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:: Search published articles ::
Showing 3 results for Baghbani-Arani

Rabee Movagharnia, Fahimeh Baghbani-Arani, Seyed Ataollah Sadat Shandiz,
Volume 22, Issue 1 (Bimonthly 2018)
Abstract

Background: Nowadays, investigations on the role of nanoparticles for diagnosis, and treatment of cancers are being increased. This study aimed at examining the cytotoxic effect of green synthesized silver nanoparticles (AgNPs) on human colon cancer (HT29) and normal (HEK293) cells using the Artemisa tournefortiana extract.
Materials and Methods: In the current study, the green synthesis of AgNPs was conducted using the A. tournefortiana extract. Then, the characterization of fabricated AgNPs was performed by ultraviolet-visible (UV-vis) spectroscopy, X-ray diffraction (XRD), and transmission electron microscopy (TEM) methods. The HT29 and HEK293 cell lines were treated with different concentrations of synthesized AgNPs for 24 hours and the viability of cells and half-maximal inhibitory concentration) IC50( were calculated by the MTT assay.
Results: The fabricated AgNPs showed the characteristic surface plasmon resonance peak at around 425 nm. The crystallographic shapes from the XRD and TEM tests showed that the AgNPs were mostly spherical in shape, having an average diameter of 22 nm. The MTT results revealed that AgNPs significantly decreased the viability of cells in dose-and time-dependent manner. The IC50 values of nanoparticles for HT29 and HEK293 cell lines, during the 24 hours, were 40.71 and 61.38 mg/mL, respectively.
Conclusion: According to the results of the current study, the green fabricated AgNPs can have a more cytotoxic effect on colon cancer cells compared to the normal cells. Thus, they can be considered as a promising strategy for the treatment of colon cancer.

Fatemeh Ghodratpour, Fahimeh Baghbani-Arani, Seyed Ataolah Sadat Shandiz,
Volume 22, Issue 6 (Bimonthly 2018)
Abstract

Background: Breast cancer is the second leading cause of cancer-related death worldwide among women. Nowadays, nanoparticles are interested as anti-cancer factors in studies related to cancer therapy. Therefore, the present study aimed to explore cytotoxic effects of zinc oxide nanoparticles (ZnONPs) and to evaluate NM23 gene expression in T47D breast cancer cells.
Materials and Methods: The cancerous T47D and normal HEK293 cell lines were treated with different concentration of ZnONPs for 24 hours and the cytotoxicity activity of ZnONPs was analyzed by the MTT assay. Then, the NM23 gene expression was evaluated using the real-time PCR method.
Results: According to MTT results, the ZnONPs significantly decreased the viability of T47D cells in dose-dependent manner. Also, the results revealed that the mRNA level of NM23 was up-regulated (7.8-fold) in cells treated with ZnONPs.
Conclusion: ZnONPs can destroy cancerous T47D cells compared to normal HEK293 cells. Furthermore, it seems that ZnONPs can modulate metastasis by enhancing the NM23 gene expression level in breast cancer T47D cells. Thus, ZnONPs can be considered as a promising strategy for the treatment of breast cancer.

Nafiseh Farhadi-Shaheni, Fahimeh Baghbani-Arani, Masoumeh Mahdavi-Ortakand,
Volume 27, Issue 2 (Bimonthly 2023)
Abstract

Background: Neurofibromatosis Type 1 (NF1) is an autosomal dominant disease caused by mutations in a tumor suppressor protein called neurofibromin. The NF1 gene consists of 60 exons and due to the large size of the NF1 gene, variation in mutations and the absence of mutation hotspots is a complex problem in genetic counselling. Considering that determining the frequency of mutations in a population contributes to effective genetic counseling and prevention of more diseases. So, this study aimed to identify the underlying genetic defect in 10 Iranian patients with neurofibromatosis type 1.
Materials and Methods: After collecting blood from patients and genomic DNA extraction, 9 high mutability exons were analyzed by PCR and sequencing methods. Finally, sequenced exons and reference exons were compared using the bioinformatic tools, and mutations were identified.
Results: Among 10 evaluated patients six different mutations were detected. These mutations included two deletions (c.1458-1459 delAA, c.1541-1542 delAG in 13 & 14 exons, respectively), and four substitution mutations. The c.5172 G>A, c.3871-2 A>G, and c.3867 C>T mutations were reported for the first time in this study.
Conclusions: The results of this study implied that there are various mutations in this disease and the most reliable method for NF1 mutation analysis is DNA sequencing.


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