J 2022

Disulfiram increases the efficacy of 5-fluorouracil in organotypic cultures of colorectal carcinoma

HENDRYCH, Michal; Kamila ŘÍHOVÁ; Barbora ADAMOVÁ; Vojtěch HRADIL; Marek STIBOREK et al.

Basic information

Original name

Disulfiram increases the efficacy of 5-fluorouracil in organotypic cultures of colorectal carcinoma

Authors

HENDRYCH, Michal; Kamila ŘÍHOVÁ; Barbora ADAMOVÁ; Vojtěch HRADIL; Marek STIBOREK; Petr VLČEK; Markéta HERMANOVÁ; Jana VAŠÍČKOVÁ; Petr BENEŠ; Jan ŠMARDA; Viktor KANICKÝ; Jan PREISLER and Jarmila NAVRÁTILOVÁ

Edition

PHARMACOTHERAPY, Paris, ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER, 2022, 0753-3322

Other information

Language

English

Type of outcome

Article in a journal

Country of publisher

France

Confidentiality degree

is not subject to a state or trade secret

References:

Marked to be transferred to RIV

Yes

RIV identification code

RIV/00216224:14310/22:00127468

Organization

Přírodovědecká fakulta – Repository – Repository

EID Scopus

Keywords in English

Disulfiram/copper; 5-fluorouracil; Synergism; Organotypic culture; Spheroid; Colorectal carcinoma

Links

GA18-16583S, research and development project. LX22NPO5102, research and development project. MUNI/A/1325/2021, interní kód Repo. MUNI/A/1408/2021, interní kód Repo.
Changed: 29/2/2024 04:00, RNDr. Daniel Jakubík

Abstract

In the original language

Drug efficacy determined in preclinical research is difficult to transfer to clinical practice. This is mainly due to the use of oversimplified models omitting the effect of the tumor microenvironment and the presence of various cell types participating in the formation of tumors in vivo. In this study, we used robust three-dimensional models including spheroids grown from colon cancer cell lines and organotypic cultures prepared from the colorectal carcinoma tissue to test novel therapeutic strategies. We developed a multi-modal approach combining bright-field and fluorescence microscopy for evaluating drug effects on organotypic cultures. Combined treatment with 5-fluorouracil and disulfiram/copper efficiently eliminated cancer cells in these 3D models. Moreover, disulfiram/copper down-regulated the expression of markers associated with 5-fluorouracil resistance, such as thymidylate synthase and CD133/CD44. Thus, we propose combined therapy of 5-fluorouracil and disulfiram/copper for further testing as a treatment for colorectal carcinoma. In addition, we show that organotypic cultures are suitable models for anti-cancer drug testing.

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