Correlation of matrix metalloproteinase suppressor genes RECK, VEGF, and CD105 with angiogenesis and biological behavior in esophageal squamous cell carcinoma

• Published in: World journal of gastroenterology : WJG Vol. 13; no. 45; pp. 6076 - 6081
• Main Author: Li, Sheng-Lei
• Format: Journal Article
• Language: English
• Published: United States Department of Pathology, The First Affiliated Hospital Zhengzhou University 07.12.2007; He'nan Key Laboratory of Tumor Pathology,Zhengzhou 450052, He'nan Province, China
• Subjects: Adult; Aged; Antigens, CD - metabolism; Carcinoma, Squamous Cell - blood supply; Carcinoma, Squamous Cell - diagnosis; Carcinoma, Squamous Cell - metabolism; CD105; Early Diagnosis; Endoglin; Esophageal Neoplasms - blood supply; Esophageal Neoplasms - diagnosis; Esophageal Neoplasms - metabolism; Esophagus - pathology; Female; Gene Expression; GPI-Linked Proteins; Humans; Hyperplasia - diagnosis; Hyperplasia - metabolism; Male; Membrane Glycoproteins - metabolism; Middle Aged; Neoplasm Metastasis; Neovascularization, Pathologic - metabolism; Prognosis; Receptors, Cell Surface - metabolism; Vascular Endothelial Growth Factor A - metabolism; 半胱氨酸; 抑制基因; 生物学行为; 食管癌; Immunohistochemistry; Reversion inducing cysteine rich protein with Kazal motifs; Esophageal squamous cell carcinoma; CD105; Microvessel density; Vascular endothelial growth factor
• ISSN: 1007-9327; 2219-2840
• DOI: 10.3748/wjg.13.6076

AIM： To explore the expression of reversion inducing cysteine-rich protein with Kazal motifs （RECK）, vascular endothelial growth factor （VEGF） and endoglin （CD105） protein and its correlation with occurrence, development, invasion and metastasis in esophageal squamous cell carcinoma （ESCC）. METHODS： Streptavidin-peroxidase （SP） immunohistochemistry was used to detect expression of RECK and VEGF in 62 cases of ESCC, 31 cases of adjacent atypical hyperplastic epithelium and 62 cases of normal esophageal epithelium. CD105 Mb was used to assess microvessel density （MVD）. RESULTS： The expression of RECK was closely correlated with histological grade, infiltrative depth and lymphatic metastasis in ESCC （P 〈 0.05）. The expression of RECK decreased during cancer development： normal esophageal epithelium （85.5%, 53/62）, adjacent atypical hyperplastic epithelium （71.0%, 22/31）, and carcinoma （59.7%, 37/62）. There was a significant difference among the groups （P 〈 0.05）. The expression of VEGF protein was closely correlated with infiltrative depth and lymphatic metastasis in ESCC （P 〈 0.05）. The expression of VEGF protein increased during cancer development： normal esophageal epithelium （29.0%, 18/62）, adjacent atypical hyperplastic epithelium （54.8%, 17/31）, and carcinoma （67.7%, 42/62）. There was a significant difference among the groups （P 〈 0.05）. MVDCD105 increased in accordance with histological grade, butthere was no significant difference （grade Ⅰ, 36.92 ± 10.85; grade Ⅱ, 37.65 ± 9.50; and grade Ⅲ, 38.06 ± 12.19）. The MVDCD105 was closely correlated with infiltration and lymphatic metastasis in ESCC （P 〈 0.05）. The expression of RECK was inversely correlated with the expression of VEGF and CD105.CONCLUSION： RECK, VEGF and CD105 play important roles in the infiltration, metastasis and carcinogenesis in esophageal carcinoma. Angiogenesis in ESCC may be promoted by over-expression of CD105.