首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Ethanolic Extracts from Azadirachta indica Leaves Modulate Transcriptional Levels of Hormone Receptor Variant in Breast Cancer Cell Lines
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Ethanolic Extracts from Azadirachta indica Leaves Modulate Transcriptional Levels of Hormone Receptor Variant in Breast Cancer Cell Lines

机译:印A(Azadirachta indica)叶的乙醇提取物调节乳腺癌细胞株中激素受体变异的转录水平。

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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 μg/mL of DCM and 1.0 μg/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 µg/mL (P < 0.001) for EA, and 0.03125 µg/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.
机译:乳腺癌(BC)涵盖了许多具有不同生物学和行为特征的实体,受到肿瘤分子复杂性的青睐。印度印za(印em)呈酚类化合物,表明其作为抗肿瘤化合物的潜力。本研究旨在评估MCF10,MCF7和MDA-MB-231乳腺癌细胞系对通过二氯甲烷(DCM)和乙酸乙酯(EA)获得的印obtained叶(EENL)乙醇提取物的细胞应答。使用MTT分析法评估了提取物对MCF 10A,MCF7和MDA-MB-231的抗增殖活性,分别为24小时和48小时。通过qPCR定量分析ESR1,ESR2,AR,AR-V1,AR-V4和AR-V7的转录本,其中0.03125μg/ mL的DCM和1.0μg/ mL的EA进行48小时。 EENL在果蝇上进行了单独测试,然后与阿霉素一起测试。在不影响MCF 10A的情况下,对肿瘤细胞系的抗增殖作用对于EA为1.0 µg / mL(P <0.001),对于DCM为0.03125 µg / mL(P <0.0001),两者均在48小时后达到。治疗后AR-V7的转录水平增加。体内试验表明,EENL在阿霉素(DXR)较高的浓度下诱导较少的肿瘤。 MDA-MB-231肿瘤谱系中AR-V7的行为表明了肿瘤生物学中涉及的新途径,这可能对癌症具有治疗价值。

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