• 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

ATF3在前列腺癌抑制中的新作用。

Emerging roles of ATF3 in the suppression of prostate cancer.

作者信息

Wang Ziyan, Yan Chunhong

机构信息

GRU Cancer Center.

GRU Cancer Center; Department of Biochemistry and Molecular Biology; Medical College of Georgia; Georgia Regents University; Augusta, GA USA.

出版信息

Mol Cell Oncol. 2015 Feb 3;3(1):e1010948. doi: 10.1080/23723556.2015.1010948. eCollection 2016 Jan.

DOI:10.1080/23723556.2015.1010948
PMID:27308526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4845162/
Abstract

Stress response mediator activating transcription factor 3 (ATF3) engages in diverse oncogenic pathways including the androgen receptor signaling essential for prostatic proliferation. In line with frequent downregulation of ATF3 expression in human prostate cancers, we have provided the first genetic evidence supporting the role of ATF3 as a tumor suppressor in a subset of prostate cancers with PTEN dysfunction.

摘要

应激反应介质激活转录因子3(ATF3)参与多种致癌途径,包括对前列腺增殖至关重要的雄激素受体信号传导。鉴于ATF3在人类前列腺癌中经常下调,我们提供了首个遗传学证据,支持ATF3在一部分具有PTEN功能障碍的前列腺癌中作为肿瘤抑制因子的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ce/4845162/c2915985223e/kmco-03-01-1010948-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ce/4845162/c2915985223e/kmco-03-01-1010948-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ce/4845162/c2915985223e/kmco-03-01-1010948-g001.jpg

相似文献

1
Emerging roles of ATF3 in the suppression of prostate cancer.ATF3在前列腺癌抑制中的新作用。
Mol Cell Oncol. 2015 Feb 3;3(1):e1010948. doi: 10.1080/23723556.2015.1010948. eCollection 2016 Jan.
2
Loss of ATF3 promotes Akt activation and prostate cancer development in a Pten knockout mouse model.在Pten基因敲除小鼠模型中,ATF3缺失会促进Akt激活及前列腺癌发展。
Oncogene. 2015 Sep 17;34(38):4975-84. doi: 10.1038/onc.2014.426. Epub 2014 Dec 22.
3
The expression of transcription factor activating transcription factor 3 in the human prostate and its regulation by androgen in prostate cancer.转录因子激活转录因子3在人前列腺中的表达及其在前列腺癌中受雄激素的调控
J Urol. 2006 Apr;175(4):1517-22. doi: 10.1016/S0022-5347(05)00651-8.
4
Loss of ATF3 promotes hormone-induced prostate carcinogenesis and the emergence of CK5(+)CK8(+) epithelial cells.ATF3缺失促进激素诱导的前列腺癌发生以及CK5(+)CK8(+)上皮细胞的出现。
Oncogene. 2016 Jul 7;35(27):3555-64. doi: 10.1038/onc.2015.417. Epub 2015 Nov 2.
5
The tumor metastasis suppressor gene Drg-1 down-regulates the expression of activating transcription factor 3 in prostate cancer.肿瘤转移抑制基因Drg-1下调前列腺癌中激活转录因子3的表达。
Cancer Res. 2006 Dec 15;66(24):11983-90. doi: 10.1158/0008-5472.CAN-06-0943.
6
Upregulation of miR-153 promotes cell proliferation via downregulation of the PTEN tumor suppressor gene in human prostate cancer.miR-153 的上调通过下调抑癌基因 PTEN 促进人前列腺癌细胞的增殖。
Prostate. 2013 May;73(6):596-604. doi: 10.1002/pros.22600. Epub 2012 Oct 11.
7
Botanical Formulation HX109 Ameliorates TP-Induced Benign Prostate Hyperplasia in Rat Model and Inhibits Androgen Receptor Signaling by Upregulating Ca/CaMKKβ and ATF3 in LNCaP Cells.植物配方 HX109 可改善 TP 诱导的大鼠良性前列腺增生模型,并通过上调 LNCaP 细胞中的 Ca/CaMKKβ 和 ATF3 抑制雄激素受体信号通路。
Nutrients. 2018 Dec 7;10(12):1946. doi: 10.3390/nu10121946.
8
Roles of the RAF/MEK/ERK and PI3K/PTEN/AKT pathways in malignant transformation and drug resistance.RAF/MEK/ERK和PI3K/PTEN/AKT信号通路在恶性转化和耐药中的作用。
Adv Enzyme Regul. 2006;46:249-79. doi: 10.1016/j.advenzreg.2006.01.004. Epub 2006 Jul 18.
9
Regulation of androgen receptor signaling by PTEN (phosphatase and tensin homolog deleted on chromosome 10) tumor suppressor through distinct mechanisms in prostate cancer cells.在前列腺癌细胞中,PTEN(第10号染色体缺失的磷酸酶及张力蛋白同源物)肿瘤抑制因子通过不同机制对雄激素受体信号进行调控。
Mol Endocrinol. 2004 Oct;18(10):2409-23. doi: 10.1210/me.2004-0117. Epub 2004 Jun 17.
10
Lovastatin-induced apoptosis is mediated by activating transcription factor 3 and enhanced in combination with salubrinal.洛伐他汀诱导的细胞凋亡是由激活转录因子 3 介导的,并与 salubrinal 联合增强。
Int J Cancer. 2014 Jan 15;134(2):268-79. doi: 10.1002/ijc.28369. Epub 2013 Aug 1.

引用本文的文献

1
A panel of three serum microRNAs as a potential diagnostic biomarker for renal cell carcinoma.一组三种血清微小RNA作为肾细胞癌的潜在诊断生物标志物。
Sci Rep. 2025 May 25;15(1):18135. doi: 10.1038/s41598-025-01225-6.
2
Activating transcription factor 3 is an antitumor gene synergizing with growth differentiation factor 15 to modulate cell growth in human bladder cancer.激活转录因子3是一种抗肿瘤基因,与生长分化因子15协同作用,调节人膀胱癌中的细胞生长。
Biomed J. 2024 Jun 27;48(2):100756. doi: 10.1016/j.bj.2024.100756.
3
Combating castration-resistant prostate cancer by co-targeting the epigenetic regulators EZH2 and HDAC.

本文引用的文献

1
Loss of ATF3 promotes Akt activation and prostate cancer development in a Pten knockout mouse model.在Pten基因敲除小鼠模型中,ATF3缺失会促进Akt激活及前列腺癌发展。
Oncogene. 2015 Sep 17;34(38):4975-84. doi: 10.1038/onc.2014.426. Epub 2014 Dec 22.
2
The activating transcription factor 3 protein suppresses the oncogenic function of mutant p53 proteins.激活转录因子 3 蛋白抑制突变型 p53 蛋白的致癌功能。
J Biol Chem. 2014 Mar 28;289(13):8947-59. doi: 10.1074/jbc.M113.503755. Epub 2014 Feb 19.
3
ATF3 suppresses metastasis of bladder cancer by regulating gelsolin-mediated remodeling of the actin cytoskeleton.
通过靶向表观遗传调节剂 EZH2 和 HDAC 来对抗去势抵抗性前列腺癌。
PLoS Biol. 2023 Apr 27;21(4):e3002038. doi: 10.1371/journal.pbio.3002038. eCollection 2023 Apr.
4
Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.用 ACRJ-PC28 扩展前列腺癌细胞系谱,这是一种源自非洲裔加勒比患者的 AR 阴性神经内分泌细胞系。
Cancer Res Commun. 2022 Nov;2(11):1355-1371. doi: 10.1158/2767-9764.crc-22-0245. Epub 2022 Nov 7.
5
Post-prostatic-massage urine exosomes of men with chronic prostatitis/chronic pelvic pain syndrome carry prostate-cancer-typical microRNAs and activate proto-oncogenes.慢性前列腺炎/慢性盆腔疼痛综合征患者前列腺按摩后尿液外泌体携带前列腺癌典型 microRNAs 并激活原癌基因。
Mol Oncol. 2023 Mar;17(3):445-468. doi: 10.1002/1878-0261.13329. Epub 2022 Nov 17.
6
Induces Apoptosis of Human Ovarian Cancer Cells via ATF3-Mediated Regulation of Foxo3a by Tip60.通过 Tip60 介导的 ATF3 对 Foxo3a 的调控诱导人卵巢癌细胞凋亡。
J Microbiol Biotechnol. 2022 Apr 28;32(4):493-503. doi: 10.4014/jmb.2109.09030.
7
ATF3 promotes the serine synthesis pathway and tumor growth under dietary serine restriction.ATF3 促进丝氨酸合成途径,并在饮食丝氨酸限制下促进肿瘤生长。
Cell Rep. 2021 Sep 21;36(12):109706. doi: 10.1016/j.celrep.2021.109706.
8
ATF3 Suppresses Growth and Metastasis of Clear Cell Renal Cell Carcinoma by Deactivating EGFR/AKT/GSK3β/β-Catenin Signaling Pathway.激活转录因子3通过失活表皮生长因子受体/蛋白激酶B/糖原合成酶激酶3β/β-连环蛋白信号通路抑制肾透明细胞癌的生长和转移
Front Cell Dev Biol. 2021 Mar 19;9:618987. doi: 10.3389/fcell.2021.618987. eCollection 2021.
9
ATF3 downmodulates its new targets IFI6 and IFI27 to suppress the growth and migration of tongue squamous cell carcinoma cells.ATF3 下调其新靶标 IFI6 和 IFI27,抑制舌鳞癌细胞的生长和迁移。
PLoS Genet. 2021 Feb 4;17(2):e1009283. doi: 10.1371/journal.pgen.1009283. eCollection 2021 Feb.
10
Toward Regulatory Effects of Curcumin on Transforming Growth Factor-Beta Across Different Diseases: A Review.姜黄素对不同疾病中转化生长因子-β的调节作用综述
Front Pharmacol. 2020 Dec 14;11:585413. doi: 10.3389/fphar.2020.585413. eCollection 2020.
转录激活因子 3 通过调控凝溶胶蛋白介导的细胞骨架重构抑制膀胱癌转移。
Cancer Res. 2013 Jun 15;73(12):3625-37. doi: 10.1158/0008-5472.CAN-12-3879. Epub 2013 Mar 27.
4
The stress response mediator ATF3 represses androgen signaling by binding the androgen receptor.应激反应介质 ATF3 通过与雄激素受体结合来抑制雄激素信号。
Mol Cell Biol. 2012 Aug;32(16):3190-202. doi: 10.1128/MCB.00159-12. Epub 2012 Jun 4.
5
Reciprocal feedback regulation of PI3K and androgen receptor signaling in PTEN-deficient prostate cancer.PTEN 缺陷型前列腺癌中 PI3K 和雄激素受体信号的相互反馈调节。
Cancer Cell. 2011 May 17;19(5):575-86. doi: 10.1016/j.ccr.2011.04.008.
6
MDM2 mediates ubiquitination and degradation of activating transcription factor 3.MDM2 介导激活转录因子 3 的泛素化和降解。
J Biol Chem. 2010 Aug 27;285(35):26908-26915. doi: 10.1074/jbc.M110.132597. Epub 2010 Jun 30.
7
Systems biology approaches identify ATF3 as a negative regulator of Toll-like receptor 4.系统生物学方法确定ATF3为Toll样受体4的负调控因子。
Nature. 2006 May 11;441(7090):173-8. doi: 10.1038/nature04768.
8
ATF3 regulates the stability of p53: a link to cancer.活化转录因子3调控p53的稳定性:与癌症的关联
Cell Cycle. 2006 May;5(9):926-9. doi: 10.4161/cc.5.9.2714. Epub 2006 May 1.
9
Activating transcription factor 3, a stress sensor, activates p53 by blocking its ubiquitination.激活转录因子3作为一种应激传感器,通过阻止p53的泛素化来激活它。
EMBO J. 2005 Jul 6;24(13):2425-35. doi: 10.1038/sj.emboj.7600712. Epub 2005 Jun 2.
10
A self-enabling TGFbeta response coupled to stress signaling: Smad engages stress response factor ATF3 for Id1 repression in epithelial cells.一种与应激信号传导相关的自激活转化生长因子β反应:Smad与应激反应因子ATF3结合,以抑制上皮细胞中的Id1。
Mol Cell. 2003 Apr;11(4):915-26. doi: 10.1016/s1097-2765(03)00109-6.