Unknown

Dataset Information

0

Lupeol synergizes with 5-fluorouracil to combat c-MET/EphA2 mediated chemoresistance in triple negative breast cancer.


ABSTRACT: Triple-negative breast cancer (TNBC) is the most elusive subtype of breast cancer that encounters treatment dilemmas owing to the paucity of druggable targets. We found hyperactivation of c-MET and ephrin type-A receptor 2 (EphA2) in patients treated with 5FU driven chemotherapy which correlated with lower disease-free survival. However, silencing of both these genes resulted in a marked decrease in the invasive, migratory, and tumorigenic potential of TNBC cells, indicating that a dual target strategy is actionable. Lupeol is a phytochemical, with potent anticancer efficacy and minimal side effects in preclinical studies. A synergistic strategy with 5FU and Lupeol elicited promising anticancer responses in vitro, in vivo, and in patient-derived ex vivo tumor culture models. This synergistic regimen is effective, even in the presence of HGF, which mechanistically orchestrates the activation of c-MET and EphA2. These data lay the foundation for the clinical validation of this combination therapy for TNBC patients.

SUBMITTER: Mitra D 

PROVIDER: S-EPMC10692664 | biostudies-literature | 2023 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications

Lupeol synergizes with 5-fluorouracil to combat c-MET/EphA2 mediated chemoresistance in triple negative breast cancer.

Mitra Debarpan D   Saha Depanwita D   Das Gaurav G   Mukherjee Rimi R   Banerjee Samir S   Alam Neyaz N   Mustafi Saunak Mitra SM   Nath Partha P   Majumder Anuj A   Majumder Biswanath B   Murmu Nabendu N  

iScience 20231104 12


Triple-negative breast cancer (TNBC) is the most elusive subtype of breast cancer that encounters treatment dilemmas owing to the paucity of druggable targets. We found hyperactivation of c-MET and ephrin type-A receptor 2 (EphA2) in patients treated with 5FU driven chemotherapy which correlated with lower disease-free survival. However, silencing of both these genes resulted in a marked decrease in the invasive, migratory, and tumorigenic potential of TNBC cells, indicating that a dual target s  ...[more]

Similar Datasets

| S-EPMC7970221 | biostudies-literature
| S-EPMC8750327 | biostudies-literature
| S-EPMC12023887 | biostudies-literature
| S-EPMC4661576 | biostudies-literature
| S-EPMC9065442 | biostudies-literature
| S-EPMC8405615 | biostudies-literature
| S-EPMC5342523 | biostudies-literature
| S-EPMC4008525 | biostudies-literature
| S-EPMC7731897 | biostudies-literature
| S-EPMC6132060 | biostudies-literature