| Literature DB >> 32404409 |
Madeline T Olson1,2, Nicholas E Wojtynek1,2, Geoffrey A Talmon2,3, Thomas C Caffrey1,2, Prakash Radhakrishnan1,2,3,4, Quan P Ly2,5, Michael A Hollingsworth1,2,3,4, Aaron M Mohs6,4,7,8.
Abstract
Surgical resection is currently the only potentially curative option for patients with pancreatic cancer. However, the 5-year survival rate after resection is only 25%, due in part to high rates of R1 resections, in which cells are left behind at the surgical margin, resulting in disease recurrence. Fluorescence-guided surgery (FGS) has emerged as a method to reduce incomplete resections and improve intraoperative assessment of cancer. Mucin-16 (MUC16), a protein biomarker highly overexpressed in pancreatic cancer, is a potential target for FGS. In this study, we developed a fluorescent MUC16-targeted antibody probe, AR9.6-IRDye800, for image-guided resection of pancreatic cancer. We demonstrated the efficacy of this probe to bind human pancreatic cancer cell lines in vitro and in vivo In an orthotopic xenograft model, AR9.6-IRDye800 exhibited superior fluorescence enhancement of tumors and lower signal in critical background organs in comparison to a nonspecific IgG control. The results of this study suggest that AR9.6-IRDye800 has potential for success as a probe for FGS in pancreatic cancer patients, and MUC16 is a feasible target for intraoperative imaging. ©2020 American Association for Cancer Research.Entities:
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Year: 2020 PMID: 32404409 PMCID: PMC8009292 DOI: 10.1158/1535-7163.MCT-20-0033
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261