Protein O-fucosyltransferase 1: a potential diagnostic marker and therapeutic target for human oral cancer.

IF 4.9 3区 医学 Q1 ONCOLOGY International journal of oncology Pub Date : 2013-12-01 Epub Date: 2013-09-23 DOI:10.3892/ijo.2013.2110
Satoshi Yokota, Katsunori Ogawara, Ryota Kimura, Fumie Shimizu, Takao Baba, Yasuyuki Minakawa, Morihiro Higo, Atsushi Kasamatsu, Yosuke Endo-Sakamoto, Masashi Shiiba, Hideki Tanzawa, Katsuhiro Uzawa
{"title":"Protein O-fucosyltransferase 1: a potential diagnostic marker and therapeutic target for human oral cancer.","authors":"Satoshi Yokota,&nbsp;Katsunori Ogawara,&nbsp;Ryota Kimura,&nbsp;Fumie Shimizu,&nbsp;Takao Baba,&nbsp;Yasuyuki Minakawa,&nbsp;Morihiro Higo,&nbsp;Atsushi Kasamatsu,&nbsp;Yosuke Endo-Sakamoto,&nbsp;Masashi Shiiba,&nbsp;Hideki Tanzawa,&nbsp;Katsuhiro Uzawa","doi":"10.3892/ijo.2013.2110","DOIUrl":null,"url":null,"abstract":"<p><p>Protein O-fucosyltransferase 1 (POFUT1) is the enzyme that adds O-fucose through O-glycosidic linkage to conserved serine or threonine residues in the epidermal growth factor-like repeats of a number of cellular surface and secreted proteins. Our previous study using microarray technology showed that significant upregulation of POFUT1 occurs in oral squamous cell carcinoma (OSCC)-derived cell lines compared to human normal oral keratinocytes. The aim of the present study was to examine the status of POFUT1 mRNA and protein expression in OSCC-derived cell lines and human primary OSCCs. POFUT1 mRNA was upregulated significantly (P<0.05 for both comparisons) in five OSCC-derived cell lines and primary OSCCs using quantitative reverse transcriptase-polymerase chain reaction. Immunohistochemistry data indicated that POFUT1 protein expression levels were consistent with mRNA expression status in OSCC-derived cell lines and primary OSCCs. Furthermore, POFUT1 expression status was correlated significantly (P=0.048) with the primary tumor size. The proliferation of POFUT1 knockdown cells was inhibited significantly compared with that of control cells. These results indicated that POFUT1 expression can contribute to cancer progression and that POFUT1 may serve as a diagnostic marker and a therapeutic target for OSCCs. </p>","PeriodicalId":14175,"journal":{"name":"International journal of oncology","volume":"43 6","pages":"1864-70"},"PeriodicalIF":4.9000,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3892/ijo.2013.2110","citationCount":"31","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3892/ijo.2013.2110","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/9/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 31

Abstract

Protein O-fucosyltransferase 1 (POFUT1) is the enzyme that adds O-fucose through O-glycosidic linkage to conserved serine or threonine residues in the epidermal growth factor-like repeats of a number of cellular surface and secreted proteins. Our previous study using microarray technology showed that significant upregulation of POFUT1 occurs in oral squamous cell carcinoma (OSCC)-derived cell lines compared to human normal oral keratinocytes. The aim of the present study was to examine the status of POFUT1 mRNA and protein expression in OSCC-derived cell lines and human primary OSCCs. POFUT1 mRNA was upregulated significantly (P<0.05 for both comparisons) in five OSCC-derived cell lines and primary OSCCs using quantitative reverse transcriptase-polymerase chain reaction. Immunohistochemistry data indicated that POFUT1 protein expression levels were consistent with mRNA expression status in OSCC-derived cell lines and primary OSCCs. Furthermore, POFUT1 expression status was correlated significantly (P=0.048) with the primary tumor size. The proliferation of POFUT1 knockdown cells was inhibited significantly compared with that of control cells. These results indicated that POFUT1 expression can contribute to cancer progression and that POFUT1 may serve as a diagnostic marker and a therapeutic target for OSCCs.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
蛋白O-聚焦转移酶1:人类口腔癌的潜在诊断标志物和治疗靶点。
蛋白O-聚焦转移酶1 (POFUT1)是一种通过O-糖苷连锁将O-聚焦添加到许多细胞表面和分泌蛋白的表皮生长因子样重复序列中的保守丝氨酸或苏氨酸残基上的酶。我们之前使用微阵列技术的研究表明,与人类正常口腔角质形成细胞相比,口腔鳞状细胞癌(OSCC)衍生细胞系中POFUT1的显著上调。本研究的目的是检测POFUT1 mRNA和蛋白在oscc衍生细胞系和人原代oscc中的表达状况。POFUT1 mRNA表达显著上调(P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
9.60
自引率
0.00%
发文量
157
审稿时长
2.1 months
期刊介绍: The main aim of Spandidos Publications is to facilitate scientific communication in a clear, concise and objective manner, while striving to provide prompt publication of original works of high quality. The journals largely concentrate on molecular and experimental medicine, oncology, clinical and experimental cancer treatment and biomedical research. All journals published by Spandidos Publications Ltd. maintain the highest standards of quality, and the members of their Editorial Boards are world-renowned scientists.
期刊最新文献
Advances in the study of the breast carcinoma exosomal microRNAs: From basic mechanisms to clinical applications (Review). [Corrigendum] The p85α regulatory subunit of PI3K mediates cAMP‑PKA and retinoic acid biological effects on MCF7 cell growth and migration. Emerging roles of RNA m6A modification in multiple myeloma pathogenesis and treatment resistance (Review). [Corrigendum] Podoplanin‑mediated TGF‑β‑induced epithelial‑mesen‑ chymal transition and its correlation with bHLH transcription factor DEC in TE‑11 cells. Role of SPAG6 in regulating physiological functions and tumorigenesis (Review).
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1