Expression of cell adhesion molecules in oesophageal carcinoma and its prognostic value

被引:83
作者
Nair, KS
Naidoo, R
Chetty, R
机构
[1] Univ KwaZulu Natal, Nelson R Mandela Sch Med, Doris Duke Med Res Inst, Pfizer Mol Biol Res Facil, ZA-4013 Congella, South Africa
[2] Univ Hlth Network, Toronto Med Labs, Dept Pathol, Toronto, ON M5G 2M9, Canada
[3] Univ Toronto, Toronto, ON M5G 2M9, Canada
关键词
D O I
10.1136/jcp.2004.018036
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Oesophageal carcinoma remains a disease of poor prognosis. Surgical cure rates are compromised by the fact that most patients are diagnosed at a late stage of disease because of the delayed onset of symptoms, by which time metastases and organ infiltration may have already occurred. Thus, invasion and metastases play a key role in influencing patient survival, and the search for novel treatments may therefore hinge on gaining insight into the mechanisms controlling these processes. It has been established that the initial step in the metastatic cascade is the detachment of tumour cells from the primary tumour via dysregulation of normal cell-cell and cell-matrix interactions. Distinct proteins known as cell adhesion molecules (CAMs) mediate these interactions. In recent years, a plethora of information has contributed to the in depth understanding of these molecules. This review provides a brief description of five families of CAMs (cadherins, integrins, CD44, immunoglobulin superfamily, and selectins) and highlights their altered expression in relation both to prognosis and tumour behaviour in squamous cell carcinoma and adenocarcinoma of the oesophagus.
引用
收藏
页码:343 / 351
页数:9
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