Green tea polyphenol stimulates cancer preventive effects of celecoxib in human lung cancer cells by upregulation of GADD153 gene
暂无分享,去创建一个
[1] F. Rizzi,et al. CHEMOPREVENTION OF HUMAN PROSTATE CANCER (PCA) BY ORAL ADMINISTRATION OF GREEN TEA CATECHINS (GTCS) IN HIGH-GRADE PIN (HGPIN) SUBJECTS: A PRELIMINARY REPORT FROM A 1-YEAR PROOF-OF-PRINCIPLE STUDY , 2006 .
[2] I. Weinstein,et al. Modulation of signal transduction by tea catechins and related phytochemicals. , 2005, Mutation research.
[3] F. Shibasaki,et al. Expression of Phosphorylated Ser70 of Bcl-2 Correlates with Malignancy in Human Colorectal Neoplasms , 2005, Clinical Cancer Research.
[4] Yue Wu,et al. Endoplasmic reticulum stress signal mediators are targets of selenium action. , 2005, Cancer research.
[5] Maria R. Garling,et al. Oncogenic Ras-mediated downregulation of Gadd153/CHOP is required for Ras-induced cellular transformation , 2005, Oncogene.
[6] M. Corazzari,et al. Fenretinide: a p53-independent way to kill cancer cells. , 2005, Biochemical and biophysical research communications.
[7] V. Adhami,et al. Green tea constituent epigallocatechin‐3‐gallate selectively inhibits COX‐2 without affecting COX‐1 expression in human prostate carcinoma cells , 2005, International journal of cancer.
[8] H. Eguchi,et al. Combination of IFN-α and 5-Fluorouracil Induces Apoptosis through IFN-α/β Receptor in Human Hepatocellular Carcinoma Cells , 2005 .
[9] F. Khuri,et al. Death receptor regulation and celecoxib-induced apoptosis in human lung cancer cells. , 2004, Journal of the National Cancer Institute.
[10] D. Scott,et al. Curcumin-induced GADD153 gene up-regulation in human colon cancer cells. , 2004, Carcinogenesis.
[11] K. Chisholm,et al. Tamoxifen and epigallocatechin gallate are synergistically cytotoxic to MDA-MB-231 human breast cancer cells , 2004, Anti-cancer drugs.
[12] W. Hsueh,et al. Signaling pathways involved in induction of GADD45 gene expression and apoptosis by troglitazone in human MCF-7 breast carcinoma cells , 2004, Oncogene.
[13] S. Oyadomari,et al. hsp70-DnaJ chaperone pair prevents nitric oxide- and CHOP-induced apoptosis by inhibiting translocation of Bax to mitochondria , 2004, Cell Death and Differentiation.
[14] Y. Rustum,et al. Selective Modulation of the Therapeutic Efficacy of Anticancer Drugs by Selenium Containing Compounds against Human Tumor Xenografts , 2004, Clinical Cancer Research.
[15] R. Hopkins,et al. Induction of GADD gene expression by phenethylisothiocyanate in human colon adenocarcinoma cells , 2003, Journal of cellular biochemistry.
[16] S. Taniguchi,et al. New TNF-alpha releasing inhibitors as cancer preventive agents from traditional herbal medicine and combination cancer prevention study with EGCG and sulindac or tamoxifen. , 2003, Mutation research.
[17] H. Tideman,et al. Upregulation of GADD153 expression in the apoptotic signaling of N‐(4‐hydroxyphenyl)retinamide (4HPR) , 2002, International journal of cancer.
[18] Young-Suk Won,et al. GADD153-mediated Anticancer Effects of N-(4-Hydroxyphenyl)retinamide on Human Hepatoma Cells* , 2002, The Journal of Biological Chemistry.
[19] H. Fujiki,et al. Lung cancer prevention with (-)-epigallocatechin gallate using monitoring by heterogeneous nuclear ribonucleoprotein B1. , 2002, International journal of oncology.
[20] A. Gartel,et al. The role of the cyclin-dependent kinase inhibitor p21 in apoptosis. , 2002, Molecular cancer therapeutics.
[21] K. Miyamoto,et al. Activation of peroxisome proliferator-activated receptor-γ stimulates the growth arrest and DNA-damage inducible 153 gene in non-small cell lung carcinoma cells , 2002, Oncogene.
[22] M. Masuda,et al. Effects of epigallocatechin-3-gallate on growth, epidermal growth factor receptor signaling pathways, gene expression, and chemosensitivity in human head and neck squamous cell carcinoma cell lines. , 2001, Clinical cancer research : an official journal of the American Association for Cancer Research.
[23] H. Fujiki,et al. Modulation of gene expression by (-)-epigallocatechin gallate in PC-9 cells using a cDNA expression array. , 2001, Biological & pharmaceutical bulletin.
[24] E V Maytin,et al. Stress-inducible transcription factor CHOP/gadd153 induces apoptosis in mammalian cells via p38 kinase-dependent and -independent mechanisms. , 2001, Experimental cell research.
[25] T. Aw,et al. Gadd153 Sensitizes Cells to Endoplasmic Reticulum Stress by Down-Regulating Bcl2 and Perturbing the Cellular Redox State , 2001, Molecular and Cellular Biology.
[26] K. Sugimachi,et al. Direct IFNluence of interferon-gamma on proliferation and cell-surface antigen expression of non-small cell lung cancer cells. , 2000, Lung cancer.
[27] F. Hobbs,et al. Identification of a Novel Inhibitor of Mitogen-activated Protein Kinase Kinase* , 1998, The Journal of Biological Chemistry.
[28] D. Kültz,et al. Hyperosmolality Causes Growth Arrest of Murine Kidney Cells , 1998, The Journal of Biological Chemistry.
[29] Xiaozhong Wang,et al. CHOP is implicated in programmed cell death in response to impaired function of the endoplasmic reticulum. , 1998, Genes & development.
[30] E. A. O'neill,et al. Kinetic mechanism for p38 MAP kinase. , 1997, Biochemistry.
[31] A. Komori,et al. Mechanisms of Growth Inhibition of Human Lung Cancer Cell Line, PC‐9, by Tea Polyphenols , 1997, Japanese journal of cancer research : Gann.
[32] S. Steinberg,et al. Altered cJUN expression: an early event in human lung carcinogenesis. , 1996, Cancer research.
[33] B. Neel,et al. Evidence for impaired retinoic acid receptor-thyroid hormone receptor AF-2 cofactor activity in human lung cancer , 1995, Molecular and cellular biology.
[34] D. Ron,et al. CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. , 1992, Genes & development.
[35] J. Fargnoli,et al. Mammalian genes coordinately regulated by growth arrest signals and DNA-damaging agents , 1989, Molecular and cellular biology.
[36] T. Sugimura,et al. Antitumor promoting activity of (−)‐epigallocatechin gallate, the main constituent of “Tannin” in green tea , 1987 .
[37] W. Frishman. Cardiovascular Risk Associated With Celecoxib in a Clinical Trial for Colorectal Adenoma Prevention , 2006 .
[38] H. Fujiki,et al. Translational research on TNF-alpha as an endogenous tumor promoter and green tea as cancer preventive in humans. , 2005, Journal of environmental science and health. Part C, Environmental carcinogenesis & ecotoxicology reviews.
[39] H. Fujiki,et al. Cancer Prevention with Green Tea Polyphenols for the General Population, and for Patients Following Cancer Treatment , 2005 .
[40] H. Fujiki. Green tea: Health benefits as cancer preventive for humans. , 2005, Chemical record.
[41] Y. Ohkura,et al. Combination cancer chemoprevention with green tea extract and sulindac shown in intestinal tumor formation in Min mice , 2001, Journal of Cancer Research and Clinical Oncology.
[42] H. Fujiki,et al. Synergistic effects of (--)-epigallocatechin gallate with (--)-epicatechin, sulindac, or tamoxifen on cancer-preventive activity in the human lung cancer cell line PC-9. , 1999, Cancer research.