# 64Cu2+ Complexes of Tripodal Amine Ligands’ In Vivo Tumor and Liver Uptakes and Intracellular Cu Distribution in the Extrahepatic Bile Duct Carcinoma Cell Line TFK-1: A Basic Comparative Study

**Authors:** Mitsuhiro Shinada, Masashi Takahashi, Chika Igarashi, Hiroki Matsumoto, Fukiko Hihara, Tomoko Tachibana, Masakazu Oikawa, Hisashi Suzuki, Ming-Rong Zhang, Tatsuya Higashi, Hiroaki Kurihara, Yukie Yoshii, Yoshihiro Doi

PMC · DOI: 10.3390/ph17070820 · 2024-06-21

## TL;DR

This study compares how different copper complexes affect tumor and liver uptake in a mouse model of bile duct cancer, aiming to improve cancer treatment.

## Contribution

The study introduces a comparative analysis of three tripodal amine ligands for 64Cu2+ complexes to enhance tumor targeting and reduce liver accumulation.

## Key findings

- 64Cu2+-Tren and 64Cu2+-Dien showed higher tumor uptake than 64Cu2+-TPMA and free 64Cu2+ ions.
- Liver uptake was inversely correlated with tumor uptake among the tested 64Cu2+ complexes.
- Micro-PIXE analysis confirmed that 64Cu2+-Tren delivered the highest nuclear uptake in vitro.

## Abstract

Copper (Cu) is a critical element for cancer cell proliferation and considerably accumulates in the nucleus. 64Cu2+ is an anticancer radiopharmaceutical that targets the copper requirement of cancer cells. However, intravenously injected 64Cu2+ ions primarily accumulate in the liver. Ligand complexation of 64Cu2+ may be a promising method for increasing tumor delivery by reducing liver uptake. In this study, we used three tripodal amine ligands [tris(2-aminoethyl)amine (Tren), diethylenetriamine (Dien), and tris(2-pyridylmethyl)amine (TPMA)] to enclose 64Cu2+ ions and compared their in vivo tumor and liver uptakes using a tumor-bearing xenograft mouse model of the extrahepatic bile duct carcinoma cell line TFK-1. We examined intracellular Cu distribution using microparticle-induced X-ray emission (micro-PIXE) analysis of these compounds. 64Cu2+-Tren and 64Cu2+-Dien showed higher tumor uptake than 64Cu2+-TPMA and 64Cu2+ ions in TFK-1 tumors. Among the three 64Cu2+ complexes and 64Cu2+ ions, liver uptake was inversely correlated with tumor uptake. Micro-PIXE analysis showed that in vitro cellular uptake was similar to in vivo tumor uptake, and nuclear delivery was the highest for 64Cu2+-Tren. Conclusively, an inverse correlation between tumor and liver uptake was observed using three 64Cu2+ complexes of tripodal amine ligands and 64Cu2+ ions. These results provide useful information for the future development of anticancer 64Cu radiopharmaceuticals.

## Linked entities

- **Chemicals:** Copper (PubChem CID 23978), 64Cu2+ (PubChem CID 71510780), tris(2-aminoethyl)amine (PubChem CID 77731), diethylenetriamine (PubChem CID 8111), tris(2-pyridylmethyl)amine (PubChem CID 379259)
- **Diseases:** extrahepatic bile duct carcinoma (MONDO:0003090)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** Extrahepatic Bile Duct Carcinoma (MESH:D001651), Tumor (MESH:D009369)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** TFK-1 — Homo sapiens (Human), Cholangiocarcinoma, Cancer cell line (CVCL_2214)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11280065/full.md

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Source: https://tomesphere.com/paper/PMC11280065