The concealed side of caspases: beyond a killer of cells.

Cell Mol Life Sci

Institute of Environmental Medicine, Karolinska Institutet, Stockholm, SE-171 77, Sweden.

Published: December 2024

AI Article Synopsis

  • Caspases, known for their role in cell death and apoptosis, have been found to also play important roles in cell growth, differentiation, and cancer progression.
  • Deregulated caspases can lead to various health issues, including cancer, inflammation, neurodegenerative diseases, and skin disorders.
  • Current research is exploring both caspase inhibition for therapy and the potential benefits of caspase induction in treatments, while addressing the challenges associated with side effects and understanding their evolutionary significance.

Article Abstract

Since the late 20th century, researchers have known that caspases are a pillar of cell death, particularly apoptosis. However, recent advances in cell biology have unraveled the multiple roles of caspases. These enzymes have an unconventional role in cell proliferation, differentiation, and invasion. As a result, caspase deregulation can fuel the fire of cancer, incite flames of inflammation, flare neurodegenerative disorders, and exacerbate skin pathologies. Several therapeutic approaches toward caspase inhibition have been investigated, but can caspase inhibitors harness the maladaptive effect of these proteases without causing significant side effects? A few studies have exploited caspase induction for cancer or adoptive cell therapies. Here, we provide a compelling picture of caspases, starting with their evolution, their polytomous roles beyond cell death, the flaws of their deregulation, and the merits of targeting them for therapeutic implications. Furthermore, we provide a deeper understanding of the evolution of caspase-related research up to the current era, pinpointing the role of caspases in cell survival and aiding in the development of effective caspase-targeted therapies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11615176PMC
http://dx.doi.org/10.1007/s00018-024-05495-7DOI Listing

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