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组织激肽释放酶相关肽酶4(KLK4),一种三阴性乳腺癌中的新型生物标志物。

Tissue kallikrein-related peptidase 4 (KLK4), a novel biomarker in triple-negative breast cancer.

作者信息

Yang Feng, Aubele Michaela, Walch Axel, Gross Eva, Napieralski Rudolf, Zhao Shuo, Ahmed Nancy, Kiechle Marion, Reuning Ute, Dorn Julia, Sweep Fred, Magdolen Viktor, Schmitt Manfred

出版信息

Biol Chem. 2017 Sep 26;398(10):1151-1164. doi: 10.1515/hsz-2017-0122.

Abstract

Triple-negative breast cancer (TNBC), lacking the steroid hormone receptors ER and PR and the oncoprotein HER2, is characterized by its aggressive pattern and insensitivity to endocrine and HER2-directed therapy. Human kallikrein-related peptidases KLK1-15 provide a rich source of serine protease-type biomarkers associated with tumor growth and cancer progression for a variety of malignant diseases. In this study, recombinant KLK4 protein was generated and affinity-purified KLK4-directed polyclonal antibody pAb587 established to allow localization of KLK4 protein expression in tumor cell lines and archived formalin-fixed, paraffin-embedded TNBC tumor tissue specimens. For this, KLK4 protein expression was assessed by immunohistochemistry in primary tumor tissue sections (tissue microarrays) of 188 TNBC patients, mainly treated with anthracycline- or CMF-based polychemotherapy. KLK4 protein is localized in the cytoplasm of tumor and stroma cells. In this patient cohort, elevated stroma cell KLK4 expression, but not tumor cell KLK4 expression, is predictive for poor disease-free survival by univariate analysis (hazard ratio: 2.26, p=0.001) and multivariable analysis (hazard ratio: 2.12, p<0.01). Likewise, univariate analysis revealed a trend for statistical significance of elevated KLK4 stroma cell expression for overall survival of TNBC patients as well.

摘要

三阴性乳腺癌(TNBC)缺乏类固醇激素受体ER和PR以及癌蛋白HER2,其特点是侵袭性强,对内分泌治疗和HER2靶向治疗不敏感。人激肽释放酶相关肽酶KLK1 - 15为多种恶性疾病提供了丰富的丝氨酸蛋白酶类生物标志物来源,这些标志物与肿瘤生长和癌症进展相关。在本研究中,制备了重组KLK4蛋白并建立了亲和纯化的KLK4定向多克隆抗体pAb587,以确定KLK4蛋白在肿瘤细胞系以及存档的福尔马林固定、石蜡包埋的TNBC肿瘤组织标本中的表达定位。为此,通过免疫组织化学方法评估了188例主要接受基于蒽环类或CMF的多药化疗的TNBC患者原发肿瘤组织切片(组织芯片)中的KLK4蛋白表达。KLK4蛋白定位于肿瘤细胞和基质细胞的细胞质中。在该患者队列中,单因素分析(风险比:2.26,p = 0.001)和多因素分析(风险比:2.12,p < 0.01)显示,基质细胞KLK4表达升高而非肿瘤细胞KLK4表达升高可预测无病生存期较差。同样,单因素分析也显示,TNBC患者总体生存中KLK4基质细胞表达升高也有统计学意义的趋势。

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