Angiogenesis in cancer of unknown primary: clinicopathological study of CD34, VEGF and TSP-1
Creators
- 1. Sarcoma Unit, Royal Marsden Hospital, London (United Kingdom)
- 2. Medical Oncology Department, Ioannina University Hospital, Ioannina (Greece)
- 3. Department of Pathology, Ioannina University Hospital, Ioannina (Greece)
- 4. Medical Oncology Department, Patras University Hospital, Rion (Greece)
- 5. Medical Oncology Department, School of Medicine, Aristotle's University of Thessaloniki (Greece)
- 6. Laboratory of Biochemistry, School of Medicine, University of Ioannina, Ioannina (Greece)
- 7. Biomedical Research Institute-Foundation for Research and technology (BRI-FORTH), Ioannina (Greece)
Description
Cancer of unknown primary remains a mallignancy of elusive biology and grim prognosis that lacks effective therapeutic options. We investigated angiogenesis in cancer of unknown primary to expand our knowledge on the biology of these tumors and identify potential therapeutic targets. Paraffin embedded archival material from 81 patients diagnosed with CUP was used. Tumor histology was adenocarcinoma (77%), undifferentiated carcinoma (18%) and squamous cell carcinoma (5%). The tissue expression of CD34, VEGF and TSP-1 was assessed immunohistochemically by use of specific monoclonal antibodies and was analyzed against clinicopathological data. VEGF expression was detected in all cases and was strong in 83%. Stromal expression of TSP-1 was seen in 80% of cases and was strong in 20%. The expression of both proteins was not associated with any clinical or pathological parameters. Tumor MVD was higher in tumors classified as unfavorable compared to more favorable and was positively associated with VEGF and negatively with TSP-1. Angiogenesis is very active and expression of VEGF is almost universal in cancers of unknown primary. These findings support the clinical investigation of VEGF targeted therapy in this clinical setting
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-5-25; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC555600Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 5
- Journal Page Range
- p. 25
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46082290
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANGIOGENESIS; CARCINOMAS; HISTOLOGY; MONOCLONAL ANTIBODIES; NEOPLASMS; PARAFFIN; PATIENTS; PROTEINS; THERAPY; TOTAL SUSPENDED PARTICULATES
- Descriptors DEC
- ALKANES; ANTIBODIES; DISEASES; HYDROCARBONS; MEDICINE; NEOPLASMS; ORGANIC COMPOUNDS; OTHER ORGANIC COMPOUNDS; PARTICLES; PARTICULATES; WAXES
Optional Information
- Copyright
- Copyright (c) 2005 Karavasilis et al
- Notes
- PMCID: PMC555600; PUBLISHER-ID: 1471-2407-5-25; PMID: 15743540; OAI: oai:pubmedcentral.nih.gov:555600; licensee BioMed Central Ltd.