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间充质干细胞表达 TRAIL 作为针对致敏肿瘤的靶向治疗。

Mesenchymal Stem Cell Expressing TRAIL as Targeted Therapy against Sensitised Tumour.

机构信息

Stem Cell Laboratory, Haematology Unit, Cancer Research Centre, Institute for Medical Research, Kuala Lumpur 50588, Malaysia.

UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia.

出版信息

Int J Mol Sci. 2018 Jul 27;19(8):2188. doi: 10.3390/ijms19082188.

Abstract

Tapping into the ability of engineered mesenchymal stem cells (MSCs) to mobilise into the tumour has expanded the scope of cancer treatment. Engineered MSCs expressing tumour necrosis factor (TNF)-related apoptosis inducing ligand (MSC-TRAIL) could serve as a platform for an efficient and targeted form of therapy. However, the presence of cancer stem cells (CSCs) that are resistant to TRAIL and apoptosis may represent a challenge for effective treatment. Nonetheless, with the discovery of small molecular inhibitors that could target CSCs and tumour signalling pathways, a higher efficacy of MSC-TRAIL mediated tumour inhibition can be achieved. This might pave the way for a more effective form of combined therapy, which leads to a better treatment outcome. In this review, we first discuss the tumour-homing capacity of MSCs, its effect in tumour tropism, the different approach behind genetically-engineered MSCs, and the efficacy and safety of each agent delivered by these MSCs. Then, we focus on how sensitisation of CSCs and tumours using small molecular inhibitors can increase the effect of these cells to either TRAIL or MSC-TRAIL mediated inhibition. In the conclusion, we address a few questions and safety concerns regarding the utilization of engineered MSCs for future treatment in patients.

摘要

利用工程间充质干细胞 (MSCs) 向肿瘤迁移的能力已经扩展了癌症治疗的范围。表达肿瘤坏死因子 (TNF)-相关凋亡诱导配体 (MSC-TRAIL) 的工程 MSC 可以作为高效靶向治疗的平台。然而,具有抵抗 TRAIL 和凋亡的癌症干细胞 (CSCs) 的存在可能代表有效治疗的挑战。尽管如此,随着能够针对 CSCs 和肿瘤信号通路的小分子抑制剂的发现,MSC-TRAIL 介导的肿瘤抑制的疗效可以得到提高。这可能为更有效的联合治疗铺平道路,从而带来更好的治疗效果。在这篇综述中,我们首先讨论了 MSCs 的肿瘤归巢能力、其在肿瘤趋向性中的作用、基因工程 MSCs 背后的不同方法,以及这些 MSCs 传递的每种药物的疗效和安全性。然后,我们重点关注如何使用小分子抑制剂来敏化 CSCs 和肿瘤,以增加这些细胞对 TRAIL 或 MSC-TRAIL 介导的抑制的作用。在结论中,我们针对将工程 MSC 用于未来患者治疗提出了一些问题和安全关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aefa/6121609/880d5f34dc91/ijms-19-02188-g001.jpg

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