A novel pathway combining calreticulin exposure and ATP secretion in immunogenic cancer cell death

Adverse Renal Effects of Immune Checkpoint Inhibitors: A Narrative Review

Wanchoo, R., Karam, S., Uppal, N. N., Barta, V. S., Deray, G., Devoe, C., Launay‐Vacher, V., Jhaveri, K. D., & on behalf of Cancer and Kidney International Network Workgroup on Immune Checkpoint Inhibitors (2017) · American Journal of Nephrology · doi:10.1159/000455014 · Cited by 15,320

Photodynamic therapy of cancer: An update

Agostinis, P., Berg, K., Cengel, K. A., Foster, T. H., Girotti, A. W., Gollnick, S. O., Hahn, S. M., Hamblin, M. R., Juzeniene, A., Kessel, D., et al. (2011) · CA: A Cancer Journal for Clinicians · doi:10.3322/caac.20114 · Cited by 5,145

Anthracyclines: Molecular Advances and Pharmacologic Developments in Antitumor Activity and Cardiotoxicity

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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

Photodynamic therapy and anti-tumour immunity

Castaño, A. P., Mróz, P., & Hamblin, M. R. (2006) · Nature reviews. Cancer · doi:10.1038/nrc1894 · Cited by 2,685

STRING 8--a global view on proteins and their functional interactions in 630 organisms

Jensen, L. J., Kuhn, M., Stark, M., Chaffron, S., Creevey, C. J., Muller, J., Doerks, T., Julien, P., Roth, A. C., Simonovic, M., et al. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn760 · Cited by 2,475

Activation of the NLRP3 inflammasome in dendritic cells induces IL-1β–dependent adaptive immunity against tumors

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PI3K pathway alterations in cancer: variations on a theme

Yuan, T. L., & Cantley, L. C. (2008) · Oncogene · doi:10.1038/onc.2008.245 · Cited by 1,845

Nucleotides 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

Cell-Surface Calreticulin Initiates Clearance of Viable or Apoptotic Cells through trans-Activation of LRP on the Phagocyte

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Integrating conventional and antibody-based targeted anticancer treatment into immunotherapy

Xu, M. M., Pu, Y., Weichselbaum, R. R., & Fu, Y. (2016) · Oncogene · doi:10.1038/onc.2016.231 · Cited by 21

Out of the frying pan and into the fire: damage-associated molecular patterns and cardiovascular toxicity following cancer therapy

Klee, N., McCarthy, C. G., Quinones, P. M., & Webb, R. C. (2017) · Therapeutic Advances in Cardiovascular Disease · doi:10.1177/1753944717729141 · Cited by 23

Hypoxia-mediated activation of hypoxia-inducible factor-1α in triple-negative breast cancer: A review

Liu, L., Bai, J., Hu, L., & Jiang, D. (2023) · Medicine · doi:10.1097/md.0000000000035493 · Cited by 23

Unfolding innate mechanisms in the cancer microenvironment: The emerging role of the mesenchyme

Koliaraki, V., Henriques, A. R., Prados, A., & Kollias, G. A. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20190457 · Cited by 20

Redaporfin induces immunogenic cell death by selective destruction of the endoplasmic reticulum and the Golgi apparatus

Gomes-da-Silva, L. C., Zhao, L., Arnaut, L. G., Kroemer, G., & Kepp, O. (2018) · Oncotarget · doi:10.18632/oncotarget.25798 · Cited by 20

Dual-organelle targeted photosensitizer with AIE characteristics for triple-negative breast cancer photodynamic therapy via apoptosis and immunogenic cell death

Wen, W., Li, J., Shang, W., Zhuang, Z., Deng, X., Yan, X., Xie, D., Chen, C., Zhao, Z., Tang, B. Z., et al. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.101828 · Cited by 19

A pH‐Sensitive Nanosized Covalent–Organic Polymer for Enhanced Tumor Photodynamic Immunotherapy by Hypoxia Relief and STAT3 Inhibition

Lei, L., Dai, W., Zhao, J., Jiang, A., Peng, H., Jin, Q., Li, X., & Tang, Z. (2025) · Advanced Science · doi:10.1002/advs.202504860 · Cited by 19

DAMP signaling networks: from receptors to diverse pathophysiological functions

Chen, R., Zou, J., Zhong, X. Y., Liu, J., Kang, R., & Tang, D. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.07.047 · Cited by 26

A Bioinformatic Approach for the Identification of Molecular Determinants of Resistance/Sensitivity to Cancer Thermotherapy

Düzgün, M. B., Theofilatos, K., Georgakilas, A. G., & Pavlopoulou, A. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/4606219 · Cited by 19

The “Yin and Yang” of Unfolded Protein Response in Cancer and Immunogenic Cell Death

Rufo, N., Yang, Y., Vleeschouwer, S. D., & Agostinis, P. (2022) · Cells · doi:10.3390/cells11182899 · Cited by 21

Chromomycin A5 induces bona fide immunogenic cell death in melanoma

Florêncio, K. G. D., Edson, E. A., Fernandes, K. S. D. S., Luiz, J. P. M., Pinto, F. D. C. L., Pessoa, O. D. L., Cunha, F. Q., Machado‐Neto, J. A., & Wilke, D. V. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.941757 · Cited by 20

PKHB1 peptide induces antiviral effects through induction of immunogenic cell death in herpes simplex keratitis

He, Y., Wang, C., Liang, Q., Guo, R., Jiang, J., Shen, W., & Hu, K. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1048978 · Cited by 19

Role of Natural Products in Combating Cancer

Barreto, C., & Jandus, A. (2022) · Cancer Insight · doi:10.58567/ci01010003 · Cited by 19

Immunogenicity of cancer cells: An overview

Singh, T., Bhattacharya, M., Mavi, A. K., Gulati, A., Rakesh, Sharma, N. K., Gaur, S., & Kumar, U. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110952 · Cited by 20

PERK and filamin A in actin cytoskeleton remodeling at ER-plasma membrane contact sites

van Vliet, A. R., & Agostinis, P. (2017) · Molecular & Cellular Oncology · doi:10.1080/23723556.2017.1340105 · Cited by 19

In vitro PUVA treatment triggers calreticulin exposition and HMGB1 release by dying T lymphocytes in GVHD: New insights in extracorporeal photopheresis

Coppard, C., Hannani, D., Humbert, M., Gauthier, V., Plumas, J., Merlin, É., Gabert, F. M., & Chaperot, L. (2019) · Journal of Clinical Apheresis · doi:10.1002/jca.21698 · Cited by 19

Editorial: Immunogenic Cell Death in Cancer: From Benchside Research to Bedside Reality

Garg, A. D., & Agostinis, P. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00110 · Cited by 20

Expanding the role of interventional oncology for advancing precision immunotherapy of solid tumors

Kimura, Y., Ghosn, M., Cheema, W., Adusumilli, P. S., Solomon, S. B., & Srimathveeralli, G. (2021) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2021.12.018 · Cited by 18

HSP90 inhibition acts synergistically with heat to induce a pro-immunogenic form of cell death in colon cancer cells

Mouratidis, P., & ter Haar, G. (2021) · International Journal of Hyperthermia · doi:10.1080/02656736.2021.1983036 · Cited by 17

Photodynamic therapy of melanoma with new, structurally similar, NIR-absorbing ruthenium (II) complexes promotes tumor growth control via distinct hallmarks of immunogenic cell death.

Konda, P., Roque, J. A., Lifshits, L. M., Alcos, A., Azzam, E., Shi, G., Cameron, C. G., McFarland, S. A., & Gujar, S. A. (2022) · PubMed Central · Cited by 18

Dendritic Cells Pulsed with Tumor Lysates Induced by Tetracyanotetra(aryl)porphyrazines-Based Photodynamic Therapy Effectively Trigger Anti-Tumor Immunity in an Orthotopic Mouse Glioma Model

Redkin, T. S., Sleptsova, E. E., Turubanova, V. D., Saviuk, M. O., Lermontova, S. A., Klapshina, L. G., Peskova, N. N., Balalaeva, I. V., Krysko, O., Mishchenko, T. A., et al. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15102430 · Cited by 18

WITHDRAWN: Hypericin-based Photodynamic Therapy Induces a Tumor-Specific Immune Response and an Effective DC-based cancer Immunotherapy

Zheng, Y., Yin, G., Le, V., Zhang, A., Lü, Y., Yang, M., Fei, Z., & Liu, J. (2014) · Biochemical Pharmacology · doi:10.1016/j.bcp.2014.01.036 · Cited by 17

Advancing Immunotherapy in Metastatic Breast Cancer

Mansour, M., Teo, Z. L., Luen, S. J., & Loi, S. (2017) · Current Treatment Options in Oncology · doi:10.1007/s11864-017-0478-9 · Cited by 17

Localized Microsphere/Hydrogel for Tumor Immunotherapy of Cardiac Glycoside with Minimal Toxicity

Gao, L., Zhao, M. L., Mao, Y., Zhang, L., Wang, X., Li, S., Qin, L., Xu, J. C., Hu, L., & Qiao, H. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c18693 · Cited by 16

The therapeutic mavericks: Potent immunomodulating chaperones capable of treating human diseases

Eggleton, P., Alba, J. D., Weinreich, M. A., Calias, P., Foulkes, R., & Corrigall, V. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17669 · Cited by 16

Programing Immunogenic Cell Death in Breast Tumors with Designer DNA Frameworks

Tian, T., Zhao, B., Wei, H., Sun, M., Gao, Z., Lv, M., Lei, H., Ge, Z., & Ge, G. (2023) · JACS Au · doi:10.1021/jacsau.3c00099 · Cited by 16

Immune checkpoint-targeted drug conjugates: A promising tool for remodeling tumor immune microenvironment

Choi, J., Jang, H., Choi, J., Choi, Y., Yang, Y., Shim, M. K., & Kim, S. H. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.05.031 · Cited by 16

In Vitro Testing of the Virus-Like Drug Conjugate Belzupacap Sarotalocan (AU-011) on Uveal Melanoma Suggests BAP1-Related Immunostimulatory Capacity

Ma, S., Veld, R. V. H. I. ‘., Houy, A., Stern, M., Rich, C. C., OSSENDORP, F. A., & Jager, M. J. (2023) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.64.7.10 · Cited by 16

CA9 knockdown enhanced ionizing radiation-induced ferroptosis and radiosensitivity of hypoxic glioma cells

Huang, W., He, Y., Yang, S., Xue, X., Qin, H., Sun, T., & Yang, W. (2023) · International Journal of Radiation Biology · doi:10.1080/09553002.2023.2235433 · Cited by 18

Significance of calreticulin as a prognostic factor in endometrial cancer

Xu, Q., Chen, C., Chen, G., Chen, W., Zhou, D., & Xie, Y. (2018) · Oncology Letters · doi:10.3892/ol.2018.8495 · Cited by 16

Naphthyl quinoxaline thymidine conjugate is a potent anticancer agent post UVA activation and elicits marked inhibition of tumor growth through vaccination

Yuan, Y., Wang, Z., Yang, R., Qian, T., & Zhou, Q. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.03.051 · Cited by 16

PlatinER: A Highly Potent Anticancer Platinum(II) Complex that Induces Endoplasmic Reticulum Stress Driven Immunogenic Cell Death

Tham, M. J. R., Babak, M. V., & Ang, W. H. (2020) · Angewandte Chemie · doi:10.1002/ange.202008604 · Cited by 16

Catalytic immunotherapy-photothermal therapy combination for melanoma by ferroptosis-activating vaccine based on artificial nanoenzyme

Fang, T., Ma, S., Wei, Y., Yang, J., Zhang, J., & Shen, Q. (2022) · Materials Today Chemistry · doi:10.1016/j.mtchem.2022.101308 · Cited by 16

The anticancer effect of PASylated calreticulin-targeting L-ASNase in solid tumor bearing mice with immunogenic cell death-inducing chemotherapy

Zhang, Y., Sultonova, R. D., You, S.-H., Choi, Y., Kim, S.-Y., Lee, W., Seong, J., Min, J., & Hong, Y. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115473 · Cited by 16

Current status of nanoparticle-mediated immunogenic cell death in cancer immunotherapy

Tran, T. H., & Tran, T. T. P. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113085 · Cited by 15

Endoplasmic Reticulum‐Targeting Self‐Assembly Nanosheets Promote Autophagy and Regulate Immunosuppressive Tumor Microenvironment for Efficient Photodynamic Immunotherapy

Huang, P., Liang, S., Xiang, Y., Li, M., Wang, M., & Liu, L. (2024) · Small · doi:10.1002/smll.202311056 · Cited by 15

Endoplasmic Reticulum Stress Nano‐Orchestrators for Precisely Regulated Immunogenic Cell Death as Potent Cancer Vaccines

Teng, Y., Yang, Z., Peng, Y., Yang, Y., Chen, S., Li, J., Gao, D., Sun, W., Wu, Z., Zhou, Y., et al. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202401851 · Cited by 15

Immunostimulatory Hydrogel with Synergistic Blockage of Glutamine Metabolism and Chemodynamic Therapy for Postoperative Management of Glioblastoma

Guo, Y., Jiang, T., Liang, S., Wang, A., Li, J., Jia, Y., Li, Q., Yin, J., Bai, S., & Li, J. (2025) · Advanced Science · doi:10.1002/advs.202412507 · Cited by 15

Innate recognition of apoptotic cells: novel apoptotic cell-associated molecular patterns revealed by crossreactivity of anti-LPS antibodies

Tennant, I., Pound, J. D., Marr, L. A., Willems, J. J. L. P., Petrova, S., Ford, C. A., Paterson, M., Devitt, A., & Gregory, C. D. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2012.165 · Cited by 16

Cloning, Expression, Mutagenesis Library Construction of Glycerol Dehydratase, and Binding Mode Simulation of Its Reactivase with Ligands

Jiang, W., Li, W., Hong, Y., Wang, S., & Fang, B. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-015-1906-6 · Cited by 15

Orally administered Taenia solium Calreticulin prevents experimental intestinal inflammation and is associated with a type 2 immune response

Mendlovic, F., Cruz-Rivera, M. Y., Díaz‐Gandarilla, J. A., Flores-Torres, M. A., Ávila, G., Perfiliev, M., Salazar, A. M., Arriaga‐Pizano, L., Ostrosky‐Wegman, P., & Flisser, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186510 · Cited by 22

Metabolic reprogramming by Dichloroacetic acid potentiates photodynamic therapy of human breast adenocarcinoma MCF-7 cells

Al-Karakooly, Z., Al-Anbaky, Q. A., Kannan, K., & Ali, N. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206182 · Cited by 15

cROSsing the Line: Between Beneficial and Harmful Effects of Reactive Oxygen Species in B-Cell Malignancies

Domka, K., Góral, A., & Firczuk, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01538 · Cited by 15

Sphingosine Kinase Inhibition Enhances Dimerization of Calreticulin at the Cell Surface in Mitoxantrone-Induced Immunogenic Cell Death

Nduwumwami, A. J., Hengst, J. A., & Yun, J. K. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.121.000629 · Cited by 14

Investigation of cell death mechanisms in human lymphatic endothelial cells undergoing photodynamic therapy

Wachowska, M., Osiak, A., Muchowicz, A., Gabrysiak, M., Domagała, A., Kilarski, W. W., & Gołąb, J. (2016) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2016.02.004 · Cited by 15

cRGD target liposome delivery system promoted immunogenic cell death through enhanced anticancer potency of a thymidine conjugate under UVA activation as a cancer vaccine

Yang, R., Wang, Z., Yuan, Y., Qian, T., & Zhou, Q. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.02.031 · Cited by 15

Immunogenic Cell Death Enhances Immunotherapy of Diffuse Intrinsic Pontine Glioma: From Preclinical to Clinical Studies

Liu, G., Qiu, Y., Zhang, P., Chen, Z., Chen, S., Huang, W., Wang, B., Yu, X., & Guo, D. (2022) · Pharmaceutics · doi:10.3390/pharmaceutics14091762 · Cited by 14

Combining cisplatin with Pinellia pedatisecta Schott lipid-soluble extract induces tumor immunogenic cell death in cervical cancer

Wang, C., Zhang, M., Peng, J., Zhang, M., Lu, C., Qi, X., Luo, Q., Wang, Y., & Li, G. (2024) · Phytomedicine · doi:10.1016/j.phymed.2024.155504 · Cited by 14

Gold standard assessment of immunogenic cell death induced by photodynamic therapy: From in vitro to tumor mouse models and anti-cancer vaccination strategies

Mishchenko, T. A., Balalaeva, I. V., Turubanova, V. D., Saviuk, M. O., Shilyagina, N. Y., Krysko, O., Vedunova, M. V., & Krysko, D. V. (2023) · Methods in cell biology · doi:10.1016/bs.mcb.2023.05.003 · Cited by 16

Long-Acting Nanohybrid Hydrogel Induces Persistent Immunogenic Chemotherapy for Suppressing Postoperative Tumor Recurrence and Metastasis

Li, Y., Zhu, J., Yang, Y., Chen, Y., Liu, L., Tao, J., Chen, H., & Deng, Y. (2023) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.3c00746 · Cited by 13

DAMPening Tumor Immune Escape: The Role of Endoplasmic Reticulum Chaperones in Immunogenic Chemotherapy

Cifrić, S., Turi, M., Folino, P., Clericuzio, C., Barello, F., Maciel, T., Anderson, K. C., & Gullà, A. (2024) · Antioxidants and Redox Signaling · doi:10.1089/ars.2024.0558 · Cited by 12

Cascade piezocatalytic nanoprodrug for synergistic piezocatalytic therapy and sono-activated chemotherapy-augmented immunotherapy

Zhang, T.-H., Zheng, Y., Xiang, H.-J., Chen, Y., & Wu, R. (2024) · Nano Today · doi:10.1016/j.nantod.2024.102453 · Cited by 11

Immunopathogenesis of Sjogren's syndrome: Current state of DAMPs

Ming, B., Zhu, Y., Zhong, J., & Dong, L. (2022) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2022.152062 · Cited by 13

Targeted delivery of liposomal chemoimmunotherapy for cancer treatment

Liu, Y., Han, J., Yang, B., Bhatta, R., & Wang, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1010021 · Cited by 16

Endoplasmic reticulum stress enhances the antigen-specific T cell immune responses and therapeutic antitumor effects generated by therapeutic HPV vaccines

Lee, S. Y., Oh, J. Y., Kang, T. H., Shin, H. S., Cheng, M. A., Farmer, E. A., Wu, T. ‐., & Hung, C. (2019) · Journal of Biomedical Science · doi:10.1186/s12929-019-0536-7 · Cited by 13

Successful Partnerships: Exploring the Potential of Immunogenic Signals Triggered by TMZ, CX-4945, and Combined Treatment in GL261 Glioblastoma Cells

Villamañán, L., Martínez‐Escardó, L., Arús, C., Yuste, V. J., & Candiota, A. P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073453 · Cited by 14

Schweinfurthin induces ICD without ER stress and caspase activation

Zhang, R., Neighbors, J. D., Schell, T. D., & Hohl, R. J. (2022) · OncoImmunology · doi:10.1080/2162402x.2022.2104551 · Cited by 13

Organic Semiconducting Polymers for Cancer Sonodynamic Immunotherapy

Hu, P., He, S., & Tian, H. (2025) · Polymer science & technology. · doi:10.1021/polymscitech.5c00112 · Cited by 12

Organoplatinum(II) Type II Immunogenic Cell Death Inducers Target Protein Tyrosine Phosphatase 1B to Drive Immunogenicity

Zou, J. X., Ivanov-Rostovtsev, P. A., Arakelyan, J., Babak, M. V., & Ang, W. H. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c18904 · Cited by 13

Plants-occurring Anthraquinones as Photosensitive Compounds for Photodynamic Method: A Critical Overview

Mantareva, V. N., Braikova, D., Lazarova, I., & Genova, T. (2024) · Frontiers in Bioscience-Landmark · doi:10.31083/j.fbl2905168 · Cited by 12

Endoplasmic reticulum stress-mediated autophagy contributes to 5-ethylamino-9-diethylaminobenzo[a]phenoselenazinium-mediated photodynamic therapy via the PERK–eIF2α pathway

Chen, J., Huang, J., Wang, Z., Song, X., Chen, Z., Zeng, Q., Zhou, X., Zuo, Z., Zhao, S., Chen, X., et al. (2018) · OncoTargets and Therapy · doi:10.2147/ott.s163366 · Cited by 12

Research and application of hydrostatic high pressure in tumor vaccines (Review)

Yan, S., Liu, K., Mu, L., Liu, J., Tang, W., & Liu, B. (2021) · Oncology Reports · doi:10.3892/or.2021.8026 · Cited by 12

A Benzenesulfonamide-Based Mitochondrial Uncoupler Induces Endoplasmic Reticulum Stress and Immunogenic Cell Death in Epithelial Ovarian Cancer

Bi, F., Jiang, Z., Park, W., Hartwich, T. M. P., Ge, Z., Chong, K. Y., Yang, K. B., Morrisson, M. J., Kim, D., Kim, J., et al. (2021) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-21-0396 · Cited by 12

In Vitro Generation of Murine Dendritic Cells for Cancer Immunotherapy: An Optimized Protocol

Baert, T., Garg, A. D., VINDEVOGEL, E., Hoylandt, A. V., Verbist, G., Agonistinis, P., Vergote, I. B., & Coosemans, A. (2016) · Anticancer Research · doi:10.21873/anticanres.11163 · Cited by 12

The abscopal effect induced by in situ-irradiated peripheral tumor cells in a murine GL261 brain tumor model

Zenkoh, J., Gerelchuluun, A., Wang, Y., Miwa, Y., Ohno, T., & Tsuboi, K. (2017) · Translational Cancer Research · doi:10.21037/tcr.2017.01.32 · Cited by 12

Advancements in research and clinical management of interstitial lung injury associated with ADC drugs administration in breast cancer

Zhu, J., Jiang, R., Zhang, H., Fang, Z.-R., Zhou, H., Wei, Q., & Wang, X. (2024) · Discover Oncology · doi:10.1007/s12672-024-01705-7 · Cited by 12

Endoplasmic reticulum targeting photodynamic oxidizer to boost anti-tumor immunity by intensifying immunogenic cell death in conjunction with IDO1 inhibition

Zheng, R., Chen, Z., Li, Q., Yang, N., Zhang, W., Huang, C., Zhao, L., Chen, X., Cheng, H., & Li, S. (2025) · Chinese Chemical Letters · doi:10.1016/j.cclet.2025.110865 · Cited by 11

Bibliometric analysis of research on immunogenic cell death in cancer

Zhou, Y., Hu, F., Cui, Y., Wu, H., Hu, S., & Wei, W. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1029020 · Cited by 14

Research progress on the GRP78 gene in the diagnosis, treatment and immunity of cervical cancer

Bai, Y., Wang, W., Cheng, Y., & Yang, Y. (2023) · European journal of medical research · doi:10.1186/s40001-023-01241-0 · Cited by 11

Photodynamic therapy in cancer stem cells — state of the art

Ibarra, A. M. C., Aguiar, E. M. G., Ferreira, C. B. R., Siqueira, J. M., Côrrea, L., Nunes, F. D., Franco, A. L. D. S., Cecatto, R. B., Hamblin, M. R., & Rodrigues, M. F. S. D. (2023) · Lasers in Medical Science · doi:10.1007/s10103-023-03911-1 · Cited by 11

In vitro and in vivo clearance of Rose Bengal Acetate-PhotoDynamic Therapy-induced autophagic and apoptotic cells

Panzarini, E., Inguscio, V., Tenuzzo, B. A., & Dini, L. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213494552 · Cited by 12

Combinatorial macrophage induced innate immunotherapy against Ewing sarcoma: Turning “Two Keys” simultaneously

Luo, W., Hoang, H., Miller, K. E., Zhu, H., Xu, S., Mo, X. M., Garfinkle, E. A. R., Costello, H. M., Wijeratne, S., Chemnitz, W., et al. (2024) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-024-03093-w · Cited by 10

Nanoscale metal–organic framework-mediated immunogenic cell death boosting tumor immunotherapy

Ni, W., Zhu, W., Wu, W., Chen, J., Ren, P., & Chen, F. (2022) · Materials & Design · doi:10.1016/j.matdes.2022.111068 · Cited by 10

Immunogenic cell death (ICD)-inducers in non-small-cell lung carcinoma (NSCLC): current knowledge and future perspective

Kashefizadeh, A., & Kazemizadeh, H. (2022) · Clinical & Translational Oncology · doi:10.1007/s12094-022-02949-x · Cited by 10

Oncolyic Virotherapy for Prostate Cancer: Lighting a Fire in Winter

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Upregulation of CD86 and IL-12 by rhododendrol in THP-1 cells cocultured with melanocytes through ROS and ATP

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