Halofuginone enhances the radiation sensitivity of human tumor cell lines.
暂无分享,去创建一个
[1] Jonathan Maybaum,et al. Gemcitabine sensitization by checkpoint kinase 1 inhibition correlates with inhibition of a Rad51 DNA damage response in pancreatic cancer cells , 2009, Molecular Cancer Therapeutics.
[2] J. Massagué,et al. TGFβ in Cancer , 2008, Cell.
[3] M. Anscher,et al. Small molecular inhibitor of transforming growth factor-beta protects against development of radiation-induced lung injury. , 2008, International journal of radiation oncology, biology, physics.
[4] M. Pines. Targeting TGFβ signaling to inhibit fibroblast activation as a therapy for fibrosis and cancer: effect of halofuginone , 2008, Expert opinion on drug discovery.
[5] J. Nickoloff,et al. Regulation of DNA double-strand break repair pathway choice , 2008, Cell Research.
[6] W. Plunkett,et al. H2AX phosphorylation marks gemcitabine-induced stalled replication forks and their collapse upon S-phase checkpoint abrogation , 2007, Molecular Cancer Therapeutics.
[7] M. Barcellos-Hoff,et al. New rationales for using TGFbeta inhibitors in radiotherapy , 2007, International journal of radiation biology.
[8] Inhibition of transforming growth factor-beta1 signaling attenuates ataxia telangiectasia mutated activity in response to genotoxic stress. , 2006, Cancer research.
[9] D. Lacombe,et al. Phase I and pharmacokinetic study of halofuginone, an oral quinazolinone derivative in patients with advanced solid tumours. , 2006, European journal of cancer.
[10] B. Teicher,et al. Antitransforming growth factor-beta antibody 1D11 ameliorates normal tissue damage caused by high-dose radiation. , 2006, International journal of radiation oncology, biology, physics.
[11] V. Natale,et al. H2AX phosphorylation within the G1 phase after UV irradiation depends on nucleotide excision repair and not DNA double-strand breaks. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[12] I. Bièche,et al. Halofuginone suppresses the lung metastasis of chemically induced hepatocellular carcinoma in rats through MMP inhibition. , 2006, Neoplasia.
[13] P. Harari,et al. Radiation combined with EGFR signal inhibitors: head and neck cancer focus. , 2006, Seminars in radiation oncology.
[14] P. Harari,et al. Radiation and new molecular agents, part II: targeting HDAC, HSP90, IGF-1R, PI3K, and Ras. , 2006, Seminars in radiation oncology.
[15] A. Nagler,et al. Halofuginone inhibits angiogenesis and growth in implanted metastatic rat brain tumor model--an MRI study. , 2004, Neoplasia.
[16] A. Nagler,et al. Suppression of hepatocellular carcinoma growth in mice by the alkaloid coccidiostat halofuginone. , 2004, European journal of cancer.
[17] James B. Mitchell,et al. Amelioration of Radiation-induced Fibrosis , 2004, Journal of Biological Chemistry.
[18] Y. Ogawa,et al. Histopathologic amelioration of fibroproliferative change in rat irradiated lung using soluble transforming growth factor-beta (TGF-beta) receptor mediated by adenoviral vector. , 2004, International journal of radiation oncology, biology, physics.
[19] J. Thacker,et al. The mammalian XRCC genes: their roles in DNA repair and genetic stability. , 2003, DNA repair.
[20] S. Dupont,et al. Links between Tumor Suppressors p53 Is Required for TGF-β Gene Responses by Cooperating with Smads , 2003, Cell.
[21] T. Samulski,et al. Soluble TGFbeta type II receptor gene therapy ameliorates acute radiation-induced pulmonary injury in rats. , 2002, International journal of radiation oncology, biology, physics.
[22] A. Nagler,et al. Growth inhibition of prostate cancer xenografts by halofuginone * † , 2002, The Prostate.
[23] Ruihua Chen,et al. Blockade of the effects of TGF-beta1 on mesangial cells by overexpression of Smad7. , 2002, Journal of the American Society of Nephrology : JASN.
[24] T. McGaha,et al. Halofuginone, an inhibitor of type-I collagen synthesis and skin sclerosis, blocks transforming-growth-factor-beta-mediated Smad3 activation in fibroblasts. , 2002, The Journal of investigative dermatology.
[25] James B. Mitchell,et al. Mice lacking Smad3 are protected against cutaneous injury induced by ionizing radiation. , 2002, The American journal of pathology.
[26] Junjie Chen,et al. Histone H2AX Is Phosphorylated in an ATR-dependent Manner in Response to Replicational Stress* , 2001, The Journal of Biological Chemistry.
[27] A. Nagler,et al. Halofuginone: a potent inhibitor of critical steps in angiogenesis progression , 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[28] V. Yamazaki,et al. A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage , 2000, Current Biology.
[29] M. Neeman,et al. Inhibition of neovascularization and tumor growth, and facilitation of wound repair, by halofuginone, an inhibitor of collagen type I synthesis. , 1999, Neoplasia.
[30] M. Pines,et al. Halofuginone: a novel antifibrotic therapy. , 1998, General pharmacology.
[31] Keunchil Park,et al. Expression of Transforming Growth Factor β Type II Receptor Reduces Tumorigenicity in Human Gastric Cancer Cells , 1997 .
[32] Y. Bang,et al. Expression of transforming growth factor beta type II receptor reduces tumorigenicity in human gastric cancer cells. , 1997, Cancer research.
[33] M. Anscher,et al. Normal tissue injury after cancer therapy is a local response exacerbated by an endocrine effect of TGFβ , 1995 .
[34] M. Anscher,et al. Short communication: normal tissue injury after cancer therapy is a local response exacerbated by an endocrine effect of TGF beta. , 1995, The British journal of radiology.
[35] J. Mitchell,et al. In vitro studies of Taxol as a radiation sensitizer in human tumor cells. , 1994, Journal of the National Cancer Institute.
[36] O. Halevy,et al. Halofuginone: an inhibitor of collagen type I synthesis. , 1993, Biochimica et biophysica acta.
[37] M. Anscher,et al. Transforming growth factor-beta 1 expression in irradiated liver. , 1990, Radiation research.
[38] M. Anscher,et al. Transforming growth factor-beta 1 expression in irradiated liver. , 1990, Radiation research.