尼日利亚卡拉巴非洲早期乳腺癌妇女中遗传性乳腺癌基因和胶原蛋白的免疫组织化学表达模式

Niso Udonkang, T. Ugbem, Iya Eze, E. Ofem, Akom Amaka, Solomon Johnson, David Onwineng
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引用次数: 1

摘要

非洲妇女乳腺癌的诊断年龄和基因检测的差异是引起关注的一个主要原因。常见的遗传性乳腺癌基因,如乳腺癌基因1 (BRCA1)、乳腺癌基因2 (BRCA2)和肿瘤蛋白53 (TP53或p53),以及基质中胶原沉积增加,使女性易患早期乳腺癌。本研究旨在建立Calabar大学教学医院早发性乳腺癌女性患者BRCA1、BRCA2、p53蛋白的免疫组织化学表达模式及胶原蛋白的变化。96名女性的乳腺肿瘤发生率数据来自组织病理学登记。从卡拉巴大学教学医院组织病理学实验室随机选择10个石蜡包埋的乳腺组织块,在4微米处切片,用血红素和伊红染色,胶原纤维染色,免疫组织化学染色BRCA1, BRCA2和p53蛋白表达。结果96例乳腺肿瘤患者中,≤50岁的占84.4%,>50岁的占15.6%。在10个组织中,60%为BRCA1(-)和40%为BRCA1(+), 10% BRCA2(-)和90% BRCA2(+), 30% p53(-)和70% p53(+)的蛋白表达,尽管这些并不显著。BRCA1(+)组织的染色强度明显低于BRCA2(+)组织(50.5±12.5;P =0.011), p53(+)(53.8±8.6;p = 0.040)。大多数乳腺肿瘤的胶原纤维大小显著增加,与肿瘤类型和癌的分级一致,但与BRCA或p53状态无关。综上所述,乳腺肿瘤在Calabar地区50岁以下的女性中较为常见,所选的早期乳腺癌多以BRCA1阴性表达、BRCA2和p53蛋白阳性表达以及胶原纤维沉积增加为特征。迫切需要对这些遗传性乳腺癌基因和胶原蛋白改变进行更广泛的研究,以确定早期乳腺癌发展的风险。
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Pattern of immunohistochemical expression of inherited breast cancer genes and collagen changes among African women with early breast cancer in Calabar, Nigeria
The disparity in age of diagnosis and genetic testing of breast cancer among African women is a major cause of concern. The common inherited breast cancer genes like breast cancer gene 1 (BRCA1), breast cancer gene 2 (BRCA2) and Tumour protein 53 (TP53 or p53) as well as increase collagen deposition in the stroma predispose women to early breast cancer. The aim of this study was to establish the immunohistochemical expressions patterns of BRCA1, BRCA2, and p53 proteins as well as collagen changes in females with early onset breast cancers in University of Calabar Teaching Hospital. Data on breast tumours occurrences among 96 females were obtained from the Histopathology register. Ten randomly selected paraffin wax-embedded breast tissue blocks from Histopathology laboratory, University of Calabar Teaching Hospital were sectioned at 4 micrometer, stained histologically with haematoxylin and eosin, van Gieson for collagen fibres and immunohistochemically for BRCA1, BRCA2 and p53 protein expressions. Results showed that of the 96 women with breast tumours, 84.4% were ≤50 years while 15.6% were >50 years. Among the 10 tissues, 60% were BRCA1(-) and 40% BRCA1(+), 10% BRCA2(-) with 90% BRCA2(+), and 30% p53(-) with 70% p53(+) for protein expressions, although these were not significant. The BRCA1(+) tissues had significant lower staining intensity than BRCA2(+) (50.5±12.5; p=0.011) and p53(+) (53.8±8.6; p=0.040) counterparts. Majority of the breast tumours had significant increases in collagen fibre sizes consistent with type of tumour and grade of carcinoma but was irrespective of BRCA or p53 statuses. In conclusion, breast tumours are common among women below 50 years in Calabar and the selected early breast cancers were mostly characterized by negative expressions of BRCA1, positive expressions of BRCA2 and p53 proteins as well as increase deposition of collagen fibres. There is urgent need to carryout wider studies on these inherited breast cancer genes and collagen alterations to determine the risk of early breast cancer development.
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