The role of FAK in tumor metabolism and therapy.

The role of FAK in tumor metabolism and therapy.
复制标题

DOI:
10.1016/j.pharmthera.2013.12.003
复制
发表时间:
2014-05
影响因子:
13.5
通讯作者:
Hochwald SN
Hochwald SN
中科院分区:
医学1区
文献类型:
--
作者:
Zhang J;Hochwald SN

文献摘要

参考文献

被引文献

相似文献

粘着斑激酶(FAK)在肿瘤细胞的增殖、存活和迁移中起着重要作用。改变的代谢途径通过加速葡萄糖、脂质和谷氨酰胺的加工来促进肿瘤的快速生长。除了FAK的促有丝分裂作用外,越来越多的证据支持过度活化的FAK与肿瘤发生中的异常代谢之间的关联。FAK可促进葡萄糖消耗、脂肪生成和谷氨酰胺依赖性,从而促进癌细胞增殖、运动和存活。临床研究表明,肿瘤代谢的FAK相关改变与发展实体瘤的风险增加有关。由于FAK有助于恶性表型,FAK刺激的生物能量和生物合成过程的小分子抑制可以提供一种新的方法用于肿瘤生长和侵袭的治疗干预。
Focal adhesion kinase (FAK) plays a vital role in tumor cell proliferation, survival and migration. Altered metabolic pathways fuel rapid tumor growth by accelerating glucose, lipid and glutamine processing. Besides the mitogenic effects of FAK, evidence is accumulating supporting the association between hyper-activated FAK and aberrant metabolism in tumorigenesis. FAK can promote glucose consumption, lipogenesis, and glutamine dependency to promote cancer cell proliferation, motility, and survival. Clinical studies demonstrate that FAK-related alterations of tumor metabolism are associated with increased risk of developing solid tumors. Since FAK contributes to the malignant phenotype, small molecule inhibition of FAK-stimulated bioenergetic and biosynthetic processes can provide a novel approach for therapeutic intervention in tumor growth and invasion.
DOI: 10.1007/s00204-011-0648-7
发表时间: 2011-08
影响因子: 6.1
作者:
Bernstein, Carol;Holubec, Hana;Bhattacharyya, Achyut K.;Huy Nguyen;Payne, Claire M.;Zaitlin, Beryl;Bernstein, Harris
通讯作者: Bernstein, Harris
DOI: 10.1016/j.bbrc.2009.06.088
发表时间: 2009-09-11
影响因子: 3.1
作者:
Andersson, Sandra;D'Arcy, Padraig;Sehat, Bita
通讯作者: Sehat, Bita
DOI: 10.1207/s15327914nc4501_8
发表时间: 2003-01-01
影响因子: 2.9
作者:
Fu, YM;Yu, ZX;Meadows, GG
通讯作者: Meadows, GG
DOI: 10.1046/j.1365-2184.2002.00232.x
发表时间: 2002-06-01
期刊: CELL PROLIFERATION
影响因子: 8.5
作者:
Goel, HL;Dey, CS
通讯作者: Dey, CS
DOI: 10.1042/bj2180733
发表时间: 1984-01-01
影响因子: 4.1
作者:
BROWNSEY, RW;EDGELL, NJ;DENTON, RM
通讯作者: DENTON, RM