Recoding the cancer epigenome by intervening in metabolism and iron homeostasis with mitochondria-targeted rhenium(I) complexes
Creators
- 1. MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275 (China)
Description
The development and malignancy of cancer cells are closely related to the changes of the epigenome. In this work, a mitochondria-targeted rhenium(I) complex (DFX-Re3), integrating the clinical iron chelating agent deferasirox (DFX), has been designed. By relocating iron to the mitochondria and changing the key metabolic species related to epigenetic modifications, DFX-Re3 can elevate the methylation levels of histone, DNA, and RNA. As a consequence, DFX-Re3 affects the events related to apoptosis, RNA polymerases, and T-cell receptor signaling pathways. Finally, it is shown that DFX-Re3 induces immunogenic apoptotic cell death and exhibits potent antitumor activity in vivo. This study provides a new approach for the design of novel epigenetic drugs that can recode the cancer epigenome by intervening in mitochondrial metabolism and iron homeostasis. (© 2020 Wiley‐VCH GmbH)
Additional details
Identifiers
Publishing Information
- Journal Title
- Angewandte Chemie (International Edition)
- Journal Volume
- 59
- Journal Issue
- 42
- Journal Page Range
- p. 18755-18762
- ISSN
- 1433-7851
- CODEN
- ACIEF5
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51120868
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ANTINEOPLASTIC DRUGS; APOPTOSIS; CARCINOMAS; CHELATING AGENTS; DNA; GENETICS; HISTONES; HOMEOSTASIS; IN VIVO; IRON; METABOLISM; METHYLATION; MITOCHONDRIA; RECEPTORS; RHENIUM COMPLEXES; RNA; RNA POLYMERASES; TOXICITY; TUMOR CELLS
- Descriptors DEC
- ANIMAL CELLS; BIOLOGY; CELL CONSTITUENTS; CHEMICAL REACTIONS; COMPLEXES; DISEASES; DRUGS; ELEMENTS; ENZYMES; MEMBRANE PROTEINS; METALS; NEOPLASMS; NUCLEIC ACIDS; NUCLEOTIDYLTRANSFERASES; ORGANIC COMPOUNDS; PHOSPHORUS-GROUP TRANSFERASES; POLYMERASES; PROTEINS; TRANSFERASES; TRANSITION ELEMENT COMPLEXES; TRANSITION ELEMENTS