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Exploiting the convergence of embryonic and tumorigenic signaling pathways to develop new therapeutic targets.

机译:利用胚胎和致瘤信号通路的融合来开发新的治疗靶标。

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摘要

As our understanding of embryonic stem cell biology becomes more sophisticated, the similarities between multipotent cancer cells and these totipotent precursors are increasingly striking. Both multipotent cancer cells and embryonic stem cells possess the ability to self-renew, epigenetically alter their neighboring cellular architecture, and populate a tissue mass with a phenotypically heterogeneous composition of cells. While the molecular signature of these cell types continues to be elucidated, new insights are emerging related to the convergence of embryonic and tumorigenic signaling pathways. Understanding the molecular underpinnings of these two stem cell phenotypes may lead to new therapeutic targets for the elusive cancer cell. While still in its infancy, the potential of adapting embryonic stem cells, and more specifically the factors they produce, is enormous for clinical application. Here we outline evidence that demonstrates the inductive influence of embryonic stem cells and their microenvironment to reprogram cancer cells to exhibit a more benign phenotype, with profound implications for differentiation therapy.
机译:随着我们对胚胎干细胞生物学的理解变得越来越复杂,多能癌细胞与这些全能前体之间的相似性越来越显着。多能癌细胞和胚胎干细胞都具有自我更新的能力,从表观遗传学上改变其邻近的细胞结构,并具有表型上异质的细胞组成的组织块。虽然这些细胞类型的分子标记继续得到阐明,但与胚胎和致瘤信号通路的趋同有关的新见解正在出现。了解这两种干细胞表型的分子基础可能会导致难以捉摸的癌细胞成为新的治疗靶标。尽管仍处于婴儿期,但适应胚胎干细胞的潜力,尤其是它们产生的因子,对于临床应用具有巨大的潜力。在这里,我们概述了证据,这些证据证明了胚胎干细胞及其微环境对癌细胞进行重编程以表现出更为良性的表型的诱导影响,这对于分化治疗具有深远的意义。

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