Green Tea Polyphenol Epigallocatechin-3-gallate Signaling Pathway through 67-kDa Laminin Receptor*
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Koji Yamada | Koji Yamada | H. Tachibana | Hirofumi Tachibana | Daisuke Umeda | Satomi Yano | Daisuke Umeda | S. Yano
[1] A. El'skaya,et al. Eukaryotic translation elongation factor 1 alpha: structure, expression, functions, and possible role in aminoacyl-tRNA channeling. , 1998, Progress in nucleic acid research and molecular biology.
[2] S. Ménard,et al. New insights into the metastasis‐associated 67 kD laminin receptor , 1997, Journal of cellular biochemistry.
[3] K. Kaibuchi,et al. Disruption of Rho signal transduction upon cell detachment , 2004, Journal of Cell Science.
[4] Mohammad Saleem,et al. Targeting multiple signaling pathways by green tea polyphenol (-)-epigallocatechin-3-gallate. , 2006, Cancer research.
[5] G. Pesole,et al. The 67-kDa laminin receptor originated from a ribosomal protein that acquired a dual function during evolution. , 1998, Molecular biology and evolution.
[6] M. Marra,et al. The translation elongation factor 1A in tumorigenesis, signal transduction and apoptosis: Review article , 2004, Amino Acids.
[7] S. Clarke,et al. A Novel Post-translational Modification of Yeast Elongation Factor 1A , 2000, The Journal of Biological Chemistry.
[8] Y. Surh,et al. Chemopreventive potential of epigallocatechin gallate and genistein: evidence from epidemiological and laboratory studies. , 2004, Toxicology letters.
[9] H. Saya,et al. Association of the Myosin-binding Subunit of Myosin Phosphatase and Moesin: Dual Regulation of Moesin Phosphorylation by Rho-associated Kinase and Myosin Phosphatase , 1998, The Journal of cell biology.
[10] Z. Galcheva-gargova,et al. Interaction of ZPR1 with Translation Elongation Factor-1α in Proliferating Cells , 1998, The Journal of cell biology.
[11] R. Cyr,et al. A calmodulin-sensitive interaction between microtubules and a higher plant homolog of elongation factor-1 alpha. , 1994, The Plant cell.
[12] I. Mazo,et al. Genetic suppressor elements: new tools for molecular oncology--thirteenth Cornelius P. Rhoads Memorial Award Lecture. , 1995, Cancer research.
[13] Gang Lu,et al. Possible mechanisms of the cancer-preventive activities of green tea. , 2006, Molecular nutrition & food research.
[14] J. Traugh,et al. Insulin stimulation of phosphorylation of elongation factor 1 (eEF-1) enhances elongation activity. , 1998, European journal of biochemistry.
[15] B. Ballermann,et al. The protein phosphatase-1 targeting subunit TIMAP regulates LAMR1 phosphorylation. , 2005, Biochemical and biophysical research communications.
[16] A. Somlyo,et al. Ca2+ sensitivity of smooth muscle and nonmuscle myosin II: modulated by G proteins, kinases, and myosin phosphatase. , 2003, Physiological reviews.
[17] W. Merrick,et al. Location of seven post-translational modifications in rabbit elongation factor 1 alpha including dimethyllysine, trimethyllysine, and glycerylphosphorylethanolamine. , 1989, The Journal of biological chemistry.
[18] A. Khakoo,et al. The nonintegrin laminin binding protein (p67 LBP) is expressed on a subset of activated human T lymphocytes and, together with the integrin very late activation antigen-6, mediates avid cellular adherence to laminin. , 1999, Journal of immunology.
[19] K. Kaibuchi,et al. Regulation of the Association of Adducin with Actin Filaments by Rho-associated Kinase (Rho-kinase) and Myosin Phosphatase* , 1998, The Journal of Biological Chemistry.
[20] J. Condeelis,et al. Bundling of actin filaments by elongation factor 1 alpha inhibits polymerization at filament ends , 1996, The Journal of cell biology.
[21] J. Segall,et al. Elongation factor-1 alpha is an overexpressed actin binding protein in metastatic rat mammary adenocarcinoma. , 1996, Journal of cell science.
[22] S. Ménard,et al. Prognostic significance of the 67-kilodalton laminin receptor expression in human breast carcinomas. , 1993, Journal of the National Cancer Institute.
[23] P. Ghezzi,et al. Identification by redox proteomics of glutathionylated proteins in oxidatively stressed human T lymphocytes , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[24] Hanry Yu,et al. Kinectin Anchors the Translation Elongation Factor-1δ to the Endoplasmic Reticulum* , 2003, Journal of Biological Chemistry.
[25] B. Aggarwal,et al. Targeting Signal‐Transducer‐and‐Activator‐of‐Transcription‐3 for Prevention and Therapy of Cancer , 2006, Annals of the New York Academy of Sciences.
[26] D. Hartshorne,et al. Phosphorylation of Thr695 and Thr850 on the myosin phosphatase target subunit: Inhibitory effects and occurrence in A7r5 cells , 2005, FEBS letters.
[27] Koji Yamada,et al. Epigallocatechin-3-O-gallate disrupts stress fibers and the contractile ring by reducing myosin regulatory light chain phosphorylation mediated through the target molecule 67 kDa laminin receptor. , 2005, Biochemical and biophysical research communications.
[28] Yoshiharu Matsuura,et al. Phosphorylation and Activation of Myosin by Rho-associated Kinase (Rho-kinase)* , 1996, The Journal of Biological Chemistry.
[29] Y. Fujimura,et al. A receptor for green tea polyphenol EGCG , 2004, Nature Structural &Molecular Biology.
[30] M. Tatsuka,et al. Rho-kinase contributes to diphosphorylation of myosin II regulatory light chain in nonmuscle cells , 2002, Oncogene.
[31] Giovanni Castagnetti,et al. Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: a preliminary report from a one-year proof-of-principle study. , 2006, Cancer research.
[32] N. Munshi,et al. Specific killing of multiple myeloma cells by (-)-epigallocatechin-3-gallate extracted from green tea: biologic activity and therapeutic implications. , 2006, Blood.
[33] T. Kinzy,et al. Proteasome-Mediated Degradation of Cotranslationally Damaged Proteins Involves Translation Elongation Factor 1A , 2005, Molecular and Cellular Biology.
[34] David J Newman,et al. Natural products as sources of new drugs over the period 1981-2002. , 2003, Journal of natural products.
[35] T. Gloe,et al. The 67-kDa Laminin-binding Protein Is Involved in Shear Stress-dependent Endothelial Nitric-oxide Synthase Expression* , 1999, The Journal of Biological Chemistry.
[36] K. Kaibuchi,et al. Elongation Factor-1α Is a Novel Substrate of Rho-Associated Kinase , 2000 .
[37] Xiaofeng Meng,et al. Stability, cellular uptake, biotransformation, and efflux of tea polyphenol (-)-epigallocatechin-3-gallate in HT-29 human colon adenocarcinoma cells. , 2002, Cancer research.
[38] R. Bernards,et al. A System for Stable Expression of Short Interfering RNAs in Mammalian Cells , 2002, Science.
[39] S. Maciver. Myosin II function in non-muscle cells. , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.
[40] Chung S. Yang. Inhibition of carcinogenesis by tea , 1997, Nature.
[41] D. Hartshorne,et al. Role of Protein Phosphatase Type 1 in Contractile Functions: Myosin Phosphatase* , 2004, Journal of Biological Chemistry.
[42] Koji Yamada,et al. The involvement of the 67 kDa laminin receptor-mediated modulation of cytoskeleton in the degranulation inhibition induced by epigallocatechin-3-O-gallate. , 2006, Biochemical and biophysical research communications.
[43] B. Davidson,et al. Laminin-Induced Signaling in Tumor Cells , 2004, Cancer Research.
[44] S. Ménard,et al. The 67 kDa laminin receptor as a prognostic factor in human cancer , 2004, Breast Cancer Research and Treatment.
[45] Y. Surh,et al. Cancer chemoprevention with dietary phytochemicals , 2003, Nature Reviews Cancer.
[46] I. Mazo,et al. Cloning mammalian genes by expression selection of genetic suppressor elements: association of kinesin with drug resistance and cell immortalization. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[47] M. Wilm,et al. Legionella pneumophila glucosyltransferase inhibits host elongation factor 1A , 2006, Proceedings of the National Academy of Sciences.
[48] T. Abe,et al. Diminution of 37-kDa laminin binding protein expression reduces tumour formation of murine lung cancer cells , 1999, British Journal of Cancer.
[49] D. Brautigan,et al. Inhibition of myosin/moesin phosphatase by expression of the phosphoinhibitor protein CPI-17 alters microfilament organization and retards cell spreading. , 2000, Cell motility and the cytoskeleton.