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  4. Differential expression of hyaluronan synthase 2 in breast carcinoma and its biological significance
 
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Differential expression of hyaluronan synthase 2 in breast carcinoma and its biological significance

Journal
Histopathology
Journal Volume
65
Journal Issue
3
Pages
328-339
Date Issued
2014
Author(s)
HUANG-CHUN LIEN  
Lee Y.-H.
YUNG-MING JENG  
CHING-HUNG LIN  
YEN-SHEN LU  
Yao Y.-T.
DOI
10.1111/his.12390
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84927568379&doi=10.1111%2fhis.12390&partnerID=40&md5=cdfef26cf3b7297a2ae836c20e785838
https://scholars.lib.ntu.edu.tw/handle/123456789/470177
Abstract
Aims: Hyaluronan synthase 2 (HAS2) is an enzyme in hyaluronan synthesis. Several studies have demonstrated that HAS2 plays a critical role in tumour progression in breast cancer cells. The in-situ expression patterns of HAS2 remain unclear, and the aim of this study was to determine these in order to elucidate the role of HAS2 in breast cancer. Methods and results: We examined HAS2 expression using immunohistochemistry in 244 breast carcinomas of various subtypes. We found expression of HAS2 in 30.6% of invasive ductal carcinomas (IDCs); in IDCs, HAS2 expression was correlated significantly with the triple-negative phenotype and the basal-like phenotype, and univariate and multivariate analyses indicated that it was associated with poorer overall survival. In contrast to other carcinoma subtypes, HAS2 expression was observed in up to 72.7% of metaplastic carcinomas of breast (MCB), a carcinoma subtype related to the epithelial-mesenchymal transition (EMT). Consistently, we noted up-regulated levels of HAS2 RNA and protein in TGF-β-induced EMT in MCF-10A mammary epithelial cells. Conclusion: Our findings demonstrate that HAS2 plays a role in aggressive phenotypes of primary breast carcinoma. The strong expression of HAS2 in MCB and the up-regulation of HAS2 in breast cells induced to exhibit EMT implicates an association between HAS2 expression and EMT in breast cancer. ? 2014 John Wiley & Sons Ltd.
SDGs

[SDGs]SDG1

[SDGs]SDG3

Other Subjects
hyaluronan synthase 2; hyaluronic acid; synthetase; transforming growth factor beta; unclassified drug; glucuronosyltransferase; HAS2 protein, human; RNA; transforming growth factor beta; tumor marker; Article; breast carcinoma; breast epithelium cell; cancer cell; cancer staging; cancer survival; cell culture; colloid carcinoma; epithelial mesenchymal transition; female; follow up; human; human cell; human tissue; immunofluorescence; immunohistochemistry; neuroendocrine tumor; overall survival; papillary carcinoma; phenotype; priority journal; reverse transcription polymerase chain reaction; tumor growth; tumor volume; upregulation; Western blotting; breast tumor; enzymology; genetics; Kaplan Meier method; lung carcinoma; metabolism; metaplasia; Paget nipple disease; pathology; prognosis; tumor cell line; Breast Neoplasms; Carcinoma, Ductal, Breast; Carcinoma, Lobular; Cell Line, Tumor; Epithelial-Mesenchymal Transition; Female; Glucuronosyltransferase; Humans; Immunohistochemistry; Kaplan-Meier Estimate; Metaplasia; Prognosis; RNA, Neoplasm; Transforming Growth Factor beta; Tumor Markers, Biological; Up-Regulation
Publisher
Blackwell Publishing Ltd
Type
journal article

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