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Angiogenesis and the Expression of Vascular Endothelial Growth Factors A and C in Squamous Cell Carcinoma of the Piriform Fossa
Jarrod J. Homer, MD, FRCS;
Michael G. Prentice, MRCS;
Lynn Cawkwell, PhD;
Martin Birchall, MD, FRCS;
John Greenman, PhD;
Nicholas D. Stafford, FRCS
Arch Otolaryngol Head Neck Surg. 2003;129:1110-1114.
Background Angiogenesis is essential for tumor growth and invasion. Vascular endothelial growth factor A (VEGF-A) is a prime mediator of tumor angiogenesis; VEGF-C, another member of the closely related VEGF family of proteins, has major effects on lymphatic endothelial cells and may be important in the process of lymphatic metastasis.
Objectives To evaluate the expression of these cytokines in hypopharyngeal squamous cell carcinoma and to ascertain the effects of these proteins on lymphatic metastasis and vascular angiogenesis.
Design Retrospective analysis of microvessel density and the expression of VEGF-A and VEGF-C.
Setting An academic referral center.
Subjects Thirty-four patients with stage T2 to T4 squamous cell carcinoma of the piriform fossa.
Interventions Expression of VEGF-A and VEGF-C was determined by immunohistochemistry on formalin-fixed, paraffin-embedded biopsy specimens. Angiogenesis was measured as microvessel density by staining endothelial cells for platelet-endothelial cell adhesion molecule 1/CD31.
Results Of the 34 tumors, 21 had clinicoradiologic evidence of lymphatic metastasis. Expression of VEGF-C was associated with lymphatic metastasis (P<.001), but not with microvessel density. The VEGF-A expression correlated with microvessel density (P<.001), but neither VEGF-A expression nor microvessel density was associated with lymphatic metastasis.
Conclusions The expression of VEGF-C is associated with lymphatic metastasis in squamous cell carcinoma of the piriform fossa. This is not secondary to effects on vascular angiogenesis and is hypothesized to be due to effects on lymphatic endothelial cells.
From the Department of OtolaryngologyHead and Neck Surgery, Hull Royal Infirmary, Hull, England (Drs Homer and Stafford); Department of OtolaryngologyHead and Neck Surgery, Manchester Royal Infirmary, Manchester, England (Dr Homer); Department of OtolaryngologyHead and Neck Surgery, Bristol Royal Infirmary, Bristol, England (Drs Prentice and Birchall); and Academic Department of Oncology (Dr Cawkwell) and Academic Surgical Unit (Dr Greenman), University of Hull, Hull.
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