Literature DB >> 18437888

Cell death: history and future.

Zahra Zakeri1, Richard A Lockshin.   

Abstract

Cell death was observed and understood since the 19th century, but there was no experimental examination until the mid-20th century. Beginning in the 1960s, several laboratories demonstrated that cell death was biologically controlled (programmed) and that the morphology was common and not readily explained (apoptosis). By 1990, the genetic basis of programmed cell death had been established, and the first components of the cell death machinery (caspase 3, bcl-2, and Fas) had been identified, sequenced, and recognized as highly conserved in evolution. The rapid development of the field has given us substantial understanding of how cell death is achieved. However, this knowledge has made it possible for us to understand that there are multiple pathways to death and that the commitment to die is not the same as execution. A cell that has passed the commitment stage but is blocked from undergoing apoptosis will die by another route. We still must learn much more about how a cell commits to death and what makes it choose a path to die.

Entities:  

Mesh:

Year:  2008        PMID: 18437888     DOI: 10.1007/978-1-4020-6554-5_1

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  25 in total

Review 1.  Metabolic and structural role of thiamine in nervous tissues.

Authors:  Abdoulaye Bâ
Journal:  Cell Mol Neurobiol       Date:  2008-07-19       Impact factor: 5.046

2.  Increased spontaneous apoptosis of rat primary neurospheres in vitro after experimental autoimmune encephalomyelitis.

Authors:  Mir Sajad; Jamil Zargan; Jyoti Sharma; Raman Chawla; Rajesh Arora; Sadiq Umar; Haider A Khan
Journal:  Neurochem Res       Date:  2011-03-30       Impact factor: 3.996

Review 3.  Neuronal Cell Death.

Authors:  Michael Fricker; Aviva M Tolkovsky; Vilmante Borutaite; Michael Coleman; Guy C Brown
Journal:  Physiol Rev       Date:  2018-04-01       Impact factor: 37.312

4.  Effect of thrombin fragment (TP508) on myocardial ischemia reperfusion injury in a model of type 1 diabetes mellitus.

Authors:  Louis M Chu; Robert M Osipov; Michael P Robich; Jun Feng; Michael R Sheller; Frank W Sellke
Journal:  Circulation       Date:  2010-09-14       Impact factor: 29.690

Review 5.  The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors.

Authors:  Paraskevi Xekouki; Ana Brennand; Ben Whitelaw; Karel Pacak; Constantine A Stratakis
Journal:  Horm Metab Res       Date:  2018-10-01       Impact factor: 2.936

6.  Ricinosomes predict programmed cell death leading to anther dehiscence in tomato.

Authors:  Adriano Senatore; Christopher P Trobacher; John S Greenwood
Journal:  Plant Physiol       Date:  2008-12-19       Impact factor: 8.340

Review 7.  The therapeutic effect of death: Newcastle disease virus and its antitumor potential.

Authors:  Sara Cuadrado-Castano; Maria T Sanchez-Aparicio; Adolfo García-Sastre; Enrique Villar
Journal:  Virus Res       Date:  2015-07-26       Impact factor: 3.303

8.  Effect of thrombin fragment (TP508) on myocardial ischemia-reperfusion injury in hypercholesterolemic pigs.

Authors:  Robert M Osipov; Michael P Robich; Jun Feng; Richard T Clements; Yuhong Liu; Hilary P Glazer; John Wagstaff; Cesario Bianchi; Frank W Sellke
Journal:  J Appl Physiol (1985)       Date:  2009-04-16

9.  Up-regulation of micro-RNA-221 (miRNA-221; chr Xp11.3) and caspase-3 accompanies down-regulation of the survivin-1 homolog BIRC1 (NAIP) in glioblastoma multiforme (GBM).

Authors:  W J Lukiw; J G Cui; Y Y Li; F Culicchia
Journal:  J Neurooncol       Date:  2008-08-31       Impact factor: 4.130

10.  MMPT: a thiazolidin compound inhibits the growth of lung cancer H1792 cells via Fas-mediated and caspase-dependent apoptosis pathway.

Authors:  Yun-feng Zhao; Xiu-lan Li; Yu-xi Sun; Wen Niu; Zun-li Hu; Lin Lin; Qing-zhong Kong
Journal:  Invest New Drugs       Date:  2009-05-06       Impact factor: 3.850

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