期刊文献+

KAIl基因与恶性肿瘤浸润相关性的研究

Study on correlations of KAIl gene and its TM4SF family-related members with infiltration of malignant tumors
下载PDF
导出
摘要 浸润和转移是恶性肿瘤的重要特征 ,也是引起肿瘤病例死亡的主要原因。KAIl CD82属四次跨膜超家族的成员 ,其结构为细胞膜糖蛋白。目前研究多种肿瘤中均证实了转移的肿瘤往往伴随KAIl CD82基因的表达下降或缺失 ,最新研究发现TM 4SF家族部分成员可与整合素形成复合体 ,从而调节整合素的黏附功能 ,并影响整合素介导的细胞转移。 Invasion and metastasis are two important characteristics of malignant tumor, and they are main death causes of the patients with cancer. KAIl/CD82 is a member of transmembrane 4 superfamily(TM4SF), and its structure is a glycoprotein on the cellular membrane. From recent studies on different kinds of neoplasms, it is confirmed that the metastasized tumor is often accompanied by decrease or absence in expression of KAIl/CD82 gene. Recent study showed that parts of TM4SF and integrin can form a complex, which can regulate adhesive function of integrin and influence integrin mediated cell metastasis.
出处 《国外医学(妇幼保健分册)》 2003年第6期439-443,共5页 Foreign Medical Sciences (Section of Maternal and Child Health)
基金 辽宁省科技基金项目 (981 0 50 0 1 0 4 )
关键词 KAIL/CD82 TM4SF 恶性肿瘤 转移 KAIl/CD82 TM4SF malignant tumor metastasis
  • 相关文献

参考文献26

  • 1[1]Dong J T, Isaacs W B, Barrett J C, et al. Genomic organization of the human KAIl metastasis-suppressor gene[J]. Genomics, 1997,41:25 - 32.
  • 2[2]Liu F S, Dong J T, Chen J T, et al. Frequent down-regulation and lack of mutation of the KAIl metastasis suppressor gene in epithelial ovarian carcinoma[ J ]. Gynecol Oncol, 2000,78: 10 -15.
  • 3[3]Miyazaki T, Kato H, Shitara Y, et al. Mutation and expression of the metastasis suppressor gene KAIl in esophageal squamous cell carcinoma[J]. Cancer,2000,89:955-962.
  • 4[4]Kawana Y, Komiya A, Ueda T, et al. Location of KAIl on the short arm of human chromosome 11 and frequency of allelic loss in advanced human prostate cancer [ J ]. Prostate, 1997,32: 205-213.
  • 5[5]Tagawa K, Arihiro K, Takeshima Y, et al. Down-regulation of KAIl messenger RNA expression is not associated with loss of heterozygosity of the KAIl gene region in lung adenocarcinoma [J]. Jpn J Cancer Res,1999,90:970 - 976.
  • 6[6]Jackson P, Millar D, Kingsley E, et al. Methylation of a CpG island within the promoter region of the KALL metastasis suppressor gene is not responsible for down-regulation of KAIl expression in invasive cancers or cancer cell lines [ J ]. Cancer Lett,2000,157:169 - 176.
  • 7[7]Mashimo T, Watabe M, Hirota S, et al. The expression of the KAIl gene, a tumor metastasis suppressor, is directly activated by p53[J]. Proc Natl Acad Sci USA, 1998,95:11307-11311.
  • 8[8]Mashimo T, Bandyopadhyay S, Goodarzi G, et al. Activation of the tumor metastasis suppressor gene, KAIl, by etoposide is mediated by p53 and c-Jun genes [ J ]. Biochem Biophys Res Commun, 2000,274: 370 - 376.
  • 9[9]Duriez C, Falette N, Cortes U, et al. Absence of p 53-dependent induction of metastatic suppressor KAIl gene after DNA damage[ J ]. Onco Gene, 2000,19: 2461 - 2464.
  • 10[10]Yu Y, Yang J L, Markovic B, et al. Loss of KAIl messenger RNA expression in both high-grade and invasive human bladder cancers[J]. Clin Cancer Res, 1997.3(7): 1045 - 1049.

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