A versatile technique for the in vivo imaging of human tumor xenografts using near-infrared fluorochrome-conjugated macromolecule probes

• Published in: PloS one Vol. 8; no. 12; p. e82708
• Main Authors: Suemizu, Hiroshi, Kawai, Kenji, Higuchi, Yuichiro, Hashimoto, Haruo, Ogura, Tomoyuki, Itoh, Toshio, Sasaki, Erika, Nakamura, Masato
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 17.12.2013; Public Library of Science (PLoS)
• Subjects: Albumin; Animal models; Animals; Antigens; Biology; Biomedical research; Bovine serum albumin; Cancer; Cancer metastasis; Cancer therapies; Carcinoma, Non-Small-Cell Lung - diagnosis; Carcinoma, Non-Small-Cell Lung - pathology; Cell Line, Tumor; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - diagnosis; Colorectal Neoplasms - pathology; Fluorescence; Fluorescent Dyes; Genetic modification; Genetically modified organisms; Glycine; HCT116 Cells; Heterografts; Histocompatibility antigen HLA; HLA antigens; Humans; I.R. radiation; Image processing; Imaging; Immunoglobulin G; Immunoglobulins; In vivo methods and tests; Injection; Ionizing radiation; Laboratories; Leukocytes; Liver; Liver cancer; Localization; Lung cancer; Lung diseases; Medical prognosis; Medicine; Metastases; Metastasis; Methods; Molecular Imaging - methods; Monoclonal antibodies; Neoplasm Metastasis; Neoplasm Transplantation; Neoplasms - diagnosis; Neoplasms - pathology; Non-small cell lung cancer; Non-small cell lung carcinoma; Pancreatic cancer; Pancreatic islet transplantation; Pathology; Permeability; Probes; Proteins; Red fluorescent protein; Serum albumin; Spectroscopy, Near-Infrared - methods; Transplantation; Tumors; Xenografts; Xenotransplantation; United States > US; Japan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0082708

Here, we present a versatile method for detecting human tumor xenografts in vivo, based on the enhanced permeability and retention (EPR) effect, using near-infrared (NIR) fluorochrome-conjugated macromolecule probes. Bovine serum albumin (BSA) and two immunoglobulins-an anti-human leukocyte antigen (HLA) monoclonal antibody and isotype control IgG2a-were labeled with XenoLight CF770 fluorochrome and used as NIR-conjugated macromolecule probes to study whole-body imaging in a variety of xenotransplantation mouse models. NIR fluorescent signals were observed in subcutaneously transplanted BxPC-3 (human pancreatic cancer) cells and HCT 116 (colorectal cancer) cells within 24 h of NIR-macromolecule probe injection, but the signal from the fluorochrome itself or from the NIR-conjugated small molecule (glycine) injection was not observed. The accuracy of tumor targeting was confirmed by the localization of the NIR-conjugated immunoglobulin within the T-HCT 116 xenograft (in which the orange-red fluorescent protein tdTomato was stably expressed by HCT 116 cells) in the subcutaneous transplantation model. However, there was no significant difference in the NIR signal intensity of the region of interest between the anti-HLA antibody group and the isotype control group in the subcutaneous transplantation model. Therefore, the antibody accumulation within the tumor in vivo is based on the EPR effect. The liver metastasis generated by an intrasplenic injection of T-HCT 116 cells was clearly visualized by the NIR-conjugated anti-HLA probe but not by the orange-red fluorescent signal derived from the tdTomato reporter. This result demonstrated the superiority of the NIR probes over the tdTomato reporter protein at enhancing tissue penetration. In another xenograft model, patient-derived xenografts (PDX) of LC11-JCK (human non-small cell lung cancer) were successfully visualized using the NIR-conjugated macromolecule probe without any genetic modification. These results suggested that NIR-conjugated macromolecule, preferably, anti-HLA antibody probe is a valuable tool for the detection of human tumors in experimental metastasis models using whole-body imaging.