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Turkish Journal of Biology

Abstract

Background/aim: High-grade serous ovarian cancer (HGSOC) remains one of the most aggressive forms of ovarian malignancy and frequently shows resistance to conventional therapies. This study aimed to synthesize a novel series of purine analogues, 6-[(4-substituted benzyl amine)/(4-substituted aniline)]-9-cyclopentyl purines, and evaluate their anticancer efficacy against HGSOC cell lines.

Materials and methods: We assessed the biological effects of the synthesized purine analogues on the OVCAR3, OVSAHO, and KURAMOCHI HGSOC cell lines using the sulforhodamine B assay. To investigate the mechanism of action, we conducted flow cytometry and western blot analyses, focusing on DNA replication and apoptosis.

Results: Among the tested compounds, compound 8 showed significant cytotoxic activity with IC50 values in the low micromolar range. Preliminary data from flow cytometry and western blot analyses indicated that compound 8 may inhibit DNA replication and induce apoptosis, as reflected by changes in cell viability and cell-cycle progression.

Conclusion: Compound 8 may disrupt key proliferative mechanisms in cancer cells by interfering with DNA synthesis and activating programmed cell death pathways. These findings suggest that compound 8 is a promising lead candidate for further development in ovarian cancer therapeutics.

Author ORCID Identifier

DUYGU ALTIPARMAK: 0009-0003-4130-8597

DEREN DEMİREL YAVUZ: 0009-0000-4705-9294

PINAR KUL KARADENİZLİ: 0000-0003-3639-0496

İREM DURMAZ ŞAHİN: 0000-0001-5037-7883

MERAL TUNÇBİLEK: 0000-0002-7410-0202

DOI

10.55730/1300-0152.2788

Keywords

Cytotoxicity, high-grade serous ovarian cancer, apoptosis, cell-cycle arrest, synthesis, purine analogues

First Page

29

Last Page

36

Publisher

The Scientific and Technological Research Council of Türkiye (TÜBİTAK)

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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