Modulation of MicroRNAs by Euphorbia Microsciadia Boiss in MDA-MB-231 Cell Line: New Possibilities in Breast Cancer Therapy

被引:5
作者
Mahmoudian-Sani, Mohammad-Reza [1 ]
Asadi-Samani, Majid [2 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Thalassemia & Hemoglobinopathy Res Ctr, Hlth Res Inst, Ahvaz, Iran
[2] Shahrekord Univ Med Sci, Cellular & Mol Res Ctr, Basic Hlth Sci Inst, Shahrekord, Iran
关键词
Apoptosis; breast cancer; cell cycle; euphorbia; microRNA; miR-34a; tumor suppressor; MEDICINAL-PLANTS; INDUCED APOPTOSIS; PROLIFERATION; SUPPRESSES; TARGETS; CYCLE; EXPRESSION; MIGRATION; INVASION; THERAPEUTICS;
D O I
10.2174/1574892815666200630102944
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: A large number of Euphorbia species have been evaluated for anticancer effects; however, their anticancer mechanisms have not been established up to now. Objective: The present study aimed to evaluate the effects of Euphorbia microsciadia (E. microsciadia) Boiss on the modulation of micro (mi) RNAs in MDA-MB-231 cell line. Methods: As the first step, the inhibitory concentration of hydroalcoholic extract of E. microsciadia on MDA-MB-231 cells was examined using the MTT assay, bypassing 24 and 48h from seeding. The real-time quantitative Reverse Transcription Polymerase Chain Reaction (qRT-PCR) was also utilized to determine Let-7, miR-15, miR-16, miR-29, miR-151, miR-155, miR-21, miR-146b, miR-181b, miR-221, miR-222, miR-21, and miR-146b expressions in MDA-MB-231 cells, by passing 24 and 48h from treating with the extract of E. microsciadia. Results: The results reveal the cytotoxic effects of E. microsciadia on MDA-MB-231 cell line in a dose-dependent manner. The half maximal Inhibitory Concentrations (IC50) were also equal to 275 and 240 mu g/ml for E. microsciadia, by passing 24 and 48h from the treatment, respectively. Furthermore, it was confirmed that, E. microsciadia had augmented the expression levels of Let-7, miR-15, miR-16, miR-29, and miR-34a, which lead to an increase in apoptosis. Conclusion: E. microsciadia could modulate some miRNAs involved in cell cycle arrest and apoptosis in MDA-MB-231 cell line. Accordingly, targeting miRNAs by E. microsciadia can open some newer avenues for breast cancer therapy.
引用
收藏
页码:174 / 184
页数:11
相关论文
共 84 条
[11]  
Aylward JH, 2004, Anti-cancer compounds, Patent No. [US6787161, 6787161]
[12]   In vitro growth inhibition and cytotoxicity of Euphorbia caducifolia against four human cancer cell lines and its phytochemical characterisation [J].
Bano, Shaista ;
Siddiqui, Bina Shaheen ;
Farooq, Ahsana Dar ;
Begum, Sabira ;
Siddiqui, Faheema ;
Kashif, Muhammad ;
Azhar, Mudassar .
NATURAL PRODUCT RESEARCH, 2017, 31 (24) :2936-2940
[13]  
Barnett-Itzhaki Z, 2019, MiRNA expression signature in the classification of thyroid tumors, Patent No. [US9708667, 9708667]
[14]  
Berezikov E, 2017, MiRNA and its diagnostic and therapeutic uses in diseases or conditions associated with melanoma, or in diseases or conditions associated with activated BRAF pathway, Patent No. [US20170304348, 20170304348]
[15]   Expression of microRNA-146 suppresses NF-κB activity with reduction of metastatic potential in breast cancer cells [J].
Bhaumik, D. ;
Scott, G. K. ;
Schokrpur, S. ;
Patil, C. K. ;
Campisi, J. ;
Benz, C. C. .
ONCOGENE, 2008, 27 (42) :5643-5647
[16]  
Bonci Desiree, 2010, Recent Pat Cardiovasc Drug Discov, V5, P156, DOI 10.2174/157489010793351962
[17]   MiR-15a and miR-16-1 cluster functions in human leukemia [J].
Calin, George A. ;
Cimmino, Amelia ;
Fabbri, Muller ;
Ferracin, Manuela ;
Wojcik, Sylwia E. ;
Shimizu, Masayoshi ;
Taccioli, Cristian ;
Zanesi, Nicola ;
Garzon, Ramiro ;
Aqeilan, Rami I. ;
Alder, Hansjuerg ;
Volinia, Stefano ;
Rassenti, Laura ;
Liu, Xiuping ;
Liu, Chang-gong ;
Kipps, Thomas J. ;
Negrini, Massimo ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (13) :5166-5171
[18]  
Chen Y-J, 2014, Use of compounds isolated from Euphorbia neriifolia for treating cancer and/or thrombocytopenia, Patent No. 8846768
[19]  
Choene M, 2016, MOL BIOL+, V50, P98, DOI [10.1134/S0026893316010040, 10.7868/S0026898416010043]
[20]   miR-15 and miR-16 induce apoptosis by targeting BCL2 [J].
Cimmino, A ;
Calin, GA ;
Fabbri, M ;
Iorio, MV ;
Ferracin, M ;
Shimizu, M ;
Wojcik, SE ;
Aqeilan, RI ;
Zupo, S ;
Dono, M ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :13944-13949