期刊文献+

15-脂氧合酶在肿瘤中的作用 被引量:2

The effect of 15-lipoxygenase on cancer
下载PDF
导出
摘要 15-脂氧合酶(15-LOX)是催化不饱和脂肪酸代谢的关键酶之一。人类中存有两型15-LOX:15-LOX-1和15-LOX-2,两者在催化性质、组织分布及肿瘤生物学功能上有所差异。近年来大量研究发现15-LOX在结肠癌、前列腺癌、食道癌等恶性肿瘤表达较正常组织降低,能够抑制肿瘤生长,并使其发生凋亡,在肿瘤发生发展中起着重要作用。以15-LOX为靶向的肿瘤防治及其临床应用具有广阔的前景。 As one enzyme of the lipoxygenase family, 15-lipoxygenase exerts important anticarcinogenic effects through the metabolism of polyunsaturated fatty acids. Two forms of 15-lipoxygenase occur in humans: 15-lipoxygenase-1 and 15-lipoxygenase-2. They are distinguished by their catalytic properties, tissue distribution and biological effects on tumor. Recent evidences indicate that the expression of 15-lipoxygenase was decreased in colorectal, prostate and esophageal cancer when compared with normal adjacent tissues. 15-lipoxygenase and its metabolites could inhibit the progression of cancer and induce their apoptosis. By 15-lipoxygenase-targeted research, it is possible to provide means of early detection and diagnosis of cancers and novel therapeutic options to treat or prevent cancers in the future.
作者 林芬 李建英
出处 《国际内科学杂志》 CAS 2007年第6期343-346,共4页 International Journal of Internal Medicine
基金 福建省科技人才创新基金资助项目No2002J061
关键词 15-脂氧合酶 肿瘤 凋亡 15-lipoxygenase Cancer Apoptosis
  • 相关文献

参考文献23

  • 1Xu XC,Shappel SB,Liang Z,et al.Reduced 15S-lipoxygenase expression in esophageal cancer specimens and cells and upregulation in vitro by the cyclooxygenase-1 inhibitor,NS398.Neoplasia,2003,5 (2):121-127. 被引量:1
  • 2Heslin MJ,Hawkins A,Boedefeld W,et al.Tumor-associated downregulation of 15-lipoxygenase-1 is reversed by celecoxib in colorectalcancer.Ann Surg,2005,241 (6):941-946. 被引量:1
  • 3Shureiqi I,Wu Y,Chen D,et al.The critical role of 15-lipoxygenase-1 in colorectal epithelial cell terminal differentiation and tumorigenesis.Cancer Res,2005,65 (24):11486-11492. 被引量:1
  • 4Hsi LC,Wilson LC,Eling TE,et al.Opposing effects of 15-lipoxygenasease-1 and-2 metabolites on MAPK signaling in prostate:Alteration in peroxisome proliferation-activated receptor gamma.J Biol Chem,2002,277 (43):40549-40556. 被引量:1
  • 5Kelavkar UP,Parwani AV,Shappel SB,et al.Conditional expression of human 15-lipoxygenase-1 in mouse prostate induces prostatic intraepithelial neoplasia:the FLiMP mouse model.Neoplasia,2006,8 (6):510-522. 被引量:1
  • 6Shureiqi I,Xu X,Chen D,et al.Nonsteroidal anti-inflammatory drugs induce apoptosis in esophageal cancer cells by restoring 15-lipoxygenase-1 expression.Cancer Res,2001,61 (12):4879-4884. 被引量:1
  • 7He TC,Chan TA,Vogelstein B,et al.PPARdelta is an APC-regulated target of nonsteroidal antiinflammatory drugs.Cell,1999,99(3):335-345. 被引量:1
  • 8Hsi LC,Xi X,Lotan R,et al.The Histone deacetylase inhibitor suberoylanilide hydroxamic acid induces apoptosis via induction of 15-lipoxygenase-1 in colorectal cancer cells.Cancer Res,2004,64(23):8778-8781. 被引量:1
  • 9Hennig R,Rao S,Büchler MW,et al.Decreased 15-lipoxygenase-1 (15-LOX-1) expression in human pancreatic adenocarcinoma.Pancreatology,2003,3:247. 被引量:1
  • 10Kim JS,Baek SJ,Botton FG Jr,et al.Overexpression of 15-lipoxygenase-1 induces growth arrest through phosphorylation of p53 in humancolorectal cancer cells.Mol Cancer Res,2005,3(9):511-517. 被引量:1

同被引文献20

  • 1燕贞,吴拥军,吴逸明.细胞色素P450 2D6与吸烟所致肺癌易感性的关系研究[J].卫生研究,2007,36(1):112-113. 被引量:4
  • 2谭庆平,胡建安.5-脂氧合酶与肿瘤的关系研究进展[J].毒理学杂志,2007,21(2):142-146. 被引量:4
  • 3Andre E, I-Iou K W. The presence of a lipid oxidase in soybean, Glycine soya [ J ]. Lieb C R Acad Sci, 1932,194:645 - 647. 被引量:1
  • 4Masoumeh T Y, Fatemeh K T, Vahid S, et al. Induc- tion of apoptosis by trichostatin A in human breast cancer cell lines:Involvement of 15-Lox-1 [ J]. Tumor Biol,2013,34:241 - 249. 被引量:1
  • 5Bondock S, Metwally M A. Thiochroman-4-ones:Synthe- sis and reactions [ J ]. J Sulfur Chem,2008,29:623 - 653. 被引量:1
  • 6Naki T A, Bejak V, Meegan M J, et al. Synthesis and antifungal activity of some 3-benzylidenechroman-4-ones, 3-benzylidenethlochroman-4-ones and 2-benzylidene-l-te- tralones [ J ]. Eur J Med Chem, 1990,2,5:455 - 462. 被引量:1
  • 7Igarashi M, Midorikawa H. Asymmetric epoxidatlon of L-methyl alkylidenecyanoacetates [ J ]. Bull Chem Soc Jpn, 1967,40:2624 - 2624. 被引量:1
  • 8Laird A D, Vajkoczy P, Shawver L K, et al. SU6668 is a potent antiangiogenic and antitumor agent that in- duces regression of established tumors [ J ]. Cancer Res ,2000,60:4152 - 4160. 被引量:1
  • 9Mendel D, Laird A, Smolich B, et al. Development of SU5416, a selective small molecule inhibitor of VEGF receptor tyrosine kinase activity, as an anti-angiogenesis agent[ J]. Anti-Cancer Drug Des,2000,15( 1 ) :29 -41. 被引量:1
  • 10Stephen K, Carter. Clinical strategy for the develop- ment of angiogenesis inhibitors [ J ]. Oneologist, 2000, 5(1) :51 -54. 被引量:1

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部