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首页> 外文期刊>Molecular cancer therapeutics >The Discovery and Preclinical Development of ASG-5ME, an Antibody-Drug Conjugate Targeting SLC44A4-Positive Epithelial Tumors Including Pancreatic and Prostate Cancer
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The Discovery and Preclinical Development of ASG-5ME, an Antibody-Drug Conjugate Targeting SLC44A4-Positive Epithelial Tumors Including Pancreatic and Prostate Cancer

机译:ASG-5ME的发现和临床前开发,ASG-5ME是靶向药物(包括胰腺癌和前列腺癌)的SLC44A4阳性上皮肿瘤的药物-缀合物

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摘要

Here, we report the development of an antibody-drug conjugate, ASG-5ME, which targets the solute carrier receptor SLC44A4. SLC44A4 is a member of a family of putative choline transporters that we show to be markedly upregulated in a variety of epithelial tumors, most notably prostate and pancreatic cancer. SLC44A4 is normally expressed on the apical surface of secretory epithelial cells, but in cancer we show expression is not restricted to the luminal surface in advanced and undifferentiated tumors. ASG-5ME consists of a human IgG2 anti-SLC44A4 antibody conjugated through a cleavable linker to the microtubule-disrupting agent monomethylauristatin E. It has potent antitumor activity in both cell line-and patient-derived xenograft models of pancreatic and prostate cancers. Combination studies with ASG5-ME and nab-paclitaxel demonstrated combination effect in both pancreatic and prostate tumor models. Altogether, the data presented here suggest that ASG-5ME may have the potential to offer a new therapeutic option for the treatment of pancreatic and prostate cancers. (C) 2016 AACR.
机译:在这里,我们报告了靶向溶质载体受体SLC44A4的抗体-药物偶联物ASG-5ME的开发。 SLC44A4是假定的胆碱转运蛋白家族的成员,我们发现它在多种上皮肿瘤(尤其是前列腺癌和胰腺癌)中显着上调。 SLC44A4通常在分泌性上皮细胞的顶端表面表达,但在癌症中,我们显示表达不限于晚期和未分化肿瘤的腔表面。 ASG-5ME由人IgG2抗SLC44A4抗体组成,该抗体通过可裂解的接头与微管破坏剂monomethylauristatin E偶联。它在胰腺癌和前列腺癌的细胞系和患者来源异种移植模型中均具有有效的抗肿瘤活性。与ASG5-ME和nab-紫杉醇的联合研究证明了在胰腺和前列腺肿瘤模型中的联合作用。总体而言,此处提供的数据表明,ASG-5ME可能具有为胰腺癌和前列腺癌的治疗提供新的治疗选择的潜力。 (C)2016 AACR。

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