The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Induction of Autophagy during Extracellular Matrix Detachment Promotes Cell Survival
Open accessAbstract
Autophagy has been proposed to promote cell death during lumen formation in three-dimensional mammary epithelial acini because numerous autophagic vacuoles are observed in the dying central cells during morphogenesis. Because these central cells die due to extracellular matrix (ECM) deprivation (anoikis), we have directly interrogated how matrix detachment regulates autophagy. Detachment induces autophagy in both nontumorigenic epithelial lines and in primary epithelial cells. RNA interference-mediated depletion of autophagy regulators (ATGs) inhibits detachment-induced autophagy, enhances apoptosis, and reduces clonogenic recovery after anoikis. Remarkably, matrix-detached cells still exhibit autophagy when apoptosis is blocked by Bcl-2 overexpression, and ATG depletion reduces the clonogenic survival of Bcl-2-expressing cells after detachment. Finally, stable reduction of ATG5 or ATG7 in MCF-10A acini enhances luminal apoptosis during morphogenesis and fails to elicit long-term luminal filling, even when combined with apoptotic inhibition mediated by Bcl-2 overexpression. Thus, autophagy promotes epithelial cell survival during anoikis, including detached cells harboring antiapoptotic lesions.
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
“Anoikis, a form of apoptosis caused by inappropriate cell/ECM interactions, has been reported in the formation of the lumen during the development of various secretory glands such as mammary and salivary glands.[20,21]”
From Autophagy, not apoptosis, plays a role in lumen formation of eccrine gland organoids (2022) · cites this paper as [21]
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
LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.
Kabeya, Y., Mizushima, N., Ueno, T., Yamamoto, A., Kirisako, T., Noda, T., Kominami, E., Ohsumi, Y., & Yoshimori, T. (2000) · The EMBO Journal · doi:10.1093/emboj/19.21.5720 · Cited by 6,605
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214
Dissemination and growth of cancer cells in metastatic sites
Chambers, A. F., Groom, A. C., & MacDonald, I. C. (2002) · Nature reviews. Cancer · doi:10.1038/nrc865 · Cited by 4,018
Levine, B., & Klionsky, D. J. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00099-1 · Cited by 3,728
Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
Pattingre, S., Tassa, A., Qu, X., Garuti, R., Liang, X. H., Mizushima, N., Packer, M., Schneider, M. D., & Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.07.002 · Cited by 3,536
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
Disruption of epithelial cell-matrix interactions induces apoptosis
Frisch, S., & Francis, H. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.124.4.619 · Cited by 3,276
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
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
Research works printed but not linked: 2
- Frisch S. M., 1999, Methods Mol. Biol, 129, 251
- Ogier-Denis E., 2003, Biochim. Biophys. Acta, 1603, 113
Cited by
Sorted by citations
Items 101–200 of 558
Sun, K., Deng, W.-J., Zhang, S., Cai, N., Jiao, S., Song, J., & Wei, L. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-35 · Cited by 123
“ATGs deletion enhanced apoptosis, and reduced clonogenic recovery after anoikis [67].”
BackgroundFu, X., Shi, Y., Zhou, J., Peng, Y., Liu, W., Shi, G., Gao, Q., Wang, X., Song, K., Fan, J., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.10.012 · Cited by 118
Targeting Autophagy in Breast Cancer
Cocco, S., Leone, A., Piezzo, M., Caputo, R., Lauro, V. D., Rella, F. D., Fusco, G., Capozzi, M., Gioia, G. D., Budillon, A., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217836 · Cited by 120
The regulation of cancer cell death and metabolism by extracellular matrix attachment
Buchheit, C. L., Rayavarapu, R. R., & Schafer, Z. T. (2012) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2012.04.007 · Cited by 115
Zheng, K., Li, Y., Wang, S., Wang, X., Liao, C., Hu, X., Fan, L., Kang, Q., Zeng, Y., Wu, X., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1192751 · Cited by 114
Tang, F., Hu, P., Yang, Z., Xue, C. H., Gong, J., Sun, S., Liu, S., Zhang, S., Li, Z., Yang, C., et al. (2017) · Oncology Reports · doi:10.3892/or.2017.5635 · Cited by 115
At a glance: A history of autophagy and cancer
Wen, X., & Klionsky, D. J. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.11.005 · Cited by 116
“Autophagy was first proposed to promote cell survival during extracellular matrix detachment in a 2008 study from Jayanta Debnath’s lab [105].”
BackgroundThe double-edged sword of AMPK signaling in cancer and its therapeutic implications
Jeon, S., & Hay, N. (2015) · Archives of Pharmacal Research · doi:10.1007/s12272-015-0549-z · Cited by 119
“Recently, several groups have shown that matrix detachment that can occur during solid tumor growth and metastasis, can also activate AMPK (Jeon et al. 2012; Fung et al. 2008; Ng et al. 2012; Hindupur et al. 2014).”
BackgroundWu, Y. C., Wu, W. K. K., Li, Y., Yu, L., Li, Z. J., Wong, C. C. M., Li, H. T., Sung, J. J. �., & Cho, C. H. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.03.051 · Cited by 113
Wilson, E. N., Bristol, M. L., Di, X. M., Maltese, W. A., Koterba, K. L., Beckman, M. J., & Gewirtz, D. A. (2011) · Hormones and Cancer · doi:10.1007/s12672-011-0081-7 · Cited by 111
Autophagy in adhesion and migration
Kenific, C. M., Wittmann, T., & Debnath, J. (2016) · Journal of Cell Science · doi:10.1242/jcs.188490 · Cited by 113
“Because autophagy protects cells from detachment-induced cell death (termed anoikis) (Fung et al., 2008), these findings support the hypothesis that autophagymediated degradation of RhoA promotes resistance to anoikis by limiting focal adhesion maturation and tension at unanchored integrin sites in detached cells.”
BackgroundSelf-citationA perspective on the role of autophagy in cancer
Ariosa, A., Lahiri, V., Lei, Y., Yang, Y., Yin, Z., Zhang, Z., & Klionsky, D. J. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2021.166262 · Cited by 115
Regulation of Tumor Cell Dormancy by Tissue Microenvironments and Autophagy
Sosa, M. S., Bragado, P., Debnath, J., & Aguirre‐Ghiso, J. A. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-1445-2_5 · Cited by 111
Self-citationEffects of propofol on the development of cancer in humans
Xu, Y., Pan, S., Jiang, W., Xue, F., & Zhu, X. (2020) · Cell Proliferation · doi:10.1111/cpr.12867 · Cited by 105
Sirtuins' control of autophagy and mitophagy in cancer
Aventaggiato, M., Vernucci, E., Barreca, F., Russo, M. A., & Tafani, M. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107748 · Cited by 103
Fanfone, D., Wu, Z., Mammi, J., Berthenet, K., Neves, D., Weber, K., Halaburkova, A., Virard, F., Bunel, F., Jamard, C., et al. (2022) · eLife · doi:10.7554/elife.73150 · Cited by 105
“Nonetheless, cancer cells developed strategies to evade anoikis such as overly activated Ras/ERK and PI3K/Akt pathways, engaging the tyrosine kinase receptor TrkB, inactivation of E- cadherin and p53 or enhanced autophagy (de Sousa Mesquita et al., 2017; Douma et al., 2004; Derksen et al., 2006; Fung et al., 2008; Cha…”
BackgroundWhat is the malignant nature of human ductal carcinoma in situ?
Espina, V. A., & Liotta, L. A. (2010) · Nature reviews. Cancer · doi:10.1038/nrc2950 · Cited by 110
“Autophagy has been shown to be a key regulator of survival in cells that are deprived of an anchoring substratum, and may have an important role for cell survival in any anchorage-independent stat”
Statins, autophagy and cancer metastasis
Zhang, J., Yang, Z., Xie, L., Xu, L., Xu, D., & Liu, X. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.11.001 · Cited by 105
“Suppression of β1 integrin signaling induces autophagy and facilitates dormancy in the MMTV–PyMT model of breast cancer [82; 87].”
BackgroundRibeiro, F. A. P., Noguti, J., Oshima, C. T. F., & Ribeiro, D. A. (2014) · PubMed · Cited by 103
Regulation of autophagy and chloroquine sensitivity by oncogenic RAS in vitro is context-dependent
Morgan, M. J., Gamez, G., Menke, C., Hernandez, A. L., Thorburn, J., Gidan, F., Staskiewicz, L., Morgan, S. C., Cummings, C. T., Maycotte, P., et al. (2014) · Autophagy · doi:10.4161/auto.32135 · Cited by 103
Autophagy Inhibition Delays Early but Not Late-Stage Metastatic Disease
Barnard, R., Regan, D. P., Hansen, R. J., Maycotte, P., Thorburn, A. M., & Gustafson, D. L. (2016) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.116.233908 · Cited by 103
“Other studies have also indicated that autophagy inhibition may not necessarily alter migration or invasion, but does impact anchorage-independent growth (Fung et al., 2008; Macintosh et al., 2012; Peng et al., 2013).”
BackgroundDectin-1–Dependent LC3 Recruitment to Phagosomes Enhances Fungicidal Activity in Macrophages
Tam, J. M., Mansour, M. K., Khan, N. S., Seward, M., Puranam, S., Tanne, A., Sokolovska, A., Becker, C. E., Acharya, M., Baird, M. A., et al. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiu290 · Cited by 101
“BG beads and GFP-LC3 colocalized, as shown by yellow rings in the phagosome, indicating that BG beads were sufficient to recruit LC3 to the phagosome (Figure 2B).”
BackgroundInfluentialSahni, S., Bae, D.-H., Lane, D. J. R., Kovačević, Ž., Kalinowski, D. S., Jansson, P. J., & Richardson, D. R. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529511 · Cited by 101
“Studies have shown that autophagy plays a protective role in cells undergoing anoikis due to extracellular matrix detachment, as observed in metastatic cells (71).”
BackgroundVollrath, J. T., Sechi, A. S., Dreser, A., Katona, I., Wiemuth, D., Vervoorts, J., Dohmen, M., Chandrasekar, A., Prause, J. U., Brauers, E., et al. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.243 · Cited by 104
Mirzoeva, O. K., Hann, B. C., Hom, Y. K., Debnath, J., Aftab, D. T., Shokat, K. M., & Korn, W. M. (2011) · Journal of Molecular Medicine · doi:10.1007/s00109-011-0774-y · Cited by 100
“05 cells stably expressing a GFP-LC3 fusion construct [18].”
Self-citationEGFR tyrosine kinase inhibition induces autophagy in cancer cells
Fung, C., Chen, X., Grandis, J. R., & Duvvuri, U. (2012) · Cancer Biology & Therapy · doi:10.4161/cbt.22002 · Cited by 101
“GFP-LC3 T-24 stable cell line was created using retroviral transduction of transgenes as previously described.(8) The pBabe GFP-LC3 plasmid was a kind gift of Dr Jayanta Debnath.”
MethodSelf-citationAutophagy in Brain Tumors: A New Target for Therapeutic Intervention
Kaza, N., Kohli, L., & Roth, K. A. (2011) · Brain Pathology · doi:10.1111/j.1750-3639.2011.00544.x · Cited by 98
“Following extracellular matrix detachment, autophagy has been shown to protect cells from anoikis (26).”
BackgroundRaudenská, M., Balvan, J., & Masařík, M. (2021) · Molecular Cancer · doi:10.1186/s12943-021-01423-6 · Cited by 99
HBx induces HepG-2 cells autophagy through PI3K/Akt–mTOR pathway
Wang, P., Guo, Q., Wang, Z., & Qian, H. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1457-x · Cited by 96
Horbinski, C., Mojesky, C., & Kyprianou, N. (2010) · American Journal Of Pathology · doi:10.2353/ajpath.2010.091270 · Cited by 97
Loss of Atg12, but not Atg5, in pro-opiomelanocortin neurons exacerbates diet-induced obesity.
Malhotra, R., Warne, J. P., Salas, E., Xu, A. W., & Debnath, J. (2015) · PubMed Central · doi:10.1080/15548627.2014.998917 · Cited by 94
“The anti-LC3 antibody generated in our laboratory has been described previously and is now commercially available (EMDMillipore, ABC232).(35) Other antibodies used for immunoblotting include: SQSTM1 (Progen, GP62-C), NBR1 (Novus, NBP1–71703), ATG12 (Cell Signaling Technology, 4180), ATG5 (Novus, NB110–53818), TUBA (Si…”
MethodSelf-citationAutophagy as a Potential Therapy for Malignant Glioma
Escamilla-Ramírez, Á., Castillo‐Rodríguez, R. A., Zavala-Vega, S., Jiménez‐Farfán, D., Anaya‐Rubio, I., Briseño, E., Palencia, G., Guevara, P., Cruz-Salgado, A., Sotelo, J., et al. (2020) · Pharmaceuticals · doi:10.3390/ph13070156 · Cited by 94
Effect of hydroxychloroquine and characterization of autophagy in a mouse model of endometriosis
Ruiz, A., Rockfield, S., Taran, N., Haller, E. M., Engelman, R. W., Flores, I., Panina‐Bordignon, P., & Nanjundan, M. (2016) · Cell Death and Disease · doi:10.1038/cddis.2015.361 · Cited by 92
“Epithelial cells normally undergo anoikis, a mechanism of programmed cell death, upon detachment from the extracellular matrix.(8) One mechanism that we propose could potentially alter the anoikis response in endometrial cells is autophagy.”
BackgroundThe Interconnections between Autophagy and Integrin-Mediated Cell Adhesion
Vlahakis, A., & Debnath, J. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.11.027 · Cited by 89
“Autophagy is induced by a diverse array of insults in addition to nutrient deprivation, which includes ER stress, hypoxia, and remarkably, the loss of cell attachment to the extracellular matrix (ECM) [3].”
BackgroundInfluentialSelf-citationBeclin1 Modulates Bone Homeostasis by Regulating Osteoclast and Chondrocyte Differentiation
Arai, A., Kim, S., Goldshteyn, V., Kim, T., Park, N.-H., Wang, C., & Kim, R. H. (2019) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3756 · Cited by 89
“The pBABEpuro GFP‐LC3 (plasmid #22405), pQCXIH‐Beclin1‐HA WT (plasmid #46993), pQCXIH‐Beclin1‐HA S‐A (plasmid #46994), and pQCXIH‐Beclin1‐HA S‐D (plasmid #46995) were purchased from Addgene (Cambridge, MA, USA).((17,18)) The retroviral vector pLPCX‐Beclin1‐HA WT was generated by inserting a DNA fragment encoding Becli…”
Jo, Y. K., Kim, S. C., Park, I. J., Park, S. J., Jin, D., Hong, S., Cho, D., & Kim, J. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052705 · Cited by 96
“Autophagy induction by detachment from the extracellular matrix assists tumor cell survival during anoikis, which contributes to dissemination and metastasis [25,26].”
Backgroundp53 Is a Master Regulator of Proteostasis in SMARCB1-Deficient Malignant Rhabdoid Tumors
Carugo, A., Minelli, R., Sapio, L., Soeung, M., Carbone, F., Robinson, F. S., Tepper, J., Chen, Z., Lovisa, S., Svelto, M., et al. (2019) · Cancer Cell · doi:10.1016/j.ccell.2019.01.006 · Cited by 94
Grkovic, S., O׳Reilly, V. C., Han, S., Hong, M., Baxter, R. C., & Firth, S. M. (2012) · Oncogene · doi:10.1038/onc.2012.264 · Cited by 90
Metabolic reprogramming ensures cancer cell survival despite oncogenic signaling blockadePreprint
Lue, H.-W., Podolak, J., Kolahi, K. S., Cheng, L. C., Rao, S. A. M., Garg, D., Xue, C.-H., Rantala, J., Tyner, J. W., Thornburg, K. L. R., et al. (2017) · Genes & Development · doi:10.1101/gad.305292.117 · Cited by 90
Aβ1-42 monomers or oligomers have different effects on autophagy and apoptosis
Guglielmotto, M., Monteleone, D., Piras, A., Valsecchi, V., Tropiano, M., Ariano, S., Fornaro, M., Vercelli, A., Puyal, J., Arancio, O., et al. (2014) · Autophagy · doi:10.4161/auto.30001 · Cited by 90
“On the contrary, the disruption of the BCL2-BECN1 complex may be a mechanism through which cells promote autophagy during different stress conditions.(37,38) Thus, in some circumstances, such as nutrient deprivation or hypoxia, it has been reported that inhibition of autophagy is followed by an accelerated cell death…”
BackgroundRab35 GTPase recruits NDP52 to autophagy targets
Minowa‐Nozawa, A., Nozawa, T., Okamoto‐Furuta, K., Kohda, H., & Nakagawa, I. (2017) · The EMBO Journal · doi:10.15252/embj.201796463 · Cited by 89
“TBC1D10A, Rab35, and NDP52 were mutated by site-directed mutagenesis using PrimeSTAR Mutagenesis Basal Kit (Takara). pBABE-puro-GFP-LC3 (plasmid 22405), which was generated by Fung et al (2008), was purchased from Addgene.”
Wang, S.-F., Wu, M.-Y., Cai, C.-Z., Li, M., & Lu, J. (2016) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2016.10.069 · Cited by 88
Proteasome inhibition: A new therapeutic strategy to cancer treatment
Wu, W. K. K., Cho, C. H., Lee, C. W., Wu, K., Fan, D., Yu, J. Q., & Sung, J. J. �. (2010) · Cancer Letters · doi:10.1016/j.canlet.2009.12.002 · Cited by 88
“Furthermore, it protects cancer cells from the accumulation of damaged organelles or protein aggregates [113], the loss of interaction with the extracellular matrix [114] and the toxicity of cancer therapies [115].”
BackgroundAutophagic and Apoptotic Pathways as Targets for Chemotherapy in Glioblastoma
Trejo‐Solís, C., Serrano‐García, N., Escamilla-Ramírez, Á., Castillo‐Rodríguez, R. A., Jiménez‐Farfán, D., Palencia, G., Calvillo, M., Lemus, M. A. A., Flores‐Nájera, A., Cruz-Salgado, A., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123773 · Cited by 87
“AMPK is activated in EMC cell detaching, sustaining growth, and/or preventing apoptosis [152].”
BackgroundWang, K., Liu, X., Liu, Q., Ho, I. H. T., Wei, X., Yin, T., Zhan, Y., Zhang, W., Zhang, W., Chen, B., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02880-5 · Cited by 88
Autophagy in breast cancer and its implications for therapy.
Jain, K., Paranandi, K. S., Sridharan, S., & Basu, A. (2013) · PubMed Central · Cited by 84
Mechanisms of redox metabolism and cancer cell survival during extracellular matrix detachment
Hawk, M. A., & Schafer, Z. T. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm117.000260 · Cited by 82
“For example, ECM-detached cells undergo autophagy (13), which involves the catabolism of intracellular organelles and can serve as both a survival mechanism under conditions of nutrient starvation (14) or an alternative form of cell death if left unchecked (15).”
BackgroundCoupienne, I., Bontems, S., Dewaele, M., Rubio, N., Habraken, Y., Fulda, S., Agostinis, P., & Piette, J. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.12.015 · Cited by 83
“Debnath [23] (Department of Pathology and Biomedical”
Chiarelli, N., Ritelli, M., Zoppi, N., & Colombi, M. (2019) · Genes · doi:10.3390/genes10080609 · Cited by 82
“Cell detachment from the ECM activates the autophagy pathway that, in turn, protects cells from anoikis [90].”
BackgroundThe Importance of Autophagy Regulation in Breast Cancer Development and Treatment
Zarzynska, J. M. (2014) · BioMed Research International · doi:10.1155/2014/710345 · Cited by 82
Repurposing Drugs in Oncology (ReDO)—clarithromycin as an anti-cancer agent
Nuffel, A. M. T. V. (2015) · ecancermedicalscience · doi:10.3332/ecancer.2015.513 · Cited by 83
“Autophagy is also upregulated during extracellular matrix (ECM) detachment which is required for metastasis [101].”
BackgroundSundararaman, A., Amirtham, U., & Rangarajan, A. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.731257 · Cited by 81
“Recent work from our laboratory (6) and that of others (7, 8, 25) has demonstrated AMPK activation upon matrix deprivation and its role in anoikis resistance.”
BackgroundTargeting autophagy in breast cancer
Maycotte, P. (2014) · World Journal of Clinical Oncology · doi:10.5306/wjco.v5.i3.224 · Cited by 84
PTK6 Regulates IGF-1-Induced Anchorage-Independent Survival
Irie, H. Y., Shrestha, Y., Selfors, L. M., Frye, F., Iida, N., Wang, Z., Zou, L., Yao, J., Lu, Y., Epstein, C. B., et al. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011729 · Cited by 80
“Interestingly, inhibition of autophagy enhances apoptotic cell death in MCF-10A cells [33], suggesting that autophagy promotes epithelial cell survival, rather than cell”
The Evolving, Multifaceted Roles of Autophagy in Cancer
Liu, J., & Debnath, J. (2016) · Advances in cancer research · doi:10.1016/bs.acr.2016.01.005 · Cited by 82
Self-citationMetabolism during ECM Detachment: Achilles Heel of Cancer Cells?
Mason, J. A., Hagel, K. R., Hawk, M. A., & Schafer, Z. T. (2017) · Trends in Cancer · doi:10.1016/j.trecan.2017.04.009 · Cited by 78
Autophagy induced during apoptosis degrades mitochondria and inhibits type I interferon secretion
Lindqvist, L., Frank, D. O., McArthur, K., Dite, T. A., Lazarou, M., Oakhill, J. S., Kile, B. T., & Vaux, D. L. (2017) · Cell Death and Differentiation · doi:10.1038/s41418-017-0017-z · Cited by 82
The role of autophagy in cancer: from molecular mechanism to therapeutic window
Jalali, P., Shahmoradi, A., Samii, A., Mazloomnejad, R., Hatamnejad, M. R., Saeed, A., Namdar, A., & Salehi, Z. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1528230 · Cited by 89
“While melanoma metastases revealed enhanced LC3B staining as compared to original tumor samples with the same characteristics (268, 270, 271).”
Bustos, S. O., Antunes, F., Rangel, M. C., & Chammas, R. J. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.606436 · Cited by 79
“One of the first associations between autophagy and the invasion process was evidenced by the capacity of epithelial cells to evade anoikis via autophagy, what enabled cancer cells migration and invasion (108).”
BackgroundThe Multifaceted Functions of Autophagy in Breast Cancer Development and Treatment
Niklaus, N. J., Tokarchuk, I., Zbinden, M., Schläfli, A. M., Maycotte, P., & Tschan, M. P. (2021) · Cells · doi:10.3390/cells10061447 · Cited by 78
“Thus, detachment-mediated anoikis induces autophagic activity that protects the cells from apoptosis even in cells that already exhibit anti-apoptotic signaling [44,45] (Figure 3).”
BackgroundAutophagy and Crohn's Disease: At the Crossroads of Infection,Inflammation, Immunity, and Cancer
Brest, P., Corcelle–Termeau, E., Césaro, A., Chargui, A., Belaïd, A., Klionsky, D. J., Vouret‐Craviari, V., Hébuterne, X., Hofman, P. M., & Mograbi, B. (2010) · Current Molecular Medicine · doi:10.2174/156652410791608252 · Cited by 85
Mutant p53 as a Regulator and Target of Autophagy
Shi, Y., Norberg, E., & Vakifahmetoglu-Norberg, H. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.607149 · Cited by 77
Autophagy regulation in cancer development and therapy.
White, E. J., Martín, V., Liu, J.-L., Klein, S. R., Piya, S., Gomez‐Manzano, C., Fueyo-Margareto, J., & Jiang, H. (2011) · Europe PMC (PubMed Central) · Cited by 76
The Multifaceted Roles of Autophagy in Tumors—Implications for Breast Cancer
Debnath, J. (2011) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-011-9223-3 · Cited by 78
“Autophagy is induced in both non-transformed and oncogene-transformed cells following matrix detachment, which protects these cells from anoikis [26,65].”
Self-citationOncogenic Ras differentially regulates metabolism and anoikis in extracellular matrix-detached cells
Mason, J. A., Davison-Versagli, C. A., Leliaert, A. K., Pape, D. J., McCallister, C. M., Zuo, J.-L., Durbin, S., Buchheit, C. L., Zhang, S., & Schafer, Z. T. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.15 · Cited by 72
Extracellular Matrix Regulation of Metabolism and Implications for TumorigenesisPreprint
Grassian, A. R., Coloff, J. L., & Brugge, J. S. (2011) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2011.76.010967 · Cited by 80
“Combined inhibition of apoptosis and autophagy is unable to prevent the death of ECM-detached cells, and consistent with the prosurvival function of autophagy, inhibition of autophagy accelerates ECM detachmentinduced cell death and decreases replating ability (Fung et al. 2008).”
BackgroundStarobinets, H., Ye, J., Broz, M. L., Barry, K. C., Goldsmith, J., Marsh, T., Rostker, F., Krummel, M. F., & Debnath, J. (2016) · Journal of Clinical Investigation · doi:10.1172/jci85705 · Cited by 74
“tide between human, rat, and mouse (40), which is also commer-”
BackgroundSelf-citationLiss, V., Liebl, D., Zhang, Y., Rajashekar, R., Chlanda, P., Giesker, K., Chikkaballi, D., & Hensel, M. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004374 · Cited by 76
“pBABEpuro GFP-LC3 GFP-LC3b [55], Addgene 22405, U05784”
Bidirectional extracellular matrix signaling during tissue morphogenesis
Gjorevski, N., & Nelson, C. M. (2009) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2009.10.013 · Cited by 73
“For example, lack of integrin engagement has been shown to induce autophagy during cavitation of the lumen of mammary epithelial acini [13,14].”
BackgroundParker, K. H., Horn, L. A., & Ostrand‐Rosenberg, S. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3hi0715-305r · Cited by 73
“The role of autophagy in promoting tumor progression is well established and has been attributed to its ability to increase the survival of tumor cells [3, 42].”
BackgroundSingla, M., & Bhattacharyya, S. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.07.070 · Cited by 70
Patergnani, S., Missiroli, S., Morciano, G., Perrone, M., Mantovani, C. M., Anania, G., Fiorica, F., Pinton, P., & Giorgi, C. (2021) · Cancers · doi:10.3390/cancers13225622 · Cited by 77
V-ATPase Inhibition Regulates Anoikis Resistance and Metastasis of Cancer Cells
Schempp, C. M., von Schwarzenberg, K., Schreiner, L., Kubisch, R., Müller, R., Wagner, E., & Vollmar, A. M. (2014) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-13-0484 · Cited by 73
“It has been shown that inhibition of autophagy increased caspase-3 activity in detached cells (19).”
BackgroundChen, N., & Debnath, J. (2013) · Autophagy · doi:10.4161/auto.24870 · Cited by 71
Self-citationAutophagy in the “inflammation-carcinogenesis” pathway of liver and HCC immunotherapy
Yu, S., Wang, Y., Li, J., Claret, F. X., Li, Q., Tian, T., Liang, X., Ruan, Z., Jiang, L., Yao, Y., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.09.049 · Cited by 72
Ferraresi, A., Esposito, A., Girone, C., Vallino, L., Salwa, A., Ghezzi, I., Thongchot, S., Vidoni, C., Dhanasekaran, D. N., & Isidoro, C. (2021) · Cells · doi:10.3390/cells10113213 · Cited by 70
“On one side, autophagy hampers the early phases of metastasization by degrading EMTassociated markers [43] and reversing the EMT process [44], on the other hand it supports the survival of cancer cells that have already undergone EMT by preventing anoikis [45].”
BackgroundRubio, N., Coupienne, I., Valentin, E. D., Heirman, I., Grooten, J., Piette, J. G., & Agostinis, P. (2012) · Autophagy · doi:10.4161/auto.20763 · Cited by 70
Satyavarapu, E. M., Das, R., Mandal, C., Mukhopadhyay, A., & Mandal, C. (2018) · Cell Death & Disease · doi:10.1038/s41419-018-0989-8 · Cited by 69
RetractedCrosstalk Between ROS and Autophagy in Tumorigenesis: Understanding the Multifaceted Paradox
Hasan, A., Rizvi, S. F., Parveen, S., Pathak, N., Nazir, A., & Mir, S. S. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.852424 · Cited by 77
Li, S., Chen, Y., Zhang, Y., Jiang, X., Jiang, Y., Qin, X., Yang, H., Wu, C., & Liu, Y. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27149 · Cited by 68
Jo, Y. K., Roh, S. A., Lee, H., Park, N. Y., Choi, E. S., Oh, J., Park, S. J., Shin, J. H., Suh, Y., Lee, E. K., et al. (2016) · Cancer Letters · doi:10.1016/j.canlet.2016.11.002 · Cited by 66
Zhang, X., Wang, L., Ireland, S., Ahat, E., Li, J., Bekier, M. E., Zhang, Z., & Wang, Y. (2019) · Autophagy · doi:10.1080/15548627.2019.1596480 · Cited by 67
Identification of a novel AMPK-PEA15 axis in the anoikis-resistant growth of mammary cells
Hindupur, S. K., Andugulapati, S. B., Saxena, M. T., Pandey, S., Sreenivasamurthy, S. G. S., Heda, N., Kumar, M. V., Mukherjee, G., Dey, D., & Rangarajan, A. (2014) · Breast Cancer Research · doi:10.1186/s13058-014-0420-z · Cited by 68
“Also, increased levels of phosphorylated (p)AMPK was reported in MCF10A immortalized mammary epithelial cells subjected to matrix detachment [18], suggesting that AMPK signaling may be involved in the survival and growth of HMECs in suspension.”
BackgroundThe Emerging Roles of Autophagy in Human Diseases
Lei, Y., & Klionsky, D. J. (2021) · Biomedicines · doi:10.3390/biomedicines9111651 · Cited by 68
“When detachment from the ECM occurs, oxidative stress activates EIF2AK3/PERK, which induces autophagy through promoting the expression level of some essential ATG genes [108], activating AMPK and inhibiting MTOR complex 1 (MTORC1) [109] and the induced autophagy protects the cell from anoikis [108,110].”
BackgroundMolecular Mechanisms of Autophagy in Cancer Development, Progression, and Therapy
Vitto, V. A. M., Bianchin, S., Zolondick, A. A., Pellielo, G., Rimessi, A., Chianese, D., Yang, H., Carbone, M., Pinton, P., Giorgi, C., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10071596 · Cited by 73
“demonstrated that autophagy promotes epithelial cell survival during anoikis through the stable reduction of ATG5 or ATG7 in MCF-10A [100].”
BackgroundInfluentialAltman, B. J., Wofford, J. A., Zhao, Y., Coloff, J. L., Ferguson, E. C., Wieman, H. L., Swearingen, A. E. D. V., Ilkayeva, O., & Rathmell, J. C. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-08-0829 · Cited by 64
“These findings are consistent with the view that apoptosis occurs to prevent cells from surviving long-term in the absence of growth factors (Lum et al., 2005a; Degenhardt et al., 2006; Fung et al., 2008) and further show that autophagy augments this apoptotic stress.”
BackgroundDeng, Z., Wang, H., Liu, J., Deng, Y., & Zhang, N. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03890-7 · Cited by 70
“Induction of autophagy promoted cell survival in detached nontransformed epithelial cells and primary fibroblasts [19, 20].”
BackgroundSGK1 signaling promotes glucose metabolism and survival in extracellular matrix detached cells
Mason, J. A., Cockfield, J. A., Pape, D. J., Meissner, H., Sokolowski, M. T., White, T. C., Valentín López, J. C., Liu, J., Liu, X., Martínez-Reyes, I., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108821 · Cited by 64
Shtutman, M. S., Baig, M. S., Levina, E. M., Hurteau, G. J., Lim, C., Broude, E. V., Nikiforov, M. A., Harkins, T. T., Carmack, C. S., Ding, Y., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103842108 · Cited by 64
“Retroviral vector expressing GFP-LC3 (21) was obtained from Addgene.”
BackgroundMethodInfluentialAdhesion-mediated apoptosis resistance in cancer
Westhoff, M., & Fulda, S. (2009) · Drug Resistance Updates · doi:10.1016/j.drup.2009.08.001 · Cited by 66
The miR-290-295 cluster suppresses autophagic cell death of melanoma cells
Chen, Y., Liersch, R., & Detmar, M. J. (2012) · Scientific Reports · doi:10.1038/srep00808 · Cited by 65
Saha, M., Kumar, S., Bukhari, S., Andugulapati, S. B., Kumar, P., Hindupur, S. K., & Rangarajan, A. (2018) · Cancer Research · doi:10.1158/0008-5472.can-17-2090 · Cited by 66
“Further, the catabolic process of autophagy, which is also known to regulate energy balance, plays a key role in anoikis-resistance [29].”
BackgroundAnoikis evasion in inflammatory breast cancer cells is mediated by Bim-EL sequestration
Buchheit, C. L., Angarola, B. L., Steiner, A., Weigel, K. J., & Schafer, Z. T. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.209 · Cited by 63
Current questions and possible controversies in autophagy
Lindqvist, L., Simon, A. K., & Baehrecke, E. H. (2015) · Cell Death Discovery · doi:10.1038/cddiscovery.2015.36 · Cited by 62
Autophagy and cancer cell metabolism
Anderson, C. M., & Macleod, K. F. (2019) · International review of cytology · doi:10.1016/bs.ircmb.2019.06.002 · Cited by 63
“This role in promoting metastasis may be explained in part by the role of autophagy in promoting survival following matrix detachment that occurs during progression to invasive cancer (Avivar-Valderas et al., 2013; Fung et al., 2008).”
BackgroundAutophagy and Mitophagy Promotion in a Rat Model of Endometriosis
Siracusa, R., D’Amico, R., Impellizzeri, D., Cordaro, M., Peritore, A. F., Gugliandolo, E., Crupi, R., Salinaro, A. T., Raffone, E., Genovese, T., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105074 · Cited by 61
“In normal conditions, upon detachment from the extracellular matrix, epithelial cells undergo anoikis [10].”
BackgroundElzinga, B. M., Nyhan, M. J., Crowley, L. C., O’Donovan, T. R., Cahill, M. R., & McKenna, S. L. (2013) · American Journal of Hematology · doi:10.1002/ajh.23428 · Cited by 61
Paul, S., Ghosh, S., Mandal, S., Sau, S., & Pal, M. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003376 · Cited by 61
“The level of ATG7, a HSF1 target (53) and an E1 ubiquitin ligase involved in the autophagosome formation (54), was also monitored.”
BackgroundPetibone, D. M., Majeed, W., & Casciano, D. A. (2016) · Journal of Applied Toxicology · doi:10.1002/jat.3393 · Cited by 63
Liu, Y., Munoz, N. M., Tsai, A., Logan, T. M., & Ma, T. (2016) · Stem Cells · doi:10.1002/stem.2510 · Cited by 60
Metadata
- Authors
- Fung, C., Lock, R., Gao, S., Salas, E., & Debnath, J.
- Affiliations
- University of California, San Francisco (US)
- Harvard University (US)
- *Department of Pathology and
- ORCID
- Debnath, Jayanta
- Venue
- Molecular Biology of the Cell
- Published
- 2008-03
- Volume
- 19
- Issue
- 3
- Pages
- 797-806
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC2262959
- OpenAlex
- W2039403501
- Cited by
- 558
- References
- 52
- Citations by year
- 2026: 10 · 2025: 20 · 2024: 15 · 2023: 26 · 2022: 33 · 2021: 45 · 2020: 41 · 2019: 35 · 2018: 36 · 2017: 23 · 2016: 40 · 2015: 37 · 2014: 44 · 2013: 43 · 2012: 28
- FWCI
- 9.86
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Biology of the Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Howard Hughes Medical Institute
- American Association for Cancer Research
- National Institutes of Health
- Genentech
- University of California, San Francisco
- National Cancer Institute (K08CA098419)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- autophagy, anoikis, extracellular matrix detachment, lumen formation, epithelial morphogenesis, apoptosis, Bcl-2, ATG5, ATG7, clonogenic survival, autophagy-related genes, mammary tumor cells
- MeSH terms
- Autophagy-Related Protein 5, Autophagy-Related Protein 7, Animals, Autophagy, Cell Adhesion, Cell Line, Cell Survival, Dogs, Epidermal Growth Factor, Epithelial Cells, Extracellular Matrix, Fibroblasts, Humans, Microtubule-Associated Proteins, Apoptosis, Proto-Oncogene Proteins c-bcl-2, Ubiquitin-Activating Enzymes, Mice, ErbB Receptors
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