1994•Thermal Medicine(Japanese Journal of Hyperthermic Oncology)Open access

Hyperthermia Combined with Dipyridamole Enhance the Cytotoxicity of 5-Fluorouracil both in Vitro and in Vivo.

Sadaaki Inutsuka, Hideo Baba, Hideya Takeuchi, Yoshihisa Sakaguchi, Tetsuya Kusumoto, Yoshihiko Maehara, Keizō Sugimachi

Open full text 0 citations

Abstract

The combined effect of 5-FU, DP, and HT was investigated both in vitro and in vivo. When HeLa and B16 melanoma cells were exposed concomitantly ti heat (43' C, 40min) and DP (2.5 μg/ml), the cytotoxicity of 5-FU (0.1 μg/ml) was sugnificantly enhanced determined with colonergic assay. SDI test also revealed that this trimodality treatment was more cytotoxic to B16 melanoma cells and human cancer tissues than 5-FU alone.Growth of B16 melanoma that had been implanted subcutaneously was inhibited by DP (100mg/kg), and 5-FU (13.2mg/kg), when compared with 5-FU alone.Hyperthermia (HT) and dipyridamole (DP) augment the cytotoxicity of 5-fluorouracil (5-FU) in vitro and in vivo. The combination therapy of 5-FU, DP and HT is thought to be useful toward malignant diseases.

Open-access reader

About this research paper

What this paper is about

The combined effect of 5-FU, DP, and HT was investigated both in vitro and in vivo. When HeLa and B16 melanoma cells were exposed concomitantly ti heat (43' C, 40min) and DP (2.5 μg/ml), the cytotoxicity of 5-FU (0.1 μg/ml) was sugnificantly enhanced determined with colonergic assay. SDI test also revealed that this trimodality treatment was more cytotoxic to B16 melanoma cells and human cancer tissues than 5-FU alone.Growth of B16 melanoma that had been implanted subcutaneously was inhibited by DP (100mg/kg), and 5-FU (13.2mg/kg), when compared with 5-FU alone.Hyperthermia (HT) and dipyridamole (DP) augment the cytotoxicity of 5-fluorouracil (5-FU) in vitro and in vivo. The combination therapy of 5-FU, DP and HT is thought to be useful toward malignant diseases.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The combined effect of 5-FU, DP, and HT was investigated both in vitro and in vivo. When HeLa and B16 melanoma cells were exposed concomitantly ti heat (43' C, 40min) and DP (2.5 μg/ml), the cytotoxicity of 5-FU (0.1 μg/ml) was sugnificantly enhanced determined with colonergic assay. SDI test also revealed that this trimodality treatment was more cytotoxic to B16 melanoma cells and human cancer tissues than 5-FU alone.Growth of B16 melanoma that had been implanted subcutaneously was inhibited by DP (100mg/kg), and 5-FU (13.2mg/kg), when compared with 5-FU alone.Hyperthermia (HT) and dipyridamole (DP) augment the cytotoxicity of 5-fluorouracil (5-FU) in vitro and in vivo. The combination therapy of 5-FU, DP and HT is thought to be useful toward malignant diseases.

Key concepts: In vivo, Cytotoxicity, In vitro, Dipyridamole, Hyperthermia, HeLa, Melanoma, Pharmacology

Related papers

Back to paper searchBrowse research topicsOriginal source
Hyperthermia Combined with Dipyridamole Enhance the Cytotoxicity of 5-Fluorouracil both in Vitro and in Vivo. — Research Paper | ScholarLens