Literature DB >> 12623359

Antivascular therapy of cancer: DMXAA.

Bruce C Baguley1.   

Abstract

The vascular endothelium of tumour tissue, which differs in several ways from that of normal tissues, is a potential target for selective anticancer therapy. By contrast with antiangiogenic agents, antivascular agents target the endothelial cells of existing tumour blood vessels, causing distortion or damage and consequently decreasing tumour blood flow. DMXAA (5,6-dimethylxanthenone-4-acetic acid), a low-molecular-weight drug, has a striking antivascular and in some cases curative effect in experimental tumours. Its action on vascular endothelial cells seems to involve a cascade of events leading to induction of tumour haemorrhagic necrosis. These events include both direct and indirect effects, the latter involving the release of further vasoactive agents, such as serotonin, tumour necrosis factor, other cytokines, and nitric oxide from host cells. Phase I clinical trials of DMXAA have been completed and the next challenge to face is how the antivascular effect of this drug should be exploited for the treatment of human cancer.

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Year:  2003        PMID: 12623359     DOI: 10.1016/s1470-2045(03)01018-0

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  41 in total

1.  The role of funding and policies on innovation in cancer drug development.

Authors:  P Kanavos; R Sullivan; G Lewison; W Schurer; S Eckhouse; Z Vlachopioti
Journal:  Ecancermedicalscience       Date:  2010-02-03

2.  Comparative outcomes of squamous and non-squamous non-small cell lung cancer (NSCLC) patients in phase II studies of ASA404 (DMXAA) - retrospective analysis of pooled data.

Authors:  Mark J McKeage; Michael B Jameson
Journal:  J Thorac Dis       Date:  2010-12       Impact factor: 2.895

3.  Aminolevulinic acid-photodynamic therapy combined with topically applied vascular disrupting agent vadimezan leads to enhanced antitumor responses.

Authors:  Allison Marrero; Theresa Becker; Ulas Sunar; Janet Morgan; David Bellnier
Journal:  Photochem Photobiol       Date:  2011-06-13       Impact factor: 3.421

4.  Antivascular ultrasound therapy extends survival of mice with implanted melanomas.

Authors:  Andrew K W Wood; Susan M Schultz; William M-F Lee; Ralph M Bunte; Chandra M Sehgal
Journal:  Ultrasound Med Biol       Date:  2010-04-09       Impact factor: 2.998

5.  5,6-Dimethylxanthenone-4-acetic acid (DMXAA) activates stimulator of interferon gene (STING)-dependent innate immune pathways and is regulated by mitochondrial membrane potential.

Authors:  Daniel Prantner; Darren J Perkins; Wendy Lai; Mark S Williams; Shruti Sharma; Katherine A Fitzgerald; Stefanie N Vogel
Journal:  J Biol Chem       Date:  2012-10-01       Impact factor: 5.157

Review 6.  The unique characteristics of tumor vasculature and preclinical evidence for its selective disruption by Tumor-Vascular Disrupting Agents.

Authors:  Dietmar W Siemann
Journal:  Cancer Treat Rev       Date:  2010-06-08       Impact factor: 12.111

7.  Control of cervicovaginal HPV-16 E7-expressing tumors by the combination of therapeutic HPV vaccination and vascular disrupting agents.

Authors:  Qi Zeng; Shiwen Peng; Archana Monie; Ming Yang; Xiaowu Pang; Chien-Fu Hung; T-C Wu
Journal:  Hum Gene Ther       Date:  2011-03-09       Impact factor: 5.695

8.  Mouse, but not human STING, binds and signals in response to the vascular disrupting agent 5,6-dimethylxanthenone-4-acetic acid.

Authors:  Joseph Conlon; Dara L Burdette; Shruti Sharma; Numana Bhat; Mikayla Thompson; Zhaozhao Jiang; Vijay A K Rathinam; Brian Monks; Tengchuan Jin; T Sam Xiao; Stefanie N Vogel; Russell E Vance; Katherine A Fitzgerald
Journal:  J Immunol       Date:  2013-04-12       Impact factor: 5.422

9.  Enhancement of the action of the antivascular drug 5,6-dimethylxanthenone-4-acetic acid (DMXAA; ASA404) by non-steroidal anti-inflammatory drugs.

Authors:  L-C Steve Wang; Lai-Ming Ching; James W Paxton; Philip Kestell; Rachel Sutherland; Li Zhuang; Bruce C Baguley
Journal:  Invest New Drugs       Date:  2008-08-12       Impact factor: 3.850

10.  Acute vascular disruption by 5,6-dimethylxanthenone-4-acetic Acid in an orthotopic model of human head and neck cancer.

Authors:  Mukund Seshadri; Karoly Toth
Journal:  Transl Oncol       Date:  2009-08-18       Impact factor: 4.243

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