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1.
Braz. j. med. biol. res ; 42(7): 593-598, July 2009. ilus, tab
Artigo em Inglês | LILACS | ID: lil-517801

RESUMO

Blood and lymphatic vessel proliferation is essential for tumor growth and progression. Most colorectal carcinomas develop from adenomas (adenoma-carcinoma sequence) in a process due to accumulation of molecular genetic alterations. About 5% of adenomatous polyps are expected to become malignant, but data on the differential angiogenic patterns of these lesions in patients with and without concomitant cancer are missing. The aim of the present study is to compare the angiogenic and lymphatic patterns of adenomatous polyps from patients with and without sporadic cancer. Thirty adenomatous polyps (15 from patients with another principal malignant lesion, and 15 from patients without cancer) were submitted to immunohistochemical staining for CD105 (marker for neoangiogenesis) and D2-40 (marker for lymphatic endothelium). Microvessel density and total vascular area were determined by computer image analysis to quantify the immunostained and total areas, and to assess the number of microvessels. Adenomas from patients with carcinoma showed significantly higher values of total vascular area determined by immunostaining for CD105 (cutoff value = 4386 µm²; P = 0.019) and of lymphatic microvessel density determined by immunostaining with D2-40 (cutoff value = 11.5; P = 0.041) when compared with those from patients without cancer. The present data indicate a significant increase in blood microvascular area and in lymphatic microvascular counts in adenomas removed from patients with cancer.


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Pólipos Adenomatosos/patologia , Neoplasias Colorretais/patologia , Linfangiogênese/fisiologia , Neovascularização Patológica/patologia , Pólipos Adenomatosos/irrigação sanguínea , Pólipos Adenomatosos/química , Anticorpos Monoclonais/análise , Antígenos CD/análise , Biomarcadores/análise , Neoplasias Colorretais/irrigação sanguínea , Neoplasias Colorretais/química , Imuno-Histoquímica , Vasos Linfáticos/química , Vasos Linfáticos/patologia , Microcirculação , Estudos Retrospectivos , Receptores de Superfície Celular/análise
2.
Braz J Med Biol Res ; 42(7): 593-8, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19466284

RESUMO

Blood and lymphatic vessel proliferation is essential for tumor growth and progression. Most colorectal carcinomas develop from adenomas (adenoma-carcinoma sequence) in a process due to accumulation of molecular genetic alterations. About 5% of adenomatous polyps are expected to become malignant, but data on the differential angiogenic patterns of these lesions in patients with and without concomitant cancer are missing. The aim of the present study is to compare the angiogenic and lymphatic patterns of adenomatous polyps from patients with and without sporadic cancer. Thirty adenomatous polyps (15 from patients with another principal malignant lesion, and 15 from patients without cancer) were submitted to immunohistochemical staining for CD105 (marker for neoangiogenesis) and D2-40 (marker for lymphatic endothelium). Microvessel density and total vascular area were determined by computer image analysis to quantify the immunostained and total areas, and to assess the number of microvessels. Adenomas from patients with carcinoma showed significantly higher values of total vascular area determined by immunostaining for CD105 (cutoff value = 4386 microm(2); P = 0.019) and of lymphatic microvessel density determined by immunostaining with D2-40 (cutoff value = 11.5; P = 0.041) when compared with those from patients without cancer. The present data indicate a significant increase in blood microvascular area and in lymphatic microvascular counts in adenomas removed from patients with cancer.


Assuntos
Pólipos Adenomatosos/patologia , Neoplasias Colorretais/patologia , Linfangiogênese/fisiologia , Neovascularização Patológica/patologia , Pólipos Adenomatosos/irrigação sanguínea , Pólipos Adenomatosos/química , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Monoclonais/análise , Anticorpos Monoclonais Murinos , Antígenos CD/análise , Biomarcadores/análise , Neoplasias Colorretais/irrigação sanguínea , Neoplasias Colorretais/química , Endoglina , Feminino , Humanos , Imuno-Histoquímica , Vasos Linfáticos/química , Vasos Linfáticos/patologia , Masculino , Microcirculação , Pessoa de Meia-Idade , Receptores de Superfície Celular/análise , Estudos Retrospectivos
3.
Anal Quant Cytol Histol ; 26(4): 201-6, 2004 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15457672

RESUMO

OBJECTIVE: To evaluate 3-dimensional parameters and bidimensional microvascular quantification in the different morphologic presentations of colorectal adenomas. STUDY DESIGN: A study was carried out, including 102 neoplastic colorectal lesions obtained by endoscopy or surgical resection. For the analysis of angiogenesis, immunohistochemistry, digital image analysis, microvascular quantification and stereology were used. RESULTS: Microvascular quantification, volume and microvascular length estimate rose gradually with high grade dysplasia as compared to the low grade ones (P < .001). There was no significant difference in angiogenesis between polypoid and nonpolypoid colorectal adenomas in terms of quantification and microvascular length estimate. CONCLUSION: The use of digital image analysis and stereology added greater objectivity and effectiveness to angiogenic evaluation because they allowed accurate segmentation of hypervascular areas, representation of the characteristic 3-dimensional morphology of the vascular supply and identification of differences in microvascularization in the developmental stages of colorectal cancer. However, no significant relation could be found between macroscopic type and angiogenesis, suggesting that angiogenesis may contribute little to morphogenesis of colorectal adenomas.


Assuntos
Adenoma/patologia , Pólipos Adenomatosos/patologia , Neoplasias Colorretais/patologia , Citometria por Imagem/métodos , Neovascularização Patológica/patologia , Adenoma/irrigação sanguínea , Pólipos Adenomatosos/irrigação sanguínea , Neoplasias Colorretais/irrigação sanguínea , Humanos , Processamento de Imagem Assistida por Computador , Microcirculação/patologia
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