1.Mucin gene family and its role in diagnosis of pancreas neoplasms.
Chinese Journal of Pathology 2006;35(2):113-116
Adenocarcinoma, Papillary
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diagnosis
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metabolism
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Carcinoma, Pancreatic Ductal
;
diagnosis
;
metabolism
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Cystadenoma, Mucinous
;
diagnosis
;
metabolism
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Gene Expression Regulation, Neoplastic
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Humans
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Mucins
;
classification
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genetics
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metabolism
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Pancreas
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metabolism
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Pancreatic Neoplasms
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diagnosis
;
metabolism
2.Pathology of mammary mucinous carcinoma and its molecular markers.
Wei ZHANG ; Yun NIU ; Tong-xian ZHANG ; Shan LIU ; Fen LIU
Chinese Journal of Pathology 2013;42(11):777-779
Adenocarcinoma, Mucinous
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classification
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metabolism
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pathology
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Biomarkers, Tumor
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metabolism
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Breast Neoplasms
;
classification
;
metabolism
;
pathology
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Carcinoma, Ductal, Breast
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pathology
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Carcinoma, Intraductal, Noninfiltrating
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pathology
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Female
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Humans
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Lymphatic Metastasis
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Mucin-1
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metabolism
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Mucin-2
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metabolism
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Mucins
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metabolism
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WT1 Proteins
;
metabolism
3.Expression of mucin glycoproteins and cytokeratins in intrahepatic cholangiocarcinoma.
Shi-mei ZHAO ; Xiong-zeng ZHU ; Yuan JI ; Jun HOU
Chinese Journal of Pathology 2008;37(11):749-753
OBJECTIVETo compare the immunoprofiles of intrahepatic cholangiocarcinoma and metastatic colorectal adenocarcinoma for mucin glycoproteins (including MUC1, MUC2, MUC5AC and MUC6) and cytokeratins (including CK7, CK19 and CK20), and to assess their diagnostic value.
METHODSOne hundred cases of intrahepatic cholangiocarcinoma and 21 cases of metastatic colorectal adenocarcinoma were enrolled into the study. Immunohistochemical study for MUC1, MUC2, MUC5AC, MUC6, CK7, CK19 and CK20 was carried out in all cases by EnVision method.
RESULTSIn intrahepatic cholangiocarcinoma, the expression rates of MUC1, MUC2, MUC5AC and MUC6 were 61.0%, 2.0%, 22.0% and 8.0% respectively, as compared to 57.1%, 47.6%, 19.0% and 23.8% respectively in metastatic colorectal adenocarcinoma. On the other hand, the expression rates of CK7, CK19 and CK20 in intrahepatic cholangiocarcinoma were 73.0%, 53.0% and 15.0% respectively, in contrast to 14.3%, 90.5% and 85.7% respectively in metastatic colorectal adenocarcinoma. The difference in expressions of MUC2, MUC6, CK7 and CK20 carried statistical significance.
CONCLUSIONSThe immunoprofile for mucin glycoproteins and cytokeratins provides important clues in distinguishing between intrahepatic cholangiocarcinoma and metastatic colorectal adenocarcinoma to liver. The immunophenotype of MUC2-/MUC6-/CK7+/CK20- indicates the diagnosis of intrahepatic cholangiocarcinoma, while MUC2+/MUC6+/CK7-/CK20+ suggests the possibility of metastatic colorectal adenocarcinoma.
Adenocarcinoma ; metabolism ; pathology ; Aged ; Bile Duct Neoplasms ; genetics ; metabolism ; pathology ; Bile Ducts, Intrahepatic ; pathology ; Biomarkers, Tumor ; analysis ; Cholangiocarcinoma ; genetics ; metabolism ; pathology ; Colorectal Neoplasms ; metabolism ; pathology ; Female ; Glycoproteins ; metabolism ; Humans ; Keratins ; metabolism ; Male ; Middle Aged ; Mucins ; metabolism ; Neoplasm Staging ; classification
4.Mucin histochemistry by paradoxical concanavalin A staining in early gastric carcinomas.
Kyung Ja CHO ; Ha Hye MYONG ; Ja June JANG
Journal of Korean Medical Science 1991;6(2):119-125
Phenotypic expression of tumor cells was investigated in 33 early gastric carcinomas by mucin histochemistry using paradoxical concanavalin A staining. This staining method had been developed to differentiate 3 classes of mucins located at various sites of the alimentary tract. Twenty-five (76%) tumors contained mixtures of neutral or acid class II mucin and class III mucin, suggesting the origin of multipotential stem cells. The surface mucous cell expression was more dominant than the pyloric gland or intestinal phenotypes in the well-and poorly differentiated adenocarcinomas. The intestinal properties of the tumor cells were noted not only in the well-differentiated but also in the poorly differentiated or signet ring cell carcinomas, not closely being related to the presence of background intestinal metaplasia. Signet ring cell carcinomas revealed a distinct pattern of mucin histochemistry compared with the other types.
Adenocarcinoma/metabolism/pathology
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Adenocarcinoma, Mucinous/metabolism/pathology
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Cell Differentiation
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Concanavalin A
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Histocytochemistry
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Humans
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Intestines/pathology
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Metaplasia
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Mucins/classification/*metabolism
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Staining and Labeling/*methods
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Stem Cells/metabolism/pathology
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Stomach Neoplasms/*metabolism/pathology
5.Draft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans.
Jinhwa KONG ; Jungim WON ; Jeehee YOON ; UnJoo LEE ; Jong Il KIM ; Sun HUH
The Korean Journal of Parasitology 2016;54(6):751-758
This study aimed at constructing a draft genome of the adult female worm Toxocara canis using next-generation sequencing (NGS) and de novo assembly, as well as to find new genes after annotation using functional genomics tools. Using an NGS machine, we produced DNA read data of T. canis. The de novo assembly of the read data was performed using SOAPdenovo. RNA read data were assembled using Trinity. Structural annotation, homology search, functional annotation, classification of protein domains, and KEGG pathway analysis were carried out. Besides them, recently developed tools such as MAKER, PASA, Evidence Modeler, and Blast2GO were used. The scaffold DNA was obtained, the N50 was 108,950 bp, and the overall length was 341,776,187 bp. The N50 of the transcriptome was 940 bp, and its length was 53,046,952 bp. The GC content of the entire genome was 39.3%. The total number of genes was 20,178, and the total number of protein sequences was 22,358. Of the 22,358 protein sequences, 4,992 were newly observed in T. canis. Following proteins previously unknown were found: E3 ubiquitin-protein ligase cbl-b and antigen T-cell receptor, zeta chain for T-cell and B-cell regulation; endoprotease bli-4 for cuticle metabolism; mucin 12Ea and polymorphic mucin variant C6/1/40r2.1 for mucin production; tropomodulin-family protein and ryanodine receptor calcium release channels for muscle movement. We were able to find new hypothetical polypeptides sequences unique to T. canis, and the findings of this study are capable of serving as a basis for extending our biological understanding of T. canis.
Adult
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B-Lymphocytes
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Base Composition
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Classification
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DNA
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Female
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Genome*
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Genomics
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Humans
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Larva Migrans, Visceral*
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Metabolism
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Mucins
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Peptides
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Protein Structure, Tertiary
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Receptors, Antigen, T-Cell
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RNA
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Ryanodine Receptor Calcium Release Channel
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T-Lymphocytes
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Toxocara canis*
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Toxocara*
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Transcriptome
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Ubiquitin-Protein Ligases