MARC 主機 00000nam a2200553 i 4500 001 978-981-10-3233-2 003 DE-He213 005 20170315105341.0 006 m o d 007 cr nn 008maaau 008 170315s2017 si s 0 eng d 020 9789811032332|q(electronic bk.) 020 9789811032318|q(paper) 024 7 10.1007/978-981-10-3233-2|2doi 040 GP|cGP|erda 041 0 eng 050 4 QP624.75.P74 072 7 MFN|2bicssc 072 7 MED107000|2bisacsh 072 7 SCI029000|2bisacsh 082 04 572.86|223 245 00 RUNX proteins in development and cancer /|cedited by Yoram Groner, Yoshiaki Ito, Paul Liu, James C. Neil, Nancy A. Speck, Andre van Wijnen 264 1 Singapore :|bSpringer Singapore :|bImprint: Springer, |c2017 300 1 online resource (xx, 515 pages) :|billustrations, digital ;|c24 cm 336 text|btxt|2rdacontent 337 computer|bc|2rdamedia 338 online resource|bcr|2rdacarrier 347 text file|bPDF|2rda 490 1 Advances in experimental medicine and biology,|x0065-2598 ;|vvolume 962 505 0 RUNX in invertebrates -- Structure and biophysics of CBFb/ RUNX and its transcription products -- Covalent modification of RUNX proteins: structure affects function -- The role of Runx1 in embryonic blood cell formation -- RUNX1 structure and function in blood cell development -- Roles of Runx2 in skeletal development -- Roles of Runx genes in nervous system development -- Runx family genes in tissue stem cell dynamics -- Roles of RUNX1 enhancer in normal hematopoiesis and leukemogenesis -- RUNX1-ETO leukemia -- Clinical relevance of RUNX1 and CBFB alterations in acute myeloid leukemia and other hematological disorders -- Mechanism of ETV6-RUNX1 leukemia -- ETV6-RUNX1+ acute lymphoblastic leukemia in identical twins -- Molecular basis and targeted inhibition of CBFb-SMMHC acute myeloid leukemia -- The RUNX genes as conditional oncogenes: insights from retroviral targeting and mouse models -- RUNX1 and CBFb mutations and activities of their wild-type alleles in AML -- Roles of RUNX in B cell immortalization -- Roles of RUNX in solid tumors -- RUNX3 and p53: How two tumor suppressors cooperate against oncogenic Ras -- Runx3 and cell fate decisions in pancreas cancer -- RUNX genes in breast cancer and the mammary lineage -- Runx3 in immunity, inflammation and cancer -- Roles of RUNX complexes in immune cell development -- CBFb and HIV infection -- Roles of RUNX in Hippo pathway signaling -- Roles of RUNX in hypoxia-induced responses and angiogenesis -- The emerging roles of RUNX transcription factors in Epithelial- Mesenchymal Transition -- Regulatory role of RUNX1 and RUNX3 in the maintenance of genomic integrity 520 This volume provides the reader with an overview of the diverse functions of the RUNX family of genes. As highlighted in the introduction and several of the 29 chapters, humans and other mammals have three RUNX genes that are known to play specific roles in blood, bone and neuronal development. However, their evolutionary history has recently been traced back to unicellular organisms and their involvement in many well-known signaling pathways (Wnt, TGFb, Notch, Hippo) is indicative of a more general function in cell biology. Their documented roles in cell fate decisions include control of proliferation, differentiation, survival, senescence and autophagy. The pleiotropic effects of RUNX in development are mirrored in cancer, where RUNX genes can function as oncogenes that collaborate strongly with Myc family oncogenes or as tumour suppressor genes. In the latter role, they display hallmarks of both 'gatekeepers' that modulate p53 responses and 'caretakers' that protect the genome from DNA damage. Several chapters focus on the importance of these genes in leukemia research, where RUNX1 and CBFB are frequently affected by chromosomal translocations that generate fusion oncoproteins, while recent studies suggest wider roles for RUNX modulation in solid cancers. Moreover, RUNX genes are intimately involved in the development and regulation of the immune system, while emerging evidence suggests a role in innate immunity to infectious agents, including HIV. At the biochemical level, the RUNX family can serve as activators or repressors of transcription and as stable mediators of epigenetic memory through mitosis. Not surprisingly, RUNX activity is controlled at multiple levels, this includes miRNAs and a plethora of post- translational modifications. Several chapters highlight the interplay between the three mammalian RUNX genes, where cross-talk and partial functional redundancies are evident. Finally, structural analysis of the RUNX/CBFB interaction has led to the development of small molecule inhibitors that provide exciting new tools to decipher the roles of RUNX in development and as targets for therapy. This volume provides a compendium and reference source that will be of broad interest to cancer researchers, developmental biologists and immunologists 650 0 DNA-binding proteins|xCancer|xResearch 650 0 Life sciences 650 14 Biomedicine 650 24 Gene Function 650 24 Oncology 650 24 Protein Science 700 1 Groner, Yoram,|eeditor 700 1 Ito, Yoshiaki,|eeditor 700 1 Liu, Paul,|eeditor 700 1 Neil, James C.,|eeditor 700 1 Speck, Nancy A.,|eeditor 700 1 Wijnen, Andre van,|eeditor 710 2 SpringerLink (Online service) 773 0 |tSpringer eBooks 830 0 Advances in experimental medicine and biology ;|vvolume 962 856 40 |uhttp://dx.doi.org/10.1007/978-981-10-3233-2 912 Springer|b110608094615
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