| Literature DB >> 27550944 |
Michael Mattie1, Arthur Raitano2, Kendall Morrison2, Karen Morrison2, Zili An2, Linnette Capo2, Alla Verlinsky2, Monica Leavitt2, Jimmy Ou2, Rossana Nadell2, Hector Aviña2, Claudia Guevara2, Faisal Malik2, Ruth Moser3, Steven Duniho3, Jeffrey Coleman2, Ying Li2, Daniel S Pereira2, Fernando Doñate2, Ingrid B J Joseph2, Pia Challita-Eid2, Dennis Benjamin3, David R Stover2.
Abstract
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 ASG-5ME 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. Mol Cancer Ther; 15(11); 2679-87. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27550944 DOI: 10.1158/1535-7163.MCT-16-0225
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261