Division of General Medical Sciences-Oncology, Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH 44106, United States.
Cell Signal. 2011 Jun;23(6):951-62. doi: 10.1016/j.cellsig.2010.10.015. Epub 2010 Nov 6.
Tumorigenesis is in many respects a process of dysregulated cellular evolution that drives malignant cells to acquire six phenotypic hallmarks of cancer, including their ability to proliferate and replicate autonomously, to resist cytostatic and apoptotic signals, and to induce tissue invasion, metastasis, and angiogenesis. Transforming growth factor-β (TGF-β) is a potent pleiotropic cytokine that functions as a formidable barrier to the development of cancer hallmarks in normal cells and tissues. Paradoxically, tumorigenesis counteracts the tumor suppressing activities of TGF-β, thus enabling TGF-β to stimulate cancer invasion and metastasis. Fundamental gaps exist in our knowledge of how malignant cells overcome the cytostatic actions of TGF-β, and of how TGF-β stimulates the acquisition of cancer hallmarks by developing and progressing human cancers. Here we review the molecular and cellular mechanisms that underlie the ability of TGF-β to mediate tumor suppression in normal cells, and conversely, to facilitate cancer progression and disease dissemination in malignant cells.
肿瘤发生在许多方面是一个失调的细胞进化过程,它促使恶性细胞获得癌症的六个表型特征,包括自主增殖和复制、抵抗细胞周期停滞和细胞凋亡信号以及诱导组织侵袭、转移和血管生成的能力。转化生长因子-β(TGF-β)是一种有效的多效细胞因子,它作为一种强大的屏障,阻止正常细胞和组织中癌症特征的发展。矛盾的是,肿瘤发生会对抗 TGF-β 的肿瘤抑制作用,从而使 TGF-β能够刺激癌症的侵袭和转移。我们对恶性细胞如何克服 TGF-β的细胞周期停滞作用,以及 TGF-β如何通过发展和进展人类癌症来刺激获得癌症特征的分子和细胞机制知之甚少。在这里,我们回顾了 TGF-β介导正常细胞肿瘤抑制的分子和细胞机制,以及相反地,促进恶性细胞中癌症进展和疾病传播的机制。