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c-Met抑制剂MSC2156119J有效抑制肝癌模型中的肿瘤生长。

The c-Met Inhibitor MSC2156119J Effectively Inhibits Tumor Growth in Liver Cancer Models.

作者信息

Bladt Friedhelm, Friese-Hamim Manja, Ihling Christian, Wilm Claudia, Blaukat Andree

机构信息

EMD Serono, and Merck Serono Research and Development, Merck KGaA, Darmstadt 64293, Germany.

出版信息

Cancers (Basel). 2014 Aug 19;6(3):1736-52. doi: 10.3390/cancers6031736.

Abstract

The mesenchymal-epithelial transition factor (c-Met) is a receptor tyrosine kinase with hepatocyte growth factor (HGF) as its only high-affinity ligand. Aberrant activation of c-Met is associated with many human malignancies, including hepatocellular carcinoma (HCC). We investigated the in vivo antitumor and antimetastatic efficacy of the c-Met inhibitor MSC2156119J (EMD 1214063) in patient-derived tumor explants. BALB/c nude mice were inoculated with MHCC97H cells or with tumor fragments of 10 patient-derived primary liver cancer explants selected according to c-Met/HGF expression levels. MSC2156119J (10, 30, and 100 mg/kg) and sorafenib (50 mg/kg) were administered orally as single-agent treatment or in combination, with vehicle as control. Tumor response, metastases formation, and alpha fetoprotein (AFP) levels were measured. MSC2156119J inhibited tumor growth and induced complete regression in mice bearing subcutaneous and orthotopic MHCC97H tumors. AFP levels were undetectable after 5 weeks of MSC2156119J treatment, and the number of metastatic lung foci was reduced. Primary liver explant models with strong c-Met/HGF activation showed increased responsiveness to MSC2156119J, with MSC2156119J showing similar or superior activity to sorafenib. Tumors characterized by low c-Met expression were less sensitive to MSC2156119J. MSC2156119J was better tolerated than sorafenib, and combination therapy did not improve efficacy. These findings indicate that selective c-Met/HGF inhibition with MSC2156119J is associated with marked regression of c-Met high-expressing tumors, supporting its clinical development as an antitumor treatment for HCC patients with active c-Met signaling.

摘要

间充质上皮转化因子(c-Met)是一种受体酪氨酸激酶,肝细胞生长因子(HGF)是其唯一的高亲和力配体。c-Met的异常激活与许多人类恶性肿瘤相关,包括肝细胞癌(HCC)。我们研究了c-Met抑制剂MSC2156119J(EMD 1214063)在患者来源的肿瘤外植体中的体内抗肿瘤和抗转移疗效。将BALB/c裸鼠接种MHCC97H细胞或根据c-Met/HGF表达水平选择的10个患者来源的原发性肝癌外植体的肿瘤片段。MSC2156119J(10、30和100mg/kg)和索拉非尼(50mg/kg)作为单药治疗或联合给药,以溶媒作为对照。测量肿瘤反应、转移形成和甲胎蛋白(AFP)水平。MSC2156119J抑制了皮下和原位MHCC97H肿瘤小鼠的肿瘤生长并诱导了完全消退。MSC2156119J治疗5周后AFP水平检测不到,肺转移灶数量减少。c-Met/HGF激活强烈的原发性肝外植体模型对MSC2156119J的反应性增加,MSC2156119J显示出与索拉非尼相似或更好的活性。以c-Met低表达为特征的肿瘤对MSC2156119J不太敏感。MSC2156119J的耐受性优于索拉非尼,联合治疗并未提高疗效。这些发现表明,用MSC2156119J选择性抑制c-Met/HGF与c-Met高表达肿瘤的显著消退相关,支持其作为具有活跃c-Met信号的HCC患者的抗肿瘤治疗药物进行临床开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5357/4190565/fa4973331cab/cancers-06-01736-g001.jpg

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