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本文引用的文献

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Induction therapy with autologous mesenchymal stem cells in living-related kidney transplants: a randomized controlled trial.自体间充质干细胞诱导治疗活体亲属肾移植:一项随机对照试验。
JAMA. 2012 Mar 21;307(11):1169-77. doi: 10.1001/jama.2012.316.
2
Analysis of exosome release and its prognostic value in human colorectal cancer.分析人结直肠癌细胞外泌体的释放及其预后价值。
Genes Chromosomes Cancer. 2012 Apr;51(4):409-18. doi: 10.1002/gcc.21926.
3
Breast-cancer stem cells-beyond semantics.乳腺癌干细胞——超越语义学。
Lancet Oncol. 2012 Jan;13(1):e43-8. doi: 10.1016/S1470-2045(11)70191-7.
4
Exosomes and immune surveillance of neoplastic lesions: a review.外泌体与肿瘤病变的免疫监视:综述
Biotech Histochem. 2012 Apr;87(3):161-8. doi: 10.3109/10520291003659042. Epub 2012 Jan 4.
5
Human neural stem cell tropism to metastatic breast cancer.人神经干细胞向转移性乳腺癌的趋化性。
Stem Cells. 2012 Feb;30(2):314-25. doi: 10.1002/stem.784.
6
Moving from the laboratory bench to patients' bedside: considerations for effective therapy with stem cells.从实验室工作台到患者床边:干细胞有效治疗的考虑因素。
Clin Transl Sci. 2011 Oct;4(5):380-6. doi: 10.1111/j.1752-8062.2011.00283.x.
7
Understanding tumor-stroma interplays for targeted therapies by armed mesenchymal stromal progenitors: the Mesenkillers.通过武装间充质基质祖细胞理解肿瘤-基质相互作用以用于靶向治疗:Mesenkillers。
Am J Cancer Res. 2011;1(6):787-805. Epub 2011 May 28.
8
AMD3100-mediated production of interleukin-1 from mesenchymal stem cells is key to chemosensitivity of breast cancer cells.AMD3100 介导的间充质干细胞产生白细胞介素-1 是乳腺癌细胞化疗敏感性的关键。
Am J Cancer Res. 2011;1(6):701-15. Epub 2011 Jun 25.
9
Cancer stem cells: targets and potential biomarkers for radiotherapy.肿瘤干细胞:放疗的靶点和潜在生物标志物。
Clin Cancer Res. 2011 Dec 1;17(23):7224-9. doi: 10.1158/1078-0432.CCR-10-2639. Epub 2011 Oct 5.
10
Molecular targeting of malignant glioma cells with an EphA2-specific immunotoxin delivered by human bone marrow-derived mesenchymal stem cells.通过人骨髓间充质干细胞递送 EphA2 特异性免疫毒素对恶性神经胶质瘤细胞进行分子靶向治疗。
Cancer Lett. 2011 Dec 22;312(2):168-77. doi: 10.1016/j.canlet.2011.07.035. Epub 2011 Aug 17.

癌症干细胞会影响未来对干细胞治疗的投资吗?

Would cancer stem cells affect the future investment in stem cell therapy.

作者信息

Rameshwar Pranela

机构信息

Pranela Rameshwar, Department of Medicine, UMDNJ-New Jersey Medical School, 185 South Orange Ave, MSB, Room E-579, Newark, NJ 07103, United States.

出版信息

World J Exp Med. 2012 Apr 20;2(2):26-9. doi: 10.5493/wjem.v2.i2.26.

DOI:10.5493/wjem.v2.i2.26
PMID:24520530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3905576/
Abstract

The common goal within the overwhelming interests in stem cell research is to safely translate the science to patients. Although there are various methods by which this goal can be reached, this editorial emphasizes the safety of mesenchymal stem cell (MSC) transplant and possible confounds by the growing information on cancer stem cells (CSCs). There are several ongoing clinical trials with MSCs and their interactions with CSCs need to be examined. The rapid knowledge on MSCs and CSCs has now collided with regards to the safe treatment of MSCs. The information discussed on MSCs can be extrapolated to other stem cells with similar phenotype and functions such as placenta stem cells. MSCs are attractive for cell therapy, mainly due to reduced ethical concerns, ease in expansion and reduced ability to be transformed. Also, MSCs can exert both immune suppressor and tissue regeneration simultaneously. It is expected that any clinical trial with MSCs will take precaution to ensure that the cells are not transformed. However, going forward, the different centers should be aware that MSCs might undergo oncogenic events, especially as undifferentiated cells or early differentiated cells. Another major concern for MSC therapy is their ability to promote tumor growth and perhaps, to protect CSCs by altered immune responses. These issues are discussed in light of a large number of undiagnosed cancers.

摘要

干细胞研究的众多利益相关方的共同目标是将相关科学成果安全地应用于患者。虽然实现这一目标有多种方法,但本社论强调了间充质干细胞(MSC)移植的安全性以及癌症干细胞(CSC)相关信息不断增加可能带来的混淆因素。目前有多项关于MSC的临床试验正在进行,其与CSC的相互作用需要进行研究。关于MSC和CSC的快速知识如今在MSC的安全治疗方面产生了冲突。文中讨论的关于MSC的信息可以外推到具有相似表型和功能的其他干细胞,如胎盘干细胞。MSC对细胞治疗具有吸引力,主要是因为伦理问题较少、易于扩增且转化能力较低。此外,MSC可以同时发挥免疫抑制和组织再生作用。预计任何关于MSC的临床试验都会采取预防措施,以确保细胞不会发生转化。然而,展望未来,不同的研究中心应该意识到MSC可能会发生致癌事件,尤其是作为未分化细胞或早期分化细胞时。MSC治疗的另一个主要问题是它们促进肿瘤生长的能力,以及可能通过改变免疫反应来保护CSC的能力。鉴于大量未被诊断的癌症,对这些问题进行了讨论。