
The study revealed that targeted treatments for acute promyelocytic leukemia, a rare form of blood cancer, cause a cascade of molecular events leading to cellular senescence and recovery. This action model could be activated in other types of cancers.
The PML/RARA protein causes the proliferation of cancer cells in patients affected by acute promyelocytic leukemia. Existing targeted treatments combining a hormone (retinoic acid) and a poison (arsenic) result in permanent recovery for the majority of patients, without having a precise understanding of their action on cancer cells. Previous work by Hugues de Thé’s team has shown that the combination of arsenic and retinoic acid causes destruction of the PML/RARA protein and the elimination of leukemic stem cells. However, the link between these two events had yet to be understood.
The new research contributed the factors needed to understand that recovery. It demonstrated the unexpected involvement of a cascade of events leading to senescence. The aim of the treatment is to reach this final aging stage of the cells in order to render them incapable of multiplying.
During this targeted treatment, the researchers showed that the p53 protein, which determines cell death and survival, triggers senescence through the involvement of PML nuclear bodies. These spherical structures are present in normal cells but are disorganized by PML/RARA in leukemia. The treatment reorganizes them, activating p53 and triggering senescence. In this cascade of events (treatment, PML/RARA degradation, reformation of nuclear bodies, p53 activation), only one link has to be missing to block all the therapeutic effects.
It is this phenomenon that enables the elimination of diseased cells and leads to total recovery of the patient, using only combined retinoic acid/arsenic treatment. The absence of chemotherapy avoids many severe side effects.
This understanding of the cellular and molecular mechanism of recovery from acute promyelocytic leukemia opens prospects for activating this same PML/p53 pathway in other types of cancers.
Date: January 14, 2014
Source: Inserm
Filed Under: Drug Discovery