1.Association of microvessel density and blood vessel invasion with the prognosis in rectal carcinoma at stages I to II.
Yong-jian ZHOU ; Qin YE ; Hui-shan LU ; Ying-hong YANG ; Guo-xian GUAN ; Chang-ming HUANG ; Chuan WANG ; Jie ZHANG
Chinese Journal of Gastrointestinal Surgery 2010;13(7):516-519
OBJECTIVETo investigate the possibility of microvessel density (MVD) and blood vessel invade (BVI) as the indexes in predicting prognosis of rectal carcinoma at stages I to II.
METHODSTumor tissues from 380 patients who underwent resection of stage I or II rectal cancer were analyzed for MVD and BVI by immunohistochemical S-P method with anti-CD105 and anti-CD 34 antibody. Binary and multivariable Cox regression was applied to indicate independent factors associated with overall survival.
RESULTSCD105 was present in the neovascularity of the cancer tissue but not in the normal tissue, while CD34 was present in the tumor tissue and the normal tissue. BVI on CD34 staining was significantly higher than that on HE staining. Multivariable analysis revealed that TNM stage, CD34-BVI, histologic type, and CD105-MDV were independent risk factors to predict the possibility of poor prognosis of stage I or II rectal cancer. CD34-BVI or CD105-MVD positivity had a hazard ratio of 4.483 (95% confidence interval 2.861-7.026) for mortality.
CONCLUSIONThe expressions of CD34-BVI and CD105-MVD are independent factors to predict the possibility of poor survival of stage I or II rectal carcinoma. Detection of CD105-MVD combined with CD34-BVI may help predict clinical outcome and design further individualized adjuvant treatment.
Adult ; Aged ; Aged, 80 and over ; Antigens, CD ; metabolism ; Antigens, CD34 ; metabolism ; Endoglin ; Female ; Humans ; Male ; Microvessels ; pathology ; Middle Aged ; Neoplasm Staging ; Neovascularization, Pathologic ; pathology ; Prognosis ; Receptors, Cell Surface ; metabolism ; Rectal Neoplasms ; blood supply ; diagnosis ; pathology
2.Perfusion Parameters of Dynamic Contrast-Enhanced Magnetic Resonance Imaging in Patients with Rectal Cancer: Correlation with Microvascular Density and Vascular Endothelial Growth Factor Expression.
Yeo Eun KIM ; Joon Seok LIM ; Junjeong CHOI ; Daehong KIM ; Sungmin MYOUNG ; Myeong Jin KIM ; Ki Whang KIM
Korean Journal of Radiology 2013;14(6):878-885
OBJECTIVE: To determine whether quantitative perfusion parameters of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) correlate with immunohistochemical markers of angiogenesis in rectal cancer. MATERIALS AND METHODS: Preoperative DCE-MRI was performed in 63 patients with rectal adenocarcinoma. Transendothelial volume transfer (Ktrans) and fractional volume of the extravascular-extracellular space (Ve) were measured by Interactive Data Language software in rectal cancer. After surgery, microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression scores were determined using immunohistochemical staining of rectal cancer specimens. Perfusion parameters (Ktrans, Ve) of DCE-MRI in rectal cancer were found to be correlated with MVD and VEGF expression scores by Spearman's rank coefficient analysis. T stage and N stage (negative or positive) were correlated with perfusion parameters and MVD. RESULTS: Significant correlation was not found between any DCE-MRI perfusion parameters and MVD (rs = -0.056 and p = 0.662 for Ktrans; rs = -0.103 and p = 0.416 for Ve), or between any DCE-MRI perfusion parameters and the VEGF expression score (rs = -0.042, p = 0.741 for Ktrans ; r = 0.086, p = 0.497 for Ve) in rectal cancer. TN stage showed no significant correlation with perfusion parameters or MVD (p > 0.05 for all). CONCLUSION: DCE-MRI perfusion parameters, Ktrans and Ve, correlated poorly with MVD and VEGF expression scores in rectal cancer, suggesting that these parameters do not simply denote static histological vascular properties.
Adult
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Aged
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Aged, 80 and over
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Contrast Media/*diagnostic use
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Female
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Follow-Up Studies
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Humans
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Immunohistochemistry
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Magnetic Resonance Imaging/*methods
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Male
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Middle Aged
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Neoplasm Staging
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Neovascularization, Pathologic/diagnosis/metabolism
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Rectal Neoplasms/blood supply/*diagnosis/metabolism
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Retrospective Studies
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Tumor Markers, Biological/biosynthesis
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Vascular Endothelial Growth Factor A/*biosynthesis