期刊文献+

CD44V6和β-catenin与骨肉瘤关系的研究进展 被引量:1

Expressions of CD44V6 and β-catenin in osteosarcoma and their clinical significance
下载PDF
导出
摘要 CD44V6与β-catenin是两种重要的细胞黏附分子(cell adhesion molecules,CAMs),通过介导细胞与细胞、细胞与基质间的相互作用,参与多细胞生物的多种生理及病理过程,是近年来研究的热点。CD44V6主要分布于上皮源性细胞和肿瘤细胞,介导异质细胞间的黏附,与细胞的集聚、淋巴细胞的再循环、淋巴细胞的激活、细胞的迁移、细胞间的信号传导及肿瘤细胞的侵袭、转移密切相关;β-catenin介导同质细胞间的黏附,在脊椎动物的身体形成和发育及肿瘤的发生、发展及侵袭转移过程中起重要作用。已有研究证明,CD44V6、β-catenin在多种恶性肿瘤如骨肉瘤、乳腺癌、胃癌及结直肠癌中表达增高,其表达水平与肿瘤细胞的浸润、转移能力成正相关。因此,CD44V6与β-cate-nin能反映肿瘤细胞的增殖活性及肿瘤的恶性程度,可以作为肿瘤恶性表型的标志,尤其可以作为肿瘤的辅助性诊断及预测转移的指标之一。 CD44V6 and β-catenin are currently viewed as two important adhesive molecules that mediate the interaction of cell with cell, and cell with matrix,and affect various physiologic and pathologic processes. CD44V6 locates mainly at epitheliod and tumor cells, and may play an important role in some processes,such as cell adhesion, aggregation, lymphocytic recirculation and activation, cell migration, signal transduction and the metastasis of tumor cells. β-catenin has been proved to promote the cell adhesion, invasion and metastasis of some cancers, meanwhile, overexpress in many tumors including osteosarcoma, breast carcinoma, digestive tract cancers. These results suggest, therefore, CD44V6 and βcatenin may be taken as tumor markers that reflect proliferation activity and progression of cancer cells, and predict the prognosis of tumors.
作者 李成存 李敏
出处 《中华肿瘤防治杂志》 CAS 2008年第1期76-79,共4页 Chinese Journal of Cancer Prevention and Treatment
关键词 骨肉瘤 抗原 CD44 细胞支架蛋白质类 综述文献 osteosarcoma antigens, CD44 cytoskeletal proteins review literature
  • 相关文献

参考文献28

  • 1Underhill C B, Green S J, Tarone P. The hyaluronate receptor is identical to a glycoprotein of Mr 85000 (gp85) as show by a monoclonal antibody that interferes with binding activity[J]. J Biol Chem, 1987, 262(27): 13142-13146.
  • 2Mckallip R J, Do Y, Fisher M T, et al. Role of CD44 in activation-induced cell death: CD44-deficient mice exhibit enhanced T cell response to conventional and supertigens[J]. Lnt Immund, 2002, 14(9): 1015-1026.
  • 3Allouche M, Charrad R S, Bettaieb A, et al. Ligation of the CD44 adhession molecule inhibits drug-induced apoptosis in human myeloid leukemia cell[J]. Blood, 2000, 96(3): 1187- 1190.
  • 4Hogerkorp C M, Bilke S, Breslin T, et al. CD44-stimulatied human B cell expression transcripts specifically involved in im munomodulation and inflammation as analyzed by DNA microrrays[J]. Blood, 2003, 102(6): 2307-2313.
  • 5Bassarova A V, Torlakovic E, Sedloev T, et al. Simultaneous bilateral breast carcinoma: Histopathological characteristics and CD44/catenin-cadherin profile[J]. Histol Histopathol, 2005, 20(3) :791--799.
  • 6Bendardaf R, Elzagheid A, Lamlum H, et al. E-cadherin, CD44S and CD44V6 correlate with tumor differentiation in colorectalcancer[J]. OncolRep, 2005, 13 (5): 831-835.
  • 7Hong S C, Song J Y, Lee J K, et al. Significance of CD44V6 expression in gynecologic malignancies[J]. J Obstet Gynaecol Res, 2006, 32(4): 379-386.
  • 8金鲁明,张海涛,郭成浩.乳腺癌组织中CD44V6和整合素α5β1的表达及其意义[J].中华肿瘤防治杂志,2006,13(18):1409-1411. 被引量:6
  • 9辛榕,郭乔楠,冯俊明.粘附分子CD44、CD44V3、CD44V6及PCNA在人骨肉瘤中的表达及其临床意义[J].第三军医大学学报,2003,25(10):874-876. 被引量:11
  • 10Carvalho R, Milne A N, Polak M, et al. A novel region of amplification at 11p12--13 in gastric cancer, revealed by representational difference analysis is associated with overexpression of CD44V6, especially in early-onset gastric carcinomas[J]. Genes Chromosomes Cancer, 2006, 45 (10): 967-975.

二级参考文献44

  • 1皋岚湘,丁华野.新版WHO乳腺浸润性癌组织学类型的特点概述[J].中华病理学杂志,2004,33(4):382-384. 被引量:17
  • 2刘子君.骨与关节病理学[M].北京:人民卫生出版社,1994.149-151.
  • 3[7]Wielenga V J, Heider K H, Offerhaus G J, et al. Expression of CD44-variant proteins in human colorectal cancer is related to tumor progression[J]. Cancer Res, 1993,53:4754-4756.
  • 4[8]Kuryu M, Ozaki T, Nishida K, et al. Expression of CD44-variants in osteosarcoma[J]. J Cancer Res Clin Oncol, 1999,125(11):646-652.
  • 5Kugler A. Matrix metalloproteinases and their inhibitors[J].Anticancer Res, 1999,19(2C) : 1589-1592.
  • 6Goodison S, Urquidi V, Tarin D. CD44 cell adhesion molecules[J].Mol Pathol,1999,52(4):189-196.
  • 7Davidson B, Goldberg I, Kopolovic J, et al. Expression of matrix metalioproteinase-9 in squamous cell cardnoma of the uterine cervix-clinicopathologic study using immunohistochemistry and mRNA in situ hybridization[J].Gynecol Oncol, 1999.72(3) : 380-386.
  • 8Kainz C, Tempfer C, Kohlberger P, et al. Immunohistocemical detection of adhesion molecule CD44 splice variants in lymph node metastases of cervical cancer[J].Int J Cancer, 1996,69(3) :170-173.
  • 9Inoue Y, Abe K, Obata K, et al. Immunohistochemical studies on matrix metalloproteinase-9 (MMP-9) and type Ⅳ collagen in endometrial carcinoma[J].J Obstet Gynaecol Res, 1997,23(2) :139-145.
  • 10Iurlaro M, Loverro G, Vacca A, et al. Angiogenesis extent and expression of matrix metalloproteinase-2 and-9 correlate with upgrading and myometrial invasion in endometrial carcinoma[J].Eur J Clin Invest, 1999,29(9) :793-801.

共引文献25

同被引文献13

引证文献1

二级引证文献3

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