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首页> 外文期刊>Gynecologic Oncology: An International Journal >Immunohistochemical expression of Annexin A2 and S100A proteins in patients with bulky stage IB-IIA cervical cancer treated with neoadjuvant chemotherapy
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Immunohistochemical expression of Annexin A2 and S100A proteins in patients with bulky stage IB-IIA cervical cancer treated with neoadjuvant chemotherapy

机译:新辅助化学疗法治疗大块IB-IIA期宫颈癌患者Annexin A2和S100A蛋白的免疫组织化学表达

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Objective: Abnormal expression of Annexin A2 and S100A proteins has been reported to induce sensitivity/resistance to chemotherapy in a variety of cancers. The aim of this study was to evaluate the significance of Annexin A2 and S100A protein expression to predict response to neoadjuvant chemotherapy and prognostic significance of these protein expressions in bulky stage IB-IIA cervical cancer patients. Methods: Paired tumor samples (pre- and post-chemotherapy) were obtained from 68 patients who were treated with cisplatin-based neoadjuvant chemotherapy and radical hysterectomy at our hospital from 2006 to 2011. The expression of Annexin A2 and S100A proteins was analyzed by immunohistochemistry. Results: Thirty-six patients were identified as chemotherapy-response and 32 were non-response. (a). Protein expression in tumor cells: (1). Exposure of tumor cells to chemotherapy results in a change of Annexin A2 and S100A expression (P < 0.05). (2). Annexin A2, S100A8 and S100A9 protein expression correlates with tumor response to chemotherapy (P < 0.05). (b). Protein expression in stromal cells: (1). Expression of Annexin A2, S100A8 and S100A9 was increased, but S100A2 and S100A4 was decreased after exposure to chemotherapy (P < 0.05). (2). Only S100A4 expression was associated with response to chemotherapy (P < 0.05). Multivariate analysis revealed that tumor size (P = 0.022), differentiation (P = 0.000), Annexin A2 expression in stromal cells (P = 0.009), and S100A8 expression in tumor cells (P = 0.008) were independent prognostic factors for progression-free survival of cervical cancer patients. Conclusions: Expression of some of the measured proteins in tumor and stromal cells correlates with chemotherapy exposure, response to therapy, and progression-free survival.
机译:目的:据报道,膜联蛋白A2和S100A蛋白的异常表达可诱导多种癌症对化疗的敏感性/耐药性。这项研究的目的是评估膜联蛋白A2和S100A蛋白表达在预测新辅助化疗反应中的意义以及这些蛋白表达在IB-IIA子宫颈癌患者中的预后意义。方法:收集2006年至2011年在我院行顺铂新辅助化疗和根治性子宫切除术的68例患者的配对肿瘤样品(化疗前后)。采用免疫组织化学分析Annexin A2和S100A蛋白的表达。 。结果:36例患者被确认为化疗有反应,32例为无反应。 (一种)。肿瘤细胞中的蛋白质表达:(1)。肿瘤细胞暴露于化疗导致膜联蛋白A2和S100A表达的改变(P <0.05)。 (2)。 Annexin A2,S100A8和S100A9蛋白表达与肿瘤对化学疗法的反应相关(P <0.05)。 (b)。基质细胞中的蛋白质表达:(1)。暴露于化疗后,膜联蛋白A2,S100A8和S100A9的表达增加,但S100A2和S100A4的表达减少(P <0.05)。 (2)。仅S100A4表达与对化疗的反应相关(P <0.05)。多变量分析显示,肿瘤大小(P = 0.022),分化(P = 0.000),基质细胞中膜联蛋白A2表达(P = 0.009)和肿瘤细胞中S100A8表达(P = 0.008)是无进展的独立预后因素宫颈癌患者的生存率。结论:肿瘤和基质细胞中某些被测蛋白的表达与化疗暴露,对治疗的反应和无进展生存有关。

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