绘制作为乳腺癌中肿瘤-免疫细胞通讯关键调节因子的 MicroRNA 功能图谱及潜在治疗策略

Aimi Syamima Abdul Manap, Aini Athirah Wisham, Fei Wen Wong, Huda Raihanah Ahmad Najmi, Zhi Fei Ng, Rubaiyat Siddique Diba
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摘要

在女性中,乳腺癌是发病率最高的癌症,出现转移会大大降低预后,降低总体生存率。深入了解癌细胞转化、随后向身体其他部位扩散以及免疫系统监测肿瘤生长的生物机制,将有助于开发更高效的靶向疗法。微小核糖核酸(miRNA)在肿瘤细胞和免疫细胞之间的相互作用中起着关键作用,有助于肿瘤细胞逃避免疫系统并促进癌症进展。此外,miRNA 还影响转移的形成,包括转移部位的建立和肿瘤细胞向迁移表型的转化。具体来说,这些基因的表达失调与癌基因和抑癌基因的异常表达有关,从而促进了肿瘤的发展。本研究旨在简明扼要地概述 miRNA 在乳腺癌中的意义和功能,重点关注 miRNA 作为肿瘤抑制因子参与抗肿瘤免疫反应以及作为致癌基因参与转移形成的情况。此外,由于 miRNAs 能够调节促进或抑制癌变的特定通路,因此具有作为基因治疗靶点的巨大潜力。本文将重点介绍基于 miRNA 疗法的最新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping the function of MicroRNAs as a critical regulator of tumor-immune cell communication in breast cancer and potential treatment strategies
Among women, breast cancer ranks as the most prevalent form of cancer, and the presence of metastases significantly reduces prognosis and diminishes overall survival rates. Gaining insights into the biological mechanisms governing the conversion of cancer cells, their subsequent spread to other areas of the body, and the immune system’s monitoring of tumor growth will contribute to the advancement of more efficient and targeted therapies. MicroRNAs (miRNAs) play a critical role in the interaction between tumor cells and immune cells, facilitating tumor cells’ evasion of the immune system and promoting cancer progression. Additionally, miRNAs also influence metastasis formation, including the establishment of metastatic sites and the transformation of tumor cells into migratory phenotypes. Specifically, dysregulated expression of these genes has been associated with abnormal expression of oncogenes and tumor suppressor genes, thereby facilitating tumor development. This study aims to provide a concise overview of the significance and function of miRNAs in breast cancer, focusing on their involvement as tumor suppressors in the antitumor immune response and as oncogenes in metastasis formation. Furthermore, miRNAs hold tremendous potential as targets for gene therapy due to their ability to modulate specific pathways that can either promote or suppress carcinogenesis. This perspective highlights the latest strategies developed for miRNA-based therapies.
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