Estradiol modulated colorectal cancer stem cells bioactivity and interaction with endothelial cells
Estradiol modulated colorectal cancer stem cells bioactivity and interaction with endothelial cells
نویسندگان: آرزو رضائی نژاد زمانی , مهدی احمدی , آیدا پویافر , حسام سقائی باقری , شیرین صابریان پور , امیر مهدی زاده حقیقی , مهدی طالبی , رضا رهبرقاضی
کلمات کلیدی: Human cancer stem cells, Estradiol, Survival and proliferation, Migration, Paracrine activity, Endothelial affinity
نشریه: 22959 , 2020 , 257 , 2020
| نویسنده ثبت کننده مقاله |
رضا رهبرقاضی |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز سلولهای بنیادی |
| کد مقاله |
72925 |
| عنوان فارسی مقاله |
Estradiol modulated colorectal cancer stem cells bioactivity and interaction with endothelial cells |
| عنوان لاتین مقاله |
Estradiol modulated colorectal cancer stem cells bioactivity and interaction with endothelial cells |
| ناشر |
14 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
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| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
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| This study aimed to evaluate the modulatory role of sex-related hormone estradiol on cancer stem cells with the origin of colorectal adenocarcinoma in vitro. Cancer stem cells were incubated with 100 nM estradiol for 48 h. The cell survival rate was analyzed using the MTT assay. Immunocytochemistry staining of Ki-67 and Inhibin and Apoptosis PCR array were done to measure proliferation/apoptosis. Cell migration was monitored via the Transwell Migration assay. The expression of exosome biogenesis genes was measured using a real-time PCR assay. The fatty acid profile was monitored using gas chromatography. The level of FAK, SQSTM1, ER, and SIRT1 was examined using Western blotting. Cancer stem-endothelial cell interaction was investigated using Surface Plasmon Resonance assay. Data showed no significant differences in cancer stem cell viability and proliferation between control and estradiol-treated groups (p>0.05). PCR array highlighted the up-regulation of both pro- and anti-apoptosis effectors in the treatment group compared to the control cells (p<0.05). Cell migration capacity was increased after treatment with estradiol (p<0.001). Both exocytosis and exosome biogenesis were decreased in cancer stem cells exposed to estradiol (p<0.05). Data showed the reduction of palmitic acid, and increase of Palmitoleic and Linolenic acids in estradiol-treated cells. Estrogen induced estrogen receptor, SQSTM1 proteins and decreased SIRT1 factor after 48 h. Surface Plasmon Resonance revealed the suppression of cancer stem-endothelial cell interaction and affinity. Estradiol could change the migration, juxtacrine and paracrine activities of cancer stem cells, showing the importance of sex-related hormones in the dynamic of cancer development. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Estradiol.pdf | 1399/04/31 | 2624360 | دانلود |