Evaluation of Anticancer and Cytotoxic Effects of Genistein on PC3 Prostate Cell Line under Three-Dimensional Culture Medium


Journal

Iranian biomedical journal
ISSN: 2008-823X
Titre abrégé: Iran Biomed J
Pays: Iran
ID NLM: 9814853

Informations de publication

Date de publication:
01 11 2022
Historique:
aheadofprint: 20 11 2022
entrez: 20 11 2022
pubmed: 21 11 2022
medline: 25 11 2022
Statut: epublish

Résumé

Prostate cancer is a major cause of disease and mortality among men. Genistein (GNT) is an isoflavone found naturally in legumes. Isoflavones, a subset of phytoestrogens, are structurally similar to mammalian estrogens. This study aimed to evaluate the anticancer and cytotoxic effects of GNT on PC3 cell line under three dimensional (3D) culture medium. The 3D culture was created by encapsulating the PC3 cells in alginate hydrogel. MTT assay, neutral red uptake, comet assay, and cytochrome C assay were used to study the anticancer and cytotoxic effects of GNT at 120, 240, and 480 μM concentrations. Also, nitric oxide (NO), catalase, and glutathione assay levels were determined to evaluate the effect of GNT on the cellular stress. The culture medium was used as the negative control. GNT reduced the production of cellular NO and increased the production of catalase and glutathione, confirming the results of the NO test. Evaluation of the toxicity effect of GNT at the concentrations of 120, 240, and 480 μM using comet assay showed that this chemical agent induces apoptosis in PC3 cells in a dose-dependent manner. As the level of cytochrome C in PC3 cells treated with different concentrations of GNT was not significantly different from that of the control, GNT could induce apoptosis in PC3 cells through the non-mitochondrial pathway. The findings of this study disclose that the anticancer effect of GNT on PC3 cells under 3D culture conditions could increase the effectiveness of treatment. Also, the cell survival rate is dependent on GNT concentration.

Sections du résumé

Background
Prostate cancer is a major cause of disease and mortality among men. Genistein (GNT) is an isoflavone found naturally in legumes. Isoflavones, a subset of phytoestrogens, are structurally similar to mammalian estrogens. This study aimed to evaluate the anticancer and cytotoxic effects of GNT on PC3 cell line under three dimensional (3D) culture medium.
Methods
The 3D culture was created by encapsulating the PC3 cells in alginate hydrogel. MTT assay, neutral red uptake, comet assay, and cytochrome C assay were used to study the anticancer and cytotoxic effects of GNT at 120, 240, and 480 μM concentrations. Also, nitric oxide (NO), catalase, and glutathione assay levels were determined to evaluate the effect of GNT on the cellular stress. The culture medium was used as the negative control.
Results
GNT reduced the production of cellular NO and increased the production of catalase and glutathione, confirming the results of the NO test. Evaluation of the toxicity effect of GNT at the concentrations of 120, 240, and 480 μM using comet assay showed that this chemical agent induces apoptosis in PC3 cells in a dose-dependent manner. As the level of cytochrome C in PC3 cells treated with different concentrations of GNT was not significantly different from that of the control, GNT could induce apoptosis in PC3 cells through the non-mitochondrial pathway.
Conclusion
The findings of this study disclose that the anticancer effect of GNT on PC3 cells under 3D culture conditions could increase the effectiveness of treatment. Also, the cell survival rate is dependent on GNT concentration.

Identifiants

pubmed: 36403104
doi: 10.52547/ibj.3711
pmc: PMC9763873
doi:

Substances chimiques

Antineoplastic Agents 0
Catalase EC 1.11.1.6
Cytochromes c 9007-43-6
Genistein DH2M523P0H
Culture Media 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

380-8

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Auteurs

Seyedeh Masoumeh Khamesi (SM)

Department of Medical Radiation Engineering, Central Tehran Branch, Islamic Azad University, Tehran, Iran.

Mehdi Salehi Barough (M)

Department of Medical Radiation Engineering, Central Tehran Branch, Islamic Azad University, Tehran, Iran.

Jamil Zargan (J)

Department of Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran.

Mohsen Shayesteh (M)

Department of Physics, Imam Hossein University, Tehran, Iran.

Nooshin Banaee (N)

Department of Medical Radiation Engineering, Central Tehran Branch, Islamic Azad University, Tehran, Iran.

Ashkan Haji Noormohammadi (A)

Department of Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran.

Hani Keshavarz Alikhani (H)

Department of Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran.

Mohsen Mousavi (M)

Department of Biology, Faculty of Basic Science, Imam Hossein University, Tehran, Iran.

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Classifications MeSH