Summary of ssbd-repos-000187

SSBD:database
URL

Name
ssbd-repos-000187 (187-Tsuboi-TumorDyn)
URL
DOI
-

Title
Fluorescence images of breast tumor-bearing mouse treated with or without Kadcyla for different time.
Description
-
Submited Date
-
Release Date
2022-11-23
Updated Date
-
License
Funding information
-
File formats
Data size
26.1 MB

Organism
Homo sapiens, Mus musculus
Strain
-
Cell Line
-
Genes
-
Proteins
-

GO Molecular Function (MF)
-
GO Biological Process (BP)
tumor suppressor
GO Cellular Component (CC)
-
Study Type
-
Imaging Methods
fluorescence microscopy

Method Summary
-
Related paper(s)

Setsuko Tsuboi, Takashi Jin (2020) Shortwave-infrared (SWIR) fluorescence molecular imaging using indocyanine green-antibody conjugates for the optical diagnostics of cancerous tumours., RSC advances, Volume 10, Number 47, pp. 28171-28179

Published in 2020 Jul 27 (Electronic publication in July 28, 2020, midnight )

(Abstract) Recently, shortwave-infrared (SWIR, 1000-1400 nm) fluorescence imaging has attracted much attention due to the higher contrast and sensitivity with deeper penetration depths compared to conventional visible and near-infrared (NIR) fluorescence imaging. For the SWIR fluorescence imaging, the development of fluorescent probes emitting over 1000 nm is necessary. So far, a variety of SWIR fluorescent probes based on single-walled carbon nanotubes, quantum dots, rare-metal doped nanomaterials, and organic dyes have been developed. However, there are a very limited number of biocompatible SWIR fluorescent probes, which can be used to biomedical applications. Among NIR and SWIR fluorescent probes, indocyanine green (ICG) is the only fluorescent dye approved by US Food and Drug Administration (FDA) for clinical use. Although ICG has a fluorescence maximum at a NIR region (ca. 830 nm), ICG emits in the SWIR region over 1000 nm. Here, we present ICG-based SWIR fluorescence molecular imaging for the highly-sensitive optical detection of breast and skin tumours in mice. As SWIR fluorescent molecular-imaging probes, we synthesized ICG-antibody conjugates, which prepared from anti-HER2 antibody (Herceptin), anti-EGFR antibody (Erbitux), anti-VEGFR-2 antibody (Cyramza), and anti-PD-L1 antibody (anti-PD-L1 ab). The present SWIR molecular imaging probes specifically accumulated to the breast and skin tumours, and their SWIR fluorescence images (>1000 nm) showed 1.5-2.0 times higher contrast than NIR tumour images taken at 830 nm. We show that the SWIR fluorescence imaging using ICG-antibody conjugates can be used for the elucidation of expression level of cancer-specific membrane proteins, HER2, EGFR, VEGFR-2, and PD-L1 in vivo. We also show that the SWIR fluorescence imaging enables quantitative analysis of the change in the size of tumour treated with an anti-cancer drug, Kadcyla. Our findings suggest that the SWIR fluorescence molecular imaging using ICG-antibody conjugates has potential to use for the optical diagnostics of cancerous tumors in medical and clinical fields.

Contact(s)
Takashi Jin
Organization(s)
RIKEN , Center for Biosystems Dynamics Research , Laboratory for Developmental Dynamics
Image Data Contributors
Quantitative Data Contributors

Download files
Download zipped files