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1.
Zhonghua Kou Qiang Yi Xue Za Zhi ; 57(11): 1102-1112, 2022 Nov 09.
Article in Chinese | MEDLINE | ID: mdl-36379888

ABSTRACT

Pathological diagnosis of salivary gland tumors is one of the most challenging areas in all head and neck surgical pathology. The classification of salivary gland tumors was updated in the 5th edition of the World Health Organization Classification of Head and Neck Tumours, most of which were based on their molecular pathological characteristerics. This new classification features a description of several new entitiesamong benign and malignant neoplasms, salivary gland tumors with updated naming or diagnostic criteria, and lesions deleted from this section, etc.This present review focuses on the updates and changes in the new classification of salivary gland tumors, and provides some reference for head and neck surgeons and pathologists.


Subject(s)
Head and Neck Neoplasms , Salivary Gland Neoplasms , Humans , Salivary Gland Neoplasms/classification , Salivary Gland Neoplasms/pathology , Salivary Glands , World Health Organization
3.
Eur Rev Med Pharmacol Sci ; 24(11): 6064-6071, 2020 06.
Article in English | MEDLINE | ID: mdl-32572921

ABSTRACT

OBJECTIVE: Studies have found that hsa_circ_103809, a newly discovered circRNA in recent years, can serve as an oncogene involved in the progression of hepatocellular carcinoma. However, its role in gastric cancer (GCa) remains elusive. The aim of this study was to reveal the molecular mechanism of hsa_circ_103809 affecting the process of GCa, thus providing new ideas for its treatment. PATIENTS AND METHODS: Hsa_circ_103809 expression in GCa and adjacent tissues specimens were studied by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) analysis, and its effect on the prognosis of GCa patients was analyzed. In GCa cells lines, hsa_circ_103809 was knocked down by small interfering RNA, and GCa cell metastasis ability was detected by cell wound healing test and transwell assay. Finally, the potential target gene of hsa_circ_103809 was predicted through bioinformatics website and verified by Luciferase assay. RESULTS: Hsa_circ_103809 showed an increased expression both in GCa tissues and cell lines, predicting a poor prognosis of GCa patients. Meanwhile, the invasive and migration capacities of GCa cells were remarkably reduced after the knockdown of hsa_circ_103809. Bioinformatics website predicted that there existed binding sites of hsa_circ_103809 on microRNA-101-3p, and Luciferase assay verified that hsa_circ_103809 can adsorb microRNA-101-3p. In GCa tissues, qPCR detected a significantly reduced expression of microRNA-101-3p, which was negatively correlated with that of hsa_circ_103809. In addition, the knockdown of hsa_circ_103809 enhanced microRNA-101-3p expression in GCa cell lines. Subsequent in vitro experiments further detected that the overexpression of hsa_circ_103809 partially reversed the inhibitory effect of microRNA-101-3p overexpression on GCa cell migration ability and invasiveness. CONCLUSIONS: Hsa_circ_103809, highly expressed in GCa, may promote the migration capacity of GCa cells by adsorbing microRNA-101-3p and thus become a new therapeutic target for GCa.


Subject(s)
Cell Movement , MicroRNAs/metabolism , Neoplasm Invasiveness , RNA, Circular/metabolism , Stomach Neoplasms/metabolism , Binding Sites , Cell Proliferation , Cells, Cultured , Humans , MicroRNAs/genetics , RNA, Circular/genetics , Stomach Neoplasms/pathology
4.
Neurosci Lett ; 372(3): 200-3, 2004 Dec 06.
Article in English | MEDLINE | ID: mdl-15542240

ABSTRACT

Apoptosis is thought to play a role in neuronal pathology in schizophrenia. Recently, the GSN gene was reported to have anti-apoptotic properties. In a genome-wide expression analysis on schizophrenia, GSN was also found to be significantly down-regulated in schizophrenia. All the hints suggest that GSN is a novel candidate gene in occurrence of schizophrenia. In this work, we genotyped 3 SNPs around the GSN locus in 493 sets of the Han Chinese trio sample using allele-specific PCR. A weak association or a marginally positive result was detected (0.05 for P-value of the overtransmitted haplotype and 0.02 for a global P-value).


Subject(s)
Gelsolin/genetics , Schizophrenia/genetics , Adult , China/epidemiology , Cohort Studies , Female , Genetic Linkage , Genotype , Haplotypes , Heterozygote , Humans , Male , Polymorphism, Single Nucleotide/genetics , Psychiatric Status Rating Scales , Reverse Transcriptase Polymerase Chain Reaction , Schizophrenic Psychology
5.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 17(3): 136-8, 1997 Mar.
Article in Chinese | MEDLINE | ID: mdl-9863075

ABSTRACT

OBJECTIVE: To investigate the curative effect of integrated traditional and western medicine (TCM-WM) therapy on hepatolenticular degeneration (HLD). METHODS: Eighty patients with HLD were divided randomly into two groups (TCM-WM group and WM group), TCM-WM group (40 cases) were given orally dimercaptosuccinic acid (DMSA) and Gandou ([symbol: see text]) decoction for 1 month. The efficacy was compared with that of 40 cases treated with DMSA as the control. The changes of urinary trace and macro-elements before and after treatment were observed. RESULTS: The total effective rate of TCM-WM group was significantly higher than that of WM group (P < 0.05), especially more patients with hepatic type responded well to treatment with TCM-WM than with only chelating agent DMSA. Urinary trace and macro-elements were all obviously elevated in patients of two groups after treatment (P < 0.01). CONCLUSION: TCM-WM therapy appears extremely promising as new cupruretic method for treatment of HLD. It is particularly suitable for treating the patient with hepatic type.


Subject(s)
Drugs, Chinese Herbal/therapeutic use , Hepatolenticular Degeneration/drug therapy , Adolescent , Adult , Chelating Agents/therapeutic use , Child , Copper/urine , Female , Hepatolenticular Degeneration/urine , Humans , Male , Succimer/therapeutic use
6.
World J Gastroenterol ; 3(4): 260-2, 1997 Dec 15.
Article in English | MEDLINE | ID: mdl-27053888

ABSTRACT

AIM: To further explore the etiological mechanism of Wilson's disease (WD) by comparing the changes of biliary trace elements and its clinical phenotype. METHODS: WD patients with different types and conditions (n = 20), non-WD patients with chronic liver damage (n = 22), and healthy volunteers (n = 10; used as controls) were studied. Biliary samples were taken by duodenal drainage. Atom absorption spectrophotometer was used to assay the copper and zinc content of each sample. RESULTS: In WD, the copper content and copper/zinc ratio of biliary juice were evidently lower than those of non-WD patients with chronic liver damage and of healthy controls (F = 14.76, 25.4; 14.92, 26.2 respectively; P < 0.01), while the biliary zinc level had no significant difference from the two non-WD control groups (P > 0.05). There were significant differences in biliary copper excretion among patients with different types and conditions (F = 3.75, P < 0.05; F = 6.20, P < 0.01). CONCLUSION: Copper excretion by liver and the biliary system decreases obviously in WD, which plays a key role in the phenotypic copper retention, and the biliary copper retention is closely related with the severity of hepatic injury and illness.

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