TY - JOUR
T1 - Molecular mechanisms of vascular smooth muscle cell growth
AU - Hafizi, Sassan
AU - Chester, Adrian H.
AU - Yacoub, Magdi H.
PY - 1997/11/1
Y1 - 1997/11/1
N2 - In recent years, much progress has been made in elucidating the complex but orchestrated series of molecular events that drives a vascular smooth muscle cell to undergo proliferation. These events are initiated by mitogenic stimuli, such as platelet-derived growth factor binding to its receptor and triggering an intracellular signal transduction cascade, leading ultimately to cell-cycle progression and cell division. The signaling pathways that take place in response to both hyperplastic and hypertrophic agents, which include the mitogen-activated protein kinase and p70 S6 kinase, are discussed. In addition, novel protein kinase mediators, such as phosphatidylinositol 3-kinase and protein kinase B, and mechanisms that have recently been implicated in vascular smooth muscle cell growth are described.
AB - In recent years, much progress has been made in elucidating the complex but orchestrated series of molecular events that drives a vascular smooth muscle cell to undergo proliferation. These events are initiated by mitogenic stimuli, such as platelet-derived growth factor binding to its receptor and triggering an intracellular signal transduction cascade, leading ultimately to cell-cycle progression and cell division. The signaling pathways that take place in response to both hyperplastic and hypertrophic agents, which include the mitogen-activated protein kinase and p70 S6 kinase, are discussed. In addition, novel protein kinase mediators, such as phosphatidylinositol 3-kinase and protein kinase B, and mechanisms that have recently been implicated in vascular smooth muscle cell growth are described.
UR - http://www.scopus.com/inward/record.url?scp=0030729397&partnerID=8YFLogxK
U2 - 10.1097/00001573-199711000-00001
DO - 10.1097/00001573-199711000-00001
M3 - Literature review
C2 - 9429819
AN - SCOPUS:0030729397
SN - 0268-4705
VL - 12
SP - 495
EP - 503
JO - Current Opinion in Cardiology
JF - Current Opinion in Cardiology
IS - 6
ER -