Synthesis, Characterization and Apoptosis Capabilities of a Novel Naphthoquinone‐Derived Compound in Triple‐Negative Breast Cancer

Author:

Adacan Kaan1,Gokmen Zeliha2,Okan Akar Remzi13,Ozyıldız Zeynep2,Dinçer Hatice4,Karakaş Didem56,Ulukaya Engin13ORCID

Affiliation:

1. Istinye University Molecular Cancer Research Center (ISUMKAM) 34010 Istanbul Türkiye

2. Department of Chemistry, Faculty of Engineering Istanbul University-Cerrahpasa 34452 Istanbul Türkiye

3. Department of Clinical Biochemistry Faculty of Medicine Istinye University 34010 Istanbul Türkiye

4. Department of Cancer Biology and Pharmacology Health Sciences Institute Istinye University 34010 Istanbul Türkiye

5. Department of Molecular Biology and Genetics Faculty of Engineering and Natural Sciences Istinye University 34010 Istanbul Türkiye

6. Pancreatic Cancer Research Center Acibadem University 34755 Istanbul Türkiye

Abstract

AbstractBreast cancer is the most frequently diagnosed cancer in women and the second leading cause of cancer‐related deaths. Because triple‐negative breast cancer (TNBC) is highly resistant to clinically employed drugs, developing new drugs and treatment approaches is imperative. Naphthoquinone compounds potentially induce cancer cell death, and their clinical derivatives have been widely used as medicines. This study presents the synthesis and structure of a newly substituted naphthoquinone compound, as determined by spectroscopic techniques, then assesses the compound‘s ability to induce cell death on the MDA‐MB‐231 cell line using SRB viability testing, flow cytometry, and Western Blotting. The study also examines the compound‘s inhibition of cell migration through a scratch assay. The study discovered that the compound demonstrated an antigrowth/cytotoxic impact at concentrations of 3.12 μM and beyond. The cytotoxicity may have been caused by elevated reactive oxygen species, which resulted in DNA damage. The mode of cell death was apoptotic, confirmed by the translocation of phosphatidylserine, the activation of caspases, and the disruption of the mitochondrial membrane potential. The compound seems promising as a new anti‐malignant agent to be used for the treatment of breast cancer and deserves further attention for proof‐of‐concept in animal studies.

Publisher

Wiley

Subject

General Chemistry

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