Tomita Y, Watanabe H, Kobayashi H, Nishiyama T, Tsuji S, Imai K, Abo T, Fujiwara M, Sato S
Department of Urology, Niigata University School of Medicine, Japan.
Am J Pathol. 1993 Jul;143(1):191-8.
Immunohistochemical examination demonstrated expression of intercellular adhesion molecule-1 (ICAM-1) on 17 of 44 transitional cell cancers (TCCs) but not on normal transitional cells. ICAM-1 was frequently expressed in higher stage tumors, especially in those with abundant immune cells scattered within tumor. Analysis of infiltrating immune cells showed that they were composed mainly of T lymphocytes and a smaller number of macrophages bearing the lymphocyte function-associated antigen-1 (LFA-1). Expression of ICAM-1 on transitional cell cancer cell lines was augmented by in vitro treatment with interferon-gamma, tumor necrosis factor-alpha, and interleukin-1 beta. Furthermore, Northern blot analysis revealed higher quantities of a 3.3-kb RNA in T24 cells exposed to interferon-gamma or tumor necrosis factor-alpha. These results suggest that the expression of ICAM-1 on transitional cell cancers might be modified by cytokines produced by infiltrating immune cells, which might facilitate immune responses against cancer cells.
免疫组化检查显示,44例移行细胞癌(TCC)中有17例表达细胞间黏附分子-1(ICAM-1),而正常移行细胞不表达。ICAM-1在较高分期的肿瘤中频繁表达,尤其是在肿瘤内散在大量免疫细胞的肿瘤中。对浸润免疫细胞的分析表明,它们主要由T淋巴细胞和少量携带淋巴细胞功能相关抗原-1(LFA-1)的巨噬细胞组成。用γ干扰素、肿瘤坏死因子-α和白细胞介素-1β体外处理后,移行细胞癌细胞系上ICAM-1的表达增强。此外,Northern印迹分析显示,暴露于γ干扰素或肿瘤坏死因子-α的T24细胞中3.3-kb RNA的量更高。这些结果表明,浸润免疫细胞产生的细胞因子可能会改变ICAM-1在移行细胞癌上的表达,这可能会促进针对癌细胞的免疫反应。