Eine Plattform für die Wissenschaft: Bauingenieurwesen, Architektur und Urbanistik
Eine Plattform für die Wissenschaft: Bauingenieurwesen, Architektur und Urbanistik
Effects and mechanisms of betulinic acid on improving EGFR TKI‐resistance of lung cancer cells
Epidermal growth factor receptor (EGFR) mutations have been identified in approximately 55% of lung cancer patients in Taiwan. Gefitinib (Iressa) and Erlotinib (Tarceva) are the first‐generation targeting drugs to patients with EGFR gene mutants a work by inhibiting tyrosine kinase activity. However, resistance in EGFR‐mutated patients to first‐generation tyrosine kinase inhibitor (TKI) therapy after 8‐11 months of treatment has occurred. Betulinic acid (BetA) is a pentacyclic triterpenoid natural product derived from widespread plants. BetA has been reported to have a cytotoxic effect in several cancers. The purpose of this study is to investigate the effects and mechanisms of BetA on dampening EGFR TKI‐resistance of lung cancer cells. Our study has demonstrated by MTT assay that combining BetA and an EGFR TKI increased the cytotoxicity against EGFR TKI‐resistance lung cancer cells. Based on flow cytometry, combination treatments of BetA with an EGFR TKI enhanced Sub‐G1 accumulation, induced apoptosis and induced mitochondrial membrane potential loss. Using western blotting, BetA and EGFR TKI combined treatments inhibited cell cycle related protein and triggered apoptosis‐ and autophagy‐ related protein expression. Taken together, our data suggests that a target therapy combining BetA with an EGFR TKI improves drug efficacy in EGFR TKI‐resistant lung cancer cells.
Effects and mechanisms of betulinic acid on improving EGFR TKI‐resistance of lung cancer cells
Epidermal growth factor receptor (EGFR) mutations have been identified in approximately 55% of lung cancer patients in Taiwan. Gefitinib (Iressa) and Erlotinib (Tarceva) are the first‐generation targeting drugs to patients with EGFR gene mutants a work by inhibiting tyrosine kinase activity. However, resistance in EGFR‐mutated patients to first‐generation tyrosine kinase inhibitor (TKI) therapy after 8‐11 months of treatment has occurred. Betulinic acid (BetA) is a pentacyclic triterpenoid natural product derived from widespread plants. BetA has been reported to have a cytotoxic effect in several cancers. The purpose of this study is to investigate the effects and mechanisms of BetA on dampening EGFR TKI‐resistance of lung cancer cells. Our study has demonstrated by MTT assay that combining BetA and an EGFR TKI increased the cytotoxicity against EGFR TKI‐resistance lung cancer cells. Based on flow cytometry, combination treatments of BetA with an EGFR TKI enhanced Sub‐G1 accumulation, induced apoptosis and induced mitochondrial membrane potential loss. Using western blotting, BetA and EGFR TKI combined treatments inhibited cell cycle related protein and triggered apoptosis‐ and autophagy‐ related protein expression. Taken together, our data suggests that a target therapy combining BetA with an EGFR TKI improves drug efficacy in EGFR TKI‐resistant lung cancer cells.
Effects and mechanisms of betulinic acid on improving EGFR TKI‐resistance of lung cancer cells
Ko, Jiunn‐Liang (Autor:in) / Lin, Ching‐Hsiung (Autor:in) / Chen, Heng‐Chung (Autor:in) / Hung, Wei‐Heng (Autor:in) / Chien, Peng‐Ju (Autor:in) / Chang, Hui‐Yi (Autor:in) / Wang, Bing‐Yen (Autor:in)
Environmental Toxicology ; 33 ; 1153-1159
01.11.2018
7 pages
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
Cellular Origins of EGFR‐Driven Lung Cancer Cells Determine Sensitivity to Therapy
| Wiley | 2021
| British Library Online Contents | 2019
| British Library Online Contents | 2014
Antitumor drug effect of betulinic acid mediated by polyethylene glycol modified liposomes
| British Library Online Contents | 2016
Antitumor drug effect of betulinic acid mediated by polyethylene glycol modified liposomes
| British Library Online Contents | 2016