Literature DB >> 16243712

The priming/completion paradigm to explain growth factor-dependent cell cycle progression.

Andrius Kazlauskas1.   

Abstract

Approximately 50 years ago, researchers established conditions to maintain cells in tissue culture: Likely et al. (1952), Scherer et al. (1953), Eagle (1955). This simple model system set the stage for discovery of growth factors and the signaling systems that they engage to mediate cellular responses such as proliferation. The purpose of this review is to present the original view of how growth factors regulate cell cycle progression and an updated (priming/completion) version of how growth factors advance resting cells through the cell cycle.

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Year:  2005        PMID: 16243712     DOI: 10.1080/08977190500096020

Source DB:  PubMed          Journal:  Growth Factors        ISSN: 0897-7194            Impact factor:   2.511


  4 in total

1.  Disruption of platelet-derived growth factor-dependent phosphatidylinositol 3-kinase and phospholipase Cγ 1 activity abolishes vascular smooth muscle cell proliferation and migration and attenuates neointima formation in vivo.

Authors:  Evren Caglayan; Marius Vantler; Olli Leppänen; Felix Gerhardt; Lenard Mustafov; Henrik Ten Freyhaus; Kai Kappert; Margarete Odenthal; Wolfram H Zimmermann; Michelle D Tallquist; Stephan Rosenkranz
Journal:  J Am Coll Cardiol       Date:  2011-06-21       Impact factor: 24.094

2.  Two phases of mitogenic signaling unveil roles for p53 and EGR1 in elimination of inconsistent growth signals.

Authors:  Yaara Zwang; Aldema Sas-Chen; Yotam Drier; Tal Shay; Roi Avraham; Mattia Lauriola; Efrat Shema; Efrat Lidor-Nili; Jasmine Jacob-Hirsch; Ninette Amariglio; Yiling Lu; Gordon B Mills; Gideon Rechavi; Moshe Oren; Eytan Domany; Yosef Yarden
Journal:  Mol Cell       Date:  2011-05-20       Impact factor: 17.970

3.  "Competence" progress.

Authors:  David F Stern
Journal:  Mol Cell       Date:  2011-05-20       Impact factor: 17.970

4.  Two waves of the nuclear phospholipase C activity in serum-stimulated HL-60 cells during G(1) phase of the cell cycle.

Authors:  Vesna Lukinovic-Skudar; Katarina Matkovic; Hrvoje Banfic; Dora Visnjic
Journal:  Biochim Biophys Acta       Date:  2007-02-13
  4 in total

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