Overexpression of vascular endothelial growth factor and its receptors in bronchial dypslasia demonstrated by quantitative RT-PCR analysis
Autor: | Michio Sugita, Jerry Haney, Daniel T. Merrick, T. Kennedy, Wilbur A. Franklin, Robert L. Keith, Sheila Petrunich, York E. Miller |
---|---|
Rok vydání: | 2005 |
Předmět: |
Vascular Endothelial Growth Factor A
Pulmonary and Respiratory Medicine Cancer Research Pathology medicine.medical_specialty Lung Neoplasms Angiogenesis Biopsy Enzyme-Linked Immunosorbent Assay medicine.disease_cause Neovascularization chemistry.chemical_compound medicine Humans Neoplasm Invasiveness Lung cancer Neovascularization Pathologic Reverse Transcriptase Polymerase Chain Reaction business.industry Gene Expression Profiling Smoking respiratory system medicine.disease Immunohistochemistry Up-Regulation respiratory tract diseases Vascular endothelial growth factor Receptors Vascular Endothelial Growth Factor Oncology chemistry Tumor progression Dysplasia Disease Progression RNA medicine.symptom business Carcinogenesis Precancerous Conditions |
Zdroj: | Lung Cancer. 48:31-45 |
ISSN: | 0169-5002 |
DOI: | 10.1016/j.lungcan.2004.07.049 |
Popis: | Neoangiogenesis is required for the growth of invasive lung carcinoma, however, the role of angiogenesis in the progression of premalignant changes to carcinoma of the lung is less clear. We have evaluated vascular endothelial growth factor (VEGF) expression and microvessel densities (MVDs) in 62 bronchoscopic biopsies from normal, reactive (basal cell hyperplasia (BCH)) and dysplastic bronchial epithelium and in tissue from twenty-seven invasive lung carcinomas in an effort to demonstrate angiogenic activity in these preneoplastic lesions and determine whether it is associated with increased bronchial epithelial VEGF expression. MVDs and VEGF RNA expression measured by quantitative RT-PCR were found to be elevated in comparison to normal bronchial tissue in bronchial dysplasias and invasive lung carcinomas but not in basal cell hyperplasias. Immunohistochemical (IHC) analyses revealed that expression of VEGF arose predominantly from bronchial epithelium. ELISA analysis of lung tumor tissue showed that elevated VEGF protein expression correlated with VEGF RNA levels (r=0.59, p=0.004). Increased expression of VEGF RNA was also found in histologically normal bronchial mucosa from patients with either dysplasia at other sites or a history of heavy tobacco use suggesting a possible field effect in regard to the elaboration of VEGF. Furthermore, analysis of VEGF isoforms and VEGF receptors by semi-quantitative RT-PCR in dysplastic and invasive lesions revealed characteristic altered patterns of expression in dysplasia and early cancer as compared to normal tissue. These results indicate that angiogenesis develops early in lung carcinogenesis and is associated with overexpression of VEGF. |
Databáze: | OpenAIRE |
Externí odkaz: |