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本文引用的文献

1
Overexpression of sirt7 exhibits oncogenic property and serves as a prognostic factor in colorectal cancer.Sirt7 过表达在结直肠癌中表现出致癌特性,并作为一个预后因素。
Clin Cancer Res. 2014 Jul 1;20(13):3434-45. doi: 10.1158/1078-0432.CCR-13-2952. Epub 2014 Apr 25.
2
Intracellular distribution of human SIRT7 and mapping of the nuclear/nucleolar localization signal.人源 SIRT7 的细胞内分布及核仁定位信号的作图。
FEBS J. 2013 Jul;280(14):3451-66. doi: 10.1111/febs.12346. Epub 2013 Jun 20.
3
Altered expression of SIRT gene family in head and neck squamous cell carcinoma.SIRT基因家族在头颈部鳞状细胞癌中的表达改变。
Tumour Biol. 2013 Jun;34(3):1847-54. doi: 10.1007/s13277-013-0726-y. Epub 2013 Mar 12.
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From sirtuin biology to human diseases: an update.从长寿蛋白生物学到人类疾病:最新进展。
J Biol Chem. 2012 Dec 14;287(51):42444-52. doi: 10.1074/jbc.R112.402768. Epub 2012 Oct 18.
5
Sirtuin7 oncogenic potential in human hepatocellular carcinoma and its regulation by the tumor suppressors MiR-125a-5p and MiR-125b.Sirtuin7 致癌潜能在人肝癌和它的章程由肿瘤遏抑 MiR-125a-5p 和 MiR-125b。
Hepatology. 2013 Mar;57(3):1055-67. doi: 10.1002/hep.26101. Epub 2013 Feb 11.
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Rejuvenating sirtuins: the rise of a new family of cancer drug targets.激活沉默信息调节因子:新一代癌症药物靶点的崛起。
Curr Pharm Des. 2013;19(4):614-23. doi: 10.2174/138161213804581954.
7
The controversial role of Sirtuins in tumorigenesis - SIRT7 joins the debate.Sirtuins 在肿瘤发生中的争议性作用——SIRT7 加入争论。
Cell Res. 2013 Jan;23(1):10-2. doi: 10.1038/cr.2012.112. Epub 2012 Jul 31.
8
SIRT7 links H3K18 deacetylation to maintenance of oncogenic transformation.SIRT7 将 H3K18 去乙酰化与致癌转化的维持联系起来。
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Functional proteomics establishes the interaction of SIRT7 with chromatin remodeling complexes and expands its role in regulation of RNA polymerase I transcription.功能蛋白质组学确立了 SIRT7 与染色质重塑复合物的相互作用,并扩展了其在 RNA 聚合酶 I 转录调控中的作用。
Mol Cell Proteomics. 2012 May;11(5):60-76. doi: 10.1074/mcp.A111.015156.
10
Sirtuins as regulators of metabolism and healthspan.沉默调节蛋白作为代谢和寿命的调节剂。
Nat Rev Mol Cell Biol. 2012 Mar 7;13(4):225-238. doi: 10.1038/nrm3293.

Sirt7的高表达可作为乳腺癌不良预后的一个预测指标。

High expression of Sirt7 served as a predictor of adverse outcome in breast cancer.

作者信息

Geng Qian, Peng Haoyu, Chen Fengsheng, Luo Rongcheng, Li Rong

机构信息

Cancer Center, Southern Medical University Guangzhou 510315, China ; Traditional Chinese Medicine-Integrated Hospital, Southern Medical University Guangzhou 510315, China.

Cancer Center, Southern Medical University Guangzhou 510315, China ; Department of Oncology, Nanfang Hospital, Southern Medical University Guangzhou 510515, China.

出版信息

Int J Clin Exp Pathol. 2015 Feb 1;8(2):1938-45. eCollection 2015.

PMID:25973086
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4396261/
Abstract

OBJECTIVE

Sirt7, as one of the seven Sirtuin family members, which plays distinct roles in cancer progression, is bringing emerging attention due to its oncogenic characteristic. The expression of Sirt7 in breast cancer remained unclear, and the aim of this study was to elucidate its role in breast cancer.

METHODS

A total of 188 cases included in this study were immunohistochemically evaluated for Sirt7, and western blot assay was used to assess its expression in breast cell lines as well as 36 breast cancer tissues and 36 paired non-cancerous tissues.

RESULTS

Upregulation of Sirt7 was found in breast cancer cell lines and breast cancer tissues (P < 0.001) by western blot analysis. Sirt7 was highly expressed in breast cancer tissue samples (67.8%) compared to adjacent normal breast tissues (31.8%) by immunohistochemical assay. It was also observed that the high expression level of Sirt7 was significantly correlated with high histological grade (P = 0.039) and negatively related to overall survival (P = 0.006). Sirt7 proved to be an independent prognostic factor (P = 0.007) in breast cancer.

CONCLUSIONS

Sirt7 expression was implicated with high histological grade and independently predicted poor clinical outcome in patients with breast cancer, suggesting that Sirt7 might play a role in the malignant progression of breast cancer.

摘要

目的

Sirt7作为沉默调节蛋白家族的七个成员之一,在癌症进展中发挥着不同作用,因其致癌特性而受到越来越多的关注。Sirt7在乳腺癌中的表达尚不清楚,本研究旨在阐明其在乳腺癌中的作用。

方法

本研究共纳入188例患者,采用免疫组织化学方法评估Sirt7的表达,并通过蛋白质印迹分析评估其在乳腺癌细胞系以及36例乳腺癌组织和36例配对的癌旁组织中的表达。

结果

蛋白质印迹分析发现乳腺癌细胞系和乳腺癌组织中Sirt7表达上调(P < 0.001)。免疫组织化学分析显示,与邻近正常乳腺组织(31.8%)相比,Sirt7在乳腺癌组织样本中高表达(67.8%)。还观察到Sirt7的高表达水平与高组织学分级显著相关(P = 0.039),与总生存期呈负相关(P = 0.006)。Sirt7被证明是乳腺癌的独立预后因素(P = 0.007)。

结论

Sirt7的表达与高组织学分级有关,并独立预测乳腺癌患者的不良临床结局,提示Sirt7可能在乳腺癌的恶性进展中起作用。