Gardner M J, Jones L M, Catterall J B, Turner G A
Department of Clinical Biochemistry, Medical School, Newcastle upon Tyne, UK.
Cancer Lett. 1995 May 8;91(2):229-34. doi: 10.1016/0304-3835(95)03743-g.
A major route for the spread of ovarian cancer is by the attachment of tumour cells to the mesothelium lining in the peritoneal cavity. The expression of various adhesion molecules has been measured on freshly-prepared mesothelial cells, two mesothelial cells lines and 13 established ovarian tumour cell lines. The integrins beta 1 and beta 3, ICAM-1, and CD44 were detected on all mesothelial preparations and on many or all of the tumour lines. VCAM-I was expressed exclusively on the mesothelial cells and Lewis x was expressed on half of the tumour lines. There was low or no expression of sialyl Le(x), sialyl Le(a), integrins alpha 4, beta 1, beta 4, or E and P selectins. Only CD44 expression was significantly affected by trypsin treatment. From the known interactions of adhesion molecules, the results suggest that CD44, and beta 1 and beta 3 integrins may be important in tumour/mesothelial interactions.
卵巢癌的一个主要传播途径是肿瘤细胞附着于腹膜腔的间皮衬里。已对新鲜制备的间皮细胞、两种间皮细胞系和13种已建立的卵巢肿瘤细胞系上各种粘附分子的表达进行了检测。在所有间皮制剂以及许多或所有肿瘤系中均检测到整合素β1和β3、细胞间粘附分子-1(ICAM-1)以及CD44。血管细胞粘附分子-1(VCAM-1)仅在间皮细胞上表达,而Lewis x在一半的肿瘤系中表达。唾液酸化Lewis x(sialyl Le(x))、唾液酸化Lewis a(sialyl Le(a))、整合素α4、β1、β4或E及P选择素的表达较低或无表达。只有CD44的表达受到胰蛋白酶处理的显著影响。从粘附分子的已知相互作用来看,结果表明CD44以及β1和β3整合素可能在肿瘤/间皮相互作用中起重要作用。