Literature DB >> 17975549

Big wheel keeps on turning: apoptosome regulation and its role in chemoresistance.

B Fadeel1, A Ottosson, S Pervaiz.   

Abstract

Apoptosis, a form of programmed cell death, enables organisms to maintain tissue homeostasis through deletion of extraneous cells and also serves as a means to eliminate potentially harmful cells. Numerous stress signals have been shown to engage the intrinsic pathway of apoptosis, with the release from mitochondria of proapoptotic factors such as cytochrome c and the subsequent formation of a cytosolic complex between apoptotic protease-activating factor-1 (Apaf-1) and procaspase-9, known as the apoptosome. Recent studies have led to the identification of an array of factors that control the formation and activation of the apoptosome under physiological conditions. Moreover, deregulation of apoptosome function has been documented in various forms of human cancer, and may play a role in both carcinogenesis and chemoresistance. We discuss how the apoptosome is regulated in normal and disease states, and how targeting of apoptosome-dependent, post-mitochondrial stages of apoptosis may serve as a rational approach to cancer treatment.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17975549     DOI: 10.1038/sj.cdd.4402265

Source DB:  PubMed          Journal:  Cell Death Differ        ISSN: 1350-9047            Impact factor:   15.828


  30 in total

1.  The emerging role of matrix metalloproteases of the ADAM family in male germ cell apoptosis.

Authors:  Ricardo D Moreno; Paulina Urriola-Muñoz; Raúl Lagos-Cabré
Journal:  Spermatogenesis       Date:  2011-07-01

Review 2.  Cellular mechanisms controlling caspase activation and function.

Authors:  Amanda B Parrish; Christopher D Freel; Sally Kornbluth
Journal:  Cold Spring Harb Perspect Biol       Date:  2013-06-01       Impact factor: 10.005

3.  Protein kinase RNA/FADD/caspase-8 pathway mediates the proapoptotic activity of the RNA-binding protein human antigen R (HuR).

Authors:  Christopher von Roretz; Imed-Eddine Gallouzi
Journal:  J Biol Chem       Date:  2010-03-30       Impact factor: 5.157

4.  Apoptotic-induced cleavage shifts HuR from being a promoter of survival to an activator of caspase-mediated apoptosis.

Authors:  C von Roretz; X Jin Lian; A M Macri; N Punjani; E Clair; O Drouin; V Dormoy-Raclet; J F Ma; I-E Gallouzi
Journal:  Cell Death Differ       Date:  2012-09-07       Impact factor: 15.828

5.  The adenosine A3 receptor agonist Cl-IB-MECA induces cell death through Ca²⁺/ROS-dependent down regulation of ERK and Akt in A172 human glioma cells.

Authors:  Thae Hyun Kim; Yong Keun Kim; Jae Suk Woo
Journal:  Neurochem Res       Date:  2012-08-10       Impact factor: 3.996

Review 6.  Targeting cell death signaling in colorectal cancer: current strategies and future perspectives.

Authors:  Bruno Christian Koehler; Dirk Jäger; Henning Schulze-Bergkamen
Journal:  World J Gastroenterol       Date:  2014-02-28       Impact factor: 5.742

Review 7.  Mitochondrial and postmitochondrial survival signaling in cancer.

Authors:  Neelu Yadav; Dhyan Chandra
Journal:  Mitochondrion       Date:  2013-12-10       Impact factor: 4.160

8.  Transportin 2 regulates apoptosis through the RNA-binding protein HuR.

Authors:  Christopher von Roretz; Angelo M Macri; Imed-Eddine Gallouzi
Journal:  J Biol Chem       Date:  2011-06-06       Impact factor: 5.157

9.  The histone deacetylase inhibitors LAQ824 and LBH589 do not require death receptor signaling or a functional apoptosome to mediate tumor cell death or therapeutic efficacy.

Authors:  Leigh Ellis; Michael Bots; Ralph K Lindemann; Jessica E Bolden; Andrea Newbold; Leonie A Cluse; Clare L Scott; Andreas Strasser; Peter Atadja; Scott W Lowe; Ricky W Johnstone
Journal:  Blood       Date:  2009-04-21       Impact factor: 22.113

10.  Androgen-Sensitized Apoptosis of HPr-1AR Human Prostate Epithelial Cells.

Authors:  Congcong Chen; Jason A Dienhart; Eric C Bolton
Journal:  PLoS One       Date:  2016-05-20       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.