent mutations in BECN1 or other essential autophagy genes (21, 22).”
Autophagy in Human Health and Disease
Choi, A. M. K., Ryter, S. W., & Levine, B. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1205406 · Cited by 2,583
Flagged first, then by citations
Cited by
Sorted by citations
Items 801–900 of 1,000
The Function of Autophagy in the Initiation, and Development of Breast Cancer
Beilankouhi, E. A. V., Valilo, M., Dastmalchi, N., Teimourian, S., & Safaralizadeh, R. (2023) · Current Medicinal Chemistry · doi:10.2174/0929867330666230503145319 · Cited by 13
Fang, J., Qian, Y. H., Chen, J., Xu, D., Cao, N., Zhu, G., Hu, W., Hu, H., Qian, N., Yang, S., et al. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvad077 · Cited by 13
NUCKS1 promotes the progression of colorectal cancer via activating PI3K/AKT/mTOR signaling pathway
Liao-Liao, Z. H. U., Jing-Jie, S. H. I., Yong-Dong, G. U. O., Yang, C., Rong-Lin, W. A. N. G., Shan-Shan, L. I., Gan, D., Pei-Xiang, M. A., Jun-Qiang, L. I., & Hai-Chuan, S. U. (2023) · Neoplasma · doi:10.4149/neo_2023_221107n1088 · Cited by 14
Wang, Y., Zuo, R., Huo, G., Han, Z., He, Y., Luo, Y., Chen, L.-W., Li, G., Cui, J., Zhu, F., et al. (2023) · The FASEB Journal · doi:10.1096/fj.202300248r · Cited by 13
Ohnami, S., Ohshima, K., Nagashima, T., Urakami, K., Shimoda, Y., Saito, J., Naruoka, A., Hatakeyama, K., Mochizuki, T., Serizawa, M., et al. (2017) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-017-2977-1 · Cited by 13
Derrone induces autophagic cell death through induction of ROS and ERK in A549 cells
Kang, M.-J., Kim, S., Kwon, E., Jo, Y. H., Lee, M. K., Lee, H.-S., Moon, D., & Kim, M.-O. (2019) · PLoS ONE · doi:10.1371/journal.pone.0218659 · Cited by 13
Kindlin‑2 suppresses cervical cancer cell migration through AKT/mTOR‑mediated autophagy induction
Wu, G., Long, Y., Lu, Y., Feng, Y., Yang, X., Xu, X., & Yao, D. (2020) · Oncology Reports · doi:10.3892/or.2020.7603 · Cited by 13
Zhong, S., Chen, H. A., Yang, S., Feng, J., & Zhou, S. (2020) · PeerJ · doi:10.7717/peerj.9621 · Cited by 13
Suppression of autophagy facilitates hydrogen gas‑mediated lung cancer cell apoptosis
Liu, L., Yan, Z., Wang, Y., Meng, J., & Chen, G. (2020) · Oncology Letters · doi:10.3892/ol.2020.11973 · Cited by 13
He, M., Yan, G., Wang, Y., Gong, R., Hong, L., Yu, S., He, X., Li, G., Du, W., Ma, T., et al. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16412 · Cited by 14
Qu, J., Zeng, C. C., Zou, T., Xu, C., Yang, X., & Lin, Z. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115566 · Cited by 15
The roles, controversies, and combination therapies of autophagy in lung cancer
Wang, Z., Zhou, C., & Yang, S. (2021) · Cell Biology International · doi:10.1002/cbin.11704 · Cited by 13
Li, J., Tang, X., Du, Y., Dong, J., Zhao, Z., Hu, H., Song, T., Guo, J., Wang, Y., Xu, T., et al. (2021) · BioMed Research International · doi:10.1155/2021/5428425 · Cited by 12
Squalene-Based Nano-Assemblies Improve the Pro-Autophagic Activity of Trehalose
Frapporti, G., Colombo, E., Ahmed, H., Assoni, G., Polito, L., Randazzo, P., Arosio, D., Seneci, P., & Piccoli, G. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14040862 · Cited by 13
DANCR promotes glioma cell autophagy and proliferation via the miR‑33b/DLX6/ATG7 axis
Yu, W., Ma, L., & Li, X. (2023) · Oncology Reports · doi:10.3892/or.2023.8476 · Cited by 13
The Current Status of the Liver Liquid Biopsy in MASH Related HCC: Overview and Future Directions
Ugonabo, O. S., Udoh, U. S., Rajan, P. K., Reeves, H., Arcand, C. M., Nakafuku, Y., Joshi, T., Finley, R., Pierre, S. V., & Sanabria, J. R. (2023) · Biomolecules · doi:10.3390/biom13091369 · Cited by 13
Gaglio, D., Valtorta, S., Ripamonti, M., Bonanomi, M., Damiani, C., Todde, S., Negri, A. S., Sanvito, F., Mastroianni, F., Campli, A. D., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.10470 · Cited by 15
Paiardi, C., Mirzoyan, Z., Zola, S., Parisi, F., Vingiani, A., Pasini, M. E., & Bellosta, P. (2017) · Genes · doi:10.3390/genes8050131 · Cited by 13
Havaki, S., Vlachou, V., Zampetidis, C., Selemenakis, P., Kotsinas, A., Mavrogonatou, E., Rizou, S. V., Kyrodimos, E., Evangelou, K., Kletsas, D., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18091920 · Cited by 14
Khan, M. W., Layden, B. T., & Chakrabarti, P. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.03.013 · Cited by 13
Chromosomal instability causes sensitivity to protein folding stress and ATP depletion
Khan, M., Shaukat, Z., Saint, R. B., & Gregory, S. L. (2018) · Biology Open · doi:10.1242/bio.038000 · Cited by 13
Autoimmune Hepatitis and Stellate Cells: An Insight into the Role of Autophagy
Golbabapour, S., Lankarani, K. B., Ghavami, S., & Geramizadeh, B. (2019) · Current Medicinal Chemistry · doi:10.2174/0929867326666190402120231 · Cited by 13
Chargui, A., Belaïd, A., Ndiaye, P. D., Imbert, V., Samson, M., Guigonis, J., Tauc, M., Peyron, J., Poujeol, P., Brest, P., et al. (2021) · Cancers · doi:10.3390/cancers13102490 · Cited by 13
Lahiri, V., Metur, S. P., Hu, Z., Song, X., Mari, M. C., Hawkins, W. D., Bhattarai, J., Delorme‐Axford, E., Reggiori, F., Tang, D., et al. (2021) · Autophagy · doi:10.1080/15548627.2021.1997305 · Cited by 14
Relationship Between Autophagy and Drug Resistance in Tumors
Hu, X., Wen, L., Li, X., & Zhu, C. (2022) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557522666220905090732 · Cited by 13
Role of Tumor Cell Intrinsic and Host Autophagy in CancerPreprint
Guo, J. Y., & White, E. (2024) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a041539 · Cited by 14
Self-citationSmall molecule disruption of RARα/NCoR1 interaction inhibits chaperone-mediated autophagy in cancer
McCabe, M., Bhattacharyya, R., Sereda, R., Santiago‐Fernández, O., Khawaja, R. R., Díaz, A., Lindenau, K. L., Ozturk, D. G., Garner, T. P., Sidoli, S., et al. (2025) · EMBO Molecular Medicine · doi:10.1038/s44321-025-00254-y · Cited by 12
Deng, X., Wang, J., Lu, C., Zhou, Y., Shen, L., Ge, A., Fan, H., & Liu, L. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1226629 · Cited by 14
Chen, Z., Chen, Z., Gao, S., Shi, J. R., Li, X., & Sun, F. (2023) · Reproductive Biology · doi:10.1016/j.repbio.2023.100846 · Cited by 12
Molecular basis and current insights of atypical Rho small GTPase in cancer
Huang, H., Wang, S., Guan, Y., Ren, J., & Liu, X. (2024) · Molecular Biology Reports · doi:10.1007/s11033-023-09140-7 · Cited by 12
Ding, X., Li, X., Jiang, Y., Li, Y., Li, H., Shang, L., Feng, G., Zhang, H., Xu, Z., Yang, L., et al. (2024) · Cancer Cell International · doi:10.1186/s12935-024-03282-9 · Cited by 14
The protective role of baicalin regulation of autophagy in cancers
Zhang, Q., Guo, S., Ge, H., & Wang, H. (2025) · Cytotechnology · doi:10.1007/s10616-024-00689-0 · Cited by 12
Lim, J. Y., & Kwan, H. Y. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.80788 · Cited by 12
Ashrafizadeh, M., Mohammadinejad, R., Tavakol, S., Ahmadi, Z., & Sahebkar, A. (2020) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520620666200619180716 · Cited by 11
Zhang, X., Deibert, C. P., Kim, W.-J., Jaman, E., Rao, A. V., Lotze, M. T., & Amankulor, N. (2020) · Cancer Gene Therapy · doi:10.1038/s41417-020-0205-8 · Cited by 13
Identification of autophagy‐related gene and lncRNA signatures in the prognosis of HNSCC
Li, Q., Wang, J., Meng, X., Chen, W., Feng, J., & Mao, J. (2021) · Oral Diseases · doi:10.1111/odi.13889 · Cited by 12
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
Yan, R.-L., Luan, C.-L., Liao, C., Liu, L., Chen, F.-Y., Chen, H., & Chen, R. (2022) · Journal of Biomedical Science · doi:10.1186/s12929-022-00815-0 · Cited by 12
Molecular Targets of Ascochlorin and Its Derivatives for Cancer Therapy
Min‐Wen, J. C., Chua, B. Y.-J., Mishra, S., Dai, X., Magae, J., Shyh‐Chang, N., Kumar, A. P., & Sethi, G. (2017) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2017.01.001 · Cited by 12
TFDP3 regulates the apoptosis and autophagy in breast cancer cell line MDA-MB-231
Ding, L., Chu, M., Jiao, Y.-S., Qi, H., Xiao, P., Li, H., Guo, Q., & Wang, Y. (2018) · PLoS ONE · doi:10.1371/journal.pone.0203833 · Cited by 12
Centrosome Amplification in Cancer Disrupts Autophagy and Sensitizes to Autophagy Inhibition
Denu, R. A., Kaur, G., Sass, M. M., Lakkaraju, A., & Burkard, M. E. (2019) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-19-0509 · Cited by 15
Feng, S., Zha, Z., Wang, Z., Yang, P., Wu, J., Li, X., Xu, Q., & Liu, Y. (2020) · Natural Product Research · doi:10.1080/14786419.2020.1739039 · Cited by 12
Li, X. M., Jung, K. E., Yim, S., Hong, D. K., Kim, C. D., Hong, J. Y., Lee, H. J., Lee, S. Y., Kim, J. E., & Park, C. W. (2020) · BioMed Research International · doi:10.1155/2020/4584626 · Cited by 12
Insights of roles played by septins in pathogenic fungi
Li, L., Zhu, X., Su, Z.-Z., Poeta, M. D., Liu, X., & Lin, F. (2021) · Virulence · doi:10.1080/21505594.2021.1933370 · Cited by 12
Xu, N., Zhao, Y., Bu, H., Tan, S., Dong, G., Liu, J., Wang, M., Jiang, J., Yuan, B., & Li, R. (2021) · Phytomedicine · doi:10.1016/j.phymed.2021.153742 · Cited by 12
Deciphering the relevance of dead box RNA helicases in gliomagenesis and autophagy
Sharma, A., Soni, N., Chaudhary, M., Jia, J., & Bissa, B. (2025) · Human Cell · doi:10.1007/s13577-025-01329-1 · Cited by 11
IL28A protein homotetramer structure is required for autolysosomal degradation of HCV-NS5A in vitro
Ma, Y.-Y., Li, J., Peng, Z., & Zhang, J. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2400-9 · Cited by 11
Huang, X., An, R.-F., & Zhang, W. (2022) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/1389557522666220217113719 · Cited by 11
Metformin regulates autophagy via LGMN to inhibit choriocarcinoma
Tu, W., Qin, M., Li, Y., Wu, W., & Tong, X. (2022) · Gene · doi:10.1016/j.gene.2022.147090 · Cited by 11
The multiple roles of autophagy in uveal melanoma and the microenvironment
Liu, B., Yao, X., Shang, Y., & Dai, J. (2024) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-023-05576-3 · Cited by 11
IGF2BP2 modulates autophagy and serves as a prognostic marker in glioma
Li, N., Deng, L., Zhang, Y., Tang, X., Lei, B., & Zhang, Q. (2024) · Ibrain · doi:10.1002/ibra.12150 · Cited by 11
Autophagy as a Therapeutic Target in Breast Tumors: The Cancer stem cell perspective
Raza, S., Siddiqui, J. A., Srivastava, A., Chattopadhyay, N., Sinha, R. A., & Chakravarti, B. (2024) · Autophagy Reports · doi:10.1080/27694127.2024.2358648 · Cited by 11
Li, X., Chaouhan, H. S., Yu, S., Wang, I., Yu, T., Chuang, Y., Chen, K., Lin, F., Chen, M. Y., Hsu, C., et al. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70400 · Cited by 13
Non-coding RNAs regulate autophagy in kidney disease: friend or foe?
Li, Y., Ma, T., Liang, X., Jin, T., Zhao, X., Huang, J., Hao, J., Liu, H., & Wang, P. (2025) · Autophagy · doi:10.1080/15548627.2025.2551683 · Cited by 11
Pang, F., Liu, C., Cui, Y., Gong, K., Liu, G., Bian, Y., Gao, X., & Zhang, D. (2019) · Europe PMC (PubMed Central) · Cited by 11
Inhibition of autophagy enhances apoptosis induced by bortezomib in AML cells
Jiang, L., Zhao, Y., & Yang, M. (2020) · Oncology Letters · doi:10.3892/ol.2020.12370 · Cited by 11
Beclin 1, LC3 and P62 Expression in Equine Sarcoids
Martano, M., Altamura, G., Power, K., Liguori, P., Restucci, B., Borzacchiello, G., & Maiolino, P. (2021) · Animals · doi:10.3390/ani12010020 · Cited by 12
Molecular and cellular functions of long non-coding RNAs in prostate and breast cancer
Zhu, Y., & Zhu, J. (2022) · Advances in clinical chemistry · doi:10.1016/bs.acc.2021.09.005 · Cited by 13
Fei, Y., Xu, J., Ge, L., Chen, L., Yu, H., Pan, L., & Chen, P. (2022) · Aging · doi:10.18632/aging.204097 · Cited by 11
Chomchoei, C., Brimson, J. M., & Brimson, S. J. (2022) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2022.2166829 · Cited by 11
Dey, D. K., Sharma, C., Vadlamudi, Y., & Kang, S. C. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121476 · Cited by 11
Hua, L., Song, Y., Min, J., Wang, R., Li, H., Zhu, L., Guo, Y., Gan, D., Li, S., Ma, P., et al. (2023) · Cancer Science · doi:10.1111/cas.15798 · Cited by 11
Safari, F., & Dadvar, F. (2023) · Tissue and Cell · doi:10.1016/j.tice.2023.102160 · Cited by 11
Role of autophagy in inhibiting the proliferation of A549 cells by type III interferon
Gao, D., Yu, X., Zhang, B., Kong, M., Fang, Y., Cai, Y., Zhu, C., Zhao, J., & Li, J. (2019) · Cell Biology International · doi:10.1002/cbin.11132 · Cited by 11
Lu, H., Zhu, C., Ruan, Y., Fan, L., Wei, K., Yang, Z., & Chen, Q. (2021) · Analytical Cellular Pathology · doi:10.1155/2021/3081491 · Cited by 11
Pirtoli, L., Belmonte, G., Toscano, M., Tini, P., & Miracco, C. (2016) · PubMed · Cited by 11
Hay-Koren, A., Bialik, S., Levin‐Salomon, V., & Kimchi, A. (2017) · Journal of Internal Medicine · doi:10.1111/joim.12616 · Cited by 12
Influence of nitric oxide signaling mechanisms in cancer
Ramírez-Patiño, R., Ávalos-Navarro, G., Figuera, L. E., Varela-Hernández, J. J., Bautista-Herrera, L., Muñoz-Valle, J., & Gallegos‐Arreola, M. P. (2022) · International Journal of Immunopathology and Pharmacology · doi:10.1177/03946320221135454 · Cited by 11
Repurposing the Antidepressant Sertraline: A Systematic Scoping Review of Its Anticancer Mechanisms
Blum, C., Dohrmann, M., McCarthy, L., McMenamin, M., & O’Callaghan, L. A. (2025) · Pharmacology Research & Perspectives · doi:10.1002/prp2.70168 · Cited by 10
Hu, J., Guo, Y., Ren, L., Zhang, H., Qin, X., Yin, F., & Liu, X. (2026) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5c01372 · Cited by 13
Lu, Y., Li, A., Liu, A., Li, M., & Wang, M. (2026) · Biomedicines · doi:10.3390/biomedicines14020416 · Cited by 10
Purvalanol A induces apoptosis and reverses cisplatin resistance in ovarian cancer
Zhang, X., Hong, S., Jiang, Y., Liu, J., Wang, Y., Peng, J., Wang, H., & Li, H. (2022) · Anti-Cancer Drugs · doi:10.1097/cad.0000000000001339 · Cited by 10
Rajan, P. K., Udoh, U. S., Nakafuku, Y., Pierre, S. V., & Sanabria, J. R. (2023) · Cells · doi:10.3390/cells12192367 · Cited by 10
Crosstalk between the mTOR pathway and primary cilia in human diseases
Prosseda, P. P., Prosseda, S. D., Tran, M., Liton, P. B., & Sun, Y. (2023) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2023.09.004 · Cited by 11
Chen, Q., Zhou, Y., Yu, M., Zhu, S., Sun, J., Du, W., Chen, Z., Tao, J., Feng, X., Zhang, Q., et al. (2024) · APOPTOSIS · doi:10.1007/s10495-024-01939-4 · Cited by 10
Wong, M. M.-T., Aziz, N. A., Ch’ng, E. S., Armon, S., Chook, J. B., Bong, J. J., Peh, S., Wu, Y. S., & Teow, S. (2024) · Journal of Molecular Histology · doi:10.1007/s10735-024-10191-8 · Cited by 10
Wnt Signaling in Hepatocellular Carcinoma: Biological Mechanisms and Therapeutic Opportunities
Zhu, Y., He, Y., & Gan, R. (2024) · Cells · doi:10.3390/cells13231990 · Cited by 10
Liu, Q., Hu, J., Li, X., Gao, H., Kong, D., & Jin, M. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.116796 · Cited by 10
Therapeutic peptides targeting the Ras superfamily
Hurd, C. A., Mott, H. R., & Owen, D. (2020) · Peptide Science · doi:10.1002/pep2.24165 · Cited by 10
Mohamed, F. E. Z. A., Jalan, R., Minogue, S., Andreola, F., Habtesion, A., Hall, A. R., Winstanley, A. M., Damink, S. W. M. O., Malagó, M., Davies, N. A., et al. (2021) · Digestive Diseases and Sciences · doi:10.1007/s10620-021-06973-9 · Cited by 10
Cui, H., Weng, Y., Ding, N., Chen, C., Wang, L., Zhou, Y., Zhang, L., Cui, Y., & Zhang, W. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.650891 · Cited by 10
Zheng, Y., He, Z., Su, Z., Wang, H., Jiang, X., Fang, X., Lu, S., & Li, Y. (2023) · Cell Biology International · doi:10.1002/cbin.12021 · Cited by 10
Kawakita, E., Yang, F., Shi, S., Takagaki, Y., Koya, D., & Kanasaki, K. (2023) · Cancers · doi:10.3390/cancers15184529 · Cited by 11
Huang, S., Hsu, W., Huang, H.-S., Yen, J.-H., Lin, M.-C., Peng, C., & Yen, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20163978 · Cited by 10
George, M. P., Gladwin, M. T., & Graham, B. B. (2020) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2020-0099tr · Cited by 10
Shi, M., Liu, Y., Huang, J., Chen, Z., Ni, C., Lü, J., Zhang, Y., Liu, Z., & Bai, J. (2022) · Biomaterials Advances · doi:10.1016/j.bioadv.2022.212919 · Cited by 10
Long-term effects of COVID-19 on cancer patients: the experience from Guy’s Cancer Centre
Monroy‐Iglesias, M. J., Tremble, K., Russell, B. A., Moss, C. L., Dolly, S. O., Sita-Lumsden, A. R., Cortellini, A., Pinato, D. J., Rigg, A. S., Karagiannis, S. N., et al. (2022) · Future Oncology · doi:10.2217/fon-2022-0088 · Cited by 10
Delaney, J. R., & Stupack, D. G. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159114 · Cited by 10
Autophagy is required for crizotinib-induced apoptosis in MET-amplified gastric cancer cells
Schroeder, R., Choi, W., Hong, D. S., & McConkey, D. J. (2017) · Oncotarget · doi:10.18632/oncotarget.18386 · Cited by 10
Selective autophagy restricts IL-9 secretion from TH9 cells: relevance in cancer growth
Benoit-Lizon, I., Jacquin, É., & Apétoh, L. (2017) · Cell Cycle · doi:10.1080/15384101.2017.1414680 · Cited by 10
Draz, H. M., Goldberg, A. A., Guns, E. S. T., Fazli, L., Safe, S. H., & Sanderson, J. T. (2018) · Investigational New Drugs · doi:10.1007/s10637-018-0595-8 · Cited by 10
Urine proteome changes in rats subcutaneously inoculated with approximately ten tumor cells
Wei, J., Meng, W., & Gao, Y. (2019) · PeerJ · doi:10.7717/peerj.7717 · Cited by 10
Zhanghuang, C., Yao, Z., Tang, H., Zhang, K., Wu, C., Li, L., Xie, Y., Yang, Z. L., & Yan, B. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.843234 · Cited by 9
Zhang, H., Meng, L., Yin, L., Fan, T., Yu, L., Han, S., Wang, L., Liang, W., Yang, X., & Sun, S. (2022) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2022.122297 · Cited by 9
Zhang, R., Hao, J., Yu, H., Wang, Z., Lan, F., Peng, Y., & Qiu, Y. (2023) · Gene · doi:10.1016/j.gene.2023.147917 · Cited by 9
Gulzar, M., Noor, S., Hasan, G. M., & Hassan, M. I. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.128725 · Cited by 10
Liu, A.-B., Liu, J., Wang, S., Ма, Л., & Zhang, J. (2024) · Cancer Cell International · doi:10.1186/s12935-024-03355-9 · Cited by 9
Drug repositioning identifies potential autophagy inhibitors for the LIR motif p62/SQSTM1 protein
Asghari, N., Saei, A. K., Cordani, M., Nayeri, Z., & Moosavi, M. (2024) · Comput. Biol. Chem. · doi:10.1016/j.compbiolchem.2024.108235 · Cited by 9
Loss of DDX24 inhibits lung cancer progression by stimulating IKBKG splicing-mediated autophagy
Sun, S., Jing, X., Tong, G., Chen, C., Xie, S., Wang, C., Chen, D., Zhao, J., Qi, Y., Zhang, W., et al. (2025) · Theranostics · doi:10.7150/thno.102425 · Cited by 9
Walweel, N., Çınar, V., Mersin, O., Macit, S., Yildiz, U., Demirel, E., Tunç, C. Ü., Ulutabanca, H., Hamurcu, Z., Durmaz, Y. Y., et al. (2025) · ACS Applied Bio Materials · doi:10.1021/acsabm.4c01778 · Cited by 9
Metadata
- Authors
- White, E.
- Corresponding author
- White, Eileen
- ORCID
- White, Eileen
- Venue
- Journal of Clinical Investigation
- Published
- 2015-01-02
- Volume
- 125
- Issue
- 1
- Pages
- 42-46
- ISSN
- 0021-9738 (ISSN-L)
- PMC
- PMC4382247
- OpenAlex
- W2055811314
- Cited by
- 1,332
- References
- 58
- Citations by year
- 2026: 63 · 2025: 68 · 2024: 111 · 2023: 116 · 2022: 129 · 2021: 158 · 2020: 157 · 2019: 138 · 2018: 142 · 2017: 132 · 2016: 92 · 2015: 24
- FWCI
- 16.89
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Clinical Investigation (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Rutgers Cancer Institute of New Jersey
- National Institutes of Health
- National Cancer Institute (R01CA053370, R37CA053370, RC1CA147961, R01CA130893, R01CA163591)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- autophagy, cancer, carcinogenesis, lysosomes, p53, mitochondrial metabolism, tumor microenvironment, starvation, cancer therapy, autophagy inhibition
- MeSH terms
- Animals, Autophagy, Humans, Neoplasms, Carcinogenesis
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