Intercellular Signaling in Development and Disease: Cell by Edward A. Dennis, Ralph A. Bradshaw

By Edward A. Dennis, Ralph A. Bradshaw

Required studying for somebody considering mobilephone signaling examine with articles written and edited via specialists within the box. This name covers disorder states corresponding to lymphoid leukemia, breast melanoma, pulmonary fibrosis, systemic sclerosis, andinflammatory bowel sickness, in addition to up to date study on signaling platforms and mutations in
transcription elements that offer new ambitions for treating disease.

  • Articles written and edited through specialists within the field
  • Thematic quantity masking sickness states similar to lymphoid leukemia, breast melanoma, pulmonary fibrosis, systemic sclerosis, and inflammatory bowel disease
  • Up-to-date study on signaling structures and mutations in transcription components that supply new pursuits for treating disease
  • Show description

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    Extra info for Intercellular Signaling in Development and Disease: Cell Signaling Collection

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    Paxillin phosphorylation at Y31 and 118 also generates binding sites for p120RasGAP, which through p190RhoGAP can contribute to local suppression of RhoA activity. Similarly, FAK/Src phosphorylation of the Arf GAP, GIT facilitates recruitment of the GIT–PIX–PAK–Nck complex into focal adhesions via interaction with the paxillin LD4 motif. The Cdc42/Rac GEF PIX can locally stimulate Rac1 and Cdc42 and trigger cytoskeleton reorganization via activation of various effector proteins including p21-activated kinase (PAK).

    This specialized form of cell death is referred to as anoikis). Normal epithelial cells acquire resistance to anoikis upon expression of certain oncogenes [91–93]. A number of studies have implicated integrin signaling to the phosphoinositide-3Ј-kinase (PI3K)–AKT pathway as a central regulator of anoikis [92]. FAK is thought to regulate anoikis by direct activation of PI3K and AKT, and perhaps indirectly via interactions with Cas/Crk/DOCK180/Rac [89]. Integrin-linked kinase (ILK) has also been implicated in signaling to AKT, although this pathway is poorly understood.

    Hehlgans S, Haase M, Cordes N. Signalling via integrins: implications for cell survival and anticancer strategies. Biochim Biophys Acta 2007;1775:163–80. 97. Howe A, Aplin AE, Alahari SK, Juliano RL. Integrin signaling and cell growth control. Curr Opin Cell Biol 1998;10:220–31. 98. Parsons JT, Slack-Davis J, Tilghman R, Roberts WG. Focal adhesion kinase: targeting adhesion signaling pathways for therapeutic intervention. Clin Cancer Res 2008;14:627–32. 99. Yamada KM, Araki M. Tumor suppressor PTEN: modulator of cell signaling, growth, migration and apoptosis.

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