Lee Yong-Hun, Schiemann William P
Case Comprehensive Cancer Center, Division of General Medical Sciences-Oncology, Case Western Reserve University, Wolstein Research Building, 2103 Cornell Road Cleveland, OH 44106.
Breast Cancer Manag. 2014;3(1):73-85. doi: 10.2217/bmt.13.74.
Transforming growth factor (TGF-β) is a multifunctional cytokine that plays essential roles in regulating mammary gland development, morphogenesis, differentiation, and involution. TGF-β also regulates mammary gland homeostasis and prevents its transformation by prohibiting dysregulated cell cycle progression, and by inducing apoptosis; it also creates cell microenvironments that readily inhibit cell migration, invasion, and metastasis. Interestingly, while early-stage mammary tumors remain sensitive to the tumor suppressing activities of TGF-β, late-stage breast cancers become insensitive to the anticancer functions of this cytokine and instead rely upon TGF-β to drive disease and metastatic progression. This switch in TGF-β function is known as the "TGF-β Paradox" and represents the rationale for developing chemotherapies to inactivate the TGF-β pathway and its oncogenic functions in late-stage breast cancers. Here we outline the molecular mechanisms that manifest the "TGF-β Paradox" and discuss the challenges associated with the development and use of anti-TGF-β agents to treat breast cancer patients.
转化生长因子(TGF-β)是一种多功能细胞因子,在调节乳腺发育、形态发生、分化和退化过程中发挥着重要作用。TGF-β还通过禁止细胞周期进展失调和诱导细胞凋亡来调节乳腺内环境稳定,并防止其发生转化;它还能创造易于抑制细胞迁移、侵袭和转移的细胞微环境。有趣的是,虽然早期乳腺肿瘤对TGF-β的肿瘤抑制活性仍保持敏感,但晚期乳腺癌对这种细胞因子的抗癌功能变得不敏感,反而依赖TGF-β来驱动疾病和转移进展。TGF-β功能的这种转变被称为“TGF-β悖论”,这也是开发化学疗法以灭活晚期乳腺癌中TGF-β信号通路及其致癌功能的理论基础。在此,我们概述了体现“TGF-β悖论”的分子机制,并讨论了开发和使用抗TGF-β药物治疗乳腺癌患者所面临的挑战。