Hsa-Mir-1225-5p 的表达限制了乳腺癌细胞株的侵袭性生物学行为

Y-Andrés Hernandez, Janeth Gonzalez, Reggie Garcia, Andrés Aristizabal-Pachón
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引用次数: 0

摘要

导言:许多遗传和生物过程都与微小RNA(miRNA)的功能有关,miRNA通过靶向信使RNA(mRNA)来调节基因表达。人们普遍认为,miRNA 在哺乳动物的疾病发展和胚胎学中发挥作用:为了进一步了解 miRNA 在致癌过程中的功能,我们对 miRNA 在癌症中的表达谱进行了研究。尽管hsa-miR-1225-5p被称为癌症中值得注意的miRNA,但它是否在乳腺癌腔内A亚型和腔内B亚型的体外进展中发挥作用尚不清楚。我们建议在乳腺癌细胞系中表达合成的 hsa-miR-1225-5p 分子,并评估其活性,以研究其在管腔型乳腺癌发展过程中的功能。从增殖、生存、迁移和侵袭等典型的癌症进展阶段来看,我们研究了 hsa-miR-1225-5p 在管腔型 A 型和 B 型乳腺癌细胞系中的作用:此外,我们还利用生物信息学数据库,深入探讨了基于目标得分的 miRNA 与 MRNA 相互作用的预测。我们的研究表明,miR-1225-5p 的表达能显著抑制管腔 A 型和 B 型乳腺癌细胞系的体外生长:结果得到了生物信息学分析和详细基因网络的支持,该网络促进了癌症进展所需的信号通路的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Expression of Hsa-Mir-1225-5p Limits the Aggressive Biological Behaviour of Luminal Breast Cancer Cell Lines.

Introduction: Numerous genetic and biological processes have been linked to the function of microRNAs (miRNAs), which regulate gene expression by targeting messenger RNA (mRNA). It is commonly acknowledged that miRNAs play a role in the development of disease and the embryology of mammals.

Method: To further understand its function in the oncogenic process, the expression of the miRNA profile in cancer has been investigated. Despite being referred to as a noteworthy miRNA in cancer, it is unknown whether hsa-miR-1225-5p plays a part in the in vitro progression of the luminal A and luminal B subtypes of breast cancer. We proposed that a synthetic hsa-miR-1225-5p molecule be expressed in breast cancer cell lines and its activity be evaluated with the aim of studying its function in the development of luminal breast cancer. In terms of the typical cancer progression stages, such as proliferation, survival, migration, and invasion, we investigated the role of hsa-miR-1225-5p in luminal A and B breast cancer cell lines.

Results: Additionally, using bioinformatics databases, we thoroughly explored the target score-based prediction of miRNA-mRNA interaction. Our study showed that the expression of miR-1225-5p significantly inhibited the in vitro growth of luminal A and B breast cancer cell lines.

Conclusion: The results were supported by a bioinformatic analysis and a detailed gene network that boosts the activation of signaling pathways required for cancer progression.

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