The importance of bystander effects in radiation therapy in melanoma skin-cancer cells and umbilical-cord stromal stem cells

被引:36
作者
Gomez-Millan, Jaime [2 ]
Santos Katz, Iana Suly [3 ]
de Araujo Farias, Virginea
Linares-Fernandez, Jose-Luis
Lopez-Penalver, Jesus
Ortiz-Ferron, Gustavo
Ruiz-Ruiz, Carmen
Javier Oliver, Francisco [5 ]
Mariano Ruiz de Almodovar, Jose [1 ,4 ]
机构
[1] Univ Granada, Ctr Invest Biomed, IBIMER, Inst Biopatol & Med Regenerativa, Granada 18100, Spain
[2] Hosp Univ Virgen de la Victoria, Unidad Gest Clin Oncol, Malaga, Spain
[3] Ctr Pesquisa & Formacao Imunol, Inst Butantan, Sao Paulo, Brazil
[4] Hosp Univ San Cecilio, Granada, Spain
[5] Inst Parasitol & Biomed Lopez Neyra, Granada, Spain
关键词
Melanoma cancer cells; Umbilical-cord stromal stem cells; Radiosensitivity; Radiation-induced bystander cell-death; Fractionation in the bystander effect; INDUCED DNA-DAMAGE; BREAST-CANCER; HUMAN FIBROBLASTS; EPITHELIAL-CELLS; DOSE-RESPONSE; NORMAL TISSUE; RADIOTHERAPY; APOPTOSIS; PATHWAYS; TRAIL;
D O I
10.1016/j.radonc.2011.11.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: To examine direct and bystander radiation-induced effects in normal umbilical-cord stromal stem cell (HCSSC) lines and in human cancer cells. Materials and methods: The UCSSC lines used in this study were obtained in our laboratory. Two cell lines (UCSSC 35 and UCSSC 37) and two human melanoma skin-cancer cells (A375 and G361) were exposed to ionizing radiation to measure acute radiation-dosage cell-survival curves and radiation-induced bystander cell-death response. Results: Normal cells, although extremely sensitive to ionizing radiation, were resistant to the bystander effect whilst tumor cells were sensitive to irradiated cell-conditioned media, showing a dose-response relationship that became saturated at relatively low doses. We applied a biophysical model to describe bystander cell-death through the binding of a ligand to the cells. This model allowed us to calculate the maximum cell death (chi(max)) produced by the bystander effect together with its association constant (K-By) in terms of dose equivalence (Gy). The values obtained for K-By in A375 and G361 cells were 0.23 and 0.29 Gy, respectively. Conclusion: Our findings help to understand how anticancer therapy could have an additional decisive effect in that the response of sub-lethally hit tumor cells to damage might be required for therapy to be successful because the survival of cells communicating with irradiated cells is reduced. (c) 2011 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 102 (2012) 450-458
引用
收藏
页码:450 / 458
页数:9
相关论文
共 63 条
[1]
Toll-like receptor 4-dependent contribution of the immune system to anticancer chemotherapy and radiotherapy [J].
Apetoh, Lionel ;
Ghiringhelli, Francois ;
Tesniere, Antoine ;
Obeid, Michel ;
Ortiz, Carla ;
Criollo, Alfredo ;
Mignot, Gregoire ;
Maiuri, M. Chiara ;
Ullrich, Evelyn ;
Saulnier, Patrick ;
Yang, Huan ;
Amigorena, Sebastian ;
Ryffel, Bernard ;
Barrat, Franck J. ;
Saftig, Paul ;
Levi, Francis ;
Lidereau, Rosette ;
Nogues, Catherine ;
Mira, Jean-Paul ;
Chompret, Agnes ;
Joulin, Virginie ;
Clavel-Chapelon, Francoise ;
Bourhis, Jean ;
Andre, Fabrice ;
Delaloge, Suzette ;
Tursz, Thomas ;
Kroemer, Guido ;
Zitvogel, Laurence .
NATURE MEDICINE, 2007, 13 (09) :1050-1059
[2]
Apoptosis control by death and decoy receptors [J].
Ashkenazi, A ;
Dixit, VM .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :255-260
[3]
Non-targeted effects as a paradigm breaking evidence [J].
Averbeck, Dietrich .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2010, 687 (1-2) :7-12
[4]
Oxidative metabolism, gap junctions and the ionizing radiation-induced bystander effect [J].
Azzam, EI ;
de Toledo, SM ;
Little, JB .
ONCOGENE, 2003, 22 (45) :7050-7057
[5]
Barcellos-Hoff MH, 2001, RADIAT RES, V156, P618, DOI 10.1667/0033-7587(2001)156[0618:ESTTMA]2.0.CO
[6]
2
[7]
A proliferation-dependent bystander effect in primary porcine and human urothelial explants in response to targeted irradiation [J].
Belyakov, OV ;
Folkard, M ;
Mothersill, C ;
Prise, KM ;
Michael, BD .
BRITISH JOURNAL OF CANCER, 2003, 88 (05) :767-774
[8]
ATR-dependent radiation-induced γH2AX foci in bystander primary human astrocytes and glioma cells [J].
Burdak-Rothkamm, S. ;
Short, S. C. ;
Folkard, M. ;
Rothkamm, K. ;
Prise, K. M. .
ONCOGENE, 2007, 26 (07) :993-1002
[9]
ATM acts downstream of ATR in the DNA damage response signaling of bystander cells [J].
Burdak-Rothkamm, Susanne ;
Rothkamm, Kai ;
Prise, Kevin M. .
CANCER RESEARCH, 2008, 68 (17) :7059-7065
[10]
DNA damaging bystander signalling from stem cells, cancer cells and fibroblasts after Cr(VI) exposure and its dependence on telomerase [J].
Cogan, Nicola ;
Baird, Duncan M. ;
Phillips, Ryan ;
Crompton, Lucy A. ;
Caldwell, Maeve A. ;
Rubio, Miguel A. ;
Newson, Roger ;
Lyng, Fiona ;
Case, C. Patrick .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2010, 683 (1-2) :1-8