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拓扑异构酶 II alpha 表达和 Ki-67 标记指数与雌激素受体阳性和人表皮生长因子受体 2 阴性乳腺癌的预后因素相关。

Topoisomerase II alpha expression and the Ki-67 labeling index correlate with prognostic factors in estrogen receptor-positive and human epidermal growth factor type-2-negative breast cancer.

机构信息

Department of Thoracic and Visceral Organ Surgery, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma, 371-8511, Japan.

出版信息

Breast Cancer. 2012 Oct;19(4):309-14. doi: 10.1007/s12282-011-0291-4. Epub 2011 Jul 2.

Abstract

BACKGROUND

Topoisomerase II alpha (Topo IIa) is involved in DNA replication and is a molecular target for anthracycline-based chemotherapy. The Ki-67 labeling index (LI) is an evaluation of tumor cell proliferation. The objective of this study was to evaluate relationships among Topo IIa expression, the Ki-67 LI, and prognostic factors in estrogen receptor (ER)-positive, human epidermal growth factor type-2 (HER2)-negative breast cancer.

MATERIALS AND METHODS

Seventy-one patients were diagnosed with ER-positive, HER2-negative breast cancer between July 2003 and December 2004. Formalin-fixed, paraffin-embedded tumor specimens were stained for Topo IIa expression and Ki-67 LI. We investigated the correlation of the level of Topo IIa expression and the Ki-67 LI with clinical factors such as age, tumor size, progesterone receptor status, nodal status, nuclear grade, and lymphovascular invasion (LVI).

RESULTS

Statistically significant differences were observed between Topo IIa overexpression, nuclear grade (p = 0.036), and LVI (p = 0.029). Topo IIa overexpression was statistically correlated with the Ki-67 LI (p < 0.0001). A statistically significant difference was observed between the Ki-67 LI and nuclear grade (p = 0.01). Survival analysis revealed the significant prognostic value of Ki-67 LI in patients with ER-positive, HER2-negative breast cancer (p = 0.003).

CONCLUSIONS

Ki-67 LI is a strong prognostic factor in ER-positive HER2-negative breast cancer. Topo IIa overexpression was significantly correlated with the Ki-67 LI, nuclear grade, and LVI. These findings suggest use of Topo IIa expression as a proliferation marker and a prognostic factor in ER-positive, HER2-negative breast cancer.

摘要

背景

拓扑异构酶 IIα(Topo IIa)参与 DNA 复制,是基于蒽环类化疗的分子靶标。Ki-67 标记指数(LI)是评估肿瘤细胞增殖的一种方法。本研究旨在评估在雌激素受体(ER)阳性、人表皮生长因子受体 2(HER2)阴性乳腺癌中,Topo IIa 表达、Ki-67 LI 与预后因素之间的关系。

材料与方法

2003 年 7 月至 2004 年 12 月期间,我们诊断了 71 例 ER 阳性、HER2 阴性乳腺癌患者。对福尔马林固定、石蜡包埋的肿瘤标本进行 Topo IIa 表达和 Ki-67 LI 的染色。我们研究了 Topo IIa 表达水平和 Ki-67 LI 与年龄、肿瘤大小、孕激素受体状态、淋巴结状态、核分级和脉管侵犯(LVI)等临床因素的相关性。

结果

Topo IIa 过表达、核分级(p=0.036)和 LVI(p=0.029)之间存在统计学显著差异。Topo IIa 过表达与 Ki-67 LI 之间存在统计学相关性(p<0.0001)。Ki-67 LI 与核分级之间存在统计学差异(p=0.01)。生存分析显示 Ki-67 LI 对 ER 阳性、HER2 阴性乳腺癌患者具有显著的预后价值(p=0.003)。

结论

Ki-67 LI 是 ER 阳性 HER2 阴性乳腺癌的一个强烈的预后因素。Topo IIa 过表达与 Ki-67 LI、核分级和 LVI 显著相关。这些发现表明,Topo IIa 表达可以作为 ER 阳性、HER2 阴性乳腺癌的增殖标志物和预后因素。

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