Antiangiogenic properties of viscum album extracts are associated with endothelial cytotoxicity

Sri Ramulu Elluru1, Jean-Paul Duong Van Huyen, Sandrine Delignat

  • 1INSERM UMRS 872, Equipe 16-Immunopathology and Therapeutic Intervention, Centre de Recherche des Cordeliers, 15 Rue de l'Ecole de Médecine, 75006 Paris, France.

Anticancer Research
|August 8, 2009
PubMed
Abstract

Insights

Viscum album (VA) Qu Spez extract significantly inhibited angiogenesis, a key process in tumor growth. Other VA extracts showed no significant effect, suggesting targeted application for cancer therapy.

Area of Science:

  • Oncology
  • Vascular Biology

Background:

  • Viscum album (VA) extracts are utilized in cancer therapy, exhibiting cytotoxicity to tumor and endothelial cells.
  • Tumor growth, sustenance, and metastasis are critically dependent on angiogenesis.
  • Inhibiting angiogenesis presents a promising therapeutic strategy for cancer treatment.

Purpose of the Study:

  • To investigate the antiangiogenic effects of different Viscum album (VA) extracts.
  • To evaluate the potential of VA extracts as inhibitors of tumor angiogenesis.

Main Methods:

  • Cytotoxicity assessed via Annexin V/propidium iodide staining in endothelial cells.
  • In vitro antiangiogenic activity evaluated by vascular formation in matrigel assays.
  • In vivo efficacy tested using matrigel plugs and systemic treatment in mice.

Main Results:

  • Combined systemic and intra-matrigel administration of VA Qu Spez extract significantly inhibited angiogenesis.
  • VA P extract demonstrated no significant impact on vessel formation.

Conclusions:

  • The findings suggest that specific Viscum album (VA) extracts, particularly VA Qu Spez, can inhibit angiogenesis.
  • These results may inform improved therapeutic strategies for cancer utilizing VA extracts targeting angiogenesis.

Related Concept Videos

Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...
Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
Cytotoxic Edema: Pathophysiology01:21

Cytotoxic Edema: Pathophysiology

Cytotoxic edema is a form of cerebral edema characterized by intracellular swelling of neurons, astrocytes, and other glial cells. It develops when the mechanisms responsible for maintaining ionic gradients across the cell membrane become impaired. Under normal physiological conditions, the sodium–potassium ATPase actively transports sodium ions out of the cell and potassium ions into the cell, preserving osmotic balance and enabling electrical signaling. This pump requires a continuous supply...