G One Ahn

Summary

Affiliation: Stanford University
Country: USA

Publications

  1. pmc Role of endothelial progenitors and other bone marrow-derived cells in the development of the tumor vasculature
    G One Ahn
    Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, 269 Campus Drive, CCSR South, Rm1255, Stanford, CA 94305 5152, USA
    Angiogenesis 12:159-64. 2009
  2. pmc Inhibition of Mac-1 (CD11b/CD18) enhances tumor response to radiation by reducing myeloid cell recruitment
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 107:8363-8. 2010
  3. pmc Matrix metalloproteinase-9 is required for tumor vasculogenesis but not for angiogenesis: role of bone marrow-derived myelomonocytic cells
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, 269 Campus Drive, CCSR South, Room 1255, Stanford, CA 94305, USA
    Cancer Cell 13:193-205. 2008
  4. ncbi request reprint Targeting tumors with hypoxia-activated cytotoxins
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305 5152, USA
    Front Biosci 12:3483-501. 2007
  5. pmc Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation
    Nicholas J Leeper
    Department of Surgery, Stanford University, 300 Pasteur Dr, Stanford, CA 94305, USA
    Arterioscler Thromb Vasc Biol 33:e1-e10. 2013
  6. pmc Influence of bone marrow-derived hematopoietic cells on the tumor response to radiotherapy: experimental models and clinical perspectives
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford, California, USA
    Cell Cycle 8:970-6. 2009
  7. pmc Optimized clostridium-directed enzyme prodrug therapy improves the antitumor activity of the novel DNA cross-linking agent PR-104
    Shie Chau Liu
    Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA
    Cancer Res 68:7995-8003. 2008

Collaborators

Detail Information

Publications7

  1. pmc Role of endothelial progenitors and other bone marrow-derived cells in the development of the tumor vasculature
    G One Ahn
    Division of Cancer and Radiation Biology, Department of Radiation Oncology, Stanford University School of Medicine, 269 Campus Drive, CCSR South, Rm1255, Stanford, CA 94305 5152, USA
    Angiogenesis 12:159-64. 2009
    ..In this review, we highlight some of the recent findings on each of these cell types by outlining some of the essential proangiogenic cytokines that these cells secrete to promote tumor angiogenesis and vasculogenesis...
  2. pmc Inhibition of Mac-1 (CD11b/CD18) enhances tumor response to radiation by reducing myeloid cell recruitment
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA
    Proc Natl Acad Sci U S A 107:8363-8. 2010
    ..Our study thus supports the rationale of using clinically available Mac-1 (CD11b/CD18) antibodies as an adjuvant therapy to radiotherapy...
  3. pmc Matrix metalloproteinase-9 is required for tumor vasculogenesis but not for angiogenesis: role of bone marrow-derived myelomonocytic cells
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, 269 Campus Drive, CCSR South, Room 1255, Stanford, CA 94305, USA
    Cancer Cell 13:193-205. 2008
    ..Our results suggest that MMP-9 could be an important target for adjunct therapy to enhance the response of tumors to radiotherapy...
  4. ncbi request reprint Targeting tumors with hypoxia-activated cytotoxins
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305 5152, USA
    Front Biosci 12:3483-501. 2007
    ....
  5. pmc Loss of CDKN2B promotes p53-dependent smooth muscle cell apoptosis and aneurysm formation
    Nicholas J Leeper
    Department of Surgery, Stanford University, 300 Pasteur Dr, Stanford, CA 94305, USA
    Arterioscler Thromb Vasc Biol 33:e1-e10. 2013
    ..As for other genes at 9p21.3, human expression quantitative trait locus studies have associated expression of the tumor suppressor gene CDKN2B with the risk haplotype, but its potential role in vascular pathobiology remains unclear...
  6. pmc Influence of bone marrow-derived hematopoietic cells on the tumor response to radiotherapy: experimental models and clinical perspectives
    G One Ahn
    Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford, California, USA
    Cell Cycle 8:970-6. 2009
    ....
  7. pmc Optimized clostridium-directed enzyme prodrug therapy improves the antitumor activity of the novel DNA cross-linking agent PR-104
    Shie Chau Liu
    Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California, USA
    Cancer Res 68:7995-8003. 2008
    ..sporogenes spores in SiHa tumor-bearing mice showed significantly improved antitumor efficacy when combined with either 5-aziridinyl-2,4-dinitrobenzamide (CB1954) or the novel dinitrobenzamide mustard prodrug, PR-104...