摘要
AIM: Angiogenesis is an important step in the growth of solid malignant tumors. A number of angiogenic factors have been found such as transforming growth factorβ1 (TGF-β1)and vascular endothelial growth factor (VEGF). However,the roles of TGFβ1 and VEGF in gastrointestinal carcinogenesis are still unclear. This study was to investigate the expressions of TGF-β1 and VEGF in gastrointestinal tract malignant tumors, as well as their association with microvessel density (MVD). At the same time, we also observed the localization of TGF-β1 and its receptor CD105 in gastric malignant tumors.METHODS: The expressions of TGF-β1 and CDL05 were detected in 55 fresh specimens of gastric carcinoma and VEGF and CD105 in 44 fresh specimens of colorectal carcinoma by immunohistochemical staining (S-ABC). TGF-β1 and CD105 in 55 gastric carcinoma tissues on the same slide were detected by using double-stain Tmmunohistochemistry (DS-ABC).RESULTS: Among the 55 cases of gastric carcinoma tissues,30 were positive for TGF-β1 (54.55 %). The MVD of TGF-β1 strong positive group (++～+++ 23.22±5.8) was significantly higher than that of weak positive group (+17.56±7.2) and negative group (- 17.46±3.9) (q=4.5, q=5.3207, respectively,P＜0.01). In the areas of high expression of TGF-β1, MVD and the expression of CD105 were also high. Among the 44 cases of colonic carcinoma tissues, 26 were positive for VEGF (59.1%). The expressions of both VEGF and CD105 (MVD)were related with the depth of invasion (F=5.438, P＜0.05;F=4.168, P=0.05), lymph node metastasis (F=10.311, P＜0.01;F=20.282, P＜0.01) and Dukes stage (F=6.196, P＜0.01;F=10.274, P＜0.01), but not with histological grade (F=0.487,P＞0.05). There was a significant correlation between the expression of VEGF and CD105 (MVD) (r=0.720, P＜0.01).CONCLUSION: Over-expression of TGF-β1 and VEGF acts as stimulating factors of angiogenesis in gastrointestinal tumors.CD105, as a receptor of TGF-β1, can regulate the biological effect of TGF-β1 in tumor angiogenesis. MVD marked by CD105 is more suitable for detecting newborn blood vessels.
AIM:Angiogenesis is an important step in the growth of solid malignant tumors.A number of angiogenic factors have been found such as transforming growth factorβ1(TGF-β1) and vascular endothelial growth factor(VEGF).However, the roles of TGFβ1 and VEGF in gastrointestinal carcinogenesis are still unclear.This study was to investigate the expressions of TGF-β1 and VEGF in gastrointestinal tract malignant tumors,as well as their association with microvessel density(MVD).At the same time,we also observed the localization of TGF-β1 and its receptor CD105 in gastric malignant tumors. METHODS:The expressions of TGF-β1 and CD105 were detected in 55 fresh specimens of gastric carcinoma and VEGF and CD105 in 44 fresh specimens of colorectal carcinoma by immunohistochemical staining(S-ABC).TGF-β1 and CD105 in 55 gastric carcinoma tissues on the same slide were detected by using double-stain Immunohistochemistry (DS-ABC). RESULTS:Among the 55 cases of gastric carcinoma tissues, 30 were positive for TGF-β1(54.55 %).The MVD of TGF-β1 strong positive group(++～+++ 23.22±5.8)was significantly higher than that of weak positive group(+17.56±7.2)and negative group(-17.46±3.9)(q=4.5,q=5.3207,respectively, P<0.01).In the areas of high expression of TGF-β1,MVD and the expression of CD105 were also high.Among the 44 cases of colonic carcinoma tissues,26 were positive for VEGF (59.1%).The expressions of both VEGF and CD105(MVD) were related with the depth of invasion(F=5.438,P<0.05; F=4.168,P=0.05),lymph node metastasis(F=10.311,P<0.01; F=20.282,P<0.01)and Dukes stage(F=6.196,P<0.01; F=10.274,P<0.01),but not with histological grade(F=0.487, P>0.05).There was a significant correlation between the expression of VEGF and CD105(MVD)(r=0.720,P<0.01).CONCLUSION: Over-expression of TGF-p1 and VEGF acts as stimulating factors of angiogenesis in gastrointestinal tumors. CD105, as a receptor of TGF-p1, can regulate the biological effect of TGF-p1 in tumor angiogenesis. MVD marked by CD105 is more suitable for detecting newborn blood vessels.
