• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

UBE2C在乳腺癌中的临床病理意义:一项基于免疫组织化学、基因芯片和RNA测序数据的研究

The clinicopathological significance of UBE2C in breast cancer: a study based on immunohistochemistry, microarray and RNA-sequencing data.

作者信息

Mo Chao-Hua, Gao Li, Zhu Xiao-Fei, Wei Kang-Lai, Zeng Jing-Jing, Chen Gang, Feng Zhen-Bo

机构信息

Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, 6 Shuangyong Road, Nanning, 530021 Guangxi Zhuang Autonomous Region China.

Department of Pathology, The Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou Worker's Hospital, 1 Liushi Road, Liuzhou, 545005 Guangxi Zhuang Autonomous Region China.

出版信息

Cancer Cell Int. 2017 Sep 25;17:83. doi: 10.1186/s12935-017-0455-1. eCollection 2017.

DOI:10.1186/s12935-017-0455-1
PMID:29021715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5613379/
Abstract

BACKGROUND

Ubiquitin-conjugating enzyme E2C (UBE2C) has been previously reported to correlate with the malignant progression of various human cancers, however, the exact molecular function of UBE2C in breast carcinoma (BRCA) remained elusive. We aimed to investigate UBE2C expression in BRCA and its clinical significance.

METHODS

The expression of UBE2C in 209 BRCA tissue samples and 53 adjacent normal tissue samples was detected using immunohistochemistry. The clinical role of UBE2C was analyzed. Public databases including the human protein atlas and Oncomine were used to assess UBE2C expression in BRCA. Moreover, the cancer genome atlas (TCGA) database was employed to investigate the prognostic value of UBE2C in BRCA.

RESULTS

The positive expression rate of UBE2C in BRCA was 70.8% (148/209), and UBE2C expression in the adjacent breast tissue was negative. The expression of UBE2C was positively correlated with tumor size (r = 0.32, P < 0.001), histological grade (r = 0.237, P = 0.001), clinical stage (r = 0.198, P = 0.004), lymph node metastasis (r = 0.155, P = 0.026), HER2 expression level (r = 0.356, P < 0.001), Ki-67 expression level (r = 0.504, P < 0.001), and P53 expression level (r = 0.32, P = 0.001). Negative correlations were found between UBE2C expression and the ER (r = - 0.403, P < 0.001) and PR (r = - 0.468, P < 0.001) status. UBE2C gene expression data from the public databases all proved that UBE2C was overexpressed in BRCA. According to the TCGA data analysis, a higher positive expression of UBE2C was associated with worse survival of BRCA patients (P = 0.0428), and data from cBioPortal indicated that 11% of all sequenced BRCA patients possessed a gene alteration of UBE2C, predominately gene amplification and mRNA regulation.

CONCLUSION

Ubiquitin-conjugating enzyme E2C might pose an oncogenic effect on the progression of BRCA.

摘要

背景

泛素结合酶E2C(UBE2C)此前已被报道与多种人类癌症的恶性进展相关,然而,UBE2C在乳腺癌(BRCA)中的确切分子功能仍不清楚。我们旨在研究UBE2C在BRCA中的表达及其临床意义。

方法

采用免疫组织化学法检测209例BRCA组织样本和53例癌旁正常组织样本中UBE2C的表达。分析UBE2C的临床作用。利用包括人类蛋白质图谱和Oncomine在内的公共数据库评估BRCA中UBE2C的表达。此外,使用癌症基因组图谱(TCGA)数据库研究UBE2C在BRCA中的预后价值。

结果

BRCA中UBE2C的阳性表达率为70.8%(148/209),而癌旁乳腺组织中UBE2C表达为阴性。UBE2C的表达与肿瘤大小(r = 0.32,P < 0.001)、组织学分级(r = 0.237,P = 0.001)、临床分期(r = 0.198,P = 0.004)、淋巴结转移(r = 0.155,P = 0.026)、HER2表达水平(r = 0.356,P < 0.001)、Ki-67表达水平(r = 0.504,P < 0.001)和P53表达水平(r = 0.32,P = 0.001)呈正相关。UBE2C表达与ER(r = -0.403,P < 0.001)和PR(r = -0.468,P < 0.001)状态呈负相关。公共数据库中的UBE2C基因表达数据均证明UBE2C在BRCA中过表达。根据TCGA数据分析,UBE2C较高的阳性表达与BRCA患者较差的生存率相关(P = 0.0428),来自cBioPortal的数据表明,所有测序的BRCA患者中有11%存在UBE2C基因改变,主要是基因扩增和mRNA调控。

结论

泛素结合酶E2C可能对BRCA的进展具有致癌作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/2f5a73b290d5/12935_2017_455_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/0ecdf006e43e/12935_2017_455_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/99b71abd0fb6/12935_2017_455_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/3ac70562e03a/12935_2017_455_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/3dbed341bd62/12935_2017_455_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/559fb3f73c6e/12935_2017_455_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/ce6763de8e4f/12935_2017_455_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/7b34b8fa83a8/12935_2017_455_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/52aa0dc630c7/12935_2017_455_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/038c67184ea4/12935_2017_455_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/d8d66ea58cc7/12935_2017_455_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/f73d9e2d806f/12935_2017_455_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/2f5a73b290d5/12935_2017_455_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/0ecdf006e43e/12935_2017_455_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/99b71abd0fb6/12935_2017_455_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/3ac70562e03a/12935_2017_455_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/3dbed341bd62/12935_2017_455_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/559fb3f73c6e/12935_2017_455_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/ce6763de8e4f/12935_2017_455_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/7b34b8fa83a8/12935_2017_455_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/52aa0dc630c7/12935_2017_455_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/038c67184ea4/12935_2017_455_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/d8d66ea58cc7/12935_2017_455_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/f73d9e2d806f/12935_2017_455_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b04/5613379/2f5a73b290d5/12935_2017_455_Fig12_HTML.jpg

相似文献

1
The clinicopathological significance of UBE2C in breast cancer: a study based on immunohistochemistry, microarray and RNA-sequencing data.UBE2C在乳腺癌中的临床病理意义:一项基于免疫组织化学、基因芯片和RNA测序数据的研究
Cancer Cell Int. 2017 Sep 25;17:83. doi: 10.1186/s12935-017-0455-1. eCollection 2017.
2
Expression of UBE2C in lung adenocarcinoma based on database analysis and its clinical significance.基于数据库分析的UBE2C在肺腺癌中的表达及其临床意义
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020;45(9):1044-1052. doi: 10.11817/j.issn.1672-7347.2020.190189.
3
The clinicopathological significance of ubiquitin-conjugating enzyme E2C, leucine-rich repeated-containing G protein-coupled receptor, WW domain-containing oxidoreductase, and vasculogenic mimicry in invasive breast carcinoma.泛素结合酶E2C、富含亮氨酸重复序列的G蛋白偶联受体、含WW结构域的氧化还原酶及血管生成拟态在浸润性乳腺癌中的临床病理意义
Medicine (Baltimore). 2019 Apr;98(16):e15232. doi: 10.1097/MD.0000000000015232.
4
Identification of overexpressed genes in hepatocellular carcinoma, with special reference to ubiquitin-conjugating enzyme E2C gene expression.肝细胞癌中过表达基因的鉴定,特别参考泛素结合酶E2C基因的表达。
Int J Cancer. 2007 Jul 1;121(1):33-8. doi: 10.1002/ijc.22605.
5
as an Immune-Related Biomarker for Breast Cancer: A Study Based on Multiple Databases.作为乳腺癌的免疫相关生物标志物:一项基于多个数据库的研究。
Chin Med Sci J. 2024 Sep 30;39(3):171-181. doi: 10.24920/004340.
6
UBE2C promotes the progression of head and neck squamous cell carcinoma.UBE2C 促进头颈部鳞状细胞癌的进展。
Biochem Biophys Res Commun. 2020 Mar 5;523(2):389-397. doi: 10.1016/j.bbrc.2019.12.064. Epub 2019 Dec 20.
7
Ubiquitin-conjugating enzyme 2C (UBE2C) is a poor prognostic biomarker in invasive breast cancer.泛素连接酶 2C(UBE2C)是浸润性乳腺癌的预后不良生物标志物。
Breast Cancer Res Treat. 2022 Apr;192(3):529-539. doi: 10.1007/s10549-022-06531-5. Epub 2022 Feb 6.
8
A Comprehensive Bioinformatics Analysis of in Cancers.在癌症中 的综合生物信息学分析。
Int J Mol Sci. 2019 May 7;20(9):2228. doi: 10.3390/ijms20092228.
9
Ubiquitin-conjugating enzyme E2C regulates apoptosis-dependent tumor progression of non-small cell lung cancer via ERK pathway.泛素结合酶E2C通过ERK途径调节非小细胞肺癌的凋亡依赖性肿瘤进展。
Med Oncol. 2015 May;32(5):149. doi: 10.1007/s12032-015-0609-8. Epub 2015 Apr 2.
10
Pathological significance of MAD2L1 in breast cancer: an immunohistochemical study and meta analysis.MAD2L1在乳腺癌中的病理意义:一项免疫组织化学研究与荟萃分析
Int J Clin Exp Pathol. 2017 Sep 1;10(9):9190-9201. eCollection 2017.

引用本文的文献

1
Comprehensive analysis of the prognosis and tumor immune microenvironment of ubiquitin-conjugating enzyme transport-related gene UBE2C in hepatocellular carcinoma.泛素结合酶转运相关基因UBE2C在肝细胞癌中的预后及肿瘤免疫微环境的综合分析
Discov Oncol. 2025 May 23;16(1):884. doi: 10.1007/s12672-025-02675-0.
2
Spatially informed graph transformers for spatially resolved transcriptomics.用于空间分辨转录组学的空间信息图变换器
Commun Biol. 2025 Apr 6;8(1):574. doi: 10.1038/s42003-025-08015-w.
3
Exploring Prognostic Gene Factors in Breast Cancer via Machine Learning.

本文引用的文献

1
MicroRNA signatures predict prognosis of patients with glioblastoma multiforme through the Cancer Genome Atlas.微小RNA特征通过癌症基因组图谱预测多形性胶质母细胞瘤患者的预后。
Oncotarget. 2017 Apr 6;8(35):58386-58393. doi: 10.18632/oncotarget.16878. eCollection 2017 Aug 29.
2
The Relation of HPV Infection and Expression of p53 and p16 Proteins in Esophageal Squamous Cells Carcinoma.人乳头瘤病毒感染与食管鳞状细胞癌中p53和p16蛋白表达的关系
J Cancer. 2017 Apr 9;8(6):1062-1070. doi: 10.7150/jca.17080. eCollection 2017.
3
MicroRNA-338-3p suppresses cell proliferation and induces apoptosis of non-small-cell lung cancer by targeting sphingosine kinase 2.
通过机器学习探索乳腺癌的预后基因因素。
Biochem Genet. 2024 Dec;62(6):5022-5050. doi: 10.1007/s10528-024-10712-w. Epub 2024 Feb 21.
4
Unique E2-binding specificity of artificial RING fingers in cancer cells.人工 RING 指在癌细胞中具有独特的 E2 结合特异性。
Sci Rep. 2024 Jan 31;14(1):2545. doi: 10.1038/s41598-024-52793-y.
5
MALAT1-regulated gene expression profiling in lung cancer cell lines.MALAT1 调控的肺癌细胞系基因表达谱。
BMC Cancer. 2023 Sep 4;23(1):818. doi: 10.1186/s12885-023-11347-7.
6
Artificial RING finger reveals unique auto-ubiquitination with E2 specificity.人工 RING 指结构揭示了具有 E2 特异性的独特的自动泛素化。
Protein Sci. 2023 Oct;32(10):e4766. doi: 10.1002/pro.4766.
7
ForestSubtype: a cancer subtype identifying approach based on high-dimensional genomic data and a parallel random forest.森林亚型:一种基于高维基因组数据和并行随机森林的癌症亚型识别方法。
BMC Bioinformatics. 2023 Jul 19;24(1):289. doi: 10.1186/s12859-023-05412-y.
8
Validation of a Disease-Free Survival Prediction Model Using UBE2C and Clinical Indicators in Breast Cancer Patients.使用UBE2C和临床指标对乳腺癌患者无病生存预测模型的验证
Breast Cancer (Dove Med Press). 2023 Apr 25;15:295-310. doi: 10.2147/BCTT.S402109. eCollection 2023.
9
UBE2S and UBE2C confer a poor prognosis to breast cancer downregulation of Numb.UBE2S和UBE2C通过下调Numb导致乳腺癌预后不良。
Front Oncol. 2023 Feb 14;13:992233. doi: 10.3389/fonc.2023.992233. eCollection 2023.
10
HO-1089 and HO-1197, Novel Herbal Formulas, Have Antitumor Effects via Suppression of PLK1 (Polo-like Kinase 1) Expression in Hepatocellular Carcinoma.新型草药配方HO - 1089和HO - 1197通过抑制肝细胞癌中PLK1(Polo样激酶1)的表达发挥抗肿瘤作用。
Cancers (Basel). 2023 Jan 30;15(3):851. doi: 10.3390/cancers15030851.
微小RNA-338-3p通过靶向鞘氨醇激酶2抑制非小细胞肺癌细胞增殖并诱导其凋亡。
Cancer Cell Int. 2017 Apr 17;17:46. doi: 10.1186/s12935-017-0415-9. eCollection 2017.
4
Human microRNA-299-3p decreases invasive behavior of cancer cells by downregulation of Oct4 expression and causes apoptosis.人类微小RNA-299-3p通过下调Oct4表达降低癌细胞的侵袭行为并引发细胞凋亡。
PLoS One. 2017 Apr 20;12(4):e0174912. doi: 10.1371/journal.pone.0174912. eCollection 2017.
5
Identification of miRNA biomarkers of pneumonia using RNA-sequencing and bioinformatics analysis.使用RNA测序和生物信息学分析鉴定肺炎的miRNA生物标志物
Exp Ther Med. 2017 Apr;13(4):1235-1244. doi: 10.3892/etm.2017.4151. Epub 2017 Feb 21.
6
Immunohistochemical Ki67 after short-term hormone therapy identifies low-risk breast cancers as reliably as genomic markers.短期激素治疗后的免疫组化Ki67与基因组标志物一样能可靠地识别低风险乳腺癌。
Oncotarget. 2017 Apr 18;8(16):26122-26128. doi: 10.18632/oncotarget.15385.
7
MicroRNA-137 inhibits growth of glioblastoma through EGFR suppression.微小RNA-137通过抑制表皮生长因子受体来抑制胶质母细胞瘤的生长。
Am J Transl Res. 2017 Mar 15;9(3):1492-1499. eCollection 2017.
8
Downregulation of sorting nexin 10 is associated with overexpression of miR-30d during liver cancer progression in rats.在大鼠肝癌进展过程中,分选连接蛋白10的下调与miR-30d的过表达相关。
Tumour Biol. 2017 Apr;39(4):1010428317695932. doi: 10.1177/1010428317695932.
9
A Circulating MicroRNA Signature Capable of Assessing the Risk of Hepatocellular Carcinoma in Cirrhotic Patients.一种能够评估肝硬化患者肝细胞癌风险的循环 microRNA 特征。
Sci Rep. 2017 Mar 31;7(1):523. doi: 10.1038/s41598-017-00631-9.
10
Suppression of microRNA-629 enhances sensitivity of cervical cancer cells to 1'S-1'-acetoxychavicol acetate via regulating RSU1.抑制微小RNA-629通过调节RSU1增强宫颈癌细胞对乙酸1'S-1'-乙酰氧基胡椒酚乙酸酯的敏感性。
Onco Targets Ther. 2017 Mar 20;10:1695-1705. doi: 10.2147/OTT.S117492. eCollection 2017.