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ASG-15ME的研发,一种靶向新型尿路上皮癌生物标志物SLITRK6的抗体药物偶联物。

Development of ASG-15ME, a Novel Antibody-Drug Conjugate Targeting SLITRK6, a New Urothelial Cancer Biomarker.

作者信息

Morrison Kendall, Challita-Eid Pia M, Raitano Arthur, An Zili, Yang Peng, Abad Joseph D, Liu Wendy, Lortie Dawn Ratay, Snyder Josh T, Capo Linnette, Verlinsky Alla, Aviña Hector, Doñate Fernando, Joseph Ingrid B J, Pereira Daniel S, Morrison Karen, Stover David R

机构信息

Agensys Inc., Santa Monica, California.

出版信息

Mol Cancer Ther. 2016 Jun;15(6):1301-10. doi: 10.1158/1535-7163.MCT-15-0570. Epub 2016 Mar 4.

Abstract

SLITRK6 is a member of the SLITRK family of neuronal transmembrane proteins that was discovered as a bladder tumor antigen using suppressive subtractive hybridization. Extensive immunohistochemistry showed SLITRK6 to be expressed in multiple epithelial tumors, including bladder, lung, and breast cancer as well as in glioblastoma. To explore the possibility of using SLITRK6 as a target for an antibody-drug conjugate (ADC), we generated a panel of fully human mAbs specific for SLITRK6. ADCs showed potent in vitro and in vivo cytotoxic activity after conjugation to Monomethyl Auristatin E or Monomethyl Auristatin F. The most potent ADC, ASG-15ME, was selected as the development candidate and given the product name AGS15E. ASG-15ME is currently in phase I clinical trials for the treatment of metastatic urothelial cancer. This is the first report that SLITRK6 is a novel antigen in bladder cancer and also the first report of the development of ASG-15ME for the treatment of metastatic bladder cancer. Mol Cancer Ther; 15(6); 1301-10. ©2016 AACR.

摘要

SLITRK6是神经元跨膜蛋白SLITRK家族的成员,它是通过抑制性消减杂交作为膀胱肿瘤抗原被发现的。广泛的免疫组化显示SLITRK6在多种上皮肿瘤中表达,包括膀胱癌、肺癌和乳腺癌以及胶质母细胞瘤。为了探索将SLITRK6用作抗体药物偶联物(ADC)靶点的可能性,我们制备了一组对SLITRK6具有特异性的全人单克隆抗体。与单甲基奥瑞他汀E或单甲基奥瑞他汀F偶联后,ADC显示出强大的体外和体内细胞毒性活性。最有效的ADC,ASG-15ME,被选为开发候选药物并赋予产品名称AGS15E。ASG-15ME目前正处于治疗转移性尿路上皮癌的I期临床试验中。这是关于SLITRK6是膀胱癌新抗原的首次报道,也是关于ASG-15ME用于治疗转移性膀胱癌开发的首次报道。《分子癌症治疗》;15(6);1301 - 1310。©2016美国癌症研究协会。

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