Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents

Our research group aimed for the optimization of pharmacologic ascorbate (Ph-Asc)-induced cancer cell death. To reduce the required time and resources needed for development, an in silico system biological approach, an already approved medication, and a mild bioactive compound were used in our previ...

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Main Authors: Dóra Varga, Anna Szentirmai, András Szarka
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Molecules
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Online Access:https://www.mdpi.com/1420-3049/30/5/1031
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author Dóra Varga
Anna Szentirmai
András Szarka
author_facet Dóra Varga
Anna Szentirmai
András Szarka
author_sort Dóra Varga
collection DOAJ
description Our research group aimed for the optimization of pharmacologic ascorbate (Ph-Asc)-induced cancer cell death. To reduce the required time and resources needed for development, an in silico system biological approach, an already approved medication, and a mild bioactive compound were used in our previous studies. It was revealed that both Ph-Asc and resveratrol (RES) caused DSBs in the DNA, and chloroquine (CQ) treatment amplified the cytotoxic effect of both Ph-Asc and RES in an autophagy independent way. In the present study, we aimed at the further clarification of the cytotoxic mechanism of Ph-Asc, CQ, and RES by comparing their DNA damaging abilities, effects on the cells’ bioenergetic status, ROS, and lipid ROS generation abilities with those of the three currently investigated compounds (menadione, RSL3, H<sub>2</sub>O<sub>2</sub>). It could be assessed that the induction of DSBs is certainly a common point of their mechanism of action; furthermore, the observed cancer cell death due to the investigated treatments are independent of the bioenergetic status. Contrary to other investigated compounds, the DNA damaging effect of CQ seemed to be ROS independent. Surprisingly, the well-known ferroptosis inducer RSL3 was unable to induce lipid peroxidation in the pancreas ductal adenocarcinoma (PDAC) Mia PaCa-2 cell line. At the same time, it induced DSBs in the DNA, and the RSL3-induced cell death could not be suspended by the well-known ferroptosis inhibitors. All these observations suggest the ferroptosis resistance of this cell line. The observed DNA damaging effect of RSL3 definitely creates a new perspective in anticancer research.
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spelling doaj-art-0bd7959fb0084452bcd4e0304584cbd52025-08-20T02:59:00ZengMDPI AGMolecules1420-30492025-02-01305103110.3390/molecules30051031Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer AgentsDóra Varga0Anna Szentirmai1András Szarka2Laboratory of Biochemistry and Molecular Biology, Department of Applied Biotechnology and Food Science, Budapest University of Technology and Economics, Szent Gellért tér 4, H-1111 Budapest, HungaryLaboratory of Biochemistry and Molecular Biology, Department of Applied Biotechnology and Food Science, Budapest University of Technology and Economics, Szent Gellért tér 4, H-1111 Budapest, HungaryLaboratory of Biochemistry and Molecular Biology, Department of Applied Biotechnology and Food Science, Budapest University of Technology and Economics, Szent Gellért tér 4, H-1111 Budapest, HungaryOur research group aimed for the optimization of pharmacologic ascorbate (Ph-Asc)-induced cancer cell death. To reduce the required time and resources needed for development, an in silico system biological approach, an already approved medication, and a mild bioactive compound were used in our previous studies. It was revealed that both Ph-Asc and resveratrol (RES) caused DSBs in the DNA, and chloroquine (CQ) treatment amplified the cytotoxic effect of both Ph-Asc and RES in an autophagy independent way. In the present study, we aimed at the further clarification of the cytotoxic mechanism of Ph-Asc, CQ, and RES by comparing their DNA damaging abilities, effects on the cells’ bioenergetic status, ROS, and lipid ROS generation abilities with those of the three currently investigated compounds (menadione, RSL3, H<sub>2</sub>O<sub>2</sub>). It could be assessed that the induction of DSBs is certainly a common point of their mechanism of action; furthermore, the observed cancer cell death due to the investigated treatments are independent of the bioenergetic status. Contrary to other investigated compounds, the DNA damaging effect of CQ seemed to be ROS independent. Surprisingly, the well-known ferroptosis inducer RSL3 was unable to induce lipid peroxidation in the pancreas ductal adenocarcinoma (PDAC) Mia PaCa-2 cell line. At the same time, it induced DSBs in the DNA, and the RSL3-induced cell death could not be suspended by the well-known ferroptosis inhibitors. All these observations suggest the ferroptosis resistance of this cell line. The observed DNA damaging effect of RSL3 definitely creates a new perspective in anticancer research.https://www.mdpi.com/1420-3049/30/5/1031reactive oxygen speciescell deathferroptosischloroquinepharmacologic ascorbateresveratrol
spellingShingle Dóra Varga
Anna Szentirmai
András Szarka
Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
Molecules
reactive oxygen species
cell death
ferroptosis
chloroquine
pharmacologic ascorbate
resveratrol
title Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
title_full Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
title_fullStr Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
title_full_unstemmed Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
title_short Research for a Common Thread: Insights into the Mechanisms of Six Potential Anticancer Agents
title_sort research for a common thread insights into the mechanisms of six potential anticancer agents
topic reactive oxygen species
cell death
ferroptosis
chloroquine
pharmacologic ascorbate
resveratrol
url https://www.mdpi.com/1420-3049/30/5/1031
work_keys_str_mv AT doravarga researchforacommonthreadinsightsintothemechanismsofsixpotentialanticanceragents
AT annaszentirmai researchforacommonthreadinsightsintothemechanismsofsixpotentialanticanceragents
AT andrasszarka researchforacommonthreadinsightsintothemechanismsofsixpotentialanticanceragents