• 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

TFDP3调节乳腺癌中的上皮-间质转化。

TFDP3 Regulates Epithelial-Mesenchymal Transition in Breast Cancer.

作者信息

Yin Kailin, Liu Yanchen, Chu Ming, Wang Yuedan

机构信息

Department of Immunology, School of Basic Medical Science, Peking University, Beijing, China.

School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Liaoning, China.

出版信息

PLoS One. 2017 Jan 23;12(1):e0170573. doi: 10.1371/journal.pone.0170573. eCollection 2017.

DOI:10.1371/journal.pone.0170573
PMID:28114432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5256886/
Abstract

Breast cancer remains a lethal disease to women due to lymph node metastasis, the tumor microenvironment, secondary resistance and other unknown factors. Several important transcription factors involved in this disease, such as PTEN, p53 and beta-catenin, have been identified and researched in-depth as candidates for targeted therapy in breast cancer. TFDP3 is a new, promising candidate for transcriptional regulation in breast cancer, although it was first identified in hepatocellular carcinoma. Here, we demonstrate that TFDP3 is expressed in a variety of malignancies, normal testis tissue and breast cancer cell lines and thus provide evidence that TFDP3 is a cancer-testis antigen. We illustrate that overexpression or silencing TFDP3 interferes with epithelial-mesenchymal transition but does not influence cell proliferation, indicating that the TFDP3 protein acts as a transcription factor during epithelial-mesenchymal transition. These data highlight that TFDP3 is expressed in breast cancer, that it is a member of the cancer-testis antigen family and that it functions as a regulator in epithelial-mesenchymal transition.

摘要

由于淋巴结转移、肿瘤微环境、继发性耐药及其他未知因素,乳腺癌对女性而言仍然是一种致命疾病。一些参与该疾病的重要转录因子,如PTEN、p53和β-连环蛋白,已被确定并作为乳腺癌靶向治疗的候选因子进行了深入研究。TFDP3是乳腺癌转录调控中一个新的、有前景的候选因子,尽管它最初是在肝细胞癌中被发现的。在此,我们证明TFDP3在多种恶性肿瘤、正常睾丸组织及乳腺癌细胞系中表达,从而提供了TFDP3是一种癌-睾丸抗原的证据。我们表明,TFDP3的过表达或沉默会干扰上皮-间质转化,但不影响细胞增殖,这表明TFDP3蛋白在上皮-间质转化过程中作为一种转录因子发挥作用。这些数据突出表明,TFDP3在乳腺癌中表达,它是癌-睾丸抗原家族的一员,并在上皮-间质转化中作为一种调节因子发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/c8db35a1ee2f/pone.0170573.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/2e8bfc3b5bad/pone.0170573.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/9d075d25940e/pone.0170573.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/926b3d7301a8/pone.0170573.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/237ed65820d5/pone.0170573.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/c75b9c4e8a69/pone.0170573.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/188c747487ee/pone.0170573.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/71e7786f9651/pone.0170573.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/c8db35a1ee2f/pone.0170573.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/2e8bfc3b5bad/pone.0170573.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/9d075d25940e/pone.0170573.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/926b3d7301a8/pone.0170573.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/237ed65820d5/pone.0170573.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/c75b9c4e8a69/pone.0170573.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/188c747487ee/pone.0170573.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/71e7786f9651/pone.0170573.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3a0/5256886/c8db35a1ee2f/pone.0170573.g008.jpg

相似文献

1
TFDP3 Regulates Epithelial-Mesenchymal Transition in Breast Cancer.TFDP3调节乳腺癌中的上皮-间质转化。
PLoS One. 2017 Jan 23;12(1):e0170573. doi: 10.1371/journal.pone.0170573. eCollection 2017.
2
TFDP3 regulates the apoptosis and autophagy in breast cancer cell line MDA-MB-231.TFDP3 调控乳腺癌细胞系 MDA-MB-231 的细胞凋亡和自噬。
PLoS One. 2018 Sep 20;13(9):e0203833. doi: 10.1371/journal.pone.0203833. eCollection 2018.
3
Effects of cancer-testis antigen, TFDP3, on cell cycle regulation and its mechanism in L-02 and HepG2 cell lines in vitro.癌胚抗原TFDP3对体外培养的L-02和HepG2细胞系细胞周期调控的影响及其机制
PLoS One. 2017 Aug 10;12(8):e0182781. doi: 10.1371/journal.pone.0182781. eCollection 2017.
4
TFDP3 was expressed in coordination with E2F1 to inhibit E2F1-mediated apoptosis in prostate cancer.TFDP3 与 E2F1 协调表达,抑制前列腺癌细胞中 E2F1 介导的细胞凋亡。
Gene. 2014 Mar 10;537(2):253-9. doi: 10.1016/j.gene.2013.12.051. Epub 2014 Jan 7.
5
TFDP3 inhibits E2F1-induced, p53-mediated apoptosis.TFDP3抑制E2F1诱导的、p53介导的细胞凋亡。
Biochem Biophys Res Commun. 2007 Sep 14;361(1):20-5. doi: 10.1016/j.bbrc.2007.06.128. Epub 2007 Jul 5.
6
TFDP3 as E2F Unique Partner, Has Crucial Roles in Cancer Cells and Testis.TFDP3作为E2F的独特伙伴,在癌细胞和睾丸中发挥关键作用。
Front Oncol. 2021 Oct 20;11:742462. doi: 10.3389/fonc.2021.742462. eCollection 2021.
7
Down-regulation of leucine zipper putative tumor suppressor 1 is associated with poor prognosis, increased cell motility and invasion, and epithelial-to-mesenchymal transition characteristics in human breast carcinoma.亮氨酸拉链假定肿瘤抑制因子 1 的下调与人类乳腺癌不良预后、增加细胞迁移和侵袭以及上皮间质转化特征相关。
Hum Pathol. 2011 Oct;42(10):1410-9. doi: 10.1016/j.humpath.2010.12.007. Epub 2011 Mar 21.
8
Wnt/β-catenin pathway is required for epithelial to mesenchymal transition in CXCL12 over expressed breast cancer cells.Wnt/β-连环蛋白信号通路在CXCL12过表达的乳腺癌细胞上皮-间质转化过程中是必需的。
Int J Clin Exp Pathol. 2015 Oct 1;8(10):12357-67. eCollection 2015.
9
Coexpression of gene Oct4 and Nanog initiates stem cell characteristics in hepatocellular carcinoma and promotes epithelial-mesenchymal transition through activation of Stat3/Snail signaling.基因Oct4和Nanog的共表达启动了肝细胞癌中的干细胞特征,并通过激活Stat3/Snail信号通路促进上皮-间质转化。
J Hematol Oncol. 2015 Mar 11;8:23. doi: 10.1186/s13045-015-0119-3.
10
The potential role of Brachyury in inducing epithelial-to-mesenchymal transition (EMT) and HIF-1α expression in breast cancer cells.Brachyury在诱导乳腺癌细胞上皮-间质转化(EMT)和缺氧诱导因子-1α(HIF-1α)表达中的潜在作用。
Biochem Biophys Res Commun. 2015 Nov 27;467(4):1083-9. doi: 10.1016/j.bbrc.2015.09.076. Epub 2015 Sep 21.

引用本文的文献

1
TFDP3 as E2F Unique Partner, Has Crucial Roles in Cancer Cells and Testis.TFDP3作为E2F的独特伙伴,在癌细胞和睾丸中发挥关键作用。
Front Oncol. 2021 Oct 20;11:742462. doi: 10.3389/fonc.2021.742462. eCollection 2021.
2
Cancer testis antigens in myelodysplastic syndromes revisited: a targeted RNA-seq approach.再探骨髓增生异常综合征中的癌胚抗原:一种靶向RNA测序方法。
Oncoimmunology. 2020 Oct 1;9(1):1824642. doi: 10.1080/2162402X.2020.1824642.
3
Possible Molecular Mechanisms for the Roles of MicroRNA-21 Played in Lung Cancer.miR-21 在肺癌中作用的可能分子机制

本文引用的文献

1
Transcriptional master regulator analysis in breast cancer genetic networks.乳腺癌基因网络中的转录主调控因子分析
Comput Biol Chem. 2015 Dec;59 Pt B:67-77. doi: 10.1016/j.compbiolchem.2015.08.007. Epub 2015 Aug 22.
2
The cyclin-dependent kinase 4/6 inhibitor palbociclib in combination with letrozole versus letrozole alone as first-line treatment of oestrogen receptor-positive, HER2-negative, advanced breast cancer (PALOMA-1/TRIO-18): a randomised phase 2 study.哌柏西利联合来曲唑与来曲唑单药一线治疗雌激素受体阳性、HER2 阴性、晚期乳腺癌(PALOMA-1/TRIO-18)的随机 2 期研究。
Lancet Oncol. 2015 Jan;16(1):25-35. doi: 10.1016/S1470-2045(14)71159-3. Epub 2014 Dec 16.
3
Technol Cancer Res Treat. 2019 Jan 1;18:1533033819875130. doi: 10.1177/1533033819875130.
4
TFDP3 regulates the apoptosis and autophagy in breast cancer cell line MDA-MB-231.TFDP3 调控乳腺癌细胞系 MDA-MB-231 的细胞凋亡和自噬。
PLoS One. 2018 Sep 20;13(9):e0203833. doi: 10.1371/journal.pone.0203833. eCollection 2018.
5
Effects of cancer-testis antigen, TFDP3, on cell cycle regulation and its mechanism in L-02 and HepG2 cell lines in vitro.癌胚抗原TFDP3对体外培养的L-02和HepG2细胞系细胞周期调控的影响及其机制
PLoS One. 2017 Aug 10;12(8):e0182781. doi: 10.1371/journal.pone.0182781. eCollection 2017.
Molecular mechanisms of epithelial-mesenchymal transition.
上皮-间质转化的分子机制。
Nat Rev Mol Cell Biol. 2014 Mar;15(3):178-96. doi: 10.1038/nrm3758.
4
TFDP3 was expressed in coordination with E2F1 to inhibit E2F1-mediated apoptosis in prostate cancer.TFDP3 与 E2F1 协调表达,抑制前列腺癌细胞中 E2F1 介导的细胞凋亡。
Gene. 2014 Mar 10;537(2):253-9. doi: 10.1016/j.gene.2013.12.051. Epub 2014 Jan 7.
5
Cause and consequence of cancer/testis antigen activation in cancer.癌症中癌/睾丸抗原激活的原因和后果。
Annu Rev Pharmacol Toxicol. 2014;54:251-72. doi: 10.1146/annurev-pharmtox-011112-140326. Epub 2013 Oct 11.
6
Personalizing the treatment of women with early breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2013.个体化治疗早期乳腺癌女性:2013 年圣加仑国际早期乳腺癌专家共识初级治疗要点。
Ann Oncol. 2013 Sep;24(9):2206-23. doi: 10.1093/annonc/mdt303. Epub 2013 Aug 4.
7
Pertuzumab, trastuzumab, and docetaxel for HER2-positive metastatic breast cancer (CLEOPATRA study): overall survival results from a randomised, double-blind, placebo-controlled, phase 3 study.帕妥珠单抗、曲妥珠单抗和多西他赛联合用于人表皮生长因子受体 2 阳性转移性乳腺癌(CLEOPATRA 研究):一项随机、双盲、安慰剂对照、3 期研究的总生存结果。
Lancet Oncol. 2013 May;14(6):461-71. doi: 10.1016/S1470-2045(13)70130-X. Epub 2013 Apr 18.
8
TGF-β signaling and epithelial-mesenchymal transition in cancer progression.TGF-β 信号通路与癌症进展中的上皮间质转化。
Curr Opin Oncol. 2013 Jan;25(1):76-84. doi: 10.1097/CCO.0b013e32835b6371.
9
Trastuzumab emtansine for HER2-positive advanced breast cancer.曲妥珠单抗-美坦新偶联物用于治疗人表皮生长因子受体 2 阳性的晚期乳腺癌。
N Engl J Med. 2012 Nov 8;367(19):1783-91. doi: 10.1056/NEJMoa1209124. Epub 2012 Oct 1.
10
The landscape of cancer genes and mutational processes in breast cancer.乳腺癌中的癌症基因和突变过程景观。
Nature. 2012 May 16;486(7403):400-4. doi: 10.1038/nature11017.