Mapping Mitotic Death: Functional Integration of Mitochondria, Spindle Assembly Checkpoint and Apoptosis

Targeting the mitotic pathways of rapidly proliferating tumor cells has been an effective strategy in traditional cancer therapy. Chemotherapeutics such as taxanes and vinca alkaloids, which disrupt microtubule function, have enjoyed clinical success; however, the accompanying side effects, toxicity...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in cell and developmental biology Vol. 6; p. 177
Main Authors Ruan, Weimei, Lim, Hong Hwa, Surana, Uttam
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 10.01.2019
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Targeting the mitotic pathways of rapidly proliferating tumor cells has been an effective strategy in traditional cancer therapy. Chemotherapeutics such as taxanes and vinca alkaloids, which disrupt microtubule function, have enjoyed clinical success; however, the accompanying side effects, toxicity and multi drug resistance remain as serious concerns. The emerging classes of inhibitors targeting mitotic kinases and proteasome face their own set of challenges. It is hoped that elucidation of the regulatory interface between mitotic checkpoints, mitochondria and mitotic death will aid the development of more efficacious anti-mitotic agents and improved treatment protocols. The links between the spindle assembly checkpoint (SAC) and mitochondrial dynamics that control the progression of anti-mitotic agent-induced apoptosis have been under investigation for several years and the functional integration of these various signaling networks is now beginning to emerge. In this review, we highlight current research on the regulation of SAC, the death pathway and mitochondria with particular focus on their regulatory interconnections.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
Edited by: Daniel Leslie Fisher, Center for the National Scientific Research (CNRS), France
Reviewed by: Song-Tao Liu, University of Toledo, United States; Christine O. Didier, INSERM U1037 Centre de Recherche en Cancérologie de Toulouse, France
This article was submitted to Cell Growth and Division, a section of the journal Frontiers in Cell and Developmental Biology
ISSN:2296-634X
2296-634X
DOI:10.3389/fcell.2018.00177