The activation of beta estrogens has been investigated due to their involvement in the suppression of MPM pathogenesis, leading to potential therapies aimed at activating the estrogen receptor.
The purpose of this project is to find effective treatments for mesothelioma based on the genetic features of the patient’s cancer, avoiding the side effects usually experienced with chemotherapy.
The purpose of this research is to evaluate drug resistance, taking a detailed look at the alterations of the tyrosine-kinase receptors which are often mutated in pleural mesothelioma.
Cancers, including MPM, contain tumor-initiating cells (TIC), which are a subpopulation of tumorigenic cells that are capable of self-renewal and differentiation and are also drug-resistant.