PURPOSE: To examine the potential radiosensitising properties of trabectedin (ET-743, Yondelis). METHODS AND MATERIALS: In vitro chemosensitivity was assessed in four tumour cell lines (DU145, HeLa, HT29, HOP62) by the crystal violet method. IC10s and IC50s were established for 1-h, 24-h and 7-day (continuous) exposure times. Radiosensitisation was evaluated by conventional colony assay. BrdUrd DNA-labelling and flow cytometry were used to analyse cell cycle kinetics. The rate of apoptotic induction was assed by annexyn-V labelling. RESULTS: Mean IC50s were 18.8 nM (10.5 - 30), 2.5 nM (1.5 - 5) and 0.25 nM (0.2-0.8) for 1 h, 24 h and continuous exposure times, respectively. HT29 and HOP62 were the most sensitive cells lines to trabectedin. Radiosensitisation was observed in DU145 and HeLa cells with a dose enhancement factor (DEF) of 1.92 and 1.77 at IC50 dose level, respectively. Trabectedin induced early S phase arrest in all cell lines studied. CONCLUSIONS: Trabectedin, at pharmacologically appropriated concentrations, harbours a significant in vitro radiosensitising effect and induces cell cycle changes and apoptosis in several human cancer cell lines. Further studies to define the clinical potential of the combination of trabectedin and radiotherapy are needed.
PURPOSE: To examine the potential radiosensitising properties of trabectedin (ET-743, Yondelis). METHODS AND MATERIALS: In vitro chemosensitivity was assessed in four tumour cell lines (DU145, HeLa, HT29, HOP62) by the crystal violet method. IC10s and IC50s were established for 1-h, 24-h and 7-day (continuous) exposure times. Radiosensitisation was evaluated by conventional colony assay. BrdUrd DNA-labelling and flow cytometry were used to analyse cell cycle kinetics. The rate of apoptotic induction was assed by annexyn-V labelling. RESULTS: Mean IC50s were 18.8 nM (10.5 - 30), 2.5 nM (1.5 - 5) and 0.25 nM (0.2-0.8) for 1 h, 24 h and continuous exposure times, respectively. HT29 and HOP62 were the most sensitive cells lines to trabectedin. Radiosensitisation was observed in DU145 and HeLa cells with a dose enhancement factor (DEF) of 1.92 and 1.77 at IC50 dose level, respectively. Trabectedin induced early S phase arrest in all cell lines studied. CONCLUSIONS: Trabectedin, at pharmacologically appropriated concentrations, harbours a significant in vitro radiosensitising effect and induces cell cycle changes and apoptosis in several humancancer cell lines. Further studies to define the clinical potential of the combination of trabectedin and radiotherapy are needed.
Authors: Alessandro Gronchi; Nadia Hindi; Josefina Cruz; Jean-Yves Blay; Antonio Lopez-Pousa; Antoine Italiano; Rosa Alvarez; Antonio Gutierrez; Inmaculada Rincón; Claudia Sangalli; Jose Luis Pérez Aguiar; Jesús Romero; Carlo Morosi; Marie Pierre Sunyach; Roberta Sanfilippo; Cleofe Romagosa; Dominique Ranchere-Vince; Angelo P Dei Tos; Paolo G Casali; Javier Martin-Broto Journal: EClinicalMedicine Date: 2019-03-11
Authors: Nadia Hindi; Irene Carrasco García; Alberto Sánchez-Camacho; Antonio Gutierrez; Javier Peinado; Inmaculada Rincón; Johanna Benedetti; Pilar Sancho; Paloma Santos; Paloma Sánchez-Bustos; David Marcilla; Victor Encinas; Sara Chacon; Cristobal Muñoz-Casares; David Moura; Javier Martin-Broto Journal: Cancers (Basel) Date: 2020-12-12 Impact factor: 6.639
Authors: David S Moura; Maria Peña-Chilet; Juan Antonio Cordero Varela; Ramiro Alvarez-Alegret; Carolina Agra-Pujol; Francisco Izquierdo; Rafael Ramos; Luis Ortega-Medina; Francisco Martin-Davila; Carolina Castilla-Ramirez; Carmen Nieves Hernandez-Leon; Cleofe Romagosa; Maria Angeles Vaz Salgado; Javier Lavernia; Silvia Bagué; Empar Mayodormo-Aranda; Luis Vicioso; Jose Emilio Hernández Barceló; Jordi Rubio-Casadevall; Ana de Juan; Maria Concepcion Fiaño-Valverde; Nadia Hindi; Maria Lopez-Alvarez; Serena Lacerenza; Joaquin Dopazo; Antonio Gutierrez; Rosa Alvarez; Claudia Valverde; Javier Martinez-Trufero; Javier Martín-Broto Journal: Mol Oncol Date: 2021-06-30 Impact factor: 6.603