Avivar-Valderas A, Wen H C, Aguirre-Ghiso J A
1] Division of Hematology and Oncology, Department of Medicine, Mount Sinai School of Medicine, New York, NY, USA [2] Department of Otolaryngology, Mount Sinai School of Medicine, New York, NY, USA [3] Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, USA.
1] Tisch Cancer Institute, Mount Sinai School of Medicine, New York, NY, USA [2] Department of Oncological Sciences, Mount Sinai School of Medicine, New York, NY, USA.
Oncogene. 2014 Nov 27;33(48):5483-90. doi: 10.1038/onc.2013.554. Epub 2014 Jan 13.
The postnatal mammary gland develops extensively through cycles of proliferation, branching, involution and remodeling. We review recent advances made in the field of stress signaling pathways and its roles in mammary gland organogenesis, how they contribute to normal organ specification and homeostasis and how its subversion by oncogenes leads to cancer. We analyze stress signaling in mammary gland biology taking into account the interrelationship with the extracellular matrix and adhesion signaling during morphogenesis. By integrating the information gathered from in vivo and three dimensional in vitro organogenesis studies, we review the novel contribution of p38(SAPK), c-Jun NH2-terminal kinase and PKR-like endoplasmic reticulum kinase (PERK) signaling pathways to the timely activation of cell death, correct establishment of polarity and growth arrest and autophagy, respectively. We also review the evidence supporting that the activation of the aforementioned stress kinases maintain breast acinar structures as part of a tumor suppressive program and that its deregulation is commonplace during breast cancer initiation.
产后乳腺通过增殖、分支、退化和重塑循环进行广泛发育。我们综述了应激信号通路领域的最新进展及其在乳腺器官发生中的作用,它们如何促进正常器官的形成和稳态,以及癌基因对其的破坏如何导致癌症。我们在形态发生过程中考虑到与细胞外基质和黏附信号的相互关系,分析了乳腺生物学中的应激信号。通过整合从体内和三维体外器官发生研究中收集的信息,我们分别综述了p38(SAPK)、c-Jun氨基末端激酶和PKR样内质网激酶(PERK)信号通路对细胞死亡的及时激活、极性的正确建立、生长停滞和自噬的新贡献。我们还综述了支持上述应激激酶的激活作为肿瘤抑制程序的一部分维持乳腺腺泡结构的证据,以及其失调在乳腺癌发生过程中很常见的证据。