In silico and in vitro investigation of anticancer effect of novel anthraquinone compound on MDA-MB-231 cells

The serious adverse effects of chemotherapeutics forced to produce new bioactive substances such as anthraquinone derivatives. This study focuses on evaluating the antiproliferative effects of a newly developed anthraquinone compound, referred to as Compound 3, against MDA-MB-231 breast cancer cells. To assess the pharmacokinetic properties of Compound 3, an in silico ADME (absorption, distribution, metabolism, and excretion) evaluation was carried out. To investigate its binding behavior with cancer-relevant proteins, molecular docking simulations and interaction analyses were performed. For assessing its antitumor activity, a series of biological assays were applied. Cell viability was determined using the MTT assay, while intracellular ROS levels were quantified with the DCFH-DA probe. Apoptotic cell death was evaluated through Annexin V/PI staining, and cell motility was studied via wound healing assays. In addition, alterations in cytoskeletal architecture were analyzed using immunofluorescence microscopy. Compound 3 exhibited stronger binding affinities (indicated by lower docking energy values) compared to reference compounds for several targets, including PCNA, CK2, LC3, and MMP2. The in vitro analysis revealed a significant selective inhibitory effect on cellular proliferation along with a marked increase in intracellular ROS levels. Apoptosis was induced by certain doses of Compound 3. Additionally, treatment resulted in decreased migratory behavior and visible disruption of actin cytoskeleton organization. The overall findings emphasize the diverse biological effects of Compound 3 on breast cancer cells, revealing promising therapeutic mechanisms for further development as a compelling candidate of an anticancer agent. Investigating the potential of a new anthraquinone derivative, Compound 3, as an anticancer agent. In silico analysis hints at promising interactions with key cancer proteins. In vitro, Compound 3 inhibits proliferation, boost ROS, induce apoptosis, and alters cell morphology.

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Publication Details

Journal
Letters in Drug Design & Discovery
Published
2025-05-01
DOI
https://doi.org/10.1016/j.lddd.2025.100052
Citations
2
Primary Topic
Phytochemistry and biological activity of medicinal plants
Type
article
Field-Weighted Citation Impact
3.50

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article

In silico and in vitro investigation of anticancer effect of novel anthraquinone compound on MDA-MB-231 cells

Ahmet Mesut Şentürk, Varol Güler, Necla Bektaş, Funda Özkök et al.
2 citations
Letters in Drug Design & Discovery
Phytochemistry and biological activity of medicinal plants
3.50
article

In silico and in vitro investigation of anticancer effect of novel anthraquinone compound on MDA-MB-231 cells

Ahmet Mesut Şentürk, Varol Güler, Necla Bektaş, Funda Özkök, Nihal Onul, Bilge Özerman Edis, Esra Sert, Sacide Pehlıvan, Başak Günçer
article en
2 citations

Abstract

The serious adverse effects of chemotherapeutics forced to produce new bioactive substances such as anthraquinone derivatives. This study focuses on evaluating the antiproliferative effects of a newly developed anthraquinone compound, referred to as Compound 3, against MDA-MB-231 breast cancer cells. To assess the pharmacokinetic properties of Compound 3, an in silico ADME (absorption, distribution, metabolism, and excretion) evaluation was carried out. To investigate its binding behavior with cancer-relevant proteins, molecular docking simulations and interaction analyses were performed. For assessing its antitumor activity, a series of biological assays were applied. Cell viability was determined using the MTT assay, while intracellular ROS levels were quantified with the DCFH-DA probe. Apoptotic cell death was evaluated through Annexin V/PI staining, and cell motility was studied via wound healing assays. In addition, alterations in cytoskeletal architecture were analyzed using immunofluorescence microscopy. Compound 3 exhibited stronger binding affinities (indicated by lower docking energy values) compared to reference compounds for several targets, including PCNA, CK2, LC3, and MMP2. The in vitro analysis revealed a significant selective inhibitory effect on cellular proliferation along with a marked increase in intracellular ROS levels. Apoptosis was induced by certain doses of Compound 3. Additionally, treatment resulted in decreased migratory behavior and visible disruption of actin cytoskeleton organization. The overall findings emphasize the diverse biological effects of Compound 3 on breast cancer cells, revealing promising therapeutic mechanisms for further development as a compelling candidate of an anticancer agent. Investigating the potential of a new anthraquinone derivative, Compound 3, as an anticancer agent. In silico analysis hints at promising interactions with key cancer proteins. In vitro, Compound 3 inhibits proliferation, boost ROS, induce apoptosis, and alters cell morphology.

Letters in Drug Design & DiscoveryVol. 22(5)
Istanbul Yeni Yüzyıl University (TR), Biruni University (TR), Istanbul University-Cerrahpaşa (TR), Istanbul Technical University (TR), Istanbul University (TR)
Istanbul Üniversitesi, Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi
Openalex Percentile: Top 8%
Phytochemistry and biological activity of medicinal plants
3.50
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