CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Mesenchymal stem cell-derived exosomes as new tools for delivery of miRNAs in the treatment of cancer.
Mesenchymal stem cell-derived exosomes as new tools for delivery of miRNAs in the treatment of cancer.
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尽管正在进行的医学研究致力于寻找多种癌症的治愈方法,但癌症仍然是全球主要死亡原因之一。化疗和免疫治疗,以及手术干预和放射治疗,是癌症治疗的关键组成部分。大多数抗癌药物是全身给药的,不仅分布到肿瘤组织,也分布到正常组织,从而可能引起副作用。
此外,由于抗癌药物的递送效率低,一些肿瘤对其无反应。因此,肿瘤靶向药物递送对于提高抗癌治疗的安全性和有效性至关重要。外泌体是细胞为相互通讯而产生的微小细胞外囊泡。MicroRNA(miRNA)、长链非编码RNA(lncRNA)、小干扰RNA(siRNA)、DNA、蛋白质和脂质是外泌体中包含的治疗性货物。近年来,多项研究聚焦于miRNA作为癌症治疗的潜在治疗要素。间充质干细胞(MSC)已知具有促血管生成、抗凋亡、抗炎和免疫调节作用。来源于MSC的外泌体作为基于MSC治疗的非细胞替代方案正日益受到欢迎,因为这种方法避免了不必要的谱系分化。
因此,更多研究聚焦于将miRNA转移至间充质干细胞(MSC),并将负载miRNA的外泌体靶向癌细胞。在此,我们首先概述了MSC的特征和潜力,以及MSC来源外泌体在癌症治疗中的应用。
最后,我们强调了利用MSC来源外泌体进行miRNA递送在癌症治疗中的应用。
Although ongoing medical research is working to find a cure for a variety of cancers, it continues to be one of the major causes of death worldwide. Chemotherapy and immunotherapy, as well as surgical intervention and radiation therapy, are critical components of cancer treatment. Most anti-cancer drugs are given systemically and distribute not just to tumor tissues but also to normal tissues, where they may cause side effects.
Furthermore, because anti-cancer drugs have a low delivery efficiency, some tumors do not respond to them. As a result, tumor-targeted drug delivery is critical for improving the safety and efficacy of anti-cancer treatment. Exosomes are microscopic extracellular vesicles that cells produce to communicate with one another. MicroRNA (miRNA), long non-coding RNA (lncRNA), small interfering RNA (siRNA), DNA, protein, and lipids are among the therapeutic cargos found in exosomes.
Recently, several studies have focused on miRNAs as a potential therapeutic element for the treatment of cancer. Mesenchymal stem cells (MSC) have been known to have angiogenic, anti-apoptotic, anti-inflammatory and immunomodulatory effects. Exosomes derived from MSCs are gaining popularity as a non-cellular alternative to MSC-based therapy, as this method avoids unwanted lineage differentiation.
Therefore more research have focused on transferring miRNAs to mesenchymal stem cells (MSC) and targeting miRNA-loaded exosomes to cancer cells.
Here, we initially gave an overview of the characteristics and potentials of MSC as well as the use of MSC-derived exosomes in cancer therapy.
Finally, we emphasized the utilization of MSC-derived exosomes for miRNA delivery in the treatment of cancer.
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