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The bad and the good of mesenchymal stem cells in cancer: Boosters of tumor growth and vehicles for targeted delivery of anticancer agents.间充质干细胞在癌症中的好坏两面:肿瘤生长的助推器和抗癌药物靶向递送的载体。
World J Stem Cells. 2010 Feb 26;2(1):5-12. doi: 10.4252/wjsc.v2.i1.5.
2
Selective targeting of genetically engineered mesenchymal stem cells to tumor stroma microenvironments using tissue-specific suicide gene expression suppresses growth of hepatocellular carcinoma.利用组织特异性自杀基因表达选择性靶向基因工程间充质干细胞至肿瘤基质微环境可抑制肝癌生长。
Ann Surg. 2011 Nov;254(5):767-74; discussion 774-5. doi: 10.1097/SLA.0b013e3182368c4f.
3
Interplay between mesenchymal stem cell and tumor and potential application.间质干细胞与肿瘤的相互作用及其潜在应用。
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Potential of Mesenchymal Stem Cell based application in Cancer.基于间充质干细胞的应用在癌症治疗中的潜力。
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Deepening a Simple Question: Can MSCs Be Used to Treat Cancer?深化一个简单的问题:间充质干细胞可用于治疗癌症吗?
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Mesenchymal Stem Cells in the Tumor Microenvironment.肿瘤微环境中的间充质干细胞。
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Mesenchymal Stromal/Stem Cells: A New Era in the Cell-Based Targeted Gene Therapy of Cancer.间充质基质/干细胞:癌症细胞靶向基因治疗的新时代。
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Mesenchymal stem cells and cancer: friends or enemies?间充质干细胞与癌症:是友还是敌?
Mutat Res. 2014 Oct;768:98-106. doi: 10.1016/j.mrfmmm.2014.01.006. Epub 2014 Feb 7.
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Mesenchymal stem cells as carriers and amplifiers in CRAd delivery to tumors.间质干细胞作为 CRAd 递送肿瘤的载体和扩增剂。
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Involvement of mesenchymal stem cells in cancer progression and metastases.间充质干细胞在癌症进展和转移中的作用。
Curr Cancer Drug Targets. 2015;15(2):88-98. doi: 10.2174/1568009615666150126154151.

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The Dynamic Roles of Mesenchymal Stem Cells in Colon Cancer.间质干细胞在结肠癌中的动态作用。
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Type I interferons exert anti-tumor effect via reversing immunosuppression mediated by mesenchymal stromal cells.I型干扰素通过逆转间充质基质细胞介导的免疫抑制发挥抗肿瘤作用。
Oncogene. 2016 Nov 17;35(46):5953-5962. doi: 10.1038/onc.2016.128. Epub 2016 Apr 25.

本文引用的文献

1
Mesenchymal stem cells modified to express lentivirus TNF-α Tumstatin(45-132) inhibit the growth of prostate cancer.转染慢病毒 TNF-α Tumstatin(45-132)的间充质干细胞抑制前列腺癌的生长。
J Cell Mol Med. 2011 Feb;15(2):433-44. doi: 10.1111/j.1582-4934.2009.00920.x.
2
Bacterial cytosine deaminase mutants created by molecular engineering show improved 5-fluorocytosine-mediated cell killing in vitro and in vivo.通过分子工程构建的细菌胞嘧啶脱氨酶突变体在体外和体内均表现出增强的5-氟胞嘧啶介导的细胞杀伤作用。
Cancer Res. 2009 Jun 1;69(11):4791-9. doi: 10.1158/0008-5472.CAN-09-0615.
3
Retroviral vector-producing mesenchymal stem cells for targeted suicide cancer gene therapy.用于靶向自杀性癌症基因治疗的逆转录病毒载体生产间充质干细胞
J Gene Med. 2009 May;11(5):373-81. doi: 10.1002/jgm.1313.
4
Assessment of therapeutic efficacy and fate of engineered human mesenchymal stem cells for cancer therapy.工程化人骨髓间充质干细胞用于癌症治疗的疗效评估及转归
Proc Natl Acad Sci U S A. 2009 Mar 24;106(12):4822-7. doi: 10.1073/pnas.0806647106. Epub 2009 Mar 5.
5
Spontaneous expression of embryonic factors and p53 point mutations in aged mesenchymal stem cells: a model of age-related tumorigenesis in mice.衰老间充质干细胞中胚胎因子的自发表达及p53点突变:小鼠年龄相关性肿瘤发生的模型
Cancer Res. 2007 Nov 15;67(22):10889-98. doi: 10.1158/0008-5472.CAN-07-2665.
6
Mesenchymal stem cells within tumour stroma promote breast cancer metastasis.肿瘤基质中的间充质干细胞促进乳腺癌转移。
Nature. 2007 Oct 4;449(7162):557-63. doi: 10.1038/nature06188.
7
Monocyte chemotactic protein-1 secreted by primary breast tumors stimulates migration of mesenchymal stem cells.原发性乳腺肿瘤分泌的单核细胞趋化蛋白-1刺激间充质干细胞迁移。
Clin Cancer Res. 2007 Sep 1;13(17):5020-7. doi: 10.1158/1078-0432.CCR-07-0731.
8
Adult human fibroblasts are potent immunoregulatory cells and functionally equivalent to mesenchymal stem cells.成人成纤维细胞是强大的免疫调节细胞,在功能上等同于间充质干细胞。
J Immunol. 2007 Aug 1;179(3):1595-604. doi: 10.4049/jimmunol.179.3.1595.
9
Adipose tissue-derived human mesenchymal stem cells mediated prodrug cancer gene therapy.脂肪组织来源的人间充质干细胞介导的前体药物癌症基因治疗。
Cancer Res. 2007 Jul 1;67(13):6304-13. doi: 10.1158/0008-5472.CAN-06-4024.
10
The participation of mesenchymal stem cells in tumor stroma formation and their application as targeted-gene delivery vehicles.间充质干细胞在肿瘤基质形成中的参与及其作为靶向基因递送载体的应用。
Handb Exp Pharmacol. 2007(180):263-83. doi: 10.1007/978-3-540-68976-8_12.

间充质干细胞在癌症中的好坏两面:肿瘤生长的助推器和抗癌药物靶向递送的载体。

The bad and the good of mesenchymal stem cells in cancer: Boosters of tumor growth and vehicles for targeted delivery of anticancer agents.

机构信息

Umberto Galderisi, Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, Temple University, Philadelphia, PA 19122, United States.

出版信息

World J Stem Cells. 2010 Feb 26;2(1):5-12. doi: 10.4252/wjsc.v2.i1.5.

DOI:10.4252/wjsc.v2.i1.5
PMID:21607110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3097917/
Abstract

In cancer biology, mesenchymal stem cells (MSCs) display aspects that can appear contradictory. On one hand, these cells possess several features which give them the ability to specifically target and then sustain cancer cells in their ability to survive the multifaceted host response against cancer. On the other hand, due to this excellent aptitude to home-in on tumor tissues, regardless their location in the host's body, MSCs are considered to be extremely selective vehicles to reach cancer cells specifically. Recently, MSC sustainment of cancer cell growth is a hot research topic. Indeed, these cells are known to sustain tumor angiogenesis and metastasis formation, to create a microenvironment favorable for cancer cell growth and to down-modulate the immune system capabilities in the host organism. On the other hand, since scientists became able to take advantage of their extremely selective capability to target cancer cells, MSCs are now also thought of in a different light. Indeed, MSCs are now considered a promising vehicle for local expression or delivery of even particularly toxic anticancer agents, ranging from Herpes Simplex Virus to locally-acting antineoplastic drugs. On this basis, investigation is now focused on how to impair the pro-neoplastic features of MSCs on one hand whilst taking advantage of their specific tropism toward cancer cells, on the other. As with the two faces of Janus, this review will concisely explore the research activity in these two apparently conflicting fields.

摘要

在癌症生物学中,间充质干细胞 (MSCs) 表现出一些看似矛盾的特征。一方面,这些细胞具有多种特性,使它们能够专门针对并维持癌细胞的生存能力,使其能够抵御宿主对癌症的多方面反应。另一方面,由于这种出色的靶向肿瘤组织的能力,无论其在宿主体内的位置如何,MSCs 被认为是专门到达癌细胞的极其特异的载体。最近,MSC 维持癌细胞生长是一个热门的研究课题。事实上,这些细胞已知能够维持肿瘤血管生成和转移形成,创造有利于癌细胞生长的微环境,并下调宿主组织中的免疫系统功能。另一方面,由于科学家们能够利用其对癌细胞的极高选择性靶向能力,MSCs 现在也被赋予了不同的看法。事实上,MSCs 现在被认为是局部表达或递送甚至特别毒性抗癌药物的有前途的载体,范围从单纯疱疹病毒到局部作用的抗肿瘤药物。在此基础上,研究重点现在集中在如何一方面削弱 MSCs 的促瘤特征,另一方面又利用其对癌细胞的特异性趋向性。就像两面神雅努斯一样,这篇综述将简要探讨这两个看似矛盾的领域的研究活动。