Ethanolic Extracts from Azadirachta indica Leaves Modulate Transcriptional Levels of Hormone Receptor Variant in Breast Cancer Cell Lines

被引:5
|
作者
Braga, Deisi L. [1 ]
Mota, Sara T. S. [1 ,2 ]
Zoia, Mariana A. P. [2 ]
Lima, Paula M. A. P. [3 ]
Orsolin, Priscila C. [3 ]
Vecchi, Lara [2 ]
Nepomuceno, Julio C. [3 ]
Furstenau, Cristina R. [4 ]
Maia, Yara C. P. [2 ]
Goulart, Luiz Ricardo [2 ,5 ]
Araujo, Thaise G. [1 ,2 ]
机构
[1] Univ Fed Uberlandia, Inst Biotechnol, Lab Genet & Biotechnol, BR-38700128 Uberlandia, MG, Brazil
[2] Univ Fed Uberlandia, Inst Biotechnol, Lab Nanobiotechnol, BR-38400902 Uberlandia, MG, Brazil
[3] Univ Ctr Patos Minas, Lab Cytogenet & Mutagenesis, BR-38700207 Patos De Minas, MG, Brazil
[4] Univ Fed Uberlandia, Inst Biotechnol, Lab Anim Cell Culture, BR-38700128 Uberlandia, MG, Brazil
[5] Univ Calif Davis, Dept Med Microbiol & Immunol, Davis, CA 95616 USA
关键词
breast cancer; Azadirachta indica; neem; ethanolic extracts; androgen receptor variant-7; ANDROGEN RECEPTOR; TUMOR-SUPPRESSOR; PROSTATE-CANCER; ANTIMICROBIAL ACTIVITIES; GROWTH-INHIBITION; SPLICE VARIANT; SOMATIC-CELLS; UP-REGULATION; EXPRESSION; NEEM;
D O I
10.3390/ijms19071879
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast Cancer (BC) encompasses numerous entities with different biological and behavioral characteristics, favored by tumor molecular complexity. Azadirachta indica (neem) presents phenolic compounds, indicating its potential as an antineoplastic compound. The present study aimed to evaluate the cellular response of MCF10, MCF7, and MDA-MB-231 breast cell lines to ethanolic extracts of neem leaves (EENL) obtained by dichloromethane (DCM) and ethyl acetate (EA) solvent. Extracts' antiproliferative activities were evaluated against MCF 10A, MCF7, and MDA-MB-231 for 24 and 48 h using MTT assay. ESR1, ESR2, AR, AR-V1, AR-V4, and AR-V7 transcripts were quantified through qPCR for 0.03125 mu g/mL of DCM and 1.0 mu g/mL for EA for 48 h. The EENL was tested on Drosophila melanogaster as a sole treatment and then also together with doxorubicin. Antiproliferative effect on tumor cell lines without affecting MCF 10A were 1.0 mu g/mL (P < 0.001) for EA, and 0.03125 mu g/mL (P < 0.0001) for DCM, both after 48 h. Transcriptional levels of AR-V7 increased after treatment. In vivo assays demonstrated that EENL induced fewer tumors at a higher concentration with doxorubicin (DXR). The behavior of AR-V7 in the MDA-MB-231 tumor lineage indicates new pathways involved in tumor biology and this may have therapeutic value for cancer.
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页数:15
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