The dark side of SIRT7.

Mol Cell Biochem

Department of Genetics and Molecular Biology, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, San Pedro Zacatenco, Gustavo A. Madero, 07480, Mexico City, Mexico.

Published: November 2024

AI Article Synopsis

  • - Sirtuin 7 (SIRT7), found mainly in the nucleolus, is involved in key cellular functions like ribosomal RNA expression, DNA repair, and stress response, and has implications for various diseases including cancer and obesity.
  • - In cancer, SIRT7 is often overexpressed and helps cancer cells thrive by promoting growth, metabolism, and adaptations to stress, affecting multiple cancer types like breast and lung cancers.
  • - The review aims to clarify SIRT7’s role in cancer development and progression, while also discussing potential drug development challenges for targeting SIRT7 activity.

Article Abstract

Sirtuin 7 (SIRT7) is a member of the sirtuin family and has emerged as a key player in numerous cellular processes. It exhibits various enzymatic activities and is predominantly localized in the nucleolus, playing a role in ribosomal RNA expression, DNA damage repair, stress response and chromatin compaction. Recent studies have revealed its involvement in diseases such as cancer, cardiovascular and bone diseases, and obesity. In cancer, SIRT7 has been found to be overexpressed in multiple types of cancer, including breast cancer, clear cell renal cell carcinoma, lung adenocarcinoma, prostate adenocarcinoma, hepatocellular carcinoma, and gastric cancer, among others. In general, cancer cells exploit SIRT7 to enhance cell growth and metabolism through ribosome biogenesis, adapt to stress conditions and exert epigenetic control over cancer-related genes. The aim of this review is to provide an in-depth understanding of the role of SIRT7 in cancer carcinogenesis, evolution and progression by elucidating the underlying molecular mechanisms. Emphasis is placed on unveiling the intricate molecular pathways through which SIRT7 exerts its effects on cancer cells. In addition, this review discusses the feasibility and challenges associated with the development of drugs that can modulate SIRT7 activity.

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Source
http://dx.doi.org/10.1007/s11010-023-04869-yDOI Listing

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