Selective elimination of senescent cells by mitochondrial targeting is regulated by ANT2

• DOI: 10.1038/s41418-018-0118-3
• Publication Date: 2018-05-21T13:03:57Z
• Authors: Sona Hubackova; Eliska Davidova; Katerina Rohlenova; Jan Stursa; Lukas Werner; Ladislav Andera; LanFeng Dong; Mikkel G. Terp; Zdenek Hodny; Henrik J. Ditzel; Jakub Rohlena; Jiri Neuzil
• Keywords: 0301 basic medicine; 570; Biomedical and clinical sciences; Antineoplastic Agents, Hormonal; Cell Survival; 610; Apoptosis; Mice, Transgenic; Mice, SCID; Transfection; Article; Mice; 03 medical and health sciences; Mice, Inbred NOD; Animals; Humans; Cellular Senescence; Cell Proliferation; Health sciences; Adenine Nucleotide Translocator 2; Xenograft Model Antitumor Assays; Mitochondria; 3. Good health; Biological sciences; Tamoxifen; Gene Knockdown Techniques; MCF-7 Cells

AbstractCellular senescence is a form of cell cycle arrest that limits the proliferative potential of cells, including tumour cells. However, inability of immune cells to subsequently eliminate senescent cells from the organism may lead to tissue damage, inflammation, enhanced carcinogenesis and development of age-related diseases. We found that the anticancer agent mitochondria-targeted tamoxifen (MitoTam), unlike conventional anticancer agents, kills cancer cells without inducing senescence in vitro and in vivo. Surprisingly, it also selectively eliminates both malignant and non-cancerous senescent cells. In naturally aged mice treated with MitoTam for 4 weeks, we observed a significant decrease of senescence markers in all tested organs compared to non-treated animals. Mechanistically, we found that the susceptibility of senescent cells to MitoTam is linked to a very low expression level of adenine nucleotide translocase-2 (ANT2), inherent to the senescent phenotype. Restoration of ANT2 in senescent cells resulted in resistance to MitoTam, while its downregulation in non-senescent cells promoted their MitoTam-triggered elimination. Our study documents a novel, translationally intriguing role for an anticancer agent targeting mitochondria, that may result in a new strategy for the treatment of age-related diseases and senescence-associated pathologies.