首页> 外文期刊>International journal of oncology >Triple-negative breast cancers express receptors for luteinizing hormone-releasing hormone (LHRH) and respond to LHRH antagonist Cetrorelix with growth inhibition
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Triple-negative breast cancers express receptors for luteinizing hormone-releasing hormone (LHRH) and respond to LHRH antagonist Cetrorelix with growth inhibition

机译:三阴性乳腺癌表达促黄体生成激素释放激素(LHRH)的受体,并对LHRH拮抗剂Cetrorelix产生生长抑制反应

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The aim of the present study was to evaluate the expression of receptors for luteinizing hormone-releasing hormone (LHRH) in human specimens of triple-negative breast cancers (TNBC). In addition, we used in vitro and in vivo models of TNBC to investigate if these receptors are suitable targets for the treatment with the LHRH antagonist Cetrorelix. Receptors for LHRH were expressed in all tumor samples and in the TNBC cell lines HCC1806 and HCC1937. The proliferation of both TNBC cell lines was significantly inhibited in vitro by 1 μM Cetrorelix. Injections of 3 mg Cetrorelix on day 1 and 21 resulted in a significant growth inhibition of HCC1806 tumors xenografted into nude mice. Tumors of mice treated with Cetrorelix expressed less mRNA for EGFR and HER3 receptors than untreated tumors. After treatment of cells with Cetrorelix a flow cytometric analysis of the cell cycle revealed a decrease in S-phase. Given the low toxicity and clinical availability of Cetrorelix, this peptide antagonist should be considered for phase II studies in patients with advanced TNBC.
机译:本研究的目的是评估三阴性乳腺癌(TNBC)人标本中促黄体生成激素释放激素(LHRH)的受体的表达。此外,我们使用了TNBC的体外和体内模型来研究这些受体是否适合用LHRH拮抗剂Cetrorelix治疗。 LHRH的受体在所有肿瘤样品以及TNBC细胞HCC1806和HCC1937中都有表达。 1μMCetrorelix在体外显着抑制了两种TNBC细胞系的增殖。在第1天和第21天注射3 mg Cetrorelix会显着抑制异种移植到裸鼠体内的HCC1806肿瘤的生长。用Cetrorelix治疗的小鼠的肿瘤表达的EGFR和HER3受体mRNA低于未治疗的肿瘤。用Cetrorelix处理细胞后,细胞周期的流式细胞仪分析显示S期减少。鉴于Cetrorelix的低毒性和临床可用性,对于晚期TNBC患者,应考虑将该肽拮抗剂用于II期研究。

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