Specific Targeting and Labeling of Colonic Polyps in CPC-APC Mice with Mucin 5AC Fluorescent Antibodies: A Model for Detection of Early Colon Cancer

Author:

Turner Michael A.12ORCID,Cox Kristin E.12ORCID,Liu Shanglei1ORCID,Neel Nicholas12,Amirfakhri Siamak12,Nishino Hiroto12,Hosseini Mojgan3,Alcantara Joshua A.4,Abd El-Hafeez Amer Ali4,Lwin Thinzar M.5ORCID,Mallya Kavita6ORCID,Pisegna Joseph R.7,Singh Satish K.89ORCID,Ghosh Pradipta410,Hoffman Robert M.1211,Batra Surinder K.6ORCID,Bouvet Michael12ORCID

Affiliation:

1. Division of Surgical Oncology, Department of Surgery, University of California San Diego, La Jolla, CA 92037, USA

2. Department of Surgery, VA San Diego Healthcare System, La Jolla, CA 92161, USA

3. Department of Pathology, University of California San Diego, La Jolla, CA 92037, USA

4. Department of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA 92037, USA

5. Department of Surgical Oncology, City of Hope National Medical Center, Duarte, CA 91010, USA

6. Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198, USA

7. Department of Gastroenterology, VA Los Angeles Healthcare System, Los Angeles, CA 90073, USA

8. Medical Service, Section of Gastroenterology, VA Boston Healthcare System, Boston, MA 02130, USA

9. Department of Medicine, Section of Gastroenterology, Boston University School of Medicine, Boston, MA 02118, USA

10. Department of Medicine, University of California San Diego, La Jolla, CA 92037, USA

11. AntiCancer, Inc., San Diego, CA 92111, USA

Abstract

Poor visualization of polyps can limit colorectal cancer screening. Fluorescent antibodies to mucin5AC (MUC5AC), a glycoprotein upregulated in adenomas and colorectal cancer, could improve screening colonoscopy polyp detection rate. Adenomatous polyposis coli flox mice with a Cdx2-Cre transgene (CPC-APC) develop colonic polyps that contain both dysplastic and malignant tissue. Mice received MUC5AC-IR800 or IRdye800 as a control IV and were sacrificed after 48 h for near-infrared imaging of their colons. A polyp-to-background ratio (PBR) was calculated for each polyp by dividing the mean fluorescence intensity of the polyp by the mean fluorescence intensity of the background tissue. The mean 25 μg PBR was 1.70 (±0.56); the mean 50 μg PBR was 2.64 (±0.97); the mean 100 μg PBR was 3.32 (±1.33); and the mean 150 μg PBR was 3.38 (±0.87). The mean PBR of the dye-only control was 2.22 (±1.02), significantly less than the 150 μg arm (p-value 0.008). The present study demonstrates the ability of fluorescent anti-MUC5AC antibodies to specifically target and label colonic polyps containing high-grade dysplasia and intramucosal adenocarcinoma in CPC-APC mice. This technology can potentially improve the detection rate and decrease the miss rate of advanced colonic neoplasia and early cancer at colonoscopy.

Funder

VA Merit Review

National Institute of Health Training

NCATS

National Cancer Institute Cancer Center Support

Publisher

MDPI AG

Subject

Microbiology (medical),Molecular Biology,General Medicine,Microbiology

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