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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Navigating the tumor microenvironment: mesenchymal stem cell-mediated delivery of anticancer agents.
Navigating the tumor microenvironment: mesenchymal stem cell-mediated delivery of anticancer agents.
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多年来,癌症科学知识显著进步,近期研究揭示了许多体现癌症多面性的标志特征。抗癌药物递送的一种新方法是利用间充质干细胞(MSC)介导递送。MSC 是非造血祖细胞,可从骨髓、牙髓、脂肪组织和胎盘/脐带血等来源获取,属于成体干细胞。MSC 主要参与组织再生,同时已发现其可优先迁移至体内多种肿瘤部位。利用 MSC 有望提高抗癌药物疗效和安全性,因为它可以提升治疗药物向肿瘤部位的递送效率。大量研究显示,经 MSC 介导递送的多种药物可在乳腺癌和甲状腺癌细胞中产生抗肿瘤作用。由于缺乏共刺激分子表达,MSC 免疫原性较低,因此异基因移植后通常无需免疫抑制。本综述阐述 MSC 介导抗癌药物递送的近期进展及其机制,并总结此前关于利用该递送系统制备和递送药物的研究。
Scientific knowledge of cancer has advanced greatly throughout the years, with most recent studies findings includes many hallmarks that capture disease's multifaceted character. One of the novel approach utilised for the delivery of anti-cancer agents includes mesenchymal stem cell mediated drug delivery. Mesenchymal stem cells (MSCs) are non-haematopoietic progenitor cells that may be extracted from bone marrow, tooth pulp, adipose tissue and placenta/umbilical cord blood dealing with adult stem cells. MSCs are mostly involved in regeneration of tissue, they have also been shown to preferentially migrate to location of several types of tumour in-vivo .
Usage of MSCs ought to improve both effectiveness and safety of anti-cancer drugs by enhancing delivery efficiency of anti-cancer therapies to tumour site. Numerous researches has demonstrated that various drugs, when delivered via mesenchymal stem cell mediated delivery can elicit anti-tumour effect of cells in cancers of breast cells and thyroid cells.
MSCs have minimal immunogenicity because to lack of co-stimulatory molecule expression, which means there is no requirement for immunosuppression after allogenic transplantation. This current review elaborates recent advancements of mesenchyma stem cell mediated drug delivery of anti-cancer agents along with its mechanism and previously reported studies of drugs manufactured via this drug delivery system.
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