Retracted: Glabridin attenuates the migratory and invasive capacity of breast cancer cells by activating microRNA-200c
العنوان: | Retracted: Glabridin attenuates the migratory and invasive capacity of breast cancer cells by activating microRNA-200c |
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المؤلفون: | Fei Jiang, Xianqing Ye, Shilong Ning, Juan Mu, Zhong Li, Yuan Li, Xingxing Wang, Lu Si |
المصدر: | Cancer Science |
بيانات النشر: | Blackwell Publishing Ltd, 2014. |
سنة النشر: | 2014 |
مصطلحات موضوعية: | Cancer Research, medicine.medical_specialty, epithelial-mesenchymal transition, Vimentin, Biology, Metastasis, chemistry.chemical_compound, Breast cancer, Internal medicine, microRNA, medicine, metastasis, This Article Has Been Retracted, Epithelial–mesenchymal transition, Gene knockdown, Mesenchymal stem cell, nutritional and metabolic diseases, glabridin, General Medicine, medicine.disease, microRNA-200c, Endocrinology, Oncology, chemistry, Cancer research, biology.protein, lipids (amino acids, peptides, and proteins), Glabridin |
الوصف: | Current treatments for breast cancer, a common malignancy in human females, are less than satisfactory because of high rates of metastasis. Glabridin (GLA), which acts through the FAK/ROS signaling pathway, has been used as an antioxidant and anti-metastatic agent. However, little is known regarding the effect of microRNA (miRNA) on GLA's anti-metastatic activity. The miRNA-200 family, which is frequently expressed at low levels in triple negative breast cancers, inhibits metastasis by blocking the epithelial–mesenchymal transition. Here, we found that GLA attenuated the migratory and invasive capacity of breast cancer cells by activating miR-200c. GLA induced the mesenchymal–epithelial transition in vitro and in vivo, as determined by increased expression of the epithelial marker, E-cadherin, and decreased expression of the mesenchymal marker, vimentin. Overexpression of miR-200c enhanced the expression of E-cadherin and decreased the expression of vimentin. Furthermore, in MDA-MB-231 and BT-549 breast cancer cells exposed to GLA, knockdown of miR-200c blocked the GLA-induced mesenchymal–epithelial transition and alleviated the GLA-induced inhibition of migration and invasion. Thus, elevation of miR-200c by GLA has considerable therapeutic potential for anti-metastatic therapy for breast cancer patients. |
اللغة: | English |
تدمد: | 1349-7006 1347-9032 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee10f0ee1a6f1d66bd4b1e571631e926 http://europepmc.org/articles/PMC4317926 |
Rights: | OPEN |
رقم الانضمام: | edsair.doi.dedup.....ee10f0ee1a6f1d66bd4b1e571631e926 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 13497006 13479032 |
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