The DOI matches its Crossref record; 81 of the 81 references it cites were found in a registry or an index.
Drug Insight: cancer therapy strategies based on restoration of endogenous cell death mechanisms
Abstract
Cell death is a normal facet of human physiology, ensuring tissue homeostasis by offsetting cell production with cell demise. Neoplasms arise in part because of defects in physiological cell death mechanisms, contributing to pathological cell expansion. Defects in normal cell death pathways also contribute to cancer progression by permitting progressively aberrant cell behaviors, while also desensitizing tumor cells to immune-mediated attack, radiation, and chemotherapy. Through basic research, much has been learned about the molecular mechanisms responsible for cell turnover and how tumors escape cell death. By exploiting this knowledge base, several innovative strategies for eradicating malignancies have materialized that are based on restoration of natural pathways for cell autodestruction. Some of these strategies have advanced into human clinical trials. Several of the current strategies based on targeting core components of the cell death machinery for cancer therapy are reviewed here, and a summary of progress toward clinical applications is provided.
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
“The first approach is based on the theory that the recognition of pathogen-associated molecular patterns (PAMPs), such as bacterial cell wall components or viral RNA, by immune cells dictates the difference between silent cell death (which occurs in the absence of a pathogen) and immunogenic cell death (which is induced by a pathogen)1.”
From Immunogenic and tolerogenic cell death (2009) · cites this paper as [1]
Citations
Cites
Hanahan, D., & Weinberg, R. A. (2000) · Cell · doi:10.1016/s0092-8674(00)81683-9 · Cited by 29,219
Danial, N. N., & Korsmeyer, S. J. (2004) · Cell · doi:10.1016/s0092-8674(04)00046-7 · Cited by 4,651
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
The Pathophysiology of Mitochondrial Cell Death
Green, D. R., & Kroemer, G. (2004) · Science · doi:10.1126/science.1099320 · Cited by 3,487
Proliferation, cell cycle and apoptosis in cancer
Evan, G. I., & Vousden, K. H. (2001) · Nature · doi:10.1038/35077213 · Cited by 3,417
An inhibitor of Bcl-2 family proteins induces regression of solid tumours
Oltersdorf, T., Elmore, S. W., Shoemaker, A. R., Armstrong, R. C., Augeri, D. J., Belli, B., Bruncko, M., Deckwerth, T. L., Dinges, J., Hajduk, P. J., et al. (2005) · Nature · doi:10.1038/nature03579 · Cited by 3,407
Self-citationMitochondrial control of cell death
Kroemer, G., & Reed, J. C. (2000) · Nature Medicine · doi:10.1038/74994 · Cited by 3,103
Self-citationIAP family proteins---suppressors of apoptosisPreprint
Deveraux, Q. L., & Reed, J. C. (1999) · Genes & Development · doi:10.1101/gad.13.3.239 · Cited by 2,535
Self-citationNF-κB in cancer: from innocent bystander to major culprit
Karin, M., Cao, Y., Greten, F. R., & Li, Z. (2002) · Nature reviews. Cancer · doi:10.1038/nrc780 · Cited by 2,476
Yue, Z., Jin, S., Yang, C., Levine, A. J., & Heintz, N. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2436255100 · Cited by 2,116
Flagged first, then by citations
Research works printed but not linked: 1
- Hyer ML et al.: The FLIP-side of Fas (CD95) signaling. Clin Cancer Res, in press
Cited by
Sorted by citations
Immunogenic and tolerogenic cell death
Green, D. R., Ferguson, T., Zitvogel, L., & Kroemer, G. (2009) · Nature Reviews Immunology · doi:10.1038/nri2545 · Cited by 1,176
Hotchkiss, R. S., Strasser, A., McDunn, J. E., & Swanson, P. E. (2009) · New England Journal of Medicine · doi:10.1056/nejmra0901217 · Cited by 1,207
Bertrand, M. J. M., Milutinovic, S., Dickson, K. M., Ho, W. C., Boudreault, A., Durkin, J. P., Gillard, J. W., Jaquith, J. B., Morris, S. J., & Barker, P. A. (2008) · Molecular Cell · doi:10.1016/j.molcel.2008.05.014 · Cited by 1,134
Essential versus accessory aspects of cell death: recommendations of the NCCD 2015
Galluzzi, L., Bravo-San Pedro, J. M., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Alnemri, E. S., Altucci, L., Andrews, D., Annicchiarico-Petruzzelli, M., et al. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.137 · Cited by 1,002
To kill a tumor cell: the potential of proapoptotic receptor agonists
Ashkenazi, A., & Herbst, R. S. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34359 · Cited by 324
Programmed Cell Death Tunes Tumor Immunity
Liu, J., Hong, M., Li, Y., Chen, D., Wu, Y., & Hu, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.847345 · Cited by 330
Dissecting lipid raft facilitated cell signaling pathways in cancer
Patra, S. K. (2007) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2007.11.002 · Cited by 318
Autophagy as a therapeutic target in cancer
Chen, N., & Karantza, V. (2011) · Cancer Biology & Therapy · doi:10.4161/cbt.11.2.14622 · Cited by 309
miR‐181b modulates multidrug resistance by targeting BCL2 in human cancer cell lines
Zhu, W., Xia, S., Wang, T., Shu, Y., & Liu, P. (2010) · International Journal of Cancer · doi:10.1002/ijc.25260 · Cited by 302
Apoptosis: A review of pro‐apoptotic and anti‐apoptotic pathways and dysregulation in disease
O'Brien, M., & Kirby, R. (2008) · Journal of Veterinary Emergency and Critical Care · doi:10.1111/j.1476-4431.2008.00363.x · Cited by 253
Mitochondrial signaling in cell death via the Bcl-2 family
Leibowitz, B. J., & Yu, J. (2010) · Cancer Biology & Therapy · doi:10.4161/cbt.9.6.11392 · Cited by 250
MicroRNA-181a sensitizes human malignant glioma U87MG cells to radiation by targeting Bcl-2
Hu (2010) · Oncology Reports · doi:10.3892/or_00000725 · Cited by 232
Tagscherer, K. E., Fassl, A., Campos, B., Farhadi, M. R., Kraemer, A., Böck, B. C., Macher‐Goeppinger, S., Radlwimmer, B., Wiestler, O. D., Herold‐Mende, C. C., et al. (2008) · Oncogene · doi:10.1038/onc.2008.259 · Cited by 218
Zhu, W., Xu, H., Zhu, D., Zhi, H., Wang, T., Wang, J., Jiang, B., Shu, Y., & Liu, P. (2011) · Cancer Chemotherapy and Pharmacology · doi:10.1007/s00280-011-1752-3 · Cited by 200
Dying cell clearance and its impact on the outcome of tumor radiotherapy
Lauber, K., Ernst, A., Orth, M., i, M. H., & Belka, C. (2012) · Frontiers in Oncology · doi:10.3389/fonc.2012.00116 · Cited by 200
Necroptotic cell death in anti‐cancer therapy
Krysko, O., Aaes, T. L., Kagan, V. E., D'Herde, K. G. M. A., Bachert, C., Leybaert, L., Vandenabeele, P., & Krysko, D. V. (2017) · Immunological Reviews · doi:10.1111/imr.12583 · Cited by 180
Degradation of Survivin by the X-linked Inhibitor of Apoptosis (XIAP)-XAF1 Complex
Arora, V. A., Cheung, H. H., Plenchette, S., Micali, O. C., Liston, P., & Korneluk, R. G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m700776200 · Cited by 163
TRAIL Agonists on Clinical Trials for Cancer Therapy: The Promises and the Challenges
Bellail, A. C., Qi, L., Mulligan, P., Chhabra, V. S., & Hao, C. (2009) · Reviews on Recent Clinical Trials · doi:10.2174/157488709787047530 · Cited by 158
miR-497 modulates multidrug resistance of human cancer cell lines by targeting BCL2
Zhu, W., Zhu, D., Lu, S., Wang, T., Wang, J., Jiang, B., Shu, Y., & Liu, P. (2012) · Medical Oncology · doi:10.1007/s12032-010-9797-4 · Cited by 189
Harnessing the complexity of DNA-damage response pathways to improve cancer treatment outcomes
Al‐Ejeh, F., Kumar, R., Wiegmans, A. P., Lakhani, S. R., Brown, M. P., & Khanna, K. K. (2010) · Oncogene · doi:10.1038/onc.2010.407 · Cited by 141
Singh, R., & Saini, N. (2012) · Journal of Cell Science · doi:10.1242/jcs.095976 · Cited by 131
Jang, G. Y., Jeon, J. H., Cho, S. Y., Shin, D. M., Kim, C. W., Jeong, E. M., Bae, H.-S., Kim, T. W., Lee, S. H., Choi, Y. H., et al. (2009) · Oncogene · doi:10.1038/onc.2009.342 · Cited by 128
The p53-cathepsin axis cooperates with ROS to activate programmed necrotic death upon DNA damage
Tu, H.-C., Ren, D., Wang, G. X., Chen, D. Y., Westergard, T. D., Kim, H., Sasagawa, S., Hsieh, J. J.-D., & Cheng, E. H. Y. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808173106 · Cited by 126
Xuan, Y., & Hu, X. (2008) · Cancer Letters · doi:10.1016/j.canlet.2008.09.029 · Cited by 120
Chang, K., Tsai, S.-Y., Wu, C.-M., Yen, C.-J., Chuang, B., & Chang, J. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-11-0796 · Cited by 117
Apoptotic pathways as a therapeutic target for colorectal cancer treatment
Abraha, A. M., & Ketema, E. B. (2016) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v8.i8.583 · Cited by 116
Schmitt, E., Paquet, C., Beauchemin, M., & Bertrand, R. (2007) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.2007.b0377 · Cited by 117
MYC-induced myeloid leukemogenesis is accelerated by all six members of the antiapoptotic BCL family
Beverly, L. J., & VARMUS, H. E. (2009) · Oncogene · doi:10.1038/onc.2008.466 · Cited by 112
Cai, S. X., Drewe, J. A., & Kemnitzer, W. E. (2009) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520610909040437 · Cited by 105
Patra, S. K., Rizzi, F., Silva, A., Rugină, D. O., & Bettuzzi, S. (2008) · PubMed · Cited by 103
Esser, A. T., Smith, K. C., Gowrishankar, T. R., & Weaver, J. C. (2007) · Technology in Cancer Research & Treatment · doi:10.1177/153303460700600402 · Cited by 101
Resveratrol sensitizes melanomas to TRAIL through modulation of antiapoptotic gene expression
Ivanov, V. N., Partridge, M. A., Johnson, G. E., Huang, S. X. L., Zhou, H., & Hei, T. K. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.12.012 · Cited by 100
Transcriptional regulation of cellular senescence
Lanigan, F., Geraghty, J. G., & Bracken, A. P. (2011) · Oncogene · doi:10.1038/onc.2011.34 · Cited by 95
Recent Insights into the Biological Action of Heavy-Ion Radiation
Hamada, N. (2009) · Journal of Radiation Research · doi:10.1269/jrr.08070 · Cited by 94
Immunogenic and Non-immunogenic Cell Death in the Tumor Microenvironment
Pitt, J. M., Kroemer, G., & Zitvogel, L. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-67577-0_5 · Cited by 98
Cerella, C., Teiten, M.-H., Radogna, F., Dicato, M. A., & Diederich, M. F. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2014.03.006 · Cited by 95
Big wheel keeps on turning: apoptosome regulation and its role in chemoresistance
Fadeel, B., Ottosson, A., & Pervaiz, S. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402265 · Cited by 95
Huang, S., & Sinicrope, F. A. (2010) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-09-1004 · Cited by 93
Krajewska, M., Smith, L. H., Rong, J., Huang, X., Hyer, M. L., Zeps, N., Iacopetta, B. J., Linke, S. P., Olson, A. H., Reed, J. C., et al. (2009) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2009.952812 · Cited by 89
Self-citationNecroptosis in tumorigenesis, activation of anti-tumor immunity, and cancer therapy
Meng, M.-B., Wang, H.-H., Cui, Y.-L., Wu, Z.-Q., Shi, Y., Zaorsky, N. G., Deng, L., Yuan, Z., Lü, Y., & Wang, P. (2016) · Oncotarget · doi:10.18632/oncotarget.10548 · Cited by 91
BH3 Mimetic Obatoclax Enhances TRAIL-Mediated Apoptosis in Human Pancreatic Cancer Cells
Huang, S., Okumura, K., & Sinicrope, F. A. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-1575 · Cited by 86
Apoptosis and cancer stem cells: Implications for apoptosis targeted therapy
Kruyt, F. A. E., & Schuringa, J. J. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.04.010 · Cited by 88
miR-503 regulates the resistance of non-small cell lung cancer cells to cisplatin by targeting Bcl-2
Qiu, T., Zhou, L. Q., Wang, T., Xu, J., Wang, J., Chen, W., Xin Min, Z. H. O. U., Huang, Z., Zhu, W., Shu, Y., et al. (2013) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2013.1439 · Cited by 85
Kemnitzer, W. E., Kuemmerle, J., Jiang, S., Zhang, H., Sirisoma, N. S., Kasibhatla, S., Crogan‐Grundy, C., Tseng, B., Drewe, J. A., & Cai, S. X. (2008) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2008.09.110 · Cited by 83
Matsuzuka, T., Rachakatla, R. S., Doi, C., Maurya, D. K., Ohta, N., Kawabata, A., Pyle, M. M., Pickel, L., Reischman, J., Marini, F. C., et al. (2010) · Lung Cancer · doi:10.1016/j.lungcan.2010.01.003 · Cited by 83
Kemnitzer, W. E., Jiang, S., Zhang, H., Kasibhatla, S., Crogan‐Grundy, C., Blais, C., Attardo, G., Denis, R. C., Lamothe, S., Gourdeau, H., et al. (2008) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2008.09.011 · Cited by 78
Mawji, I. A., Simpson, C. D., Gronda, M., Williams, M. A., Hurren, R., Henderson, C. J., Datti, A., Wrana, J. L., & Schimmer, A. D. (2007) · Cancer Research · doi:10.1158/0008-5472.can-07-1687 · Cited by 78
Beverly, L. J., Lockwood, W. W., Shah, P. P., Erdjument‐Bromage, H., & VARMUS, H. E. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119167109 · Cited by 73
Anticancer drugs affect the alternative splicing of Bcl-x and other human apoptotic genes
Shkreta, L., Froehlich, U., Paquet, É. R., Toutant, J., Elela, S. A., & Chabot, B. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-08-0192 · Cited by 69
Chen, Y., Guo, H., Du, Z., Liu, X., Che, Y., & Ye, X. (2009) · Cell Proliferation · doi:10.1111/j.1365-2184.2009.00636.x · Cited by 66
Apoptosis and Compensatory Proliferation Signaling Are Coupled by CrkI-Containing Microvesicles
Gupta, K. H., Goldufsky, J. W., Wood, S. J., Tardi, N. J., Moorthy, G. S., Gilbert, D. Z., Zayas, J. P., Hahm, E., Altintas, M. M., Reiser, J., et al. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.05.014 · Cited by 62
Pickel, L., Matsuzuka, T., Doi, C., Ayuzawa, R., Maurya, D. K., Xie, S., Berkland, C. J., & Tamura, M. (2010) · Cancer Biology & Therapy · doi:10.4161/cbt.9.4.10643 · Cited by 59
The Multifaceted Roles of the BCL-2 Family Member BOK
Naim, S., & Kaufmann, T. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.574338 · Cited by 57
Llobet‐Navàs, D., Eritja, N., Yeramian, A., Pallares, J., Sorolla, A., Domingo, M., Santacana, M., Gonzalez-Tallada, F. J., Matías‐Guiu, X., & Dolcet, X. (2010) · European Journal of Cancer · doi:10.1016/j.ejca.2009.12.025 · Cited by 55
Cell death pathology: Perspective for human diseases
Agostini, M., Tucci, P., & Melino, G. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.09.081 · Cited by 55
Ingemarsdotter, C. K., Baird, S. K., Connell, C. M., Öberg, D., Halldén, G., & McNeish, I. A. (2010) · Oncogene · doi:10.1038/onc.2010.335 · Cited by 56
Sánchez‐Pérez, T., Ortiz-Ferrón, G., & López‐Rivas, A. (2009) · Cell Death and Differentiation · doi:10.1038/cdd.2009.176 · Cited by 53
Beverly, L. J., Howell, L. A., Hernandez‐Corbacho, M. J., Casson, L. K., Chipuk, J. E., & Siskind, L. J. (2013) · Biochemical Journal · doi:10.1042/bj20130147 · Cited by 52
Yang, C., Davis, J. L., Zeng, R., Vora, P., Su, X., Collins, L. I., Vangveravong, S., Mach, R. H., Piwnica-Worms, D., Weilbaecher, K. N., et al. (2013) · Cancer Discovery · doi:10.1158/2159-8290.cd-12-0271 · Cited by 50
TAK1 kinase determines TRAIL sensitivity by modulating reactive oxygen species and cIAP
Morioka, S., Omori, E., Kajino, T., Kajino‐Sakamoto, R., Matsumoto, K., & Ninomiya‐Tsuji, J. (2009) · Oncogene · doi:10.1038/onc.2009.110 · Cited by 49
Thompson, S. M., Callstrom, M. R., Butters, K. A., Knudsen, B. E., Grande, J. P., Roberts, L. R., & Woodrum, D. A. (2014) · Lasers in Surgery and Medicine · doi:10.1002/lsm.22231 · Cited by 48
Karasic, T. B., Hei, T. K., & Ivanov, V. N. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.04.014 · Cited by 47
Genomics and Cancer Drug Resistance
Rodrigues, A. S., Dinis, J., Gromicho, M., Martins, C., Laires, A., & Rueff, J. (2012) · Current Pharmaceutical Biotechnology · doi:10.2174/138920112799857549 · Cited by 47
Antigen cross-presentation: extending recent laboratory findings to therapeutic intervention
Flinsenberg, T. W. H., Compeer, E. B., Boelens, J. J., & Boes, M. L. (2011) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2011.04411.x · Cited by 43
Karaca, B., Atmaca, H., Bozkurt, E., Kısım, A., Uzunoğlu, S., Karabulut, B., Sezgin, C., Şanlı, U. A., & Uslu, R. (2012) · Molecular Biology Reports · doi:10.1007/s11033-012-2469-z · Cited by 42
Dong, H. P., Kleinberg, L., Silins, I., Flørenes, V. A., Trope, C. G., Risberg, B. Å., Nesland, J. M., & Davidson, B. (2007) · Cancer · doi:10.1002/cncr.23140 · Cited by 42
Kemnitzer, W. E., Kuemmerle, J., Jiang, S., Sirisoma, N. S., Kasibhatla, S., Crogan‐Grundy, C., Tseng, B., Drewe, J. A., & Cai, S. X. (2009) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2009.05.012 · Cited by 41
Wang, D., Zhu, H., Zhu, Y., Liu, Y., Shen, H., Yin, R.-G., Zhang, Z., & Su, Z. (2012) · Acta Histochemica · doi:10.1016/j.acthis.2012.09.007 · Cited by 40
RetractedApoptosis regulators as targets for cancer therapy
Fernández-Luna, J. L. (2007) · Clinical & Translational Oncology · doi:10.1007/s12094-007-0103-7 · Cited by 40
Nuclear Survivin Abrogates Multiple Cell Cycle Checkpoints and Enhances Viral Oncolysis
Connell, C. M., Wheatley, S. P., & McNeish, I. A. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-0817 · Cited by 40
P2X 7 -mediated chemoprevention of epithelial cancers
Gorodeski, G. I. (2009) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728220903277249 · Cited by 38
Cell Death and Deubiquitinases: Perspectives in Cancer
Bhattacharya, S., & Ghosh, M. K. (2014) · BioMed Research International · doi:10.1155/2014/435197 · Cited by 38
Energetic heavy ions overcome tumor radioresistance caused by overexpression of Bcl-2
Hamada, N., Hara, T., Omura‐Minamisawa, M., Funayama, T., Sakashita, T., Sora, S., Yokota, Y., Nakano, T., & Kobayashi, Y. (2008) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2008.02.013 · Cited by 36
Al‐Ejeh, F., Darby, J. M., Pensa, K., Diener, K. R., Hayball, J. D., & Brown, M. P. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-0964 · Cited by 36
Ortiz-Ferrón, G., Yerbes, R., Eramo, A., López-Pérez, A. I., Maria, R. D., & López‐Rivas, A. (2008) · Cell Research · doi:10.1038/cr.2008.54 · Cited by 35
Hsieh, S., Hsu, C., He, J., Liu, C.-L., Lo, S., Chen, Y.-C., & Huang, H. (2009) · Journal of Proteome Research · doi:10.1021/pr900289g · Cited by 35
Hiss, D. C., & Gabriels, G. A. (2009) · Expert Opinion on Drug Discovery · doi:10.1517/17460440903052559 · Cited by 35
Ivanov, V. N., & Hei, T. K. (2011) · APOPTOSIS · doi:10.1007/s10495-011-0649-2 · Cited by 34
Konduri, S. D., Ticku, J., Bobustuc, G. C., Sutphin, R. M., Colon, J. F., Isley, B. A., Bhakat, K. K., Kalkunte, S. S., & Baker, C. H. (2009) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-0887 · Cited by 34
Chemotherapy Synergizes with Radioimmunotherapy Targeting La Autoantigen in Tumors
Al‐Ejeh, F., Darby, J. M., & Brown, M. P. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004630 · Cited by 33
Clearance of primary necrotic cells by non‐professional phagocytes
Schwegler, M., Wirsing, A. M., Dollinger, A. J., Abendroth, B., Putz, F., Fietkau, R., & Distel, L. V. (2015) · Biology of the Cell · doi:10.1111/boc.201400090 · Cited by 31
Micro-Economics of Apoptosis in Cancer: ncRNAs Modulation of BCL-2 Family Members
Villanova, L., Careccia, S., Maria, R. D., & Fiori, M. E. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19040958 · Cited by 31
The Bcl-w promoter is activated by β-catenin/TCF4 in human colorectal carcinoma cells
Lapham, A. S., Adams, J. E., Paterson, A. R., Lee, M., Brimmell, M., & Packham, G. (2008) · Gene · doi:10.1016/j.gene.2008.12.002 · Cited by 30
Huang, X., Huang, W., Li, L., Sun, X., Song, S., Xu, Q., Zhang, L., Wei, B., & Deng, X. (2016) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.6b00564 · Cited by 30
Cutting-Edge Apoptosis-Based Therapeutics
Fischer, U., Janssen, K., & Schulze‐Osthoff, K. (2007) · BioDrugs · doi:10.2165/00063030-200721050-00001 · Cited by 29
Schepetkin, I. A., Kirpotina, L. N., Tian, J., Khlebnikov, А. I., Ye, R. D., & Quinn, M. T. (2008) · Molecular Pharmacology · doi:10.1124/mol.108.046946 · Cited by 28
Perraud, A. (2011) · Oncology Reports · doi:10.3892/or.2011.1404 · Cited by 28
Inhibition of SREBP1 sensitizes cells to death ligands
Eberhard, Y., Gronda, M., Hurren, R., Datti, A., MacLean, N., Ketela, T., Moffat, J., Wrana, J. L., & Schimmer, A. D. (2011) · Oncotarget · doi:10.18632/oncotarget.239 · Cited by 28
Golla, K., Reddy, P. S., Bhaskar, C., & Kondapi, A. K. (2013) · Drug Delivery · doi:10.3109/10717544.2013.801051 · Cited by 28
Targeting regulated cell death pathways in cancers for effective treatment: a comprehensive review
Saxena, R., Welsh, C. M., & He, Y.-W. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2024.1462339 · Cited by 29
Shen, C., Chan, T., Chen, C.-C., Hsu, Y., Long, C., & Lai, C. (2016) · Oncotarget · doi:10.18632/oncotarget.8997 · Cited by 27
Chen, C., Hu, S., Luo, D., Zhu, S., & Zhou, C. (2013) · Oncology Reports · doi:10.3892/or.2013.2618 · Cited by 25
Verma, V. K., Singh, V., Singh, M. P., & Singh, S. M. (2009) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923970802562042 · Cited by 25
Ding, Z., Liu, Y., Li, Y., Wang, D., Zhang, J., Cui, G., Yang, X., Huang, X., Liu, F., & Shen, A. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1041688 · Cited by 24
Inhibition of novel protein kinase Cɛ augments TRAIL-induced cell death in A549 lung cancer cells
Felber, M., Sonnemann, J., & Beck, J. F. (2007) · Pathology & Oncology Research · doi:10.1007/bf02940308 · Cited by 24
Immunogenic Cell Death Role in Urothelial Cancer Therapy
Yadollahvandmiandoab, R., Jalalizadeh, M., Buosi, K., García‐Perdomo, H. A., & Reis, L. O. (2022) · Current Oncology · doi:10.3390/curroncol29090526 · Cited by 23
CD95 signaling in colorectal cancer
Hoogwater, F. J. H., Steller, E. J. A., Westendorp, B. F., Rinkes, I. H. M. B., & Kranenburg, O. (2012) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2012.03.007 · Cited by 23
Kemnitzer, W. E., Sirisoma, N. S., Jiang, S., Kasibhatla, S., Crogan‐Grundy, C., Tseng, B., Drewe, J. A., & Cai, S. X. (2009) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2009.11.025 · Cited by 23
Promising Role of Melatonin as Neuroprotectant in Neurodegenerative Pathology
Joshi, N., Biswas, J., Nath, C., & Singh, S. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8865-8 · Cited by 22
New determinates of disease progression and outcome in metastatic ovarian carcinoma.
Davidson, B., Reich, R., Trope, C. G., Wang, T., & Shih, I. (2010) · PubMed · doi:10.14670/hh-25.1591 · Cited by 22
Metadata
- Authors
- Reed, J. C.
- Affiliations
- Sanford Burnham Prebys Medical Discovery Institute (US)
- Corresponding author
- Reed, John C
- ORCID
- Reed, John C
- Venue
- Nature Clinical Practice Oncology
- Published
- 2006-07
- Volume
- 3
- Issue
- 7
- Pages
- 388-398
- ISSN
- 1743-4254 (ISSN-L)
- 1743-4262
- OpenAlex
- W2125192217
- Cited by
- 179
- References
- 81
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 4 · 2023: 3 · 2022: 2 · 2020: 5 · 2018: 2 · 2017: 7 · 2016: 5 · 2015: 14 · 2014: 7 · 2013: 9 · 2012: 11
- FWCI
- 1.97
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Clinical Practice Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- cancer therapy, cell death pathways, apoptosis, epigenetic regulators, gene therapy, tumor immune evasion, tumor progression, clinical trials, cell turnover
- MeSH terms
- Antineoplastic Agents, Clinical Trials as Topic, Humans, Mitochondria, Neoplasms, Signal Transduction, Cell Death, Apoptosis, Apoptosis Regulatory Proteins, Inhibitor of Apoptosis Proteins, TNF-Related Apoptosis-Inducing Ligand
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