این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
صفحه اصلی
درباره پایگاه
فهرست سامانه ها
الزامات سامانه ها
فهرست سازمانی
تماس با ما
JCR 2016
جستجوی مقالات
جمعه 5 دی 1404
Iranian Journal of Pediatric Hematology and Oncology
، جلد ۱۵، شماره ۱، صفحات ۳۴۷-۳۵۷
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Evaluation of Chelidonium Majus L. Alkaloid Effect on VEGF Gene Expression and Cell Apoptosis in the Burkitt Lymphoma Cell Line
چکیده انگلیسی مقاله
Background:
Burkitt lymphoma (BL) is a type of mature B-cell non-Hodgkin’s lymphoma that commonly develops in children and young adults. Vascular endothelial growth factor
(VEGF
) is acknowledged as a vital regulator of angiogenesis in both normal and disease states. In light of the adverse effects linked to chemical treatments, this study aimed to explore the anticancer effects of
Chelidonium majus
L. alkaloid on the Daudi BL cell line and to evaluate the expression of the
VEGF
gene.
Materials and Methods:
This project was an experimental study. The cytotoxic effects of the alkaloid derived from
Chelidonium majus
L. on the Daudi and normal cells were evaluated using MTT assays (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide). The induction of apoptosis in cells was measured utilizing Annexin V/propidium iodide (PI) flow cytometry. Additionally, the expression levels of the VEGF gene were determined via a Real-time PCR assay. Data were entered into SPSS, version 21. Student’s t-test and ANOVA test were used for comparisons of groups.
Results:
The 50% cytotoxic concentration (CC
50
) of the alkaloid from
Chelidonium majus
L. was found to be 56.35µg/mL in the Daudi cell. Findings from flow cytometry aligned with those from MTT assays. Real-time PCR assay results showed a significant decrease in the
VEGF
gene expression (P<0.009). Effects observed after 48 hours of treatment across various concentrations of
Chelidonium majus
L. alkaloid demonstrated dose-dependency. However, in peripheral blood mononuclear cells (PBMCs) as a control, the alkaloid did not significantly affect the expression of the
VEGF
gene (P>0.05).
Conclusion:
The alkaloid is derived from
Chelidonium majus
L. Appears to influence angiogenesis by down-regulating the
VEGF
gene expression, suggesting its potential as a complementary agent in chemotherapy for Burkitt lymphoma. However
;
further research is required to evaluate the effectiveness of the
Chelidonium majus
L. Extract as a definitive treatment for Burkitt lymphoma.
کلیدواژههای انگلیسی مقاله
Burkitt lymphoma, Chelidonium majus, Vascular endothelial growth factor
نویسندگان مقاله
| Mitra Sadeghpour Natanzi
Department of Microbiology Faculty of Biological Sciences, Islamic Azad University, North Tehran branch, Tehran, Iran
| Masoud Parsania
Associate professor, Department of Microbiology, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
| Fatemeh Ashrafi
Assistant professor, Department of Microbiology, Faculty of Biological Sciences, Islamic Azad University, North Tehran branch, Tehran, Iran
| Mohammad Hassan Pouriayevali
Assistant professor, Department of Arboviruses and Viral Hemorrhagic Fevers (National Ref Lab), Pasteur Institute of Iran, Tehran, Iran
نشانی اینترنتی
http://ijpho.ssu.ac.ir/browse.php?a_code=A-10-1137-1&slc_lang=en&sid=1
فایل مقاله
فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
انکولوژی
نوع مقاله منتشر شده
پژوهشی
برگشت به:
صفحه اول پایگاه
|
نسخه مرتبط
|
نشریه مرتبط
|
فهرست نشریات