Mechanisms and consequences of entosis

Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death

Dixon, S. J., Lemberg, K. M., Lamprecht, M. R., Skouta, R., Zaitsev, E. M., Gleason, C. E., Patel, D. N., Bauer, A. J., Cantley, A. M., Yang, W. S., et al. (2012) · Cell · doi:10.1016/j.cell.2012.03.042 · Cited by 18,691

Ferroptosis as a p53-mediated activity during tumour suppression

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Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury

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Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012

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

The Combined Functions of Proapoptotic Bcl-2 Family Members Bak and Bax Are Essential for Normal Development of Multiple Tissues

Lindsten, T., Ross, A. J., King, A., Zong, W.-X., Rathmell, J. C., Shiels, H. A., Ulrich, E., Waymire, K. G., Mahar, P., Frauwirth, K., et al. (2000) · Molecular Cell · doi:10.1016/s1097-2765(00)00136-2 · Cited by 1,489

Synchronized renal tubular cell death involves ferroptosis

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Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells

Fujiwara, T., Bandi, M., Nitta, M., Ivanova, E. V., Bronson, R. T., & Pellman, D. (2005) · Nature · doi:10.1038/nature04217 · Cited by 1,067

Minutes: Mutants of Drosophila autonomously affecting cell division rate

Morata, G., & Ripoll, P. L. (1975) · Developmental Biology · doi:10.1016/0012-1606(75)90330-9 · Cited by 983

A Nonapoptotic Cell Death Process, Entosis, that Occurs by Cell-in-Cell Invasion

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Drosophila Myc Regulates Organ Size by Inducing Cell Competition

de la Cova, C., Abril, M., Bellosta, P., Gallant, P., & Johnston, L. A. (2004) · Cell · doi:10.1016/s0092-8674(04)00214-4 · Cited by 610

Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018.

Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680

Neuronal Cell Death

Fricker, M., Tolkovsky, A. M., Borutaitė, V., Coleman, M. P., & Brown, G. C. (2018) · Physiological Reviews · doi:10.1152/physrev.00011.2017 · Cited by 1,148

Fundamental Mechanisms of Regulated Cell Death and Implications for Heart Disease

Re, D. P. D., Amgalan, D., Linkermann, A., Liu, Q., & Kitsis, R. N. (2019) · Physiological Reviews · doi:10.1152/physrev.00022.2018 · Cited by 994

Diversity and complexity of cell death: a historical review

Park, W., Wei, S., Kim, B., Kim, B., Bae, S., Chae, Y. C., Ryu, D., & Ha, K. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-01078-x · Cited by 381

Cell death mechanisms in eukaryotes

Nirmala, J. G., & Lopus, M. (2019) · Cell Biology and Toxicology · doi:10.1007/s10565-019-09496-2 · Cited by 279

Cancer metabolism in space and time: Beyond the Warburg effect

Danhier, P., Bański, P., Payen, V. L., Grasso, D., Ippolito, L., Sonveaux, P., & Porporato, P. E. (2017) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2017.02.001 · Cited by 230

Multiple cell death modalities and their key features (Review)

Yan, G., Elbadawi, M., & Efferth, T. (2020) · World Academy of Sciences Journal · doi:10.3892/wasj.2020.40 · Cited by 161

Research progress on morphology and mechanism of programmed cell death

Chen, Y., Li, X., Yang, M., & Liu, S. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06712-8 · Cited by 168

Cancer stem cell niche models and contribution by mesenchymal stroma/stem cells

Melzer, C., von der Ohe, J., Lehnert, H., Ungefroren, H., & Hass, R. (2017) · Molecular Cancer · doi:10.1186/s12943-017-0595-x · Cited by 152

Mechanisms of Regulated Cell Death: Current Perspectives

Santagostino, S. F., Assenmacher, C., Tarrant, J. C., Adedeji, A. O., & Radaelli, E. (2021) · Veterinary Pathology · doi:10.1177/03009858211005537 · Cited by 137

Chemotherapy-induced senescent cancer cells engulf other cells to enhance their survival

Tonnessen-Murray, C. A., Frey, W. D., Rao, S. G., Shahbandi, A., Ungerleider, N. A., Olayiwola, J. O., Murray, L. B., Vinson, B. T., Chrisey, D. B., Lord, C. J., et al. (2019) · Journal of Cell Biology · doi:10.1083/jcb.201904051 · Cited by 127

Mitosis can drive cell cannibalism through entosis

Durgan, J., Tseng, Y.-Y., Hamann, J. C., Domart, M.-C., Collinson, L., Hall, A., Overholtzer, M., & Florey, O. (2017) · eLife · doi:10.7554/elife.27134 · Cited by 117

Paraptosis: a unique cell death mode for targeting cancer

Hanson, S., Dharan, A., Jinsha, P. V., Pal, S., Nair, B. G., Kar, R., & Mishra, N. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1159409 · Cited by 124

Genomic instability in mutant p53 cancer cells upon entotic engulfment

Mackay, H. L., Moore, D. A., Hall, C., Birkbak, N. J., Jamal‐Hanjani, M., Karim, S. A., Phatak, V. M., Piñon, L., Morton, J. P., Swanton, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05368-1 · Cited by 110

Preliminary evidence for the presence of multiple forms of cell death in diabetes cardiomyopathy

Wei, J., Zhao, Y., Liang, H., Du, W., & Wang, L. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.08.026 · Cited by 108

Cancer cell cannibalism: Multiple triggers emerge for entosis

Durgan, J., & Florey, O. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2018.03.004 · Cited by 86

Macrophages regulate the clearance of living cells by calreticulin

Krysko, D. V., Ravichandran, K. S., & Vandenabeele, P. (2018) · Nature Communications · doi:10.1038/s41467-018-06807-9 · Cited by 84

Mitosis can drive cell cannibalism through entosis.

Durgan, J., Tseng, Y., Hamann, J. C., Domart, M., Collinson, L., Hall, A., Overholtzer, M., & Florey, O. (2017) · Figshare · doi:10.17863/cam.41122 · Cited by 81

Interrogating the relevance of mitochondrial apoptosis for vertebrate development and postnatal tissue homeostasisPreprint

Tuzlak, S., Kaufmann, T., & Villunger, A. (2016) · Genes & Development · doi:10.1101/gad.289298.116 · Cited by 73

Cell death pathologies: targeting death pathways and the immune system for cancer therapy

Pentimalli, F., Grelli, S., Daniele, N. D., Melino, G., & Amelio, I. (2018) · Genes and Immunity · doi:10.1038/s41435-018-0052-x · Cited by 69

There are only four basic modes of cell death, although there are many ad-hoc variants adapted to different situations

Liu, X., Yang, W., Guan, Z.-Z., Yu, W., Fan, B., Xu, N., & Liao, D. J. (2018) · Cell & Bioscience · doi:10.1186/s13578-018-0206-6 · Cited by 67

Entosis: The emerging face of non-cell-autonomous type IV programmed death

Martins, I., Raza, S. Q., Voisin, L., Dakhli, H., Law, F., de Jong, D., Allouch, A., Thoreau, M., Brenner, C., Deutsch, É., et al. (2017) · Biomedical Journal · doi:10.1016/j.bj.2017.05.001 · Cited by 70

Types of Cell Death from a Molecular Perspective

Hajibabaie, F., Abedpoor, N., & Mohamadynejad, P. (2023) · Biology · doi:10.3390/biology12111426 · Cited by 69

Mesenchymal stem cells generate distinct functional hybrids in vitro via cell fusion or entosis

Sottile, F., Aulicino, F., Theka, I., & Cosma, M. P. (2016) · Scientific Reports · doi:10.1038/srep36863 · Cited by 60

Transient cell-in-cell formation underlies tumor relapse and resistance to immunotherapy

Gutwillig, A., Santana-Magal, N., Farhat-Younis, L., Rasoulouniriana, D., Madi, A., Luxenburg, C., Cohen, J., Padmanabhan, K., Shomron, N., Shapira, G., et al. (2022) · eLife · doi:10.7554/elife.80315 · Cited by 59

The inducible role of autophagy in cell death: emerging evidence and future perspectives

Huang, X., Yan, H., Xu, Z., Yang, B., Luo, P., & He, Q. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02135-w · Cited by 64

Cell-in-cell structures are more potent predictors of outcome than senescence or apoptosis in head and neck squamous cell carcinomas

Schenker, H., Büttner-Herold, M. J., Fietkau, R., & Distel, L. V. (2017) · Radiation Oncology · doi:10.1186/s13014-016-0746-z · Cited by 56

Cell-in-Cell Phenomenon and Its Relationship With Tumor Microenvironment and Tumor Progression: A Review

Wang, X., Li, Y., Li, J., Li, L., Zhu, H., Chen, H., Kong, R., Wang, G., Wang, Y., Hu, J., et al. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00311 · Cited by 57

An emerging role for nanomaterials in increasing immunogenicity of cancer cell death

Mishchenko, T. A., Mitroshina, Е. V., Balalaeva, I. V., Krysko, O., Vedunova, M. V., & Krysko, D. V. (2018) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2018.11.004 · Cited by 53

Cell Fusion-Related Proteins and Signaling Pathways, and Their Roles in the Development and Progression of Cancer

Zhang, H., Ma, H., Yang, X., Fan, L., Tian, S., Niu, R., Yan, M., Zheng, M., & Zhang, S. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.809668 · Cited by 49

Different Ways to Die: Cell Death Pathways and Their Association With Spinal Cord Injury

Guha, L., Singh, N., & Kumar, H. (2023) · Neurospine · doi:10.14245/ns.2244976.488 · Cited by 48

Cell death in animal development

Ghose, P., & Shaham, S. (2020) · Development · doi:10.1242/dev.191882 · Cited by 42

The roles of GTPase-activating proteins in regulated cell death and tumor immunity

He, H., Huang, J., Wu, S., Jiang, S., Liang, L., Liu, Y., Liu, W., Xie, L., Tao, Y., Jiang, Y., et al. (2021) · Journal of Hematology & Oncology · doi:10.1186/s13045-021-01184-1 · Cited by 43

Exploring rare cellular activity in more than one million cells by a transscale scope

Ichimura, T., Kakizuka, T., Horikawa, K., Seiriki, K., Kasai, A., Hashimoto, H., Fujita, K., Watanabe, T. M., & Nagai, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-95930-7 · Cited by 40

Consecutive entosis stages in human substrate-dependent cultured cells

Garanina, A. S., Kisurina-Evgenieva, O. P., Erokhina, M. V., Смирнова, Е. А., Factor, V. M., & Онищенко, Г. Е. (2017) · Scientific Reports · doi:10.1038/s41598-017-12867-6 · Cited by 39

Rho-ROCK signaling mediates entotic cell death in tumor

Zeng, C., Zeng, B., Dong, C., Liu, J., & Xing, F. (2020) · Cell Death Discovery · doi:10.1038/s41420-020-0238-7 · Cited by 38

Comprehensive landscape of cell death mechanisms: from molecular cross-talk to therapeutic innovation in oncology

Ke, Q., Mu, Y., Hu, Y., Li, J., & Liu, J. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1611055 · Cited by 43

Novel Methylselenoesters Induce Programed Cell Death via Entosis in Pancreatic Cancer Cells

Khalkar, P., Díaz-Argelich, N., Palop, J. A., Sanmartín, C., & Fernandes, A. P. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102849 · Cited by 39

CNS-localized myeloid cells capture living invading T cells during neuroinflammation

Wasser, B., Luchtman, D. W., Löffel, J. T., Robohm, K., Birkner, K., Stroh, A., Vogelaar, C. F., Zipp, F., & Bittner, S. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20190812 · Cited by 38

TRAIL signaling promotes entosis in colorectal cancer

Bozkurt, E., Düßmann, H., Salvucci, M., Cavanagh, B., Schaeybroeck, S. V., Longley, D. B., Martin, S. J., & Prehn, J. H. M. (2021) · The Journal of Cell Biology · doi:10.1083/jcb.202010030 · Cited by 38

Regulated cell death in cancer: Mechanisms, crosstalk, and opportunities for therapy

Meng, Y., Chen, Q., Zhou, Z., & Li, M. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.218077 · Cited by 40

Entosis: the core mechanism and crosstalk with other cell death programs

Kim, S.-H., Lee, D., Kim, S. E., & Overholtzer, M. (2024) · Experimental & Molecular Medicine · doi:10.1038/s12276-024-01227-w · Cited by 35

Cell-in-Cell Structures in the Liver: A Tale of Four E’s

Davies, S. P., Terry, L. V., Wilkinson, A. L., & Stamataki, Z. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00650 · Cited by 33

Dynamin-Independent Mechanisms of Endocytosis and Receptor Trafficking

Gundu, C., Arruri, V. K., Yadav, P., Navik, U., Kumar, A., Amalkar, V. S., Vikram, A., & Gaddam, R. R. (2022) · Cells · doi:10.3390/cells11162557 · Cited by 32

Cell-cell fusions and cell-in-cell phenomena in healthy cells and cancer: Lessons from protists and invertebrates

Demin, S. Y., Berdieva, M. A., & Goodkov, A. V. (2021) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2021.03.005 · Cited by 30

Induction of entosis in prostate cancer cells by nintedanib and its therapeutic implications

Liu, J., Wang, L., Zhang, Y., Li, S., Sun, F., Wang, G., Yang, T., Dong, W., Guo, L., & Xiao, H. (2019) · Oncology Letters · doi:10.3892/ol.2019.9951 · Cited by 27

Control of non-apoptotic nurse cell death by engulfment genes in Drosophila

Timmons, A. K., Mondragon, A. A., Meehan, T. L., & McCall, K. (2016) · Fly · doi:10.1080/19336934.2016.1238993 · Cited by 24

Molecular mechanisms of tetrabromobisphenol A (TBBPA) toxicity: Insights from various biological systems

Liao, Y., Wang, Y., Lin, Y., Xiao, Y., Mohan, M., Jaman, R., Dong, H., Zhu, J., Li, X., Zhang, C., et al. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117418 · Cited by 24

LC3-associated phagocytosis of neutrophils triggers tumor ferroptotic cell death in glioblastoma

Lu, T., Yee, P. P., Chih, S. Y., Tang, M., Chen, H., Aregawi, D. G., Glantz, M., Zacharia, B. E., Wang, H., & Li, W. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00130-4 · Cited by 20

Cell death classification: A new insight based on molecular mechanisms

Dehghan, S., Kheshtchin, N., Hassannezhad, S., & Soleimani, M. (2023) · Experimental Cell Research · doi:10.1016/j.yexcr.2023.113860 · Cited by 21

RNA modifications act as regulators of cell death

Xu, L., Zhang, C., Yin, H., Gong, S., Wu, N., Ren, Z., & Zhang, Y. (2021) · RNA Biology · doi:10.1080/15476286.2021.1925460 · Cited by 19

Exploring cell death pathways in oral cancer: mechanisms, therapeutic strategies, and future perspectives

Zhao, C. (2025) · Discover Oncology · doi:10.1007/s12672-025-02022-3 · Cited by 18

The lysophosphatidic acid-regulated signal transduction network in ovarian cancer cells and its role in actomyosin dynamics, cell migration and entosis

Ojasalu, K., Lieber, S., Sokòl, A. M., Nist, A., Stiewe, T., Bullwinkel, I., Finkernagel, F., Reinartz, S., Müller‐Brüsselbach, S., Grosse, R., et al. (2023) · Theranostics · doi:10.7150/thno.81656 · Cited by 17

Role of oxeiptosis in disease mechanisms and therapeutic opportunities

Bhuvaneshwari, K., Harithpriya, K., Ganesan, K., Xu, B., & Ramkumar, K. M. (2025) · APOPTOSIS · doi:10.1007/s10495-025-02087-z · Cited by 16

The implication of ROCK 2 as a potential senotherapeutic target via the suppression of the harmful effects of the SASP: Do senescent cancer cells really engulf the other cells?

Demir, Y. D. Ş., Özdemir, A., Sucularlı, C., Benhür, E., & Ark, M. (2021) · Cellular Signalling · doi:10.1016/j.cellsig.2021.110007 · Cited by 16

Orai1 is an Entotic Ca 2+ Channel for Non‐Apoptotic Cell Death, Entosis in Cancer Development

Lee, A. R., & Park, C. Y. (2023) · Advanced Science · doi:10.1002/advs.202205913 · Cited by 14

Extracellular mycobacterial DNA drives disease progression by triggering Caspase-11-dependent pyroptosis of infected macrophagesPreprint

Varela, M., van der Vaart, M., Groenewoud, A., & Meijer, A. H. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/514125 · Cited by 16

Navigating the complexities of cell death: Insights into accidental and programmed cell death

Lotfi, M.-S., & Rassouli, F. B. (2024) · Tissue and Cell · doi:10.1016/j.tice.2024.102586 · Cited by 15

An entosis-like process induces mitotic disruption in Pals1 microcephaly pathogenesis

Sterling, N. A., Park, J. Y., Park, R., Cho, S., & Kim, S. (2023) · Nature Communications · doi:10.1038/s41467-022-35719-y · Cited by 15

The Emerging Role of Deubiquitinases in Radiosensitivity

Cao, X., Yan, Z., Chen, Z., Ge, Y., Hu, X., Peng, F., Huang, W., Zhang, P., Sun, R., Chen, J., et al. (2023) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2023.12.003 · Cited by 15

Entosis and apical cell extrusion constitute a tumor-suppressive mechanism downstream of Matriptase

Armistead, J., Hatzold, J., van Roye, A., Fahle, E., & Hammerschmidt, M. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201905190 · Cited by 12

Transcriptional Landscape of PARs in Epithelial Malignancies

Nag, J. K., & Bar‐Shavit, R. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19113451 · Cited by 12

Improving tumour budding evaluation in colon cancer by extending the assessment area in colectomy specimens

Martínez‐Ciarpaglini, C., Fernández-Sellers, C., Tarazona, N., Roselló, S., Huerta, M., Roda, D., Mongort, C., Ferrández, A., Navarro, S., & Cervantes, A. M. R. (2019) · Histopathology · doi:10.1111/his.13900 · Cited by 12

Loss of RND3/RHOE controls entosis through LAMP1 expression in hepatocellular carcinoma

Basbous, S., Dif, L., Dantzer, C., Di-Tommaso, S., Dupuy, J., Bioulac‐Sage, P., Raymond, A., Desdouets, C., Saltel, F., & Moreau, V. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06420-3 · Cited by 11

Role of tumor cell senescence in non-professional phagocytosis and cell-in-cell structure formation

Gottwald, D., Putz, F., Hohmann, N., Büttner-Herold, M. J., Hecht, M., Fietkau, R., & Distel, L. V. (2020) · BMC Molecular and Cell Biology · doi:10.1186/s12860-020-00326-6 · Cited by 12

Cigarette smoke and tumor microenvironment copromote aggressiveness of human breast cancer cells

Benoit, L., Tomkiewicz, C., Delit, M., Khider, H., Audouze, K., Kowandy, F., Bortoli, S., Barouki, R., Coumoul, X., & Koual, M. (2023) · Toxicological Sciences · doi:10.1093/toxsci/kfad013 · Cited by 10

Non‐apoptotic regulated cell death mediates reprogramming of the tumour immune microenvironment by macrophages

Sun, C., Zhan, J., Li, Y., Zhou, C., Huang, S., Zhu, X., & Huang, K. (2024) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.18348 · Cited by 9

Comprehensive analysis of regulated cell death pathways: intrinsic disorder, protein–protein interactions, and cross-pathway communication

Sorokin, O., Hause, F., Wedler, A., Alakhras, T., Bauchspiess, T., Dietrich, A., Günther, W. F., Guha, C., Obika, K. B., Kraft, J., et al. (2025) · APOPTOSIS · doi:10.1007/s10495-025-02161-6 · Cited by 14

Rare case of an oligospermic male with 46,XX/46,XY tetragametic chimerism

Magharehabed, M., Almadani, N., Askari, M., Naji, M., Akbari, A., Gourabi, H., Gilani, M. A. S., Reihani-Sabet, F., Masoudi, N., & Totonchi, M. (2019) · Andrologia · doi:10.1111/and.13290 · Cited by 9

Sphingolipid metabolism and regulated cell death in malignant melanoma

Yan, K., Zhang, W., Song, H., & Xu, X. (2024) · APOPTOSIS · doi:10.1007/s10495-024-02002-y · Cited by 8

Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion

Kojima, R., & Fussenegger, M. (2018) · Advanced Science · doi:10.1002/advs.201700971 · Cited by 8

Cell-in-Cell Structures in Gastrointestinal Tumors: Biological Relevance and Clinical Applications

Николаевна, Д. И., Ignatova, N. I., & Shirmanova, M. V. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13071149 · Cited by 7

Neutrophil Engulfment in Cancer: Friend or Foe?

Lu, T., & Li, W. (2025) · Cancers · doi:10.3390/cancers17030384 · Cited by 8

Different types of cell death in vascular diseases

Saberianpour, S., Karimi, A., Modaghegh, M.-H. S., & Ahmadi, M. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06402-0 · Cited by 9

Autophagic cell death in viral infection: Do TAM receptors play a role?

Datan, E., & Salman, S. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.10.001 · Cited by 5

Cell Death: a Molecular Perspective

Zia, Q., Azhar, A., Hassan, N., Jain, P., Singh, M., Mirza, M. A., Ali, A., Parveen, S., Hasan, S., Alothaim, A. S., et al. (2021) · Current Molecular Biology Reports · doi:10.1007/s40610-021-00146-3 · Cited by 6

The role and regulation of cell death in cancer

Quang, M. T., Nguyen, M. N., & Than, V. T. (2025) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2025.06.014 · Cited by 6

Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics

Liu, Y., Chen, Q., Xu, J., & Chi, H. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02298-y · Cited by 4

Loss of Contact Inhibition of Locomotion in the Absence of JAM-A Promotes Entotic Cell Engulfments

Schwietzer, M. F., Thölmann, S., Kummer, D., Kaschler, A., Greune, L., Thüring, E.-M., Schmidt, M. A., Gerke, V., & Ebnet, K. (2022) · iScience · doi:10.1016/j.isci.2022.105144 · Cited by 4

Molecular Perspective on Proteases: Regulation of Programmed Cell Death Signaling, Inflammation and Pathological Outcomes

Ansari, A., Ranjan, K., Kumar, A., & Pathak, C. (2025) · Journal of Molecular Pathology · doi:10.3390/jmp6040032 · Cited by 3

Mechanistic paradigms of cell death - revisited

Rana, S. V. S. (2021) · Journal of Environmental Biology · doi:10.22438/jeb/42/4/mrn-1965 · Cited by 3

Tipos de muerte celular y sus implicaciones clínicas

del Campo, S. L. C. M., González‐Espinosa, C., Ruiz-Quiñonez, A. K., & Carranza‐Aguilar, C. J. (2020) · El Residente · doi:10.35366/95960 · Cited by 7

A reliable elasticity sensing method for analysis of cell entosis using microfluidic cytometer

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Polydopamine Conjugated SiO 2 Nanoparticles As Potential Drug Carriers for Melanoma Treatment

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