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The Hippo pathway: an emerging role in urologic cancers.

TLDR
The Hippo pathway core kinases MST1/2 and LATS 1/2 in mammals phosphorylate and inactivate YAP1 signaling to prevent cancer growth.
Abstract
The Hippo pathway controls several biological processes, including cell growth, differentiation, motility, stemness, cell contact, immune cell maturation, organ size, and tumorigenesis. The Hippo pathway core kinases MST1/2 and LATS1/2 in mammals phosphorylate and inactivate YAP1 signaling. Increasing evidence indicates that loss of MST1/2 and LATS1/2 function is linked to the biology of many cancer types with poorer outcomes, likely due to the activation of oncogenic YAP1/TEAD signaling. Therefore, there is a renewed interest in blocking the YAP1/TEAD functions to prevent cancer growth. This review introduces the Hippo pathway components and examines their role and therapeutic potentials in prostate, kidney, and bladder cancer.

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Citations
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The Hippo pathway and its correlation with acute kidney injury

TL;DR: This review aims to summarize recent findings on the associations between the Hippo pathway and AKI and to identify new therapeutic targets and strategies for AKI.
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The Hippo effector YAP1/TEAD1 regulates EPHA3 expression to control cell contact and motility

TL;DR: In this paper , the authors investigated the mechanism by which MST1 regulates EPHA3 and revealed that the transcriptional regulators YAP1 and TEAD1 are crucial activators of EPHA-3 transcription.
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Integrated molecular analyses of an interferon-γ based subtype with regard to outcome, immune characteristics, and immunotherapy in bladder cancer and experimental verification

TL;DR: In this paper , the role of interferon-γ related genes (IRGs) in the prognosis and immunotherapy of bladder cancer (BC) was explored through Cox regression analyses.
References
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TL;DR: The transcriptional networks in which MITF is thought to reside are discussed and signaling pathways in the cell which impinge on MITF are described, suggesting that the notion thatMITF is involved in survival pathways during normal development as well as during neoplastic growth of melanoma is supported.
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The Uroepithelium: Not Just a Passive Barrier

TL;DR: New analysis of the uroepithelium is providing information about how detergent‐insoluble membrane/protein domains called plaques are formed at the apical plasma membrane of the surface umbrella cells, how mechanical stimuli such as pressure alter exocytic and endocytic traffic in epithelial cells such as umbrella Cells, and how changes in pressure are communicated to the underlying nervous system.
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Structural insights into the YAP and TEAD complex

TL;DR: The three-dimensional structure of the YAP-TEAD1 complex is reported, in which YAP wraps around the globular structure of TEAD1 and forms extensive interactions via three highly conserved interfaces.
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Protein kinase A activates the Hippo pathway to modulate cell proliferation and differentiation

TL;DR: It is demonstrated that cyclic adenosine monophosphate (cAMP), a second messenger downstream from Gαs-coupled receptors, acts through protein kinase A (PKA) and Rho GTPases to stimulate Lats kinases and YAP phosphorylation and reveals new insight into mechanisms of PKA in regulating a broad range of cellular functions.
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