Role of ferroptosis in the development of cancer

Role of ferroptosis in the development of cancer

Cell death is an essential biological process that plays an active role both in human embryonic development and in the onset of various diseases. Every day, about 100 billion cells die in the human body. Cell death is controlled at the molecular, genetic and biochemical levels. Normally, dead cells are absorbed by cells of the human immune system without over-activating the immune system.

However, the development of many diseases is associated with an imbalance between the death of cells and their survival. Excessively massive or intensive one-time cell death in the body or high sensitivity of cells to death can cause inflammation and lead to the development of various neurodegenerative diseases. It is important to note that the development of resistance to cell death is directly related to the development of cancer and the subsequent ineffectiveness of anticancer therapy.

Modern antitumor therapy aims to trigger cell death in cancer cells, which, when dying, will activate the immune system. Over the past decades, scientists all over the world have been actively studying the molecular mechanisms of cell death and the interaction of cancer cells with the human immune system.

Ferroptosis is one of 12 types of regulated cell death, which was discovered only in 2012. Ferroptosis is different from other types of regulated cell death, such as apoptosis and necroptosis, and is triggered by the failure of the antioxidant defense mechanisms of cells, which leads to uncontrolled peroxidation of cell membrane lipids and to the death of cancer cells. Cancer cells that die by ferroptosis emit signals through which they interact with the cells of the body's immune system, which results in either the suppression of the immune response and the progression of the tumor or in the stimulation of an antitumor immune response. This indicates the immunogenic nature of cell death and leads to the involvement of the immune system in the fight against the tumor.

The authors present some arguments that emphasize the ambiguous role of ferroptosis in the treatment of cancer. Further research directions are defined in this article that will help to answer the question: "Is ferroptosis an immunogenic or immunosuppressive form of cell death?"

Another important aspect is also demonstrated by the authors. It is related to the fact that during anticancer therapy tumor cells often acquire resistance to apoptosis, a type of cell death that is most often triggered by modern methods of chemotherapy and radiotherapy. This leads to a decrease in the effectiveness of treatment and the progression of cancer. In this case, it is important to use new methods of treatment aimed at launching alternative types of regulated cell death.

Thus, the launch of ferroptosis may help to overcome the resistance to cell death and increase the effectiveness of anti-tumor therapy. At this stage, it is too early to speak about the commercialization of these research results, since more fundamental research is required, including studies on mouse models. It is necessary to test and study in detail the feasibility of launching ferroptosis to enable the introduction of this method into clinical practice in the future.

Scientific experiments are conducted both in vitro and in vivo in mouse models. These studies are based on synergistic interaction and vast experience accumulated over many years by research teams on immunogenic cell death (led by Professor Dmitri Krysko) and on photodynamic therapy in neuro-oncology (led by Dr. Maria Vedunova).