Researchers describe a mechanism that hinders cancer cells proliferation and induces their death

Vall d’Hebron and UAB researchers studied the antitumoral action of protein kinase ERK5 inhibitor drugs, and found out they accelerate toxic autophagy.

21/12/2021

The synthesis of cellular proteins takes place at the endoplasmic reticulum. In response to different factors, such as lack of nutrients or of oxygen, endoplasmic reticulum become stressed, a process that can compromise the survival of cells. To deal with this, a process called UPR (Unfolded Protein Response) is started, to restore protein production and cellular normality. Among other strategies, UPR initiates autophagy, a biological process that allows cells to degrade and recycle defective components. However, if stress is extreme or prolonged, UPR is not enough to restore protein production, and UPR leads to a cytotoxic autophagy that activates apoptosis (cellular suicide).

UPR occurs in all the body cells, but has special relevance in tumor cells, which present high levels of endoplasmic reticulum stress. UPR and autophagy allow tumor cells to better adapt to the environment and to avoid the immune system. Consequently, tumor cells are very sensitive to reach a level of autophagy that results toxic for the cell. Hence, autophagy modulation is a new therapeutic strategy to treat cancer: drugs that induce high levels of autophagy can cause the collapse of tumor cells, as well as the activation of the apoptotic cell death program.

MAP kinase ERK5 protein controls the proliferation and survival of tumor cells, being a new therapeutic target for cancer treatment. ERK5 inhibitors have shown efficacy in different cell and tumor models, both as monotherapy and in combination with chemotherapy. However, the mechanism by which these inhibitors induce tumor cell death was unknown.

A research team from the Vall d’Hebron Research and the Universitat Autònoma de Barcelona (UAB), led by José Miguel Lizcano -affiliated with both institutions-, has uncover the mechanism by which ERK5 inhibitors cause cancer cell death. Using human tumor cell cultures of pancreatic, endometrial and cervical cancer, researchers found that ERK5 regulates tumor autophagy. Thus, ERK5 inhibitors activate endoplasmic reticulum stress and UPR (which is already elevated in tumor cells) to levels that exceed their protective effect, activating a toxic form of autophagy that finally results in apoptotic death of tumor cells (a process called cytotoxic autophagy).

"ERK5 inhibitors sensitize tumor cells to chemotherapy", explains José Miguel Lizcano, "for which our research opens a very promising line for the improvement of chemotherapy as well as for more effective strategies to tackle cancer".

The research has been recently published in Frontiers in Cell and Developmental Biology, and it was performed by Andrés Gámez-García, Idoia Bolinaga-Ayala, Guillermo Yoldi, Sergio Espinosa Gil, Nora Diéguez Martínez, Elisabet Megías-Rueda, Pau Muñoz and Jose Miguel Lizcano, members of the Protein Kinases in Cancer research group, from Vall d’Hebron Research, UAB Department of Biochemistry and Molecular Biology and UAB Institut de Neurociències de la UAB (INc-UAB).

 

Paper:

Andrés Gámez-García et al. ERK5 Inhibition Induces Autophagy-Mediated Cancer Cell Death by Activating ER Stress, Front. Cell Dev. Biol., 04 November 2021 | https://doi.org/10.3389/fcell.2021.742049

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