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      Imaging Gliomas with Nanoparticle-Labeled Stem Cells Translated title: 纳米颗粒标记干细胞对胶质瘤进行成像的最新进展

      review-article
      , ,
      Chinese Medical Journal
      Medknow Publications & Media Pvt Ltd
      Glioma, Nanoparticle, Stem Cell

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          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objective:

          Gliomas are the most common neoplasm of the central nervous system (CNS); however, traditional imaging techniques do not show the boundaries of tumors well. Some researchers have found a new therapeutic mode to combine nanoparticles, which are nanosized particles with various properties for specific therapeutic purposes, and stem cells for tracing gliomas. This review provides an introduction of the basic understanding and clinical applications of the combination of stem cells and nanoparticles as a contrast agent for glioma imaging.

          Data Sources:

          Studies published in English up to and including 2017 were extracted from the PubMed database with the selected key words of “stem cell,” “glioma,” “nanoparticles,” “MRI,” “nuclear imaging,” and “Fluorescence imaging.”

          Study Selection:

          The selection of studies focused on both preclinical studies and basic studies of tracking glioma with nanoparticle-labeled stem cells.

          Results:

          Studies have demonstrated successful labeling of stem cells with multiple types of nanoparticles. These labeled stem cells efficiently migrated to gliomas of varies models and produced signals sensitively captured by different imaging modalities.

          Conclusion:

          The use of nanoparticle-labeled stem cells is a promising imaging platform for the tracking and treatment of gliomas.

          摘要

          目的:

          胶质瘤是中枢神经系统最常见的肿瘤,传统的显像方式对其边缘显像欠佳。有学者发现可通过利用具有纳米级别尺寸和针对特定治疗目的具有多种属性的纳米颗粒与干细胞相结合,从而对胶质瘤进行示踪。本文对利用纳米颗粒标记干细胞作为胶质瘤成像的显像剂这一策略进行了文献综述,并介绍其基本原理和临床应用。

          数据源:

          本文利用PubMed数据库对包括2017年以前的文献通过“干细胞”、 “胶质瘤”、 “核磁共振”、 “核成像”以及“荧光成像”等关键词进行文献筛选。

          研究选择:

          本文对纳入了有关纳米颗粒标记干细胞对胶质瘤进行成像的基础研究和临床前研究。结果: 许多研究表明,纳米颗粒可成功地对干细胞进行标记。被标记的干细胞在不同胶质瘤模型中可有效地向胶质瘤迁移、产生信号并用多种影像学技术进行成像。

          结果:

          许多研究表明,纳米颗粒可成功地对干细胞进行标记。被标记的干细胞在不同胶质瘤模型中可有效地向胶质瘤迁移、产生信号并用多种影像学技术进行成像。

          结论:

          利用纳米颗粒标记的干细胞是一种对胶质瘤进行显像和治疗的具有应用前景的技术平台。

          Related collections

          Most cited references113

          • Record: found
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          Mechanisms and functional implications of adult neurogenesis.

          The generation of new neurons is sustained throughout adulthood in the mammalian brain due to the proliferation and differentiation of adult neural stem cells. In this review, we discuss the factors that regulate proliferation and fate determination of adult neural stem cells and describe recent studies concerning the integration of newborn neurons into the existing neural circuitry. We further address the potential significance of adult neurogenesis in memory, depression, and neurodegenerative disorders such as Alzheimer's and Parkinson's disease.
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            • Record: found
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            • Article: not found

            Concise review: mesenchymal stem/multipotent stromal cells: the state of transdifferentiation and modes of tissue repair--current views.

            Mesenchymal stem cells or multipotent stromal cells (MSCs) isolated from the bone marrow of adult organisms were initially characterized as plastic adherent, fibroblastoid cells with the capacity to generate heterotopic osseous tissue when transplanted in vivo. In recent years, MSCs or MSC-like cells have been shown to reside within the connective tissue of most organs, and their surface phenotype has been well described. A large number of reports have also indicated that the cells possess the capacity to transdifferentiate into epithelial cells and lineages derived from the neuroectoderm. The broad developmental plasticity of MSCs was originally thought to contribute to their demonstrated efficacy in a wide variety of experimental animal models of disease as well as in human clinical trials. However, new findings suggest that the ability of MSCs to alter the tissue microenvironment via secretion of soluble factors may contribute more significantly than their capacity for transdifferentiation in tissue repair. Herein, we critically evaluate the literature describing the plasticity of MSCs and offer insight into how the molecular and functional heterogeneity of this cell population, which reflects the complexity of marrow stroma as an organ system, may confound interpretation of their transdifferentiation potential. Additionally, we argue that this heterogeneity also provides a basis for the broad therapeutic efficacy of MSCs.
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              • Record: found
              • Abstract: found
              • Article: not found

              Neural stem cells display extensive tropism for pathology in adult brain: evidence from intracranial gliomas.

              One of the impediments to the treatment of brain tumors (e.g., gliomas) has been the degree to which they expand, infiltrate surrounding tissue, and migrate widely into normal brain, usually rendering them "elusive" to effective resection, irradiation, chemotherapy, or gene therapy. We demonstrate that neural stem cells (NSCs), when implanted into experimental intracranial gliomas in vivo in adult rodents, distribute themselves quickly and extensively throughout the tumor bed and migrate uniquely in juxtaposition to widely expanding and aggressively advancing tumor cells, while continuing to stably express a foreign gene. The NSCs "surround" the invading tumor border while "chasing down" infiltrating tumor cells. When implanted intracranially at distant sites from the tumor (e.g., into normal tissue, into the contralateral hemisphere, or into the cerebral ventricles), the donor cells migrate through normal tissue targeting the tumor cells (including human glioblastomas). When implanted outside the CNS intravascularly, NSCs will target an intracranial tumor. NSCs can deliver a therapeutically relevant molecule-cytosine deaminase-such that quantifiable reduction in tumor burden results. These data suggest the adjunctive use of inherently migratory NSCs as a delivery vehicle for targeting therapeutic genes and vectors to refractory, migratory, invasive brain tumors. More broadly, they suggest that NSC migration can be extensive, even in the adult brain and along nonstereotypical routes, if pathology (as modeled here by tumor) is present.
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                Author and article information

                Journal
                Chin Med J (Engl)
                Chin. Med. J
                CMJ
                Chinese Medical Journal
                Medknow Publications & Media Pvt Ltd (India )
                0366-6999
                20 March 2018
                : 131
                : 6
                : 721-730
                Affiliations
                [1]Department of Neurosurgical Oncology, The First Hospital of Jilin University, Changchun, Jilin 130021, China
                Author notes
                Address for correspondence: Prof. Gang Zhao, Department of Neurosurgical Oncology, The First Hospital of Jilin University, Changchun, Jilin 130021, China E-Mail: 1527332564@ 123456qq.com
                Article
                CMJ-131-721
                10.4103/0366-6999.226900
                5865319
                29521296
                cf92278d-a5a2-40c3-992e-55225b249e06
                Copyright: © 2018 Chinese Medical Journal

                This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

                History
                : 04 December 2017
                Categories
                Review Article

                glioma,nanoparticle,stem cell
                glioma, nanoparticle, stem cell

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