与英国乳腺癌患者相比,尼日利亚乳腺癌患者细胞增殖(KI-67)表达与预后差相关

ISRN oncology Pub Date : 2013-04-11 Print Date: 2013-01-01 DOI:10.1155/2013/675051
Ayodeji O J Agboola, Adekumbiola A F Banjo, Charles C Anunobi, Babatunde Salami, Mopelola Deji Agboola, Adewale A Musa, Christopher C Nolan, Emad A Rakha, Ian O Ellis, Andrew R Green
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引用次数: 21

摘要

背景。尼日利亚黑人妇女患乳腺癌的死亡率高于英国妇女。本研究探讨尼日利亚乳腺癌妇女细胞增殖生物标志物(Ki-67)的预后特征。材料与方法。用免疫组织化学方法研究了308例尼日利亚妇女组织微阵列(TMA)中Ki-67蛋白的表达。尼日利亚妇女表达Ki-67的肿瘤的临床病理参数、生物标志物和患者预后与英国分级匹配系列相关。结果。尼日利亚妇女的乳腺肿瘤中Ki-67高表达的比例明显更高。与英国女性相比,这些肿瘤与类固醇激素受体(ER和PgR)、p21、p27、E-cadherin、BRCA-1和Bcl-2的阴性表达显著相关(均P < 0.001),但与EGFR (P = 0.003)、p53、基础细胞角蛋白:CK56、CK14、三阴性和基础表型呈正相关(均P < 0.001)。多变量分析显示,种族也与BCSS相关,与肿瘤大小、淋巴结状态和ER状态无关。结论。Ki-67的表达导致了尼日利亚妇女与不列颠哥伦比亚省妇女BCSS的差异。因此,针对本土黑人女性BC患者的Ki-67可能会改善黑人女性BC患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cell Proliferation (KI-67) Expression Is Associated with Poorer Prognosis in Nigerian Compared to British Breast Cancer Women.

Cell Proliferation (KI-67) Expression Is Associated with Poorer Prognosis in Nigerian Compared to British Breast Cancer Women.

Cell Proliferation (KI-67) Expression Is Associated with Poorer Prognosis in Nigerian Compared to British Breast Cancer Women.

Background. Black women with breast cancer (BC) in Nigeria have higher mortality rate compared with British women. This study investigated prognostic features of cell proliferation biomarker (Ki-67) in Nigerian breast cancer women. Materials and Methods. The protein expression of Ki-67 was investigated in series of 308 Nigerian women, prepared as a tissue microarray (TMA), using immunohistochemistry. Clinic-pathological parameters, biomarkers, and patient outcome of tumours expressing Ki-67 in Nigerian women were correlated with UK grade-matched series. Results. A significantly larger proportion of breast tumours from Nigerian women showed high Ki-67 expression. Those tumours were significantly correlated with negative expression of the steroid hormone receptors (ER and PgR), p21, p27, E-cadherin, BRCA-1, and Bcl-2 (all P < 0.001), but positively associated with EGFR (P = 0.003), p53, basal cytokeratins: CK56, CK14, triple negative, and basal phenotype using Nielsen's classification (all P < 0.001) compared to UK women. Multivariate analyses showed that race was also associated with BCSS independent of tumour size, lymph node status, and ER status. Conclusion. Ki-67 expression was observed to have contributed to the difference in the BCSS in Nigerian compared with British BC women. Therefore, targeting Ki-67 in the indigenous black women with BC might improve the patient outcome in the black women with BC.

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