Roles of Apoptosis and Cellular Senescence in Cancer and Aging

Title:Roles of Apoptosis and Cellular Senescence in Cancer and Aging

Volume: 17 Issue: 4

Author(s): Claudia Cerella, Cindy Grandjenette, Mario Dicato and Marc Diederich

Affiliation:

Keywords: Aging, apoptosis, cancer, cellular senescence, stress, therapy.

Abstract: Cancer and aging are two similar processes representing the final outcome of timedependent accumulation of various irreversible dysfunctions, mainly caused by stress-induced DNA and cellular damages. Apoptosis and senescence are two types of cellular response to damages that are altered in both cancer and aging, albeit through different mechanisms. Carcinogenesis is associated with a progressive reduction in the ability of the cells to trigger apoptosis and senescence. In contrast, in aging tissues, there is an increased accumulation of senescent cells, and the nature of apoptosis deregulation varies depending on the tissue. Thus, the prevailing model suggests that apoptosis and cellular senescence function as two essential tumor-suppressor mechanisms, ensuring the health of the individual during early and reproductive stages of life, but become detrimental and promote aging later in life. The recent discovery that various anticancer agents, including canonical inducers of apoptosis, act also as inducers of cellular senescence indicates that pro-senescence strategies may have applications in cancer prevention therapy. Therefore, dissection of the mechanisms mediating the delicate balance between apoptosis and cellular senescence will be beneficial in the therapeutic exploitation of both processes in the development of future anticancer and anti-aging strategies, including minimizing the side effects of such strategies. Here, we provide an overview of the roles of apoptosis and cellular senescence in cancer and aging.

Cite this article as:

Cerella Claudia, Grandjenette Cindy, Dicato Mario and Diederich Marc, Roles of Apoptosis and Cellular Senescence in Cancer and Aging, Current Drug Targets 2016; 17 (4) . https://dx.doi.org/10.2174/1389450116666150202155915