4.6 Article

Gallic Acid: A Natural Phenolic Compound Exerting Antitumoral Activities in Colorectal Cancer via Interaction with G-Quadruplexes

期刊

CANCERS
卷 14, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/cancers14112648

关键词

G-quadruplex; phenol; gallic acid; cancer; colorectal cancer

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资金

  1. Instituto de Salud Carlos III [PI21/00497, AC18/00008]
  2. Next generation EU, Plan de Recuperacion Transformacion y Resiliencia, Agencia Estatal de Investigacion [PLEC2021-008094]
  3. Ministerio de Ciencia e Innovacion from Government of Spain [PID2019-104416RB-I00, PID2020-120481RB-I00]
  4. Ministerio de Universidades from Government of Spain [FPU16/05822, FPU17/05413, FPU20/03952]
  5. University of Almeria [FPI-201102]

向作者/读者索取更多资源

Gallic acid, as a natural phenolic compound, interacts with DNA G-quadruplexes, particularly targeting G-quadruplexes in ribosomal DNA and CMYC oncogene, leading to antitumoral effects in colorectal cancer.
Simple Summary Gallic acid, a natural phenolic compound in diet, interacts with DNA G-quadruplexes both in vitro and in vivo. In particular, gallic acid targets G-quadruplexes in ribosomal DNA and CMYC oncogene, affecting gene expression. This action leads to antitumoral effects in colorectal cancer. In a patient cohort with CRC, we demonstrate that gallic acid could be explored as a therapeutic agent. Natural phenolic compounds have gained momentum for the prevention and treatment of cancer, but their antitumoral mechanism of action is not yet well understood. In the present study, we screened the antitumoral potential of several phenolic compounds in a cellular model of colorectal cancer (CRC). We selected gallic acid (GA) as a candidate in terms of potency and selectivity and extensively evaluated its biological activity. We report on the role of GA as a ligand of DNA G-quadruplexes (G4s), explaining several of its antitumoral effects, including the transcriptional inhibition of ribosomal and CMYC genes. In addition, GA shared with other established G4 ligands some effects such as cell cycle arrest, nucleolar stress, and induction of DNA damage. We further confirmed the antitumoral and G4-stabilizing properties of GA using a xenograft model of CRC. Finally, we succinctly demonstrate that GA could be explored as a therapeutic agent in a patient cohort with CRC. Our work reveals that GA, a natural bioactive compound present in the diet, affects gene expression by interaction with G4s both in vitro and in vivo and paves the way towards G4s targeting with phenolic compounds.

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