Cansaran-Duman Demet, Tanman Ümmügülsüm, Yangın Sevcan, Atakol Orhan
Ankara University, Biotechnology Institute, Keçiören, Ankara, Turkey.
Faculty of Science, Department of Chemistry, Ankara University, Tandoğan, Ankara, Turkey.
Cytotechnology. 2020 Oct 30;72(6):855-72. doi: 10.1007/s10616-020-00430-7.
This study was designed to compare usnic acid with anti-breast cancer drug molecules (A-BCDM) routinely used in the treatment of breast cancer. The miRNA information of 17 anti-breast cancer drug used in breast cancer treatment was obtained from the Small Molecule-miRNA Network-Based Inferance (SMIR-NBI) tool. We had been determined common and different expressed miRNAs between 17 A-BCDM & usnic acid and were classified according to the common miRNAs to reveal molecular similarity. As a result of the bioinformatic analyzes, 20 common miRNAs were determined between 17 A-BCDM and usnic acid. The common miRNAs were analyzed with bioinformatic tolls for determining pathways and targets. The most common miRNAs for 6 of 17 A-BCDM and usnic acid were determined as miR-374a-5p and miR-26a-5p. We compared the anti-proliferative effect of usnic acid and one of the 17 A-BCDM that tamoxifen on MDA-MB-231 triple negative breast cancer cell with real-time cell analysis system. The real time PCR assay was carried out with miR-26a-5p for evaluate to expression level of MDA-MB-231 breast cancer cell and MCF-12A non-cancerous epithelial breast cell. As a result of study, usnic acid as novel candidate drug molecule showed high similarity ratio with 5-Fluorouracil, Sulindac Sulfide, Curcumin and Cisplatin A-BCDM used in treatment of breast cancer. miR-26a-5p as common response miRNA of usnic acid and tamoxifen was showed a decreased level of expression by validated qRT-PCR assay. The obtained from study, in addition to 17 A-BCDM, usnic acid has also the potential to be used as a candidate molecule in the treatment of breast cancer. Moreover, miR-26a-5p might be used as a biomarker in the treatment of breast cancer but further analysis is required.
本研究旨在比较扁枝衣酸与乳腺癌治疗中常规使用的抗乳腺癌药物分子(A-BCDM)。从基于小分子- miRNA网络推断(SMIR-NBI)工具中获取了用于乳腺癌治疗的17种抗乳腺癌药物的miRNA信息。我们确定了17种A-BCDM与扁枝衣酸之间共同表达和差异表达的miRNA,并根据共同的miRNA进行分类以揭示分子相似性。生物信息学分析结果显示,在17种A-BCDM和扁枝衣酸之间确定了20种共同的miRNA。使用生物信息学工具对共同的miRNA进行分析以确定其途径和靶点。17种A-BCDM中的6种与扁枝衣酸最常见的miRNA被确定为miR-374a-5p和miR-26a-5p。我们使用实时细胞分析系统比较了扁枝衣酸和17种A-BCDM之一他莫昔芬对MDA-MB-231三阴性乳腺癌细胞的抗增殖作用。用miR-26a-5p进行实时PCR检测以评估MDA-MB-231乳腺癌细胞和MCF-12A非癌性乳腺上皮细胞的表达水平。研究结果表明,扁枝衣酸作为新型候选药物分子与用于乳腺癌治疗的5-氟尿嘧啶、舒林酸硫化物、姜黄素和顺铂A-BCDM具有较高的相似率。通过验证的qRT-PCR检测显示,作为扁枝衣酸和他莫昔芬共同反应miRNA的miR-26a-5p表达水平降低。研究得出,除了17种A-BCDM外,扁枝衣酸也有潜力用作乳腺癌治疗的候选分子。此外,miR-26a-5p可能用作乳腺癌治疗的生物标志物,但需要进一步分析。