Restoring of miR-193a-5p sensitizes breast cancer cells to paclitaxel through P53 pathway

Restoring of miR-193a-5p sensitizes breast cancer cells to paclitaxel through P53 pathway


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نویسندگان: بهزاد برادران , صنم صدرالدینی , داریوش شانه بندی , خلیل حاجی اصغرزاده

کلمات کلیدی: Tumor-suppressor, Breast cancer, Proliferation, Migration, Gene expression

نشریه: 952 , 4 , 10 , 2020

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله بهزاد برادران
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمونولوژی
کد مقاله 72331
عنوان فارسی مقاله Restoring of miR-193a-5p sensitizes breast cancer cells to paclitaxel through P53 pathway
عنوان لاتین مقاله Restoring of miR-193a-5p sensitizes breast cancer cells to paclitaxel through P53 pathway
ناشر 6
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
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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Recent evidence presented the important role of microRNAs in health and disease particularly in human cancers. Among those, miR-193 family contributes as a tumor suppressor in different benign and malignant cancers like breast cancer via interaction with specific targets. On the other hand, it was stated that miR-193 is able to modulate some targets in chemoresistant cancer cells. Therefore, the aim of this study was to evaluate the potential function of miR-193a-5p and paclitaxel in the apoptosis induction by targeting P53 in breast cancer cells. Methods: At first, miR-193a-5p mimics were transfected to MDA-MB-231 breast cancer cell line which indicated the lower expression level of miR-193a-5p. Subsequently, the transfected cells were treated with paclitaxel. Then, cell viability, apoptosis, and migration were evaluated by MTT, flow cytometry and DAPI staining, and scratch-wound motility assays, respectively. Moreover, the expression levels of P53 was evaluated by qRT-PCR. Results: The expression level of miR-193a-5p was restored in MDA-MB-231 cells which profoundly inhibited the proliferation (P < 0.0001), induced apoptosis (P < 0.0001) and harnessed migration (P < 0.0001) in the breast cancer cells and more effectiveness was observed in combination with paclitaxel. Interestingly, increased miR-193a-5p expression led to a reduction in P53 mRNA, offering that it can be a potential target of miR-193a. Conclusion: Taken together, it is concluded that the combination of miR-193a-5p restoration and paclitaxel could be potentially considered as an effective therapeutic strategy to get over chemoresistance during paclitaxel chemotherapy.

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نویسنده نفر چندم مقاله
بهزاد برادرانسوم
صنم صدرالدینیچهارم
داریوش شانه بندیپنجم
خلیل حاجی اصغرزادهششم

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386-Restoring of miR-193a-5p Sensitizes Breast Cancer Cells to Paclitaxel.pdf1399/06/281591290دانلود