Bandiera A, Bonifacio D, Manfioletti G, Mantovani F, Rustighi A, Zanconati F, Fusco A, Di Bonito L, Giancotti V
Dipartimento di Biochimica, Biofisica e Chimica delle Macromolecole, Universitá degli Studi di Trieste, Italy.
Cancer Res. 1998 Feb 1;58(3):426-31.
The expression of nuclear proteins high mobility group (HMG) I and HMGY was investigated in intraepithelial and invasive lesions of the uterine cervix. Human carcinoma cell lines C-41, ME-180, and CaSki were used for testing protein expression in neoplastic cells from the cervix. Morphological grading of the dysplasias (CIN 1, CIN 2, and CIN 3) and invasive carcinomas from formalin-fixed paraffin-embedded samples parallels the degree of nuclear immunostaining obtained using a polyclonal antibody raised against the amino-terminal region of HMGI(Y) proteins. The immunostaining obtained with HMGI(Y) antibody was compared with that observed using the antibody Ki-67, and the results were similar. We suggest the use of HMGI(Y) antibody in clinical oncology as a useful marker of intraepithelial lesions and invasive carcinomas.
研究了高迁移率族(HMG)I和HMGY核蛋白在子宫颈上皮内病变和浸润性病变中的表达。使用人癌细胞系C-41、ME-180和CaSki检测子宫颈肿瘤细胞中的蛋白表达。对福尔马林固定石蜡包埋样本中的发育异常(CIN 1、CIN 2和CIN 3)及浸润性癌进行形态学分级,与使用针对HMGI(Y)蛋白氨基末端区域产生的多克隆抗体获得的核免疫染色程度平行。将用HMGI(Y)抗体获得的免疫染色与使用Ki-67抗体观察到的结果进行比较,结果相似。我们建议在临床肿瘤学中使用HMGI(Y)抗体作为上皮内病变和浸润性癌的有用标志物。