Skip to content


You're viewing the new version of our site. Please leave us feedback.

Learn more

Head & Neck Oncology

Open Access

Vascular mimicry in head and neck tumours

  • Tahwinder Upile1,
  • Waseem Jerjes1,
  • Jaspal Mahil1 and
  • Colin Hopper1
Head & Neck Oncology20091(Suppl 1):P15

Published: 28 July 2009


Angiogenesis has been extensively investigated in several tumour models; however, chemotherapeutic agents based upon these models have not been very effective. It is logical to assume this lack of efficacy is due to the host tumour interface. Furthermore, it is a reasonable hypothesis that the transition between the host vasculature and tumour is not binomial but a gradual transition from tumour and mosaic vessels to host capillaries. The existence of such pure tumour and mosaic vessels would suggest the possibility of tumour vascular mimicry in the connecting vessels.

Materials and methods

Primary and metastatic tumour cells lines were developed 'in-house' and checked to be free from mycoplasma infection. A positive control HUVEC (vascular endothelial cell line) was used. An anti-endothelial antibody was then used. The growth of the cell lines was assessed. Other tumour cell lines were then investigated for similar properties as were primary and metastatic cell lines.


Certain head and neck tumours display the phenomena of vascular mimicry when grown on collagen substrate (p < 0.001). This is more so in cell lines derived from metastases than primary tumours. This was found in some other non head and neck tumour cell lines. The cell lines had a reduced capacity to undergo vascular mimicry when exposed to specific anti-endothelial growth factor antibodies.


The phenomenon of tumour vascular mimicry has important implications for future chemotherapeutic drug design.

Authors’ Affiliations

Head & Neck Centre, University College London Hospitals


© Upile et al; licensee BioMed Central Ltd. 2009

This article is published under license to BioMed Central Ltd.