Involvement of both caspase-dependent and -independent pathways in apoptotic induction by hexaminolevulinate-mediated photodynamic therapy in human lymphoma cells
Abstract
Photodynamic therapy (PDT) is a cancer treatment based on the interaction of a photosensitizer, light and oxygen. PDT with the endogenous photosensitizer, protoporphyrin IX (PpIX) induced by 5-aminolevulinic acid (ALA) or its derivatives is a modification of this treatment modality with successful application in dermatology. However, the mechanism of cell destruction by ALA-PDT has not been elucidated. In this study a human T-cell lymphoma Jurkat cell line was treated with PDT using hexaminolevulinate (HAL, hexylester of ALA). Four hours following treatment nearly 80% of the cells exhibited typical apoptotic features. Mitochondrial pro-apoptotic proteins were evaluated by Western blots in subcellular fractionated samples. PDT caused cytosolic translocation of cytochrome c and nuclear redistribution of apoptosis-inducing factor (AIF), but the release of mitochondrial Smac/DIABLO, Omi/HtrA2 and EndoG was not observed. The release of cytochrome c was followed by the cleavage of caspase-9 and caspase-3 as well as its downstream substrates, together with oligonucleosomal DNA fragmentation. The pan-caspases inhibitor, z-VAD.fmk, prevented oligonucleosomal DNA fragmentation, but failed to inhibit PDT-mediated apoptosis. The apoptotic induction by AIF-mediated caspase-independent pathway was also found after HAL-PDT with large-scale DNA fragmentation in the presence of z-VAD.fmk. These results demonstrate that cytochrome c-mediated caspase-dependent pathway and AIF-induced caspase-independent pathway are simultaneously involved in the apoptotic induction by PDT. When the cytochrome c-induced caspase-dependent pathway is blocked, the cells go into apoptosis via AIF-mediated pathway, clearly demonstrating that the cytochrome c-mediated caspase-dependent pathway is not required for such apoptotic induction. This finding may have an impact on improved PDT effectiveness.
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PDT with hexaminolevulinate induces apoptosis via both caspase-dependent and caspase-independent pathways.
“Indeed, PDT with hexaminolevulinate has been shown to induce apoptosis via both caspase-dependent and -independent pathways [29].”
From 5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy (2023) · cites this paper as [29]
Blocking caspase-9 or -3 does not prevent PDT-induced apoptosis, suggesting involvement of cell death signaling other than the mitochondria-mediated pathway.
“Furthermore, blocking the activity of caspase-9 or -3 does not prevent PDT-induced apoptosis, suggesting the involvement of cell death signaling other than the mitochondria-mediated pathway.”
From 5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy (2023) · cites this paper as [29]
Cites
Li, P., Nijhawan, D., Budihardjo, I., Srinivasula, S. M., Ahmad, M., Alnemri, E. S., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80434-1 · Cited by 7,289 · see citing works
Dougherty, T. J., Gomer, C. J., Henderson, B. W., Jori, G., Kessel, D., Korbelik, M., Moan, J., & Peng, Q. (1998) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/90.12.889 · Cited by 4,716 · see citing works
Self-citationGomer, C. J. (1988) · Cited by 4,169 · see citing works
Molecular characterization of mitochondrial apoptosis-inducing factor
Susin, S. A., Lorenzo, H. K., Zamzami, N., Marzo, I., Snow, B. E., Brothers, G. M., Mangion, J., Jacotot, E., Costantini, P., Loeffler, M., et al. (1999) · Nature · doi:10.1038/17135 · Cited by 4,060 · see citing works
Identification and inhibition of the ICE/CED-3 protease necessary for mammalian apoptosis
Nicholson, D. W., Ali, A., Thornberry, N. A., Vaillancourt, J. P., Ding, C. K., Gallant, M., Gareau, Y., Griffin, P. R., Labelle, M., Lazebnik, Y. A., et al. (1995) · Nature · doi:10.1038/376037a0 · Cited by 3,980 · see citing works
The Pathophysiology of Mitochondrial Cell Death
Green, D. R., & Kroemer, G. (2004) · Science · doi:10.1126/science.1099320 · Cited by 3,416 · see citing works
A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD
Enari, M., Sakahira, H., Yokoyama, H., Okawa, K., Iwamatsu, A., & Nagata, S. (1998) · Nature · doi:10.1038/34112 · Cited by 3,181 · see citing works
Programmed Cell Death in Animal Development
Jacobson, M. D., Weil, M., & RAFF, M. C. (1997) · Cell · doi:10.1016/s0092-8674(00)81873-5 · Cited by 2,685 · see citing works
Verhagen, A. M., Ekert, P. G., Pakusch, M., Silke, J., Connolly, L. M., Reid, G. E., Moritz, R. L., Simpson, R. J., & Vaux, D. L. (2000) · Cell · doi:10.1016/s0092-8674(00)00009-x · Cited by 2,372 · see citing works
Liu, X., Zou, H., Slaughter, C. A., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80197-x · Cited by 1,835 · see citing works
Endonuclease G is an apoptotic DNase when released from mitochondria
Li, L. Y., Luo, X., & Wang, X. (2001) · Nature · doi:10.1038/35083620 · Cited by 1,787 · see citing works
Four deaths and a funeral: from caspases to alternative mechanisms
Leist, M., & Jäättelä, M. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35085008 · Cited by 1,585 · see citing works
Breaking the mitochondrial barrier
Martinou, J., & Green, D. R. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35048069 · Cited by 951 · see citing works
Hegde, R. P., Srinivasula, S. M., Zhang, Z., Wassell, R. P., Mukattash, R., Cilenti, L., DuBois, G. C., Lazebnik, Y. A., Zervos, A. S., Fernandes‐Alnemri, T., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109721200 · Cited by 745 · see citing works
Two Distinct Pathways Leading to Nuclear Apoptosis
Susín, S. A., Daugas, É., Ravagnan, L., Samejima, K., Zamzami, N., Loeffler, M. W., Costantini, P., Ferri, K. F., Irinopoulou, T., Prévost, M., et al. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.4.571 · Cited by 736 · see citing works
5-Aminolevulinic Acid-Based Photodynamic Therapy: Principles and Experimental Research
Peng, Q., Berg, K., Moan, J., Kongshaug, M., & Nesland, J. M. (1997) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1997.tb08549.x · Cited by 615 · see citing works
Self-citationThe Photobiology of Photodynamic Therapy: Cellular Targets and Mechanisms
Oleinick, N. L., & Evans, H. H. (1998) · Radiation Research · doi:10.2307/3579816 · Cited by 571 · see citing works
Verhagen, A. M., Silke, J., Ekert, P. G., Pakusch, M., Kaufmann, H., Connolly, L. M., Day, C. L., Tikoo, A., Burke, R., Wrobel, C. N., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m109891200 · Cited by 558 · see citing works
Liu, X., Li, P., Widłak, P., Zou, H., Luo, X., Garrard, W. T., & Wang, X. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8461 · Cited by 529 · see citing works
Arnoult, D., Gaume, B. R., Karbowski, M., Sharpe, J. C., Cecconi, F., & Youle, R. J. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg423 · Cited by 451 · see citing works
Mitochondrial photodamage and PDT-induced apoptosis
Kessel, D. H., & Luo, Y. (1998) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/s1011-1344(97)00127-9 · Cited by 316 · see citing works
Porphyrins are endogenous ligands for the mitochondrial (peripheral-type) benzodiazepine receptor.
Verma, A. M., Nye, J. S., & Snyder, S. H. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.8.2256 · Cited by 301 · see citing works
Use of 5-aminolevulinic acid esters to improve photodynamic therapy on cells in culture.
Gaullier, J., Berg, K., Peng, Q., Anholt, H., Selbo, P. K., Ma, L. W., & Moan, J. E. (1997) · PubMed · Cited by 257 · see citing works
Self-citationA mechanistic study of cellular photodestruction with 5-aminolaevulinic acid-induced porphyrin
Iinuma, S., Farshi, S., Ortel, B., & Hasan, T. (1994) · British Journal of Cancer · doi:10.1038/bjc.1994.244 · Cited by 240 · see citing works
Mitochondria and the Bcl-2 family proteins in apoptosis signaling pathways
Antonsson, B. E. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009865.70898.36 · Cited by 232 · see citing works
Phospholipase activation triggers apoptosis in photosensitized mouse lymphoma cells.
Agarwal, M. L., Larkin, H. E., Zaidi, S. I. A., Mukhtar, H., & Oleinick, N. L. (1993) · PubMed · Cited by 177 · see citing works
Apoptosis and necrosis induced with light and 5-aminolaevulinic acid-derived protoporphyrin IX
Noodt, B., Berg, K., Stokke, T., Peng, Q., & Nesland, J. (1996) · British Journal of Cancer · doi:10.1038/bjc.1996.310 · Cited by 174 · see citing works
Self-citationSnyder, S. H., Verma, A. M., & Trifiletti, R. R. (1987) · The FASEB Journal · doi:10.1096/fasebj.1.4.2820823 · Cited by 158 · see citing works
Pastorino, J. G., Simbula, G., Gilfor, E., Hoek, J. B., & Farber, J. L. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47387-5 · Cited by 132 · see citing works
Molecular, cellular, and tissue responses following photodynamic therapy
Gomer, C. J., Ferrario, A., Hayashi, N., Rucker, N., Szirth, B. C., & Murphree, A. L. (1988) · Lasers in Surgery and Medicine · doi:10.1002/lsm.1900080503 · Cited by 128 · see citing works
Stoica, B. A., Movsesyan, V. A., Knoblach, S. M., & Faden, A. I. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.02.009 · Cited by 98 · see citing works
Furre, I. E., Shahzidi, S., Lukšiené, Ž., Møller, M. T. N., Borgen, E., Morgan, J., Tkacz-Stachowska, K., Nesland, J. M., & Peng, Q. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-0510 · Cited by 84 · see citing works
Self-citationThe Role of the Mitochondrial Apoptosis Induced Channel MAC in Cytochrome c Release
Martinez‐Caballero, S., Dejean, L. M., Jonas, E. A., & Kinnally, K. W. (2005) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-005-6570-z · Cited by 64 · see citing works
Editorial: Photodynamic Therapy and Detection
Peng, Q. (2006) · Journal of Environmental Pathology Toxicology and Oncology · doi:10.1615/jenvironpatholtoxicoloncol.v25.i1-2.10 · Cited by 22 · see citing works
Self-citation- Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Molecular effectors of multiple cell death pathways initiated by photodynamic therapy
Buytaert, E., Dewaele, M., & Agostinis, P. (2007) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2007.07.001 · Cited by 749 · see citing works
New Insights into the Mechanisms for Photodynamic Therapy-Induced Cancer Cell Death
Yoo, J., & Ha, K. (2012) · International review of cytology · doi:10.1016/b978-0-12-394306-4.00010-1 · Cited by 174 · see citing works
Current Challenges and Opportunities of Photodynamic Therapy against Cancer
Huis in ‘t Veld, R. V., Heuts, J., Ma, S., Cruz, L. J., Ossendorp, F. A., & Jager, M. J. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15020330 · Cited by 159 · see citing works
Hypericin phototoxicity induces different modes of cell death in melanoma and human skin cells
Davids, L. M., Kleemann, B., Kacerovská, D., Pizinger, K., & Kidson, S. H. (2008) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2008.01.011 · Cited by 113 · see citing works
Molecular mechanisms of photodynamic therapy
Ortel, B. J. (2009) · Frontiers in bioscience · doi:10.2741/3520 · Cited by 102 · see citing works
Anand, S., Wilson, C., Hasan, T. G., & Maytin, E. V. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-0805 · Cited by 95 · see citing works
Pro-Inflammatory CXCR3 Impairs Mitochondrial Function in Experimental Non-Alcoholic Steatohepatitis
Du, J., Zhang, X., Han, J., Man, K., Zhang, Y., Chu, E. S., Nan, Y., & Yu, J. Q. (2017) · Theranostics · doi:10.7150/thno.21400 · Cited by 92 · see citing works
Photodynamic therapy regulates fate of cancer stem cells through reactive oxygen species
Zhang, Z., Wang, K., Mo, J., Xiong, L., & Wen, Y. (2020) · World Journal of Stem Cells · doi:10.4252/wjsc.v12.i7.562 · Cited by 78 · see citing works
pH-Responsive Aerobic Nanoparticles for Effective Photodynamic Therapy
Shen, L., Huang, Y., Chen, D., Qiu, F., Ma, C., Jin, X., Zhu, X., Zhou, G., & Zhang, Z. (2017) · Theranostics · doi:10.7150/thno.19546 · Cited by 78 · see citing works
Berkman (2010) · International Journal of Oncology · doi:10.3892/ijo_00000553 · Cited by 65 · see citing works
Meng, Z., Yu, B., Han, G., Liu, M., Shan, B., Dong, G., Miao, Z., Jia, N., Tan, Z., Li, B., et al. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b00352 · Cited by 59 · see citing works
Vittar, N. B. R., Awruch, J., Azizuddin, K., & Rivarola, V. A. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2010.03.019 · Cited by 57 · see citing works
Fukuhara, H., Inoue, K., Kurabayashi, A., Furihata, M., Fujita, H., Utsumi, K., Sasaki, J., & Shuin, T. (2013) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2013.03.003 · Cited by 57 · see citing works
Cell Metabolism - Cell Homeostasis and Stress Response
Bubulya, P. A. (2012) · InTech eBooks · doi:10.5772/1081 · Cited by 56 · see citing works
Yoo, J., Lim, Y., Kim, Y., & Ha, K. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.326074 · Cited by 54 · see citing works
Piplartine induces caspase-mediated apoptosis in PC-3 human prostate cancer cells
Ahn (1994) · Oncology Reports · doi:10.3892/or_00000075 · Cited by 48 · see citing works
Chen, M.-F., Huang, S.-T. J., Huang, C., Liu, P., Lin, K., Liu, C.-W., Hsieh, W., Shiu, L., & Chen, C. (2016) · BMC Cancer · doi:10.1186/s12885-016-2599-0 · Cited by 48 · see citing works
Hefti, M., Albert, I., & Luginbuehl, V. (2012) · Journal of Neuro-Oncology · doi:10.1007/s11060-012-0857-9 · Cited by 42 · see citing works
Saikosaponin a Induces Apoptosis through Mitochondria-Dependent Pathway in Hepatic Stellate Cells
Chen, C., Chen, M., Huang, S.-T. J., Huang, C., Wang, H., Hsieh, W., Huang, C., Liu, L., & Shiu, L. (2017) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x17500227 · Cited by 39 · see citing works
5-Aminolevulinic Acid as a Theranostic Agent for Tumor Fluorescence Imaging and Photodynamic Therapy
Howley, R., Chandratre, S., & Chen, B. (2023) · Bioengineering · doi:10.3390/bioengineering10040496 · Cited by 33 · see citing works
Neurogenesis in an Adult Avian Song Nucleus Is Reduced by Decreasing Caspase-Mediated Apoptosis
Thompson, C. K., & Brenowitz, E. A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5423-08.2009 · Cited by 32 · see citing works
Yang, K., Niu, T., Luo, M., Tang, L., & Kang, L. (2018) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2018.10.012 · Cited by 29 · see citing works
Shahzidi, S., Brech, A., Sioud, M., Li, X., Suo, Z., Nesland, J. M., & Peng, Q. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.07.026 · Cited by 28 · see citing works
Self-citationYiang, G., CHEN, Y.-H., Chou, P.-L., CHANG, W.-J., Wei, C.-W., & Yu, Y. (2013) · Molecular Medicine Reports · doi:10.3892/mmr.2013.1261 · Cited by 26 · see citing works
Zhang, J., Deng, L., Yao, J., Gu, P., Yang, F., Wang, X., Liu, W. Y., Zhang, Y., Xing-fa, K., Jing, X., et al. (2011) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2011.07.041 · Cited by 23 · see citing works
Sačková, V., Kuliková, L., Kello, M., Uhrinová, I., & Fedoročko, P. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms12128388 · Cited by 23 · see citing works
Einbond, L. S., Wu, H., Sandu, C., Ford, M., Mighty, J., Antonetti, V., Redenti, S., & Ma, H. (2015) · Fitoterapia · doi:10.1016/j.fitote.2015.12.005 · Cited by 23 · see citing works
Doustvandi, M. A., Mohammadnejad, F., Mansoori, B., Mohammadi, A., Navaeipour, F., Baradaran, B., & Tajalli, H. (2017) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2017.09.020 · Cited by 22 · see citing works
Intérêt et place de la thérapie photodynamique en gynécologie
Ascencio, M., Collinet, P., Cosson, M., Vinatier, D., & Mordon, S. R. (2007) · Gynécologie Obstétrique & Fertilité · doi:10.1016/j.gyobfe.2007.07.035 · Cited by 22 · see citing works
Cekaite, L., Peng, Q., Reiner, A. H., Shahzidi, S., Tveito, S., Furre, I. E., & Hovig, E. J. (2007) · BMC Genomics · doi:10.1186/1471-2164-8-273 · Cited by 21 · see citing works
Self-citationWu, J., Salva, K. A., & Wood, G. S. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.364 · Cited by 21 · see citing works
Yamamoto, M., Fujita, H., Katase, N., Inoue, K., Nagatsuka, H., Utsumi, K., Sasaki, J., & Ohuchi, H. (2013) · PubMed · doi:10.18926/amo/50408 · Cited by 21 · see citing works
Cai, H., Gu, Y., Sun, Q., Zeng, J., Dong, N., & Zhao, G. F. (2011) · Photodermatology Photoimmunology & Photomedicine · doi:10.1111/j.1600-0781.2011.00577.x · Cited by 20 · see citing works
Baglo, Y., de Sousa, M. M. L., Slupphaug, G., Hagen, L., Håvåg, S., Helander, L., Zub, K. A., Krokan, H. E., & Gederaas, O. A. (2011) · Photochemical & Photobiological Sciences · doi:10.1039/c0pp00369g · Cited by 19 · see citing works
An Update on Recent Advances of Photodynamic Therapy for Primary Cutaneous Lymphomas
Liu, W.-T., Wang, H., Yeh, Y.-H., & Wong, T. (2023) · Pharmaceutics · doi:10.3390/pharmaceutics15051328 · Cited by 17 · see citing works
Salva, K. A., & Wood, G. S. (2015) · Photochemistry and Photobiology · doi:10.1111/php.12521 · Cited by 16 · see citing works
Evaluation of ALA-PDT of ovarian cancer in the Fisher 344 rat tumor model
Ascencio, M., Delemer-Lefebvre, M., Farine, M. O., Jouve, E., Collinet, P., & Mordon, S. R. (2007) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2007.07.003 · Cited by 16 · see citing works
Salva, K. A., Kim, Y. H., Rahbar, Z., & Wood, G. S. (2018) · Photochemistry and Photobiology · doi:10.1111/php.12925 · Cited by 14 · see citing works
Čunderlı́ková, B., Vasovič, V., Randeberg, L. L., Christensen, E., Warloe, T., Nesland, J. M., & Peng, Q. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.05.020 · Cited by 14 · see citing works
Self-citationBottone, M. G., Soldani, C., Fraschini, A., Croce, A. C., Bottiroli, G. F., Camboni, T., Scovassi, A. I., & Pellicciari, C. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0538-0 · Cited by 11 · see citing works
Čunderlı́ková, B., Klučková, K., Babál, P., Mlkvý, P., & Teplický, T. (2024) · International Journal of Radiation Biology · doi:10.1080/09553002.2024.2310002 · Cited by 9 · see citing works
Chen, Y., Guo, P., Chen, L., & He, D. (2024) · Frontiers in Medicine · doi:10.3389/fmed.2024.1370396 · Cited by 10 · see citing works
Apoptotic activity of a new jasmonate analogue is associated with its induction of DNA damage
Kim (2010) · Oncology Reports · doi:10.3892/or_00000920 · Cited by 9 · see citing works
Krieg, R. C., Herr, A., Raupach, K., Ren, Q., Schwamborn, K., & Knuechel, R. (2007) · Photochemical & Photobiological Sciences · doi:10.1039/b704464j · Cited by 8 · see citing works
Hexaminolevulinate-mediated photodynamic purging of leukemia cells from BM
Čunderlı́ková, B., Vasovič, V., Sieber, F., Furre, T., Nesland, J. M., & Peng, Q. (2010) · Bone Marrow Transplantation · doi:10.1038/bmt.2009.382 · Cited by 7 · see citing works
Self-citationEspeland, K., Kleinauskas, A., Juzenas, P., Brech, A., Darvekar, S. R., Vasovič, V., Warloe, T., Christensen, E., Jahnsen, J., & Peng, Q. (2022) · Biomedicines · doi:10.3390/biomedicines10020232 · Cited by 7 · see citing works
Self-citationKulbacka, J., Choromańska, A., Drąg‐Zalesińska, M., Nowak, P., Baczyńska, D., Kotulska, M., Bednarz-Misa, I. S., Saczko, J., & Chwiłkowska, A. (2020) · Photodiagnosis and Photodynamic Therapy · doi:10.1016/j.pdpdt.2020.101775 · Cited by 6 · see citing works
Hsieh, Y., Ky, C., Lin, S.-Y., Sabu, S., Rm, H., Chi, L., Pc, L., & Yu, J. (2012) · Cell Death and Disease · doi:10.1038/cddis.2012.85 · Cited by 5 · see citing works
Cho, H.-J. (2009) · Journal of Life Science · doi:10.5352/jls.2009.19.1.009 · Cited by 5 · see citing works
Wu, S., Wang, L., Ren, X., Pan, Y., Peng, Y., Zou, X., Shi, C., & Zhang, Y. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6151 · Cited by 5 · see citing works
Does N-Acetyl Cysteine Protect Against Apoptosis in HL60 Cell Line?
Aksoy, Y., Kesik, K., & Canpınar, H. (2010) · doi:10.5072/zenodo.36398 · Cited by 3 · see citing works
Study and Application of Chou-Talalay Method for Anti-tumor Drug Combination
Shiqun, W. (2013) · The Chinese Journal of Modern Applied Pharmacy · Cited by 3 · see citing works
Gheewala, T., Hussein, M. A., & Munirathinam, G. (2023) · Journal of Pharmacy and Pharmacology · doi:10.1093/jpp/rgad083 · Cited by 2 · see citing works
Photodynamic Therapy to Eradicate Tumor Cells
Cludia, A., Ribeiro, A. P. D., Nordi, L., de Andrade, C. R., Costa, C. A. D. S., & Eduardo, C. (2012) · InTech eBooks · doi:10.5772/27408 · Cited by 2 · see citing works
Viard, M., Garg, H., Blumenthal, R., & Raviv, Y. (2009) · BMC Cell Biology · doi:10.1186/1471-2121-10-21 · Cited by 2 · see citing works
Sioud, S. S. M. (2015) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.1000212 · Cited by 1 · see citing works
Shahzidi, S. (2014) · Journal of Carcinogenesis & Mutagenesis · doi:10.4172/2157-2518.s10-008 · Cited by 1 · see citing works
Self-citationApoptotic induction by photodynamic therapy using hexaminolevulinate with a literature review
Furre, I. E., Nesland, J. M., & Peng, Q. (2009) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.823956 · Cited by 1 · see citing works
Self-citationLáser y terapia fotodinámica en el tratamiento del acné
Morales, I. (2009) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Biochemical mechanisms involved in cisplatin-induced apoptosis in malignant mesothelioma cells
Cregan, I. L. (2008) · UWA Profiles and Research Repository (UWA)
Photodynamic Therapy-Induced Oxidative Stress for Cancer Treatment
Chilakamarthi, U., Singu, P. S., & Giribabu, L. (2022) · Handbook of Oxidative Stress in Cancer: Therapeutic Aspects · doi:10.1007/978-981-16-1247-3_58-1
Photodynamic Therapy-Induced Oxidative Stress for Cancer Treatment
Chilakamarthi, U., Singu, P. S., & Giribabu, L. (2022) · Handbook of Oxidative Stress in Cancer: Therapeutic Aspects · doi:10.1007/978-981-16-5422-0_58
Mechanisms and pharmacological modulation of photodynamic therapy-induced cell death
de Klerk, D. J., Tian, J., Liu, G., Korbelik, M., Kessel, D., Chovanec, M., Khaled, Y. S., van Eijck, C. H. J., Wu, L., & Heger, M. (2026) · Pharmacological Reviews · doi:10.1016/j.pharmr.2026.100166
- Authors
- Furre, I. E., Møller, M. T. N., Shahzidi, S., Nesland, J. M., & Peng, Q.
- Affiliations
- Oslo University Hospital (NO)
- Corresponding author
- Peng, Qian
- Venue
- Apoptosis
- Published
- 2006-10-10
- Volume
- 11
- Issue
- 11
- Pages
- 2031-2042
- ISSN
- 1360-8185 (ISSN-L)
- 1573-675X
- OpenAlex
- W2037314345
- Cited by
- 66
- References
- 35
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 4 · 2022: 3 · 2020: 2 · 2018: 2 · 2017: 5 · 2016: 2 · 2015: 4 · 2014: 3 · 2013: 6 · 2012: 6
- FWCI
- 4.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- APOPTOSIS (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Photodynamic Therapy Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Physical Sciences › Engineering › Biomedical Engineering › Nanoplatforms for cancer theranostics
- Keywords
- photodynamic therapy, hexaminolevulinate, caspase-dependent pathway, apoptosis-inducing factor, cytochrome c release, caspase-9, caspase-3, T-cell lymphoma, Jurkat cells, 5-aminolevulinic acid, mitochondrial proteins, DNA fragmentation
- MeSH terms
- Amino Acid Chloromethyl Ketones, Aminolevulinic Acid, Enzyme Inhibitors, Humans, Mitochondria, Photochemotherapy, Protoporphyrins, Leukemia, T-Cell, Apoptosis, Jurkat Cells, Caspases, Cytochromes c, Apoptosis Inducing Factor, Membrane Potential, Mitochondrial
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 ›
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