TP53 缺失通过上调 NF-κB-IFN-β-MHC-Ia 信号促进骨肉瘤对 NK 细胞的抵抗
TP53 Loss Elevates NF-κB-IFN-β-MHC-Ia Signaling to Promote NK Cell Resistance in Osteosarcoma.
TP53失活是骨肉瘤(OS)发生中的关键事件,也是其侵袭性的基础,但其在肿瘤-免疫相互作用中的作用仍知之甚少。
英文原题:Signaling crosstalk between mesenchymal stem cells and tumor cells: Implications for tumor suppression or progression.
间充质干细胞(MSCs)在过去二十年中已被广泛应用于各种治疗领域,尤其是在再生医学和癌症治疗方面。
间充质干细胞(MSCs)在过去二十年中已被广泛用于各种治疗应用,尤其是在再生医学和癌症治疗中。MSCs 具有分化为中胚层和非中胚层谱系的能力,这使其成为组织工程和再生医学中的热门选择。研究表明,MSCs 具有内在的抑瘤特性,并可影响参与肿瘤发展的多种细胞的行为。此外,MSCs 具有肿瘤趋向性,并具有低免疫原性。MSCs 的固有特征,加上其进行基因操作以及负载各种抗癌治疗药物的潜力,促使研究人员将其用于不同的癌症治疗策略,却未考虑其复杂的动态生物学特性。然而,尽管具有这些理想特性,多项报道显示 MSCs 也具有支持肿瘤的特性。这些相互矛盾的结果表明 MSCs 具有复杂的本质,并警示了 MSCs 潜在治疗应用的风险。因此,研究人员在临床前和临床研究中应审慎考虑 MSCs 的生物学特性,以避免任何不良后果。本文综述了过去二十年中关于 MSCs 与癌症的临床前研究,讨论了 MSCs 的特性如何影响肿瘤进展,并解释了其抑瘤与促瘤功能背后的机制。文章还重点指出了未来研究中可靶向的关键细胞通路,以提高基于 MSCs 的癌症治疗的安全性和有效性。从这项研究中获得的见解将为MSCs的进一步临床研究以及开发更有效的癌症治疗方法铺平道路。
Mesenchymal stem cells (MSCs) have been extensively used in various therapeutic applications over the last two decades, particularly in regenerative medicine and cancer treatment. MSCs have the ability to differentiate into mesodermal and non-mesodermal lineages, which makes them a popular choice in tissue engineering and regenerative medicine. Studies have shown that MSCs have inherent tumor-suppressive properties and can affect the behavior of multiple cells contributing to tumor development. Additionally, MSCs possess a tumor tropism property and have a hypoimmune nature. The intrinsic features of MSCs along with their potential to undergo genetic manipulation and be loaded with various anticancer therapeutics have motivated researchers to use them in different cancer therapy approaches without considering their complex dynamic biological aspects. However, despite their desirable features, several reports have shown that MSCs possess tumor-supportive properties. These contradictory results signify the sophisticated nature of MSCs and warn against the potential therapeutic applications of MSCs. Therefore, researchers should meticulously consider the biological properties of MSCs in preclinical and clinical studies to avoid any undesirable outcomes. This manuscript reviews preclinical studies on MSCs and cancer from the last two decades, discusses how MSC properties affect tumor progression and explains the mechanisms behind tumor suppressive and supportive functions. It also highlights critical cellular pathways that could be targeted in future studies to improve the safety and effectiveness of MSC-based therapies for cancer treatment. The insights obtained from this study will pave the way for further clinical research on MSCs and development of more effective cancer treatments.
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