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本文引用的文献

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The eicosanoids leukotriene D4 and prostaglandin E2 promote the tumorigenicity of colon cancer-initiating cells in a xenograft mouse model.在异种移植小鼠模型中,类花生酸白三烯D4和前列腺素E2可促进结肠癌起始细胞的致瘤性。
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EMT: 2016.EMT:2016 年。
Cell. 2016 Jun 30;166(1):21-45. doi: 10.1016/j.cell.2016.06.028.
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Dehydropeptidase 1 promotes metastasis through regulation of E-cadherin expression in colon cancer.脱氢肽酶1通过调控结肠癌中E-钙黏蛋白的表达促进转移。
Oncotarget. 2016 Feb 23;7(8):9501-12. doi: 10.18632/oncotarget.7033.
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Cancer statistics, 2016.癌症统计数据,2016 年。
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EMT and tumor metastasis.上皮-间质转化与肿瘤转移
Clin Transl Med. 2015 Feb 26;4:6. doi: 10.1186/s40169-015-0048-3. eCollection 2015.
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Japanese Society for Cancer of the Colon and Rectum (JSCCR) Guidelines 2014 for treatment of colorectal cancer.日本结直肠癌学会(JSCCR)2014年结直肠癌治疗指南。
Int J Clin Oncol. 2015 Apr;20(2):207-39. doi: 10.1007/s10147-015-0801-z. Epub 2015 Mar 18.
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First Selective Small Molecule Inhibitor of FGFR4 for the Treatment of Hepatocellular Carcinomas with an Activated FGFR4 Signaling Pathway.首个用于治疗 FGFR4 信号通路激活的肝细胞癌的选择性 FGFR4 小分子抑制剂。
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KRAS and YAP1 converge to regulate EMT and tumor survival.KRAS 和 YAP1 共同调控 EMT 和肿瘤存活。
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结直肠癌中双肽酶1表达的临床病理检查

Clinicopathological examination of dipeptidase 1 expression in colorectal cancer.

作者信息

Tachibana Kazunoshin, Saito Motonobu, Imai Jun-Ichi, Ito Emi, Yanagisawa Yuka, Honma Reiko, Saito Katsuharu, Ando Jin, Momma Tomoyuki, Ohki Shinji, Ohtake Tohru, Watanabe Shinya, Waguri Satoshi, Takenoshita Seiichi

机构信息

Department of Organ Regulatory Surgery, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.

Medical-Industrial Translational Research Center, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.

出版信息

Biomed Rep. 2017 Apr;6(4):423-428. doi: 10.3892/br.2017.870. Epub 2017 Mar 8.

DOI:10.3892/br.2017.870
PMID:28413640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5374953/
Abstract

Dipeptidase 1 (DPEP1) is a zinc-dependent metalloproteinase that is fundamental in glutathione and leukotriene metabolism. was initially considered as a tumor suppressor gene in Wilms' tumor and breast cancer. However, it has been reported that DPEP1 is upregulated in colorectal cancers (CRCs) and high DPEP1 expression levels are associated with poorer patient survival. The role of genes in CRC, as well as their expression, requires investigation. Therefore, the present study investigated DPEP1 expression using reverse transcription-quantitative polymerase chain reaction or immunohistochemistry on surgically resected samples from CRC cases, and further examined the biological significance of DPEP1 by comparing the expression of the epithelial to mesenchymal transition (EMT) markers, including epithelial cadherin and Vimentin to clarify the function of DPEP1 in CRC, particularly in metastasis. The level of DPEP1 expression was identified to be significantly increased in tumorous tissue samples compared with that in non-tumorous tissue samples. In addition, increased DPEP1 mRNA expression levels were associated with positive lymph node metastasis in the included cohort. However, no positive correlations were observed between DPEP1 and EMT markers in the cohort. The results indiciates that further investigations into the upregulation of DPEP1 in colorectal carcinogenesis and the role of therapeutic or prognostic biomarkers are required.

摘要

二肽酶1(DPEP1)是一种锌依赖性金属蛋白酶,在谷胱甘肽和白三烯代谢中起重要作用。它最初在肾母细胞瘤和乳腺癌中被视为肿瘤抑制基因。然而,据报道,DPEP1在结直肠癌(CRC)中上调,且DPEP1高表达水平与患者较差的生存率相关。该基因在CRC中的作用及其表达情况需要进行研究。因此,本研究使用逆转录定量聚合酶链反应或免疫组织化学方法,对CRC病例手术切除的样本进行DPEP1表达检测,并通过比较上皮-间质转化(EMT)标志物(包括上皮钙黏蛋白和波形蛋白)的表达,进一步研究DPEP1的生物学意义,以阐明DPEP1在CRC,特别是在转移中的功能。结果发现,与非肿瘤组织样本相比,肿瘤组织样本中DPEP1表达水平显著升高。此外,在纳入的队列中,DPEP1 mRNA表达水平升高与阳性淋巴结转移相关。然而,在该队列中未观察到DPEP1与EMT标志物之间存在正相关。结果表明,需要进一步研究DPEP1在结直肠癌发生过程中的上调情况以及治疗或预后生物标志物的作用。