Novel vitamin K-dependent pathways regulating cell survival

被引:20
作者
Saxena, SP
Israels, ED
Israels, LG
机构
[1] Lovelace Resp Res Inst, Kirtland AFB, Albuquerque, NM 87115 USA
[2] Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB, Canada
[3] Univ Manitoba, Dept Pediat, Winnipeg, MB, Canada
基金
英国医学研究理事会;
关键词
apoptosis; gamma-carboxylation; Gas6; protein S; receptor tyrosine kinases; vitamin K-1-dependent proteins;
D O I
10.1023/A:1009624111275
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Historically, the vitamin K-1-dependent proteins have been associated primarily with blood coagulation and secondarily with bone formation. Recent identification of K-1-dependent proteins as specific ligands for the receptor tyrosine kinases (RTKs) that can stimulate cell replication and transformation and participate in cell survival highlighted a previously unrecognized and potentially important role for vitamin K-1 in cell signaling. Growing evidence suggests that most normal and tumor cells possess an active K-1-dependent gamma -carboxylation mechanism necessary for the production of gamma -carboxyglutamic acid (Gla)-containing proteins. Gla residues in proteins facilitate calcium-dependent protein/phospholipid interaction. Recent studies demonstrating the potentially positive effects of a vitamin K-dependent receptor:ligand system on cell growth and survival in general and the effects of the overexpression of these RTKs on malignant cell survival provide a new perspective on the role of vitamin K-1, its dependent protein ligands, and their receptors. These cumulative observations also provide an explanation for the rigidly controlled K-1 levels in the mammalian fetus and the minimal hepatic stores in the adult.
引用
收藏
页码:57 / 68
页数:12
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