Lin Hui-Kuan, Bergmann Stephan, Pandolfi Pier Paolo
Department of Pathology, Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Institute, 1275 York Avenue, New York, NY 10021, USA.
Oncogene. 2005 Aug 29;24(37):5693-700. doi: 10.1038/sj.onc.1208923.
Cellular homeostasis is tightly controlled by the various pathways that regulate cell proliferation and cell death. Breaking this balance is often associated with cancer development. The transforming growth factor-beta (TGF-beta) pathway plays an important role in cellular homeostasis by regulating cell growth inhibition, cellular senescence, differentiation and apoptosis. Deregulated TGF-beta signaling is known to be involved in a variety of human cancers, including those of the colon, pancreas, breast and prostate. While TGF-beta is a potent negative regulator of hematopoiesis, the role of aberrant TGF-beta signaling in leukemogenesis remains largely unknown. Recently, evidence demonstrating deregulated TGF-beta signaling in leukemogenesis, particularly in acute promyelocytic leukemia (APL), has started to emerge. In this review, we summarize the current progress towards the understanding of the molecular mechanisms by which aberrant TGF-beta signaling may participate in leukemogenesis.
细胞稳态由调节细胞增殖和细胞死亡的各种途径严格控制。打破这种平衡通常与癌症发展相关。转化生长因子-β(TGF-β)途径通过调节细胞生长抑制、细胞衰老、分化和凋亡在细胞稳态中发挥重要作用。已知TGF-β信号失调与多种人类癌症有关,包括结肠癌、胰腺癌、乳腺癌和前列腺癌。虽然TGF-β是造血的有效负调节因子,但异常的TGF-β信号在白血病发生中的作用仍 largely未知。最近,有证据表明TGF-β信号在白血病发生中失调,特别是在急性早幼粒细胞白血病(APL)中,这种证据已经开始出现。在这篇综述中,我们总结了目前在理解异常TGF-β信号可能参与白血病发生的分子机制方面取得的进展。