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1.
Am J Gastroenterol ; 118(2): 243-255, 2023 02 01.
Article in English | MEDLINE | ID: mdl-36563321

ABSTRACT

INTRODUCTION: Evidence on the comparative diagnostic performance of endoscopic ultrasound (EUS)-based techniques for pancreatic cystic lesions (PCLs) is limited. This network meta-analysis comprehensively compared EUS-based techniques for PCL diagnosis. METHODS: A comprehensive literature search was performed for all comparative studies assessing the accuracy of 2 or more modalities for PCL diagnosis. The primary outcome was the diagnostic efficacy for mucinous PCLs. Secondary outcomes were the diagnostic efficacy for malignant PCLs, diagnostic success rate, and adverse event rate. A network meta-analysis was conducted using the ANOVA model to assess the diagnostic accuracy of each index. RESULTS: Forty studies comprising 3,641 patients were identified. The network ranking of the superiority index for EUS-guided needle-based confocal laser endomicroscopy (EUS-nCLE) and EUS-guided through-the-needle biopsy (EUS-TTNB) were significantly higher than other techniques for differentiating mucinous PCLs; besides, EUS-TTNB was also the optimal technique in identifying malignant PCLs. The evidence was inadequate for EUS-nCLE diagnosing malignant PCLs and contrast-enhanced harmonic EUS diagnosing both mucinous and malignant PCLs. Glucose showed a high sensitivity but low specificity, and molecular analysis (KRAS, GNAS, and KRAS + GNAS mutations) showed a high specificity but low sensitivity for diagnosing mucinous PCLs. Satisfactory results were not obtained during the evaluation of the efficiency of pancreatic cyst fluid (PCF) biomarkers in detecting malignant PCLs. DISCUSSION: For centers with relevant expertise and facilities, EUS-TTNB and EUS-nCLE were better choices for the diagnosis of PCLs. Further studies are urgently required for further improving PCF biomarkers and validating the diagnostic performance of the index techniques.


Subject(s)
Pancreatic Cyst , Pancreatic Neoplasms , Humans , Network Meta-Analysis , Proto-Oncogene Proteins p21(ras) , Pancreatic Neoplasms/diagnostic imaging , Pancreatic Neoplasms/pathology , Endoscopic Ultrasound-Guided Fine Needle Aspiration/methods , Pancreatic Cyst/diagnostic imaging , Pancreatic Cyst/pathology
2.
Zhongguo Zhong Yao Za Zhi ; 30(23): 1844-8, 2005 Dec.
Article in Chinese | MEDLINE | ID: mdl-16499024

ABSTRACT

OBJECTIVE: To observe the base of the interference in correlated biotic active matter obtained multi-drug resistance induced by chemotherapy for different alkaloid, and to supervise the use in clinic to restrain the multi-drug resistant of chemotherapy, and thereby to improve the curative effect. METHOD: After bestowing subter-dosage unite chemotherapeutant to ascites S180 mouse to set up the mouse models of multi-drug resistance of S180 tumour cell, and giving the mouse matrine, terandrine, oxymatrine and berberine hydrooh loride for 4 weeks, the P170, LRP, TOPOII, Fas and apoposis were determined by flow cytometry. RESULT: Matrine and terandrine could obviously reduce the express of P170, LRP and the activation of TOPOII, and increase the ratio of the express of Fas and the apoposis of drug resistant tumour cell. And at the same time it could obviously reduce the express of intercellular adhesion molecule(CD54). CONCLUSION: Matrine and terandrine can interfere in MDR which results from chemotherapeutics by the adjustment of correlated biotic active matter, besides, the different degree of alkaloid effect with different configuration.


Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Alkaloids/pharmacology , Benzylisoquinolines/pharmacology , Drug Resistance, Multiple , Drug Resistance, Neoplasm , Quinolizines/pharmacology , Sarcoma 180/pathology , Alkaloids/isolation & purification , Animals , Apoptosis/drug effects , Benzylisoquinolines/isolation & purification , Berberine Alkaloids/isolation & purification , Berberine Alkaloids/pharmacology , DNA Topoisomerases, Type II/metabolism , Female , Male , Mice , Plants, Medicinal/chemistry , Quinolizines/isolation & purification , Random Allocation , Sarcoma 180/metabolism , Tumor Cells, Cultured , Vault Ribonucleoprotein Particles/metabolism , fas Receptor/metabolism , Matrines
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