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      K63-Linked Ubiquitination in Kinase Activation and Cancer

      Frontiers in Oncology
      Frontiers Media S.A.
      akt, traf6, phosphorylation, nf-κb, ubiquitination, tumorigenesis, protein kinase

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          Abstract

          Ubiquitination has been demonstrated to play a pivotal role in multiple biological functions, which include cell growth, proliferation, apoptosis, DNA damage response, innate immune response, and neuronal degeneration. Although the role of ubiquitination in targeting proteins for proteasome-dependent degradation have been extensively studied and well-characterized, the critical non-proteolytic functions of ubiquitination, such as protein trafficking and kinase activation, involved in cell survival and cancer development, just start to emerge, In this review, we will summarize recent progresses in elucidating the non-proteolytic function of ubiquitination signaling in protein kinase activation and its implications in human cancers. The advancement in the understanding of the novel functions of ubiquitination in signal transduction pathways downstream of growth factor receptors may provide novel paradigms for the treatment of human cancers.

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          Most cited references135

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          Cellular survival: a play in three Akts.

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            The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins.

            Selective trafficking of membrane proteins to lysosomes for destruction is required for proper cell signalling and metabolism. Ubiquitylation aids this process by specifying which proteins should be transported to the lysosome lumen by the multivesicular endosome pathway. The endosomal sorting complex required for transport (ESCRT) machinery sorts cargo labelled with ubiquitin into invaginations of endosome membranes. Then, through a highly conserved mechanism also used in cytokinesis and viral budding, it mediates the breaking off of the cargo-containing intraluminal vesicles from the perimeter membrane. The involvement of the ESCRT machinery in suppressing diseases such as cancer, neurodegeneration and infections underscores its importance to the cell.
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              A role for ubiquitin in selective autophagy.

              Ubiquitination is the hallmark of protein degradation by the 26S proteasome. However, the proteasome is limited in its capacity to degrade oligomeric and aggregated proteins. Removal of harmful protein aggregates is mediated by autophagy, a mechanism by which the cell sequesters cytosolic cargo and delivers it for degradation by the lysosome. Identification of autophagy receptors, such as p62/SQSTM1 and NBR1, which simultaneously bind both ubiquitin and autophagy-specific ubiquitin-like modifiers, LC3/GABARAP, has provided a molecular link between ubiquitination and autophagy. This review explores the hypothesis that ubiquitin represents a selective degradation signal suitable for targeting various types of cargo, ranging from protein aggregates to membrane-bound organelles and microbes.
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                Author and article information

                Journal
                Front Oncol
                Front Oncol
                Front. Oncol.
                Frontiers in Oncology
                Frontiers Research Foundation
                2234-943X
                31 January 2012
                2012
                : 2
                : 5
                Affiliations
                [1] 1simpleDepartment of Cancer Biology, The University of Texas M. D. Anderson Cancer Center Houston, TX, USA
                [2] 2simpleDepartment of Molecular and Cellular Oncology, The University of Texas M. D. Anderson Cancer Center Houston, TX, USA
                [3] 3simpleThe University of Texas Graduate School of Biomedical Sciences at Houston Houston, TX, USA
                [4] 4simpleDepartment of Genomic Medicine, The University of Texas M. D. Anderson Cancer Center Houston, TX, USA
                [5] 5simpleDepartment of Biological Science and Technology, National Chiao Tung University Hsinchu, Taiwan
                Author notes

                Edited by: Wenyi Wei, Beth Israel Deaconess Medical Center, Harvard Medical School, USA

                Reviewed by: Paolo Pinton, University of Ferrara, Italy; David Kong Ann, City of Hope National Medical Center, USA

                *Correspondence: Hui-Kuan Lin, Department of Molecular and Cellular Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA. e-mail: hklin@ 123456mdanderson.org

                This article was submitted to Frontiers in Molecular and Cellular Oncology, a specialty of Frontiers in Oncology.

                Article
                10.3389/fonc.2012.00005
                3355940
                22649774
                f914820b-1baf-4328-b557-d5e6f3b46029
                Copyright © 2012 Wang, Gao, Li, Jin, Cai, Chao and Lin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

                History
                : 15 December 2011
                : 10 January 2012
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 171, Pages: 13, Words: 12848
                Categories
                Oncology
                Review Article

                Oncology & Radiotherapy
                akt,traf6,phosphorylation,nf-κb,ubiquitination,tumorigenesis,protein kinase
                Oncology & Radiotherapy
                akt, traf6, phosphorylation, nf-κb, ubiquitination, tumorigenesis, protein kinase

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