Current Progresses in Metal-based Anticancer Complexes as Mammalian TrxR Inhibitors.

Abstract:

:Reactive oxygen species (ROS) are produced as normal products of cellular metabolism, which are essential for numerous cell biological functions. Due to aberrant metabolism, oncogenic signaling activation and mitochondrial dysfunction, cancer cells generate excessive ROS that cause severe oxidative damage, finally leading to tumor cell death. Thioredoxin reductase (TrxR), as an important ROS-scavenging enzyme, is overexpressed in various human tumors and plays an important role in regulating intracellular redox homeostasis to protect cancer cells from cell death induced by substantial ROS. Hence, TrxR has emerged as a promising target for anticancer agent development. Currently, metallodrugs with anticancer activity, especially gold- and platinum-complexes, have an enormous impact on clinical cancer chemotherapy. This review provides a comprehensive overview of various metal complexes (gold, platinum, ruthenium, rhodium, iridium, iron, palladium, silver, antimony, bismuth, tin) targeting mammalian TrxR and discusses their cytotoxicity in tumor cells.

authors

Cheng Y,Qi Y

doi

10.2174/1871520617666170213150217

subject

Has Abstract

pub_date

2017-01-01 00:00:00

pages

1046-1069

issue

8

eissn

1871-5206

issn

1875-5992

pii

ACAMC-EPUB-81738

journal_volume

17

pub_type

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