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TABLE OF CONTENTS |
September 2016 Volume 18, Issue 9 |
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Open for Submissions
npj Precision Oncology is a new open access, online-only, peer-reviewed journal committed to publishing cutting-edge scientific research in all aspects of precision oncology from basic science to translational applications, to clinical medicine. The journal is part of the Nature Partner Journals series and published in partnership with The Hormel Institute, University of Minnesota.
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News and Views | Top |
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nature.com webcasts Nature Publishing Group presents a custom webcast on: Releasable purification of monocytes for human dendritic cell generation Watch on-demand today Sponsored by: Quad Technologies | | | |
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Snail/Slug binding interactions with YAP/TAZ control skeletal stem cell self-renewal and differentiation pp917 - 929 Yi Tang, Tamar Feinberg, Evan T. Keller, Xiao-Yan Li and Stephen J. Weiss doi:10.1038/ncb3394 Weiss and colleagues report that the EMT transcription factors Snail and Slug control skeletal stem cell self-renewal and differentiation by forming transcriptional complexes with the co-activators YAP and TAZ.
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Sex hormones establish a reserve pool of adult muscle stem cells pp930 - 940 Ji-Hoon Kim, Gi-Chan Han, Ji-Yun Seo, Inkuk Park, Wookjin Park et al. doi:10.1038/ncb3401 Kim et al. demonstrate that sex hormones induce Mib1 expression in myofibres during puberty, initiating the conversion of cycling juvenile satellite cells into adult quiescent satellite cells.
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Kank2 activates talin, reduces force transduction across integrins and induces central adhesion formation pp941 - 953 Zhiqi Sun, Hui-Yuan Tseng, Steven Tan, Fabrice Senger, Laetitia Kurzawa et al. doi:10.1038/ncb3402 At sites of cell adhesion to the matrix, integrins are coupled to the actin cytoskeleton through proteins such as talin. Sun et al. now identify Kank2 as an activator of talin that reduces force transmission across focal adhesions.
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Nuclear GSK3β promotes tumorigenesis by phosphorylating KDM1A and inducing its deubiquitylation by USP22 pp954 - 966 Aidong Zhou, Kangyu Lin, Sicong Zhang, Yaohui Chen, Nu Zhang et al. doi:10.1038/ncb3396 Zhou et al. show that GSK3β phosphorylates KDM1A and induces its deubiquitylation by USP22, leading to demethylation of histone H3K4 and glioblastoma progression.
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A single dividing cell population with imbalanced fate drives oesophageal tumour growth pp967 - 978 Julia Frede, Philip Greulich, Tibor Nagy, Benjamin D. Simons and Philip H. Jones doi:10.1038/ncb3400 Frede et al. use a chemical carcinogenesis model and lineage tracing to show that oesophageal tumour growth is driven by a single proliferating cancer cell population, suggesting the absence of a hierarchy of proliferating cells in this cancer type.
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NOTCH1 mediates a switch between two distinct secretomes during senescence pp979 - 992 Matthew Hoare, Yoko Ito, Tae-Won Kang, Michael P. Weekes, Nicholas J. Matheson et al. doi:10.1038/ncb3397 Hoare et al. find that NOTCH1 regulates the switch between two distinct senescence-associated secretomes—the TGF-β pathway and pro-inflammatory cytokines—and that its inhibition promotes clearance of oncogene-induced senescent liver cells.
See also: News and Views by Schmitt
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G9a/RelB regulates self-renewal and function of colon-cancer-initiating cells by silencing Let-7b and activating the K-RAS/β-catenin pathway pp993 - 1005 Shih-Ting Cha, Ching-Ting Tan, Cheng-Chi Chang, Chia-Yu Chu, Wei-Jiunn Lee et al. doi:10.1038/ncb3395 Cha et al. report that the G9a/RelB axis represses Let-7b through DNMT3A, and sustains K-RAS and β-catenin signalling, thereby controlling the maintenance and function of colorectal-cancer-initiating cells.
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Melanoma miRNA trafficking controls tumour primary niche formation pp1006 - 1017 Shani Dror, Laureen Sander, Hila Schwartz, Danna Sheinboim, Aviv Barzilai et al. doi:10.1038/ncb3399 Dror et al. report that melanoma-derived melanosomes carry miRNAs that induce primary fibroblast reprogramming into cancer-associated fibroblasts, and also induce the formation of a pro-tumorigenic niche.
See also: News and Views by García-Silva & Peinado
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Experimental & Molecular Medicine is an open access journal to communicate experimental and translational research performed using molecular tools. Submit your manuscript. | | | |
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Letter | Top |
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The mammalian dynein–dynactin complex is a strong opponent to kinesin in a tug-of-war competition pp1018 - 1024 Vladislav Belyy, Max A. Schlager, Helen Foster, Armando E. Reimer, Andrew P. Carter et al. doi:10.1038/ncb3393 It has been unclear how the relatively weak dynein motor can counterbalance kinesin forces during microtubule-dependent transport. Belyy et al. find that binding of dynactin and BICD2 increases the strength of the dynein motor.
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