Suppr超能文献

含溴结构域和额外末端结构域家族过表达在卵巢癌中的预后作用。

Prognostic role of overexpressed Bromodomain and extra-terminal family in ovarian cancer.

作者信息

Chetry Mandika, Bhandari Adheesh, Lin Yue

机构信息

Department of Oncology, The First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.

Department of Breast Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province, China.

出版信息

J Cancer. 2022 Mar 14;13(5):1695-1705. doi: 10.7150/jca.69574. eCollection 2022.

Abstract

BET family proteins have a role as epigenetic readers to accelerate the transcription of target genes. Several studies have shown that the BET protein family played important roles in several biological processes. Although, the prognostic influence of individual BET genes family in ovarian cancer patients remains unclear. We investigated BET mRNA prognostic roles subtypes in ovarian cancer patients by means of the KM plotter database. The BET mRNA expression and protein in cancer and normal ovarian cells was determined using qRTPCR and western blot. We used the HPA database to look at the protein expression profiles in normal and cancer tissues for this study. Among BET members, mRNA expression BRD2 showed improve OS in all the ovarian malignancy patients, serous patients, stage III and IV, grade II and grade III, TP53 mutated ovarian cancer patients, as well as all patients treated with Platin based chemotherapy. As for BRD3, we found that BRD3 expression was related to better OS in endometrioid ovarian carcinoma and stage III+IV ovarian carcinoma patients, as well as all patients managed with Taxol and concurrent Taxol+Platin based chemotherapy. In addition, BRDT was associated with better OS in all ovarian carcinoma patients, grade I and grade III, all clinical stage (I+II, III+IV) patients, as well as all patients cured with Taxol and concurrent Taxol+Platin chemotherapy. We conclude that high expression of BRD2, BRD3, and BRDT predicted a better prognosis. mRNA expression of BET family is considerably associated with the prognosis of ovarian carcinoma and individual BET family gene could act as a predictive prognostic indicator in ovarian carcinoma.

摘要

BET家族蛋白作为表观遗传阅读器,可加速靶基因的转录。多项研究表明,BET蛋白家族在多个生物学过程中发挥重要作用。然而,单个BET基因家族对卵巢癌患者的预后影响仍不清楚。我们通过KM plotter数据库研究了BET mRNA在卵巢癌患者中的预后作用亚型。使用qRTPCR和蛋白质印迹法测定癌组织和正常卵巢细胞中BET mRNA表达及蛋白水平。我们使用HPA数据库查看本研究中正常组织和癌组织中的蛋白表达谱。在BET家族成员中,BRD2的mRNA表达在所有卵巢恶性肿瘤患者、浆液性患者、III期和IV期患者、II级和III级患者、TP53突变的卵巢癌患者以及所有接受铂类化疗的患者中均显示出总生存期改善。至于BRD3,我们发现BRD3表达与子宫内膜样卵巢癌和III + IV期卵巢癌患者以及所有接受紫杉醇和同时接受紫杉醇+铂类化疗的患者的较好总生存期相关。此外,BRDT与所有卵巢癌患者、I级和III级患者、所有临床分期(I + II、III + IV)患者以及所有接受紫杉醇和同时接受紫杉醇+铂类化疗治愈的患者的较好总生存期相关。我们得出结论,BRD2、BRD3和BRDT的高表达预示着较好的预后。BET家族的mRNA表达与卵巢癌的预后密切相关,单个BET家族基因可作为卵巢癌的预测性预后指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95ea/8965123/5dde8e5d7d06/jcav13p1695g001.jpg

相似文献

1
Prognostic role of overexpressed Bromodomain and extra-terminal family in ovarian cancer.
J Cancer. 2022 Mar 14;13(5):1695-1705. doi: 10.7150/jca.69574. eCollection 2022.
2
The prognostic values of the peroxiredoxins family in ovarian cancer.
Biosci Rep. 2018 Sep 5;38(5). doi: 10.1042/BSR20180667. Print 2018 Oct 31.
3
Systematic analysis of the BET family in adrenocortical carcinoma: The expression, prognosis, gene regulation network, and regulation targets.
Front Endocrinol (Lausanne). 2023 Jan 30;14:1089531. doi: 10.3389/fendo.2023.1089531. eCollection 2023.
4
Prognostic values of mRNA expression in human ovarian cancer.
Biosci Rep. 2018 Apr 27;38(2). doi: 10.1042/BSR20180108.
5
Elevated expression of Tweety homologue 3 predicts poor clinical outcomes in ovarian cancer.
J Cancer. 2021 Oct 20;12(23):7147-7157. doi: 10.7150/jca.63539. eCollection 2021.
6
Prognostic Values of Transforming Growth Factor-Beta Subtypes in Ovarian Cancer.
Biomed Res Int. 2020 Apr 12;2020:2170606. doi: 10.1155/2020/2170606. eCollection 2020.
7
Significant value of XRCC2 and XRCC9 expression in the prognosis of human ovarian carcinoma.
J Cancer. 2021 Aug 28;12(20):6254-6264. doi: 10.7150/jca.59273. eCollection 2021.
8
Bromodomain and extra-terminal inhibitors emerge as potential therapeutic avenues for gastrointestinal cancers.
World J Gastrointest Oncol. 2022 Jan 15;14(1):75-89. doi: 10.4251/wjgo.v14.i1.75.
9
The Prognostic Role of BRD4 Expression in High-Grade Serous Ovarian Cancer.
Cancers (Basel). 2024 May 22;16(11):1962. doi: 10.3390/cancers16111962.

引用本文的文献

1
Anticancer Effects of BRD4 Inhibitor in Epithelial Ovarian Cancer.
Cancers (Basel). 2024 Feb 27;16(5):959. doi: 10.3390/cancers16050959.
2
Cytoprotective, Cytotoxic and Cytostatic Roles of Autophagy in Response to BET Inhibitors.
Int J Mol Sci. 2023 Aug 11;24(16):12669. doi: 10.3390/ijms241612669.

本文引用的文献

1
Cancer statistics, 2018.
CA Cancer J Clin. 2018 Jan;68(1):7-30. doi: 10.3322/caac.21442. Epub 2018 Jan 4.
3
Targeting Cancer Cells with BET Bromodomain Inhibitors.
Cold Spring Harb Perspect Med. 2017 Jul 5;7(7):a026674. doi: 10.1101/cshperspect.a026674.
4
BET bromodomain-mediated interaction between ERG and BRD4 promotes prostate cancer cell invasion.
Oncotarget. 2016 Jun 21;7(25):38319-38332. doi: 10.18632/oncotarget.9513.
5
High level of BRD4 promotes non-small cell lung cancer progression.
Oncotarget. 2016 Feb 23;7(8):9491-500. doi: 10.18632/oncotarget.7068.
7
BRD4 promotes tumor growth and epithelial-mesenchymal transition in hepatocellular carcinoma.
Int J Immunopathol Pharmacol. 2015 Mar;28(1):36-44. doi: 10.1177/0394632015572070.
8
Bromodomain 4 protein is a predictor of survival for urothelial carcinoma of bladder.
Int J Clin Exp Pathol. 2014 Jun 15;7(7):4231-8. eCollection 2014.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验