Dreesen Oliver, Brivanlou Ali H
Laboratory of Molecular Vertebrate Embryology, The Rockefeller University, New York, NY 10021-6399, USA.
Stem Cell Rev. 2007 Jan;3(1):7-17. doi: 10.1007/s12015-007-0004-8.
Cancer cells have the ability to divide indefinitely and spread to different parts of the body during metastasis. Embryonic stem cells can self-renew and, through differentiation to somatic cells, provide the building blocks of the human body. Embryonic stem cells offer tremendous opportunities for regenerative medicine and serve as an excellent model system to study early human development. Many of the molecular mechanism underlying tumorigenesis in cancer and self-renewal in stem cells have been elucidated in the past decade. Here we present a systematic analysis of seven major signaling pathways implicated in both cancer and stem cells. We present on overview of the JAK/STAT, Notch, MAPK/ERK, PI3K/AKT, NF-kB, Wnt and TGF-beta pathways and analyze their activation status in the context of cancer and stem cells. We focus on their role in stem cell self-renewal and development and identify key molecules, whose aberrant expression has been associated with malignant phenotypes. We conclude by presenting a map of the signaling networks involved in cancer and embryonic stem cells.
癌细胞具有无限增殖的能力,并在转移过程中扩散到身体的不同部位。胚胎干细胞能够自我更新,并通过分化为体细胞,提供人体的组成部分。胚胎干细胞为再生医学提供了巨大的机会,并作为研究人类早期发育的优秀模型系统。在过去十年中,许多癌症发生和干细胞自我更新的分子机制已被阐明。在这里,我们对涉及癌症和干细胞的七个主要信号通路进行了系统分析。我们概述了JAK/STAT、Notch、MAPK/ERK、PI3K/AKT、NF-κB、Wnt和TGF-β通路,并分析了它们在癌症和干细胞背景下的激活状态。我们重点关注它们在干细胞自我更新和发育中的作用,并确定其异常表达与恶性表型相关的关键分子。最后,我们展示了一张涉及癌症和胚胎干细胞的信号网络图谱。