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Chapter 15. Vasculature-disrupting Strategies Combined with Bacterial Spores Targeting Hypoxic Regions of Solid Tumors

  1. Dietmar W. Siemann2,3
  1. G-One Ahn,
  2. J. Martin Brown

Published Online: 31 MAY 2006

DOI: 10.1002/0470035439.ch15

Vascular-Targeted Therapies in Oncology

Vascular-Targeted Therapies in Oncology

How to Cite

Ahn, G.-O. and Brown, J. M. (2006) Vasculature-disrupting Strategies Combined with Bacterial Spores Targeting Hypoxic Regions of Solid Tumors, in Vascular-Targeted Therapies in Oncology (ed D. W. Siemann), John Wiley & Sons, Ltd, Chichester, UK. doi: 10.1002/0470035439.ch15

Editor Information

  1. 2

    Shands Cancer Center, University of Florida, Gainsville, Florida, USA

  2. 3

    Research Department of Radiation Oncology, University of Florida, 2000 RW Archer Road, Gainsville, FL 32610, USA

Author Information

  1. Division of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, CCSR – South, Room 1255, 269 Campus Drive, Stanford, CA 94305-5152, USA

Publication History

  1. Published Online: 31 MAY 2006
  2. Published Print: 10 MAR 2006

ISBN Information

Print ISBN: 9780470012949

Online ISBN: 9780470035436

SEARCH

Keywords:

  • vascular disrupting agents and genetically engineered anaerobic bacteria;
  • hypoxic/necrotic area and human solid tumor;
  • vasculature-disrupting strategies;
  • clostridia as hypoxia/necrotic selective cancer therapy;
  • optimizing prodrug design;
  • ADEPT (antibody-directed) and GDEPT (gene-directed);
  • clostridial approach to enzyme/prodrug therapy (CDEPT);
  • CDEPT and vascular-disrupting agents;
  • CDEPT in combination with DMXAA

Summary

This chapter contains sections titled:

  • Hypoxia and necrosis as a selective target for cancer therapy

  • Use of Clostridia as hypoxia/necrotic selective cancer therapy

  • Advantage of CDEPT over ADEPT and GDEPT

  • Combination of CDEPT with vascular-disrupting agents

  • Clinical significance

  • References