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  4. 1GALT1 seems to promote in vitro disease progression in ovarian cancer
 
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1GALT1 seems to promote in vitro disease progression in ovarian cancer

Journal
International Journal of Gynecological Cancer
Journal Volume
27
Journal Issue
5
Pages
863-871
Date Issued
2017
Author(s)
Chou C.-H.
Huang M.-J.
Liao Y.-Y.
CHI-HAU CHEN  
MIN-CHUAN HUANG  orcid-logo
DOI
10.1097/IGC.0000000000000965
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/452897
Abstract
Objective: Aberrant glycosylation affects many cellular properties in cancers. The core 1 β1,3-galactosyltransferase (C1GALT1), an enzyme that controls the formation of mucintype O-glycans, has been reported to regulate hepatocellular and mammary carcinogenesis. This study aimed to explore the role of C1GALT1 in ovarian cancer. Methods: C1GALT1 expression was assessed in a public database based on microarray data from 1287 ovarian cancer patients and ovarian cancerous tissues. Lectin blotting and flow cytometry analysis were conducted to detect changes in O-glycans on ovarian cancer cells. Effects of C1GALT1 on cell growth, migration, and sphere formation were analyzed in C1GALT1 knockdown or overexpressing ovarian cancer cells in vitro. Expression of cancer stemnessrelated genes was analyzed by quantitative reverse transcription polymerase chain reaction. Results: High C1GALT1 expression shows a trend toward association with poor survival in ovarian cancer patients. C1GALT1 modifies O-glycan expression on surfaces and glycoproteins of ovarian cancer cells. Knockdown of C1GALT1 decreased cell growth, migration, and sphere formation of ES-2 and OVTW59-p4 cells. Conversely, overexpression of C1GALT1 promoted such malignant properties of SKOV3 cells. Furthermore, C1GALT1 regulated the expression of several cancer stemness-related genes, including CD133, CD24, Oct4, Nanog, and SNAI2, in ovarian cancer cells. Conclusions: C1GALT1 modifies O-glycan expression and enhances malignant behaviors in ovarian cancer cells, suggesting that C1GALT1 plays a role in the pathogenesis of ovarian cancer and targeting C1GALT1 could be a promising approach for ovarian cancer therapy. Copyright ? 2017 by IGCS and ESGO.
SDGs

[SDGs]SDG3

Other Subjects
CD133 antigen; CD24 antigen; core 1 beta 1,3 galactosyltransferase; galactosyltransferase; glycan; glycoprotein; lectin; o glycan; octamer transcription factor 4; sialic acid derivative; sialidase; Tn antigen; transcription factor NANOG; transcription factor Slug; unclassified drug; C1GALT1 protein, human; galactosyltransferase; glycoprotein; polysaccharide; Article; blotting; cancer cell; cancer growth; cancer patient; cancer prognosis; cancer survival; cancer tissue; carcinogenesis; cell function; cell growth; cell migration; cell surface; controlled study; female; flow cytometry; gene overexpression; gene silencing; human; human cell; human tissue; in vitro study; lectin blotting; MTT assay; ovarian cancer cell line; ovary cancer; overall survival; phenotype; priority journal; quantitative reverse transcription polymerase chain reaction; reverse transcription polymerase chain reaction; staining; Western blotting; biosynthesis; cancer stem cell; cell motion; deficiency; disease exacerbation; enzymology; gene knockdown; genetics; metabolism; ovary tumor; pathology; physiology; prognosis; tissue microarray; tumor cell line; Cell Growth Processes; Cell Line, Tumor; Cell Movement; Disease Progression; Female; Galactosyltransferases; Gene Knockdown Techniques; Glycoproteins; Humans; Neoplastic Stem Cells; Ovarian Neoplasms; Polysaccharides; Prognosis; Tissue Array Analysis
Type
journal article

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