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Stem Cells, Colorectal Cancer and Cancer Stem Cell Markers Correlations

机译:干细胞,结直肠癌与癌症干细胞标志物的相关性

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The idea of stem cells as being progenitors of cancer was initially controversial, but later supported by research in the field of leukemia and solid tumors. Afterwards, it was established that genetic abnormalities can affect the stem and progenitor cells, leading to uncontrolled replication and deregulated differentiation. These alterations will cause the changeover to cancerous stem cells (CSC) having two main characteristics: tumor initiation and maintenance. This review will focus on the colorectal cancer stem cell (CR-CSCs) theory which provides a better understanding of different tumor processes: initiation, aggressive growth, recurrence, treatment resistance and metastasis. A search in PubMed/Medline was performed using the following keywords: colorectal cancer stem cells (CR-CSCs), colorectal neoplasms stem cells, colorectal cancer stem cell (CR-CSCs) markers, etc. Electronic searches were supplemented by hand searching reference lists, abstracts and proceedings from meetings. Isolation of CR-CSCs can be achieved by targeting and selecting subpopulation of tumor cells based on expression of one or multiple cell surface markers associated with cancer self-renewal, markers as: CD133, CD166, CD44, CD24, beta1 integrin-CD29, Lgr5, EpCAM (ESA), ALDH-1, Msi-1, DCAMLK1 or EphB receptors. The identification and localization of CR-CSCs through different markers will hopefully lead to a better stratification of prognosis and treatment response, as well as the development of new effective strategies for cancer management.
机译:干细胞作为癌症的祖先的想法最初引起争议,但后来得到白血病和实体瘤领域研究的支持。此后,已经确定遗传异常会影响干细胞和祖细胞,导致不受控制的复制和分化失控。这些改变将导致向具有两个主要特征的癌干细胞(CSC)的转变:肿瘤的发生和维持。这篇综述将集中于结直肠癌干细胞(CR-CSCs)理论,该理论可以更好地理解不同的肿瘤过程:起始,侵袭性生长,复发,治疗耐药性和转移。使用以下关键字在PubMed / Medline中进行搜索:结肠直肠癌干细胞(CR-CSCs),结肠直肠肿瘤干细胞,结肠直肠癌干细胞(CR-CSCs)标记等。通过手工搜索参考列表来补充电子搜索,会议摘要和议事录。可以通过基于与癌症自我更新相关的一种或多种细胞表面标志物的表达来靶向和选择肿瘤细胞的亚群,从而实现CR-CSC的分离,这些标志物包括:CD133,CD166,CD44,CD24,beta1整合素CD29,Lgr5 ,EpCAM(ESA),ALDH-1,Msi-1,DCAMLK1或EphB受体。通过不同的标志物鉴定和定位CR-CSCs有望更好地对预后和治疗反应进行分层,并开发出新的有效癌症治疗策略。

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