Cancer cells often develop defense mechanisms which enable them to survive chemotherapy. A group of researchers from the Institutes of Pharmacology and Pathology in Bern present new solutions for preventing the development of such resistances.
Cells can break down damaged molecules as well as whole areas of the cells themselves by means of self-digestion and utilize the decomposition products resulting from this process for the production of energy and new molecules or cell parts. This process of self-digestion is called autophagy and can be considered a renovation of the cell. The generation of energy by means of autophagy plays a special role for the cells if they do not have enough nutrients, oxygen or growth factors.
However, autophagy can also be used by tumour cells in order to survive stress situations such as chemotherapy - they digest the destroyed cell parts and regenerate themselves. This makes them resistant to the therapy. Now, a group of scientists from the University of Bern under the direction of Hans-Uwe Simon from the Institute of Pharmacology has discovered that the autophagy of tumour cells can be influenced with pharmacological means. The findings reveal new therapy approaches for the treatment of cancer. The study is published today in Nature Communications.
Preventing the reanimation of tumour cells
The researchers studied the importance of autophagy for tumour cells. Often, chemotherapy alone is not able to destroy all of the tumour cells. While some of the tumour cells survive the therapy by means of autophagy, others go through a so-called «mitotic catastrophe», a state in which they are no longer able to divide. If these damaged cells do not die, they can cause cancer again.
Now, however, the group of scientists gathered by Hans-Uwe Simon has found a way to prevent the survival of cancer cells after chemotherapy. They discovered a connection between autophagy and mitotic catastrophe: when the self-digestion of cancer cells was suppressed by means of pharmaceuticals, the mitotic catastrophe directly resulted in cell death. This way, the survival mechanisms of cancer cells were eliminated.
With this method, the effectiveness of the usual chemotherapy can be significantly improved: "We hope that, based on these findings, we will be able to develop new therapies which will prevent the chemoresistance of established tumours", said Hans-Uwe Simon, the head of the study.
- Dipak Maskey, Shida Yousefi, Inès Schmid, Inti Zlobec, Aurel Perren, Robert Friis, Hans-Uwe Simon. ATG5 is induced by DNA-damaging agents and promotes mitotic catastrophe independent of autophagy. Nature Communications, 2013; 4 DOI: 10.1038/ncomms3130
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