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前列腺衍生的Ets转录因子比其他癌症相关分子显示出更好的肿瘤关联性。

Prostate derived Ets transcription factor shows better tumor-association than other cancer-associated molecules.

作者信息

Ghadersohi Ali, Odunsi Kunle, Lele Shashikant, Collins Yvonne, Greco William R, Winston Janet, Liang Ping, Sood Ashwani K

机构信息

Department of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

Oncol Rep. 2004 Feb;11(2):453-8.

PMID:14719083
Abstract

We previously reported that prostate derived Ets transcription factor (PDEF) is a breast tumor-associated molecule. To obtain further insights into PDEF expression in other human tumor types, a cDNA library database from human adult normal and tumor tissues was compiled and searched for PDEF distribution. The results showed that PDEF is present at relative higher frequencies in the cDNA libraries from brain, breast, lung and ovarian tumors in comparison to those from the corresponding normal tissues. RT/PCR analysis of PDEF expression in ovarian tumors confirmed that PDEF is expressed in 36 out of 51 (71%) ovarian tumors. Further comparison of the distribution of PDEF with other widely recognized cancer-associated molecules showed that PDEF has more restricted distributions than Her-2/neu, Bcl-2, survivin or telomerase in cDNA libraries from normal human tissues and more increased distribution than Her-2/neu, CA-125, Bcl-2, survivin and telomerase in cDNA libraries from brain (except survivin), breast, lung and ovarian tumors. These data together show a better tumor-association for PDEF and suggest that PDEF is a more suitable target for developing specific cancer therapies.

摘要

我们之前报道过,前列腺衍生的Ets转录因子(PDEF)是一种与乳腺肿瘤相关的分子。为了进一步深入了解PDEF在其他人类肿瘤类型中的表达情况,我们编制了一个来自人类成人正常组织和肿瘤组织的cDNA文库数据库,并搜索PDEF的分布情况。结果显示,与相应正常组织的cDNA文库相比,PDEF在脑、乳腺、肺和卵巢肿瘤的cDNA文库中出现的频率相对较高。对卵巢肿瘤中PDEF表达的RT/PCR分析证实,51例卵巢肿瘤中有36例(71%)表达PDEF。将PDEF的分布与其他广泛认可的癌症相关分子进行进一步比较,结果表明,在来自正常人类组织的cDNA文库中,PDEF的分布比Her-2/neu、Bcl-2、生存素或端粒酶更具局限性;而在来自脑(生存素除外)、乳腺、肺和卵巢肿瘤的cDNA文库中,PDEF的分布比Her-2/neu、CA-125、Bcl-2、生存素和端粒酶增加得更多。这些数据共同表明PDEF与肿瘤的关联性更强,并提示PDEF是开发特异性癌症治疗方法更合适的靶点。

相似文献

1
Prostate derived Ets transcription factor shows better tumor-association than other cancer-associated molecules.前列腺衍生的Ets转录因子比其他癌症相关分子显示出更好的肿瘤关联性。
Oncol Rep. 2004 Feb;11(2):453-8.
2
Prostate epithelium-derived Ets transcription factor mRNA is overexpressed in human breast tumors and is a candidate breast tumor marker and a breast tumor antigen.前列腺上皮来源的Ets转录因子mRNA在人类乳腺肿瘤中过表达,是一种候选乳腺肿瘤标志物和乳腺肿瘤抗原。
Clin Cancer Res. 2001 Sep;7(9):2731-8.
3
Prostate-derived Ets factor is overexpressed in serous epithelial ovarian tumors.前列腺源性Ets因子在浆液性上皮性卵巢肿瘤中过度表达。
Int J Gynecol Pathol. 2007 Jan;26(1):10-5. doi: 10.1097/01.pgp.0000225386.41244.bd.
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Proteomic analysis of a PDEF Ets transcription factor-interacting protein complex.一种PDEF Ets转录因子相互作用蛋白复合体的蛋白质组学分析。
J Proteome Res. 2009 Mar;8(3):1327-37. doi: 10.1021/pr800683b.
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Silibinin down-regulates prostate epithelium-derived Ets transcription factor in LNCaP prostate cancer cells.水飞蓟宾下调LNCaP前列腺癌细胞中前列腺上皮来源的Ets转录因子。
Planta Med. 2004 May;70(5):397-400. doi: 10.1055/s-2004-818965.
6
Analysis of the 2.0 A crystal structure of the protein-DNA complex of the human PDEF Ets domain bound to the prostate specific antigen regulatory site.人PDEF Ets结构域与前列腺特异性抗原调控位点结合的蛋白质-DNA复合物2.0埃晶体结构分析。
Biochemistry. 2005 May 17;44(19):7095-106. doi: 10.1021/bi047352t.
7
Pdef expression in human breast cancer is correlated with invasive potential and altered gene expression.Pdef在人类乳腺癌中的表达与侵袭潜能及基因表达改变相关。
Cancer Res. 2003 Aug 1;63(15):4626-31.
8
Prostate derived ETS factor (PDEF): a putative tumor metastasis suppressor.前列腺衍生 ETS 因子 (PDEF):一种潜在的肿瘤转移抑制因子。
Cancer Lett. 2011 Nov 1;310(1):109-17. doi: 10.1016/j.canlet.2011.06.011. Epub 2011 Jun 29.
9
STAT1 and Nmi are downstream targets of Ets-1 transcription factor in MCF-7 human breast cancer cell.信号转导和转录激活因子1(STAT1)和Nmi是Ets-1转录因子在MCF-7人乳腺癌细胞中的下游靶点。
FEBS Lett. 2005 Jul 18;579(18):3941-6. doi: 10.1016/j.febslet.2005.06.011.
10
PDEF in prostate cancer.前列腺癌中的 PDEF。
Prostate. 2012 May 1;72(6):592-6. doi: 10.1002/pros.21461. Epub 2011 Jul 27.

引用本文的文献

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AR coactivators, CBP/p300, are critical mediators of DNA repair in prostate cancer.AR 共激活因子,如 CBP/p300,是前列腺癌中 DNA 修复的关键介质。
Oncogene. 2024 Oct;43(43):3197-3213. doi: 10.1038/s41388-024-03148-4. Epub 2024 Sep 13.
2
AR coactivators, CBP/p300, are critical mediators of DNA repair in prostate cancer.雄激素受体共激活因子CBP/p300是前列腺癌DNA修复的关键介质。
bioRxiv. 2024 May 7:2024.05.07.592966. doi: 10.1101/2024.05.07.592966.
3
Upregulation of SPDEF is associated with poor prognosis in prostate cancer.SPDEF的上调与前列腺癌的不良预后相关。
Oncol Lett. 2019 Nov;18(5):5107-5118. doi: 10.3892/ol.2019.10885. Epub 2019 Sep 19.
4
ELF3, ELF5, EHF and SPDEF Transcription Factors in Tissue Homeostasis and Cancer.ELF3、ELF5、EHF 和 SPDEF 转录因子在组织稳态和癌症中的作用。
Molecules. 2018 Aug 30;23(9):2191. doi: 10.3390/molecules23092191.
5
Genome-scale analysis of DNA methylation in lung adenocarcinoma and integration with mRNA expression.肺腺癌中 DNA 甲基化的全基因组分析及其与 mRNA 表达的整合。
Genome Res. 2012 Jul;22(7):1197-211. doi: 10.1101/gr.132662.111. Epub 2012 May 21.
6
[Antiandrogen strategies in prostate cancer: reconstitution of oestrogen receptor beta].[前列腺癌中的抗雄激素策略:雌激素受体β的重构]
Urologe A. 2010 Sep;49(9):1124, 1126-8, 1130. doi: 10.1007/s00120-010-2370-0.
7
Gene expression of circulating tumour cells in breast cancer patients.乳腺癌患者循环肿瘤细胞的基因表达
Eur J Med Res. 2009 Sep 28;14(10):426-32. doi: 10.1186/2047-783x-14-10-426.
8
Global gene expression analysis identifies PDEF transcriptional networks regulating cell migration during cancer progression.全球基因表达分析确定了在癌症进展过程中调节细胞迁移的PDEF转录网络。
Mol Biol Cell. 2008 Sep;19(9):3745-57. doi: 10.1091/mbc.e08-02-0154. Epub 2008 Jun 25.
9
Prostate-derived Ets transcription factor (PDEF) downregulates survivin expression and inhibits breast cancer cell growth in vitro and xenograft tumor formation in vivo.前列腺源性Ets转录因子(PDEF)下调survivin表达,并在体外抑制乳腺癌细胞生长以及在体内抑制异种移植肿瘤形成。
Breast Cancer Res Treat. 2007 Mar;102(1):19-30. doi: 10.1007/s10549-006-9314-9. Epub 2006 Aug 8.