Multitargeting Prodrugs that Release Oxaliplatin, Doxorubicin and Gemcitabine are Potent Inhibitors of Tumor Growth and Effective Inducers of Immunogenic Cell Death

Author:

Sarkar Amrita1ORCID,Novohradsky Vojtech2ORCID,Maji Moumita1ORCID,Babu Tomer1ORCID,Markova Lenka2ORCID,Kostrhunova Hana2ORCID,Kasparkova Jana23ORCID,Gandin Valentina4ORCID,Brabec Viktor2ORCID,Gibson Dan1ORCID

Affiliation:

1. Institute for Drug Research School of Pharmacy The Hebrew University of Jerusalem Jerusalem 9112102 Israel

2. Czech Academy of Sciences Institute of Biophysics Kralovopolska 135 61200 Brno Czech Republic

3. Department of Biophysics Palacky University Slechtitelu 27 783 71 Olomouc Czech Republic

4. Dipartimento di Scienze del Farmaco Universita di Padova 35131 Padova Italy

Abstract

AbstractA multitargeting prodrug (2) that releases gemcitabine, oxaliplatin, and doxorubicin in their active form in cancer cells is a potent cytotoxic agent with nM IC50s; it is highly selective to cancer cells with mean selectivity indices to human (136) and murine (320) cancer cells. It effectively induces release of DAMPs (CALR, ATP & HMGB1) in CT26 cells facilitating more efficient phagocytosis by J774 macrophages than the FDA drugs or their co‐administration. The viability of CT26 cells co‐cultured with J774 macrophages and treated with 2 was reduced by 32 % compared to the non‐treated cells, suggesting a synergistic antiproliferative effect between the chemical and immune reactions. 2 inhibited in vivo tumor growth in two murine models (LLC and CT26) better than the FDA drugs or their co‐administration with significantly lower body weight loss. Mice inoculated with CT26 cells treated with 2 showed slightly better tumor free survival than doxorubicin.

Funder

Israel Science Foundation

Grantová Agentura České Republiky

Publisher

Wiley

Subject

General Chemistry,Catalysis

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