The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Molecular mechanisms of ATP secretion during immunogenic cell death
Open accessAbstract
The immunogenic demise of cancer cells can be induced by various chemotherapeutics, such as anthracyclines and oxaliplatin, and provokes an immune response against tumor-associated antigens. Thus, immunogenic cell death (ICD)-inducing antineoplastic agents stimulate a tumor-specific immune response that determines the long-term success of therapy. The release of ATP from dying cells constitutes one of the three major hallmarks of ICD and occurs independently of the two others, namely, the pre-apoptotic exposure of calreticulin on the cell surface and the postmortem release of high-mobility group box 1 (HMBG1) into the extracellular space. Pre-mortem autophagy is known to be required for the ICD-associated secretion of ATP, implying that autophagy-deficient cancer cells fail to elicit therapy-relevant immune responses in vivo. However, the precise molecular mechanisms whereby ATP is actively secreted in the course of ICD remain elusive. Using a combination of pharmacological screens, silencing experiments and techniques to monitor the subcellular localization of ATP, we show here that, in response to ICD inducers, ATP redistributes from lysosomes to autolysosomes and is secreted by a mechanism that requires the lysosomal protein LAMP1, which translocates to the plasma membrane in a strictly caspase-dependent manner. The secretion of ATP additionally involves the caspase-dependent activation of Rho-associated, coiled-coil containing protein kinase 1 (ROCK1)-mediated, myosin II-dependent cellular blebbing, as well as the opening of pannexin 1 (PANX1) channels, which is also triggered by caspases. Of note, although autophagy and LAMP1 fail to influence PANX1 channel opening, PANX1 is required for the ICD-associated translocation of LAMP1 to the plasma membrane. Altogether, these findings suggest that caspase- and PANX1-dependent lysosomal exocytosis has an essential role in ATP release as triggered by immunogenic chemotherapy.
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?
In the citing paper
“This said, executioner caspases can positively or negatively regulate the emission of multiple DAMPs from dying cells, including immunostimulatory [229] as well as immunosuppressive [230] factors.”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [229]
In the citing paper
“In the context of ICD, ATP is released through a cascade of events occurring downstream of caspase activation and involving: (1) the autophagy-dependent accumulation of ATP within autolysosomes (the organelles forming by the fusion of autophagosomes or amphisomes with lysosomes), (2) the relocalization of lysosomal-associated membrane protein 1 (LAMP1) to the plasma membrane, (3) ROCK1-dependent”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [229]
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
Guidelines for the use and interpretation of assays for monitoring autophagy
Klionsky, D. J., Abdalla, F. C., Abeliovich, H., Abraham, R. T., Acevedo-Arozena, A., Adeli, K., Agholme, L., Agnello, M., Agostinis, P., Aguirre-Ghiso, J. A., et al. (2012) · Autophagy · doi:10.4161/auto.19496 · Cited by 3,996
Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009
Kroemer, G., Galluzzi, L., Vandenabeele, P., Abrams, J., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., El-Deiry, W. S., Golstein, P., Green, D. R., et al. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2008.150 · Cited by 3,399
Self-citationImmunogenic Cell Death in Cancer Therapy
Kroemer, G., Galluzzi, L., Kepp, O., & Zitvogel, L. (2013) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-100008 · Cited by 3,303
Self-citationImmunogenic cell death and DAMPs in cancer therapy
Krysko, D. V., Garg, A. D., Kaczmarek, A., Krysko, O., Agostinis, P., & Vandenabeele, P. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3380 · Cited by 3,223
Calreticulin exposure dictates the immunogenicity of cancer cell death
Obeid, M., Tesniere, A., Ghiringhelli, F., Fimia, G. M., Apetoh, L., Perfettini, J.-L., Castedo, M., Mignot, G., Panaretakis, T., Casares, N., et al. (2007) · Nature Medicine · doi:10.1038/nm1523 · Cited by 3,216
Self-citationCalcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension
Uehata, M., Ishizaki, T., Satoh, H., Ono, T., Kawahara, T., Morishita, T., Tamakawa, H., Yamagami, K., Inui, J., Maekawa, M., et al. (1997) · Nature · doi:10.1038/40187 · Cited by 2,862
Galluzzi, L., Vitale, I., Abrams, J. M., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., Dawson, T. M., Dawson, V. L., El-Deiry, W. S., Fulda, S., et al. (2012) · Cell Death & Differentiation · doi:10.1038/cdd.2011.96 · Cited by 2,421
Self-citationNucleotides released by apoptotic cells act as a find-me signal to promote phagocytic clearance
Elliott, M. R., Chekeni, F. B., Trampont, P. C., Lazarowski, E. R., Kadl, A., Walk, S. F., Park, D., Woodson, R. I., Ostankovich, M., Sharma, P., et al. (2009) · Nature · doi:10.1038/nature08296 · Cited by 1,654
Combining immunotherapy and targeted therapies in cancer treatment
Vanneman, M. W., & Dranoff, G. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3237 · Cited by 1,627
Caspase-dependent immunogenicity of doxorubicin-induced tumor cell death
Casares, N., Pequignot, M. O., Tesniere, A., Ghiringhelli, F., Roux, S., Chaput, N., Schmitt, E., Hamai, A., Hervas-Stubbs, S., Obeid, M., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20050915 · Cited by 1,512
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 564
Mechanisms of primary resistance to immune checkpoint inhibitors in NSCLC
Gomatou, G., Charpidou, A. G., Li, P., Syrigos, N. K., & Gkiozos, I. (2024) · Clinical & Translational Oncology · doi:10.1007/s12094-024-03731-x · Cited by 7
Qiao, X., Ma, P., Guo, J., Sun, Y., Peng, L., Yu, N., Zuo, W., & Yang, J. (2025) · Journal of Materials Chemistry B · doi:10.1039/d5tb00305a · Cited by 7
Azizi, M., Andalib, A., & Rezaei, M. (2025) · Cancer Cell International · doi:10.1186/s12935-025-03919-3 · Cited by 7
Zhou, B., Dong, W., Fu, Y., & Jiang, Q. (2025) · Discover Oncology · doi:10.1007/s12672-025-03164-0 · Cited by 7
Shum, J., Leung, P. K., Huang, L., Lee, L. C., Yarshova, M., Cheng, L., Pan, Y., Chiang, M. W.-L., Yiu, S., Lau, K., et al. (2025) · Chemical Science · doi:10.1039/d5sc04772b · Cited by 7
Jin, X., Zeng, X., Yang, D., Yi, L., Wu, W.-L., Chen, X., Luo, X., Xu, P., Zhang, S., Zhang, S., et al. (2025) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2025.111166 · Cited by 10
Kim, N.-E., Lee, S., Park, H., Kim, S., & Kim, Y. (2024) · ACS Applied Bio Materials · doi:10.1021/acsabm.4c00941 · Cited by 7
Assessment of eIF2α phosphorylation during immunogenic cell death
Bezu, L., Humeau, J., Leduc, M., Pan, H., Kroemer, G., & Kepp, O. (2022) · Methods in cell biology · doi:10.1016/bs.mcb.2022.01.003 · Cited by 7
Self-citationEx vivo activation of dendritic cells via coacervate-mediated exogenous tumor cell lysate delivery
Seong, J., Jeong, S., Kim, S., Yun, S., Baek, Y., & Kim, K. (2023) · Biomaterials Science · doi:10.1039/d3bm00234a · Cited by 7
Stecklein, S. R., Barlow, W. E., Pusztai, L., Timms, K. M., Kennedy, R. D., Logan, G. E., Seitz, R. S., Badve, S., Gökmen‐Polar, Y., Porter, P. L., et al. (2023) · JCO Precision Oncology · doi:10.1200/po.23.00197 · Cited by 7
Purinergic Signaling Within the Tumor Microenvironment
Draganov, D., & Lee, P. P. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-47189-7_5 · Cited by 7
Studying Immunogenic Cell Death in Human Colorectal Cancer Organoids
Lisandrelli, R., Winkler, M., Trajanoski, Z., & Lamberti, G. (2025) · OncoTargets and Therapy · doi:10.2147/ott.s521346 · Cited by 6
Harnessing Genomic Stress for Antitumor Immunity
Pu, C., Tao, S., Xu, J., & Huang, M. (2020) · Antioxidants and Redox Signaling · doi:10.1089/ars.2020.8221 · Cited by 6
The Purinergic Landscape of Non-Small Cell Lung Cancer
Hreich, S. J. D., Benzaquen, J., Hofman, P. M., & Vouret‐Craviari, V. (2022) · Cancers · doi:10.3390/cancers14081926 · Cited by 6
Revisiting immunogenic cell death to improve treatment response in cancer
Shakfa, N. E., Siemens, D. R., & Koti, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821310-0.00008-5 · Cited by 6
ATP-responsive and functionalized framework nucleic acid for synergistic radio-immunotherapy
Zhang, Y., Zhan, Y., Mao, C., Guo, L., Zhao, Y., Chen, Y., & Lin, Y. (2023) · Chemical Engineering Journal · doi:10.1016/j.cej.2023.146278 · Cited by 6
Commentary: Metabolites released from apoptotic cells act as tissue messengers
Zeng, C., Shao, Z., Li, J., Pan, H., & Xing, F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01878 · Cited by 6
Solvothermal domino synthesis of an ER-targeted iron(II) complex for inducing immunogenic cell death
Tian, N., Ju, H., Hu, Q., Hou, Q., Lu, Y., Liu, Y., Huang, J., Zhu, Z., Zhang, B., Huang, J. Y., et al. (2025) · Chinese Chemical Letters · doi:10.1016/j.cclet.2025.111038 · Cited by 5
Physical ablative methods and cancer cell death: Implications for immunity and therapies
Rossi, A., & Muratori, C. (2025) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2025.104903 · Cited by 5
D’Ambrosio, L., Greco, M. E., Forte, M., Vecchio, D., Schiavon, S., Nonno, F. D., Tahir, S., Picchio, V., Cozzolino, C., Sarto, G., et al. (2025) · Biology Direct · doi:10.1186/s13062-025-00703-1 · Cited by 6
Wan, H., Ye, T., Bi, Y., Zhang, J., Wu, W., Liu, A., Sun, L., Lin, J., Chai, N., Zhang, M., et al. (2025) · Open Research (University of Surrey) · doi:10.1002/viw.20250185 · Cited by 5
Khorrami, M., Fadaie, M., Dizaji, S. R., Davoodi, A., Asghari, R., Shen, J., Rahimmanesh, I., Sethi, G., & Makvandi, P. (2026) · Journal of Nanobiotechnology · doi:10.1186/s12951-026-04286-5 · Cited by 5
Combinatorial in situ cancer vaccines: unlocking broad and enhanced antitumor responses
Chen, W., Baig, J., Choi, H., & Son, S. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02821-2 · Cited by 5
Evers, M., Song, J., & Chen, X. (2022) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-030-94004-1_4 · Cited by 5
Oliveros, A., Poleschuk, M., Cole, P. D., Boison, D., & Jang, M. (2023) · International review of neurobiology · doi:10.1016/bs.irn.2023.08.003 · Cited by 6
Jiang, Z., Maggs, L., Zhou, K. L., Zou, C., Huang, J., Wang, X., & Zhang, Y. (2025) · World Journal of Urology · doi:10.1007/s00345-025-05760-9 · Cited by 5
Toxic talk: pannexin1 channel communication as an emerging mechanism of toxicity
Vinken, M. (2022) · Toxicology · doi:10.1016/j.tox.2022.153295 · Cited by 5
Khan, N. A., Garg, A. D., Agostinis, P., & Swinnen, J. V. (2017) · Oncotarget · doi:10.18632/oncotarget.23335 · Cited by 5
Immunogenic Stress and Death of Cancer Cells in Natural and Therapy-Induced Immunosurveillance
Kepp, O., Pol, J. G., Zitvogel, L., & Kroemer, G. (2017) · Springer eBooks · doi:10.1007/978-3-319-62431-0_12 · Cited by 6
Self-citationCalreticulin Exposure in Mitotic Catastrophe
Bezu, L., Kepp, O., & Kroemer, G. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1217-0_14 · Cited by 5
Self-citationSusana Fiorentino, G., & Urueña, C. P. (2018) · Revista de la Academia Colombiana de Ciencias Exactas Físicas y Naturales · doi:10.18257/raccefyn.542 · Cited by 5
Li, Y., Li, Y., Wang, X., & Qi, Z. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.164067 · Cited by 4
Selcen, S., Wieland, L., Oliveira, T. D., Ghadimi, M. B., Conradi, L., Schneider, G., Witte, L., & Wirth, M. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02662-y · Cited by 4
Feng, F., Su, M., Liu, X., Chen, J., Liu, Q., Li, X., Zhang, X., Chen, Y., Fu, H., Chen, Z., et al. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.10.042 · Cited by 4
Autophagy Modulates Immunogenic Cell Death in Cancer
Matsushita, M., & Moriwaki, M. (2026) · Cancers · doi:10.3390/cancers18020205 · Cited by 4
Gorbacheva, V. I., Grabovoy, A. S., Marukhina, P. S., Syrocheva, A. O., & Kolesova, E. P. (2026) · Beilstein Journal of Nanotechnology · doi:10.3762/bjnano.17.27 · Cited by 4
Zhang, S., Zhang, T., Cao, Z., Yang, Y., & Lü, P. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107609 · Cited by 4
Expanding the Chemical Space of Allyl Palladates with Anticancer Properties
Schiavo, A., Baio, G., Bru, F., Guerra, I., Mechrouk, V., Achard, T., Baldissin, S., Bellemin‐Laponnaz, S., Cazin, C. S. J., Tubaro, C., et al. (2025) · European Journal of Inorganic Chemistry · doi:10.1002/ejic.202500146 · Cited by 4
LAMP1 as a Target for PET Imaging in Adenocarcinoma Xenograft Models
Ataeinia, B., Haj‐Mirzaian, A., Ben-Naim, L., Esfahani, S. A., Marcos-Vidal, A., Mahmood, U., & Heidari, P. (2025) · Pharmaceuticals · doi:10.3390/ph18081122 · Cited by 4
Targeting cancer stem cells: Dual-drug delivery systems and their role in cancer therapy
Yin, C., Chen, C., Chen, Z., Song, Z., & Li, F. (2026) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2026.126588 · Cited by 4
Nguyễn, B. L., Le, N. D., Nguyen, T. O. O., Ahn, D., Patil, B. R., Kim, B., Phung, C. D., Pham, D.-V., Lee, J. M., Hong, J., et al. (2026) · Nature Communications · doi:10.1038/s41467-025-68279-y · Cited by 4
Immunogenic cell death as a cornerstone for combination therapies with immune checkpoint blockade
Niu, Y., Zhu, S., Fu, K., Lai, Y. Y., Pan, C., Yang, Y., Li, S., Wang, X., To, K. F., Wang, F., et al. (2026) · Molecular Cancer · doi:10.1186/s12943-026-02663-0 · Cited by 4
Programming regulated cell death to engineer whole-tumor-cell vaccines for cancer immunotherapy
Guan, Y., Bai, D., Bu, N., Hao, W., & Maimaitiyiming, Y. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189640 · Cited by 4
Kongsomboonvech, A. K., García-López, L., Njume, F. N., Rodriguez, F., Souza, S. P., Rosenberg, A., & Jensen, K. D. C. (2023) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2023.1130965 · Cited by 4
Aindelis, G., Glaros, V., Fragkoulis, K., Mouchtari, A., Spyridopoulou, K., & Chlichlia, K. (2024) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-024-10330-3 · Cited by 4
Zhang, J., Sun, X., Liu, L., Zhao, X., Yang, C., Li, K., Hu, H., Qiao, M., Chen, D., & Zhao, X. (2022) · Applied Materials Today · doi:10.1016/j.apmt.2022.101518 · Cited by 4
Andrews, C. E., Zilberberg, J., Pérez‐Ollé, R., Exley, M. A., & Andrews, D. W. (2023) · Journal of Neuro-Oncology · doi:10.1007/s11060-023-04491-4 · Cited by 4
A Hydrogel Strategy to Augment Tissue Adenosine to Improve Hindlimb Perfusion
Sayegh, M. N., Cooney, K. A., Han, W. M., Wang, L., Strobel, F. H., Hansen, L., Garcı́a, A. J., & Levit, R. D. (2021) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.315428 · Cited by 4
Demontoux, L., Dérangère, V., Pilot, T., Thinselin, C., Chevriaux, A., Chalmin, F., Bouyer, F., Ghiringhelli, F., & Rébé, C. (2019) · International Journal of Cancer · doi:10.1002/ijc.32590 · Cited by 4
Chen, Y., Liu, W., Cai, Q., Pan, C., Yin, Z., Tang, Y., He, Z., Cheng, G., & Shu, L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1570040 · Cited by 3
Xu, X., & Li, X. (2025) · Breast Cancer Targets and Therapy · doi:10.2147/bctt.s545150 · Cited by 3
Antiviral humoral immunity: Enemy or ally of viral immunotherapy?
Dávola, M. E., Cormier, O., & Mossman, K. L. (2025) · Seminars in Immunology · doi:10.1016/j.smim.2025.102001 · Cited by 3
Mecchi, L., Caron, M. M. J., Welting, T. J. M., & Stoddart, M. J. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.12.029 · Cited by 3
Lv, X., Xue, J., Zhou, J., Zhao, Q., Liu, Y., Wang, L., Jiao, Y., & Qin, S. (2026) · Journal of Translational Medicine · doi:10.1186/s12967-025-07641-6 · Cited by 4
Hypoxia-responsive photosensitizer prodrug for bimodal chemo-photodynamic therapy
Qiu, A.-J., Qiu, C.-H., Xia, X.-Y., Wang, F., & Cao, Q. (2026) · Dyes and Pigments · doi:10.1016/j.dyepig.2026.113678 · Cited by 3
Lu, I., Zhang, J., Chen, X., & Wang, X. (2026) · Molecular Carcinogenesis · doi:10.1002/mc.70128 · Cited by 3
Watson, E. C. R., Shuwa, H. A., Heycock, M. W. D., Wade, J., Wang, C.-Y., Htun, M., Li, L., Niehaus, V., Baker, W., Miller, B., et al. (2026) · BMJ Immunology · doi:10.1136/bmjimm-2026-000029 · Cited by 4
Self-citationSeaver, K., Kourko, O., Gee, K., Greer, P. A., & Basta, S. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.884827 · Cited by 4
Demiya, K., Tazawa, H., Kondo, H., Kure, M., Mochizuki, Y., Komatsubara, T., Yoshida, A., Uotani, K., Hasei, J., Fujiwara, T., et al. (2024) · Molecular Therapy Oncology · doi:10.1016/j.omton.2024.200845 · Cited by 7
Jeong, D., Kim, S., Park, H., Woo, K., Choi, J., Choi, M., Shin, J., Park, S. H., Seon, M., Lee, D., et al. (2025) · Advanced Science · doi:10.1002/advs.202412393 · Cited by 3
Kwon, G., Baek, J., Kim, N., Kwon, S., Song, N., Park, S., Kim, B., & Lee, D. (2023) · Biomaterials Science · doi:10.1039/d3bm00770g · Cited by 3
Lotsberg, M. L., Chen, S., Dhakal, S., Lorens, J. B., Baguley, B. C., Chouaı̈b, S., & Engelsen, A. S. T. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819609-0.00008-0 · Cited by 3
Cell-Autonomous (Cell-Intrinsic) Stress Responses
Land, W. G. (2018) · Springer eBooks · doi:10.1007/978-3-319-78655-1_18 · Cited by 4
Hussain, M. K., Ali, R., Ahamad, S., Khan, M. F., & Saquib, M. (2023) · doi:10.1002/9781394168033.ch6 · Cited by 3
Guo, J., Lin, W., Tang, T., Liu, F., Tan, F., Qin, L., Xu, W., Li, H., Sun, Z., Cui, R., et al. (2025) · ACS Applied Nano Materials · doi:10.1021/acsanm.5c01449 · Cited by 2
A new role of RAB21 and VARP in autophagy and autophagic exocytosis of ATP
Barbosa, M. C., Reta, P. M., Nola, S., Aguilera, M. O., Galli, T., Colombo, M. I., & Fader, C. M. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2501365 · Cited by 2
Development of therapeutic cancer vaccines based on cancer immunity cycle
Zhang, J., Zheng, Y., Xu, L., Gao, J., Ou, Z., Zhu, M., & Wang, W. (2025) · Frontiers of Medicine · doi:10.1007/s11684-025-1134-6 · Cited by 2
Qiu, X., Liu, J., Song, L., Yu, H., Wu, Y., Wang, Q., Lu, M., Gu, X., Chen, B., Zhang, M., et al. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.147397 · Cited by 2
Das, M., Nayak, D. K., Patel, S., Kumar, A., Quaderi, M. A., Dandsena, P. K., Naik, L., Mishra, A., Mishra, A., Singh, R., et al. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117512 · Cited by 2
Mitochondrial respiration in peripheral blood mononuclear cells of healthy adult population
Lee, J. H., Vine, J., Balaji, L., Peradze, N., Antony, N., Wang, Y., Morton, A., Moskowitz, A., Donnino, M. W., & Liu, X. (2026) · PLoS ONE · doi:10.1371/journal.pone.0336939 · Cited by 2
Self-citationKešar, U., Markelc, B., Čemažar, M., Serša, G., Jesenko, T., & Strojan, P. (2026) · BMC Cancer · doi:10.1186/s12885-026-15674-3 · Cited by 2
Eskandani, N. A., Ghasemzaei, M., Farani, M. R., Mirzaee, D., Hatami, A., Khosravi, A. A., Ghoreishian, S. M., & Huh, Y. S. (2026) · Nano Today · doi:10.1016/j.nantod.2026.103065 · Cited by 2
HIF ‐Regulated Pannexin‐1 Channel Drives Luminal ATP Accumulation in Kidney Cysts
Skoczynski, K., Scholz, J. K., Ursu, R., Schödel, J., Grampp, S., Naas, S., Lauer, V., Schiffer, M., Büttner-Herold, M. J., Buchholz, B., et al. (2026) · The FASEB Journal · doi:10.1096/fj.202502847rr · Cited by 2
Li, C., Pang, F., Ma, Y., Bin, Y., Huang, L., Zhao, J., Huang, M., Liang, J., Zhang, L., Zhao, S., et al. (2026) · SmartMat · doi:10.1002/smm2.70095 · Cited by 2
Self-citationLC3B in Malignant Cells Correlates With Immune Infiltrate in Hypopharyngeal Squamous Cell Carcinoma
Gao, S., Chen, J., Han, X., Wei, D., Wu, Z., & Gao, C. (2020) · Technology in Cancer Research & Treatment · doi:10.1177/1533033820970664 · Cited by 2
Shields, N. J., Peyroux, E. M., Campbell, K., Mehta, S. Y., Woolley, A. G., Counoupas, C., Neumann, S., & Young, S. L. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100500 · Cited by 2
Immunogenic Cell Death in Cancer
Humeau, J., Naour, J. L., Kroemer, G., & Pol, J. G. (2023) · Interdisciplinary cancer research · doi:10.1007/16833_2022_121 · Cited by 2
Self-citationTherapeutic strategies to enhance immune response induced by multiple myeloma cells
Liu, Z., Yang, C., Liu, X., Xu, X., Zhao, X., & Fu, R. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1169541 · Cited by 4
Park, J. H., Kim, M., Yun, D. H., & Kim, Y. (2023) · ACS Applied Bio Materials · doi:10.1021/acsabm.3c00581 · Cited by 2
Yao, Y., Zhang, Q., Wei, S., Li, H., Zhou, T., Zhang, Q., Zhang, J., Zhang, J., & Wang, H. (2024) · Translational Cancer Research · doi:10.21037/tcr-23-2243 · Cited by 2
In vitro evaluation of the immunogenic potential of gramicidin S and its photocontrolled analogues
Horbatok, K., Semchuk, I., Gorbach, O. I., Khranovska, N., Kosach, V., Borysko, P., Koniev, S., Ulrich, A. S., Afonin, S., & Komarov, I. V. (2025) · RSC Medicinal Chemistry · doi:10.1039/d5md00075k · Cited by 2
Wu, L., Sun, Q., Kitani, A., Zhou, X., Mao, L., & Sang, M. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb47100812 · Cited by 2
Cancer Biology: Severe Cumulative Delayed Type Hypersensitivity Reactions
Khatami, M. (2017) · Springer eBooks · doi:10.1007/978-3-319-66475-0_6 · Cited by 2
Baines, K., & Lane, J. D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/769059 · Cited by 2
Oluremi, A. S., Kannan, K., & Ali, N. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262211031 · Cited by 1
Aria, H., Bakherad, H., Mehdipour, A. R., Azizi, M., & Rezaei, M. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116174 · Cited by 1
Liu, S., Zheng, Q., Yin, J., Huang, Y., Zou, G., Song, K., Lin, Q., You, J., Liao, Y., & Shi, B. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.173174 · Cited by 1
Disulfiram/Copper Combined with Irradiation Induces Immunogenic Cell Death in Melanoma
Wang, E., Zhang, Y., Jia, L., Lin, Z., Sun, T., Hu, P., Wang, K., Shang, Z., Guo, W. Y., Kiang, J. G., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27020980 · Cited by 2
Wu, B.-W., Wang, P.-P., Zhou, Y., Li, J.-J., Yi, Z.-X., Cheng, X.-Y., Liang, L.-J., Zuo, Y.-R., Yang, P.-W., Liu, S., et al. (2026) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2026.113290 · Cited by 1
Bozhdansky, V., Tayar, S., Kashkash, S., Bacharach, E., & Ehrlich, M. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02823-1 · Cited by 1
Li, Q., Huo, Y., Zhu, X., Cheng, Z., Sun, Y., Jin, S., Sun, M., Zhang, H., Wu, X., & Jin, Y. (2026) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.6c00191 · Cited by 1
Wang, J., Liu, C., Zhang, X., Xie, Y., Zhang, X., Wang, T. T., & Wang, L. (2026) · RSC Advances · doi:10.1039/d6ra01921h · Cited by 1
Lee, S., Jiao, A., Park, H., Hong, K. H., Ha, J., Nam, H., Kim, S., Kim, S. H., Jeong, S. D., Lee, D., et al. (2026) · Biomaterials · doi:10.1016/j.biomaterials.2026.124337 · Cited by 1
Paik, J. Y., Gajulapalli, S. R., Li, V., Park, S., Lee, Y., Orlikova-Boyer, B., Lorant, A., Christov, C., Kirsch, G., Kang, H. J., et al. (2026) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2026.119652 · Cited by 1
Zhou, Y., Lin, P., Wang, J., Huang, X., Zhang, H., Liu, J., Zhou, P., Liu, X. M., Chen, W., Sun, H., et al. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108328 · Cited by 1
Lin, T., Chen, Y., & Huang, Z. (2026) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-026-05815-7 · Cited by 1
Immunotherapy in Pancreatic Cancer; the Road Less Traveled
Leem, G., & Song, S. Y. (2016) · Immunological Disorders and Immunotherapy · doi:10.4172/idit.1000106 · Cited by 1
Weissenstein, U., Tschumi, S., Leonhard, B., & Baumgartner, S. (2025) · BMC Complementary Medicine and Therapies · doi:10.1186/s12906-025-04909-8 · Cited by 1
Treatment-Induced Breast Cancer Dormancy and Relapse
Keim, R. C. (2014) · VCU Scholars Compass (Virginia Commonwealth University) · doi:10.25772/xn3r-3633 · Cited by 1
Immunogenic clearance-mediated cancer vaccination
Nam, G., Yang, Y., & Kim, I. (2020) · Elsevier eBooks · doi:10.1016/b978-0-08-102983-1.00020-x · Cited by 1
Metadata
- Authors
- Martins, I., Wang, Y., Michaud, M., Ma, Y., Sukkurwala, A. Q., Shen, S., Kepp, O., Métivier, D., Galluzzi, L., Perfettini, J.-L., Zitvogel, L., & Kroemer, G.
- Affiliations
- Université Paris-Sud (FR)
- Institut Gustave Roussy (FR)
- Inserm (FR)
- Corresponding author
- Kroemer, G
- Venue
- Cell Death & Differentiation
- Published
- 2013-07-12
- Volume
- 21
- Issue
- 1
- Pages
- 79-91
- ISSN
- 1350-9047 (ISSN-L)
- 1476-5403
- PMC
- PMC3857631
- OpenAlex
- W1991505853
- Cited by
- 563
- References
- 61
- Citations by year
- 2026: 53 · 2025: 57 · 2024: 48 · 2023: 67 · 2022: 39 · 2021: 45 · 2020: 51 · 2019: 34 · 2018: 40 · 2017: 36 · 2016: 34 · 2015: 28 · 2014: 21 · 2013: 10
- FWCI
- 13.87
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell Death and Differentiation (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Sidaction
- European Commission
- Agence Nationale de la Recherche
- Fondation de France
- Institut National Du Cancer
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Adenosine and Purinergic Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- immunogenic cell death, ATP release, lysosomal exocytosis, LAMP1, autophagy, caspase activation, Panx1 channels, ROCK1, myosin II, immunogenic chemotherapy, anthracyclines, oxaliplatin, cancer immunotherapy
- MeSH terms
- Autophagy-Related Protein 5, Adenosine Triphosphate, Animals, Antineoplastic Agents, Cell Membrane, DNA-Binding Proteins, Humans, Lysosomes, Microtubule-Associated Proteins, Nerve Tissue Proteins, RNA-Binding Proteins, Cell Death, Connexins, HMGB1 Protein, Myosin Type II, RNA Interference, RNA, Small Interfering, Cell Line, Tumor, Mice, Lysosomal-Associated Membrane Protein 1, rho-Associated 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