In Vitro Radiosensitization of T47D and MDA-MB-231 Breast Cancer Cells with the Neoflavonoid Dalbergin | ||
| Middle East Journal of Cancer | ||
| مقاله 2، دوره 14، شماره 2 - شماره پیاپی 54، 2023، صفحه 205-218 اصل مقاله (3.84 M) | ||
| نوع مقاله: Original Article(s) | ||
| شناسه دیجیتال (DOI): 10.30476/mejc.2022.91913.1637 | ||
| نویسندگان | ||
| Fereshte Mahdizade Valojerdi* 1؛ Bahram Goliaei2؛ Nakisa Rezakhani1؛ Alireza Nikoofar3؛ Hoda Keshmiri Neghab4؛ Mohammad Hasan Soheilifar5؛ Bahareh Bigdeli2 | ||
| 1Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran | ||
| 2Department of Biophysics, Institute of Biochemistry and Biophysics, University of Tehran, Tehran, Iran | ||
| 3Department of Radiotherapy, Iran University of Medical Sciences (IUMS), Tehran, Iran | ||
| 4Department of Photo Healing and Regeneration, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran | ||
| 5Department of Medical Laser, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran | ||
| چکیده | ||
| Background: Radiotherapy is a frequently used therapeutic modality for breast cancer. Dalbergin, a natural antioxidant, inhibits carcinogens and tumor progression. In the present study, we investigated the effect of Dalbergin on the response of T47D and MDA-MB-231 breast cancer cell lines to ionizing radiation. Method: In this experimental in vitro study, doubling time of T47D and MDAMB- 231 were obtained from the growth curve. The cytotoxic effect of Dalbergin on T47D and MDA-MB-231 breast cancer cells were estimated via MTT assay. To determine the clonogenic ability, we treated T47D and MDA-MB-231 with Dalbergin for 48 h prior to irradiation, subsequent to which a colony assay was performed. Real-time polymerase chain reaction was employed to determine the gene expression level. Results: Dalbergin inhibited proliferation of T47D and MDA-MB-231 in a time and concentration-dependent manner. Additionally, the most appropriate time for the treatment of these types of cancer cells was found to be 48 h and the drug's concentration in both cell lines was different. The IC50 values of T47D and MDA-MB-231 cells were 0.001 and 0.0001 μM, respectively. Moreover, this drug radiaosensitizes both cell lines effectively compared with the radiation only. Finally, the gene expression level of p53, Bcl-2, and STAT3 were investigated in cancer cells. Conclusion: Dalbergin showed apoptotic effects probably through the STAT/p53 signaling pathway. Therefore, Dalbergin could be considered as a radiosensitizer and its effects may be owing to increased cell death. | ||
| کلیدواژهها | ||
| Dalbergin؛ Cells؛ X-rays؛ Apoptotic؛ Cell death | ||
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