Notch-1 activates estrogen receptor-alpha-dependent transcription via IKKalpha in breast cancer cells.

Abstract:

:Approximately 80% of breast cancers express the estrogen receptor-alpha (ERalpha) and are treated with anti-estrogens. Resistance to these agents is a major cause of mortality. We have shown that estrogen inhibits Notch, whereas anti-estrogens or estrogen withdrawal activate Notch signaling. Combined inhibition of Notch and estrogen signaling has synergistic effects in ERalpha-positive breast cancer models. However, the mechanisms whereby Notch-1 promotes the growth of ERalpha-positive breast cancer cells are unknown. Here, we demonstrate that Notch-1 increases the transcription of ERalpha-responsive genes in the presence or absence of estrogen via a novel chromatin crosstalk mechanism. Our data support a model in which Notch-1 can activate the transcription of ERalpha-target genes via IKKalpha-dependent cooperative chromatin recruitment of Notch-CSL-MAML1 transcriptional complexes (NTC) and ERalpha, which promotes the recruitment of p300. CSL binding elements frequently occur in close proximity to estrogen-responsive elements (EREs) in the human and mouse genomes. Our observations suggest that a hitherto unknown Notch-1/ERalpha chromatin crosstalk mediates Notch signaling effects in ERalpha-positive breast cancer cells and contributes to regulate the transcriptional functions of ERalpha itself.

journal_name

Oncogene

journal_title

Oncogene

authors

Hao L,Rizzo P,Osipo C,Pannuti A,Wyatt D,Cheung LW,Sonenshein G,Osborne BA,Miele L

doi

10.1038/onc.2009.323

subject

Has Abstract

pub_date

2010-01-14 00:00:00

pages

201-13

issue

2

eissn

0950-9232

issn

1476-5594

pii

onc2009323

journal_volume

29

pub_type

杂志文章

相关文献

ONCOGENE文献大全
  • Cloning and sequencing of the human c-abl 3' untranslated region.

    abstract::The human c-abl oncogene gives rise to different mRNA transcripts which vary primarily in that they possess alternative first exons. In the present study, we present the sequence for the human c-abl 3' untranslated region (3'utr) and show that while human and murine c-abl cDNA sequences are generally homologous, human...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Andrews DF 3rd,Tompkins CK,Hendrickson SL,Singer JW

    更新日期:1990-03-01 00:00:00

  • Overexpression of miR-489 derails mammary hierarchy structure and inhibits HER2/neu-induced tumorigenesis.

    abstract::Although it has been demonstrated that transformed progenitor cell population can contribute to tumor initiation, factors contributing to this malignant transformation are poorly known. Using in vitro and xenograft-based models, previous studies demonstrated that miR-489 acts as a tumor suppressor miRNA by targeting v...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0439-1

    authors: Patel Y,Soni M,Awgulewitsch A,Kern MJ,Liu S,Shah N,Singh UP,Chen H

    更新日期:2019-01-01 00:00:00

  • MUC1 oncoprotein mitigates ER stress via CDA-mediated reprogramming of pyrimidine metabolism.

    abstract::The Mucin 1 (MUC1) protein is overexpressed in various cancers and mediates chemotherapy resistance. However, the mechanism is not fully understood. Given that most chemotherapeutic drugs disrupt ER homeostasis as part of their toxicity, and MUC1 expression is regulated by proteins involved in ER homeostasis, we inves...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-1225-4

    authors: Olou AA,King RJ,Yu F,Singh PK

    更新日期:2020-04-01 00:00:00

  • The PI 3-kinase-Rac-p38 MAP kinase pathway is involved in the formation of signet-ring cell carcinoma.

    abstract::Signet-ring cell carcinoma is classified in poorly differentiated adenocarcinoma with an aggressive nature and a poor prognosis. We have shown that the activation of PI 3-kinase in highly differentiated adenocarcinomas induces loss of cell-cell contact and formation of vacuoles, giving phenotypes similar to those of s...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206796

    authors: Xu Q,Karouji Y,Kobayashi M,Ihara S,Konishi H,Fukui Y

    更新日期:2003-08-28 00:00:00

  • Identification of IGFBP-6 as an effector of the tumor suppressor activity of SEMA3B.

    abstract::SEMA3B, a member of class 3 semaphorins, is a tumor suppressor. Competition with vascular endothelial growth factor (VEGF)165 explains a portion of the activity, whereas the VEGF-independent mechanism was not elucidated. We employed a microarray and screened for the genes whose expression was increased by SEMA3B in NC...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2008.263

    authors: Koyama N,Zhang J,Huqun,Miyazawa H,Tanaka T,Su X,Hagiwara K

    更新日期:2008-11-20 00:00:00

  • Thrombospondin-4 mediates TGF-β-induced angiogenesis.

    abstract::TGF-β is a multifunctional cytokine affecting many cell types and implicated in tissue remodeling processes. Due to its many functions and cell-specific effects, the consequences of TGF-β signaling are process-and stage-dependent, and it is not uncommon that TGF-β exerts distinct and sometimes opposing effects on a di...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2017.140

    authors: Muppala S,Xiao R,Krukovets I,Verbovetsky D,Yendamuri R,Habib N,Raman P,Plow E,Stenina-Adognravi O

    更新日期:2017-09-07 00:00:00

  • Co-localization of the TSC2 product tuberin with its target Rap1 in the Golgi apparatus.

    abstract::Tuberin is the protein product of the tuberous sclerosis-2 (TSC2) gene, which is associated with tuberous sclerosis (TSC), a human genetic syndrome characterized by the development of tumors in a variety of tissues. We have previously shown that tuberin is a widely expressed 180 kDa protein which exhibits specific GTP...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Wienecke R,Maize JC Jr,Shoarinejad F,Vass WC,Reed J,Bonifacino JS,Resau JH,de Gunzburg J,Yeung RS,DeClue JE

    更新日期:1996-09-05 00:00:00

  • Cyclin D3 action in androgen receptor regulation and prostate cancer.

    abstract::Prostate cancer (PCa) cell proliferation is dependent on activation of the androgen receptor (AR), a ligand-dependent transcription factor. AR activation controls G1-S phase progression through fostering enhanced translation of the D-type cyclins, which promote cell cycle progression through activation of CDK4/6. Howe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210981

    authors: Olshavsky NA,Groh EM,Comstock CE,Morey LM,Wang Y,Revelo MP,Burd C,Meller J,Knudsen KE

    更新日期:2008-05-15 00:00:00

  • Cloning and characterization of a novel gene encoding a putative transmembrane protein with altered expression in some human transformed and tumor-derived cell lines.

    abstract::Identification and characterization of genes expressed in normal cells and decreased in their malignant counterparts is an important method for detecting candidate tumor suppressors. Using differential display of mRNAs from nontumorigenic infinite life span human fibroblast cell strain MSU-1.1 and an isogenic fibrosar...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202290

    authors: Qing J,Wei D,Maher VM,McCormick JJ

    更新日期:1999-01-14 00:00:00

  • ELAS1-mediated inhibition of the cyclin G1-B'γ interaction promotes cancer cell apoptosis via stabilization and activation of p53.

    abstract::Radiation therapy (RT) is useful for selectively killing cancer cells. However, because high levels of ionizing radiation (IR) are toxic to normal cells, RT cannot be applied repeatedly to cancer patients. Therefore, novel chemicals that enhance the efficacy of chemoradiotherapy (CRT) would be valuable. Here, we repor...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.47

    authors: Ohno S,Naito Y,Mukai S,Yabuta N,Nojima H

    更新日期:2015-12-03 00:00:00

  • Mutations in the catalytic subunit of class IA PI3K confer leukemogenic potential to hematopoietic cells.

    abstract::Constitutive activation of the phosphoinositide 3-kinase (PI3K)-AKT pathway is observed in up to 70% of acute myelogenous leukemia. To investigate the relevance of an intrinsic PI3K-AKT pathway activation in hematopoietic malignancies, we analysed the effect of point mutations in the catalytic (p110alpha) and regulato...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2008.40

    authors: Horn S,Bergholz U,Jücker M,McCubrey JA,Trümper L,Stocking C,Bäsecke J

    更新日期:2008-07-03 00:00:00

  • A refined molecular taxonomy of breast cancer.

    abstract::The current histoclinical breast cancer classification is simple but imprecise. Several molecular classifications of breast cancers based on expression profiling have been proposed as alternatives. However, their reliability and clinical utility have been repeatedly questioned, notably because most of them were derive...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.301

    authors: Guedj M,Marisa L,de Reynies A,Orsetti B,Schiappa R,Bibeau F,MacGrogan G,Lerebours F,Finetti P,Longy M,Bertheau P,Bertrand F,Bonnet F,Martin AL,Feugeas JP,Bièche I,Lehmann-Che J,Lidereau R,Birnbaum D,Bertucci F,de

    更新日期:2012-03-01 00:00:00

  • Frequent loss of chromosome 14 in atypical and malignant meningioma: identification of a putative 'tumor progression' locus.

    abstract::Formation of meningiomas has been associated with the loss of genetic material on chromosome 22. To approach the additional chromosomal events that underlie progression of these tumors to malignancy, we have examined several other chromosomal regions for loss of heterozygosity (LOH) in these tumors. Fifty-eight tumors...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1200853

    authors: Menon AG,Rutter JL,von Sattel JP,Synder H,Murdoch C,Blumenfeld A,Martuza RL,von Deimling A,Gusella JF,Houseal TW

    更新日期:1997-02-06 00:00:00

  • Characterization of a third ras gene, rasB, that is expressed throughout the growth and development of Dictyostelium discoideum.

    abstract::Previous reports have indicated that the cellular slime mold Dictyostelium discoideum possesses two ras genes (rasG and rasD) and one rap gene (rap1). All three genes are developmentally regulated, with each showing a different pattern of transcription during the Dictyostelium life cycle. To establish whether there ar...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Daniel J,Spiegelman GB,Weeks G

    更新日期:1993-04-01 00:00:00

  • c-Jun causes focus formation and anchorage-independent growth in culture but is non-tumorigenic.

    abstract::The RCAS retroviral vector was used to express chicken and mouse cellular Jun proteins in chicken embryo fibroblasts. Both mouse and chicken proteins induced foci of transformed cells with low to moderate efficiency compared with viral Jun, but were as effective as the viral protein in promoting anchorage-independent ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Wong WY,Håvarstein LS,Morgan IM,Vogt PK

    更新日期:1992-10-01 00:00:00

  • Loss of a single Hic1 allele accelerates polyp formation in Apc(Δ716) mice.

    abstract::Adenomatous polyposis coli (APC) gene mutations have been implicated in familial and sporadic gastrointestinal (GI) cancers. APC mutations are associated with autosomal dominant inheritance of disease in humans. Similarly, mice that contain a single mutant APC gene encoding a protein truncated at residue 716 (Apc(Δ716...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2010.633

    authors: Mohammad HP,Zhang W,Prevas HS,Leadem BR,Zhang M,Herman JG,Hooker CM,Watkins DN,Karim B,Huso DL,Baylin SB

    更新日期:2011-06-09 00:00:00

  • Simple sequence repeat polymorphism within the p53 gene.

    abstract::This report describes a new polymorphism, in intron 3 of the p53 gene, which consists of a single repeat of 16 nucleotides, absent in the published wild-type p53 gene sequence. In the Caucasian population tested (n = 82), 28% of individuals were heterozygotes for this polymorphism. Using PCR-based analysis, we were ab...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Lazar V,Hazard F,Bertin F,Janin N,Bellet D,Bressac B

    更新日期:1993-06-01 00:00:00

  • Fas signaling promotes motility and metastasis through epithelial-mesenchymal transition in gastrointestinal cancer.

    abstract::Fas signaling was reported to participate in cell apoptosis. However, this pathway has also been shown to promote tumor cell motility, leading to the hypothesis that Fas signaling may induce epithelial-mesenchymal transition (EMT) to promote metastasis. The effects of Fas-ligand (FasL) treatment and inhibition of Fas ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2012.126

    authors: Zheng HX,Cai YD,Wang YD,Cui XB,Xie TT,Li WJ,Peng L,Zhang Y,Wang ZQ,Wang J,Jiang B

    更新日期:2013-02-28 00:00:00

  • Stress signals for apoptosis: ceramide and c-Jun kinase.

    abstract::Mammalian systems respond to environmental stress by either adapting or undergoing programmed cell death. While there is general agreement that the caspase family of proteases serve as the effectors of the apoptotic death response, the signaling apparatus involved in the decision to activate the caspase system is less...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1202570

    authors: Basu S,Kolesnick R

    更新日期:1998-12-24 00:00:00

  • MSX2 is an oncogenic downstream target of activated WNT signaling in ovarian endometrioid adenocarcinoma.

    abstract::Ovarian endometrioid adenocarcinomas (OEAs) frequently exhibit constitutive activation of canonical WNT signaling, usually as a result of oncogenic mutations that stabilize and dysregulate the β-catenin protein. In previous work, we used microarray-based methods to compare gene expression in OEAs with and without dysr...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.123

    authors: Zhai Y,Iura A,Yeasmin S,Wiese AB,Wu R,Feng Y,Fearon ER,Cho KR

    更新日期:2011-10-06 00:00:00

  • Alpha-fetoprotein producing gastric cancer lacks transcription factor ATBF1.

    abstract::Alpha-fetoprotein (AFP) producing gastric cancer (AFP-GC) is very malignant and highly metastatic compared with common gastric cancer. However, the causal relationship between AFP production and the high malignancy of AFP-GC is unclear. We investigated AFP gene regulation in AFP-GC by an active transcription factor, H...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204160

    authors: Kataoka H,Miura Y,Joh T,Seno K,Tada T,Tamaoki T,Nakabayashi H,Kawaguchi M,Asai K,Kato T,Itoh M

    更新日期:2001-02-15 00:00:00

  • Alterations in the p16(INK4a) and p53 tumor suppressor genes of hTERT-immortalized human fibroblasts.

    abstract::Exogenous expression of the catalytic subunit of telomerase, hTERT, in a normal human foreskin fibroblast cell strain resulted in telomerase activity and an extended proliferative lifespan prior to a period of crisis. Three immortalized cell lines with stably maintained telomere lengths were established from cells tha...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1207440

    authors: Noble JR,Zhong ZH,Neumann AA,Melki JR,Clark SJ,Reddel RR

    更新日期:2004-04-15 00:00:00

  • Differential requirements of the MAP kinase and PI3 kinase signaling pathways in Src- versus insulin and IGF-1 receptors-induced growth and transformation of rat intestinal epithelial cells.

    abstract::There have been few studies on the specific signaling pathways involved in the transformation of epithelial cells by oncogenic protein tyrosine kinases. Here we investigate the requirement of MAP (MAPK) and phosphatidylinositol 3- (PI3K) kinases in the transformation of rat intestinal epithelial (RIE) cells by oncogen...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203911

    authors: Nguyen KT,Wang WJ,Chan JL,Wang LH

    更新日期:2000-11-09 00:00:00

  • Opposing roles of angiomotin-like-1 and zona occludens-2 on pro-apoptotic function of YAP.

    abstract::YAP (Yes-associated protein) oncogene has been found to form a stable complex with members of the Angiomotin (Amot) family of proteins, which bind WW domains of YAP and sequester the protein in the cytoplasm and junctional complexes. The Amot-mediated retention of YAP in the cytoplasm results in the inhibition of its ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.216

    authors: Oka T,Schmitt AP,Sudol M

    更新日期:2012-01-05 00:00:00

  • Mouse models in tumor suppression.

    abstract::Genetic lesions found in tumors are often targeted to the negative growth regulatory tumor suppressor genes. Much of our understanding of tumor suppressor gene function is derived from experimental manipulations in cultured cells. Recently, however, the generation of mice with germ line tumor suppressor gene mutations...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1202573

    authors: Ghebranious N,Donehower LA

    更新日期:1998-12-24 00:00:00

  • Modulation of c-myc oncogene expression by phorbol ester and interferon-gamma: appraisal by flow cytometry.

    abstract::A flow cytometric assay was developed to examine the expression of the cellular myc oncogene in relation to cell cycle in individual cells. C-myc-oncoprotein was detected by indirect immunofluorescence using a purified sheep polyclonal antibody, anti-human-myc. Specific binding of anti-human-myc was measured by flow c...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Mohamed AN,Nakeff A,Mohammad RM,KuKuruga M,al-Katib A

    更新日期:1988-10-01 00:00:00

  • Wild-type egr1/Krox24 promotes and dominant-negative mutants inhibit, pluripotent differentiation of p19 embryonal carcinoma cells.

    abstract::The zinc-finger transcription factor Krox24 was analysed for its role in differentiation in P19 embryonal carcinoma cells. Reciprocal dominant negative mutants consisting of Krox24 deleted for a crucial region of the zinc-finger domain (delta Krox24) or of the zinc-finger region alone (delta Krox24Zf) abolished the ac...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202166

    authors: Lanoix J,Mullick A,He Y,Bravo R,Skup D

    更新日期:1998-11-12 00:00:00

  • Herbimycin A accelerates the induction of apoptosis following etoposide treatment or gamma-irradiation of bcr/abl-positive leukaemia cells.

    abstract::Philadelphia chromosome (Ph)-positive leukaemia cells express the chimeric bcr/abl oncoprotein, whose deregulated protein tyrosine kinase (PTK) activity antagonizes the induction of apoptosis by DNA damaging agents. Treatment of Ph-positive K562, TOM 1 and KCL-22 cells with etoposide for 2d induced cytosolic vacuolati...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201680

    authors: Riordan FA,Bravery CA,Mengubas K,Ray N,Borthwick NJ,Akbar AN,Hart SM,Hoffbrand AV,Mehta AB,Wickremasinghe RG

    更新日期:1998-03-26 00:00:00

  • Chromosome 5p aberrations are early events in lung cancer: implication of glial cell line-derived neurotrophic factor in disease progression.

    abstract::Lung cancer is the most widely diagnosed malignancy in the world. Understanding early-stage disease will give insight into its pathogenesis. Despite the fact that pre-invasive lesions are challenging to isolate, and often yield insufficient DNA for the analysis of multiple loci, genomic profiling of such lesions will ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208643

    authors: Garnis C,Davies JJ,Buys TP,Tsao MS,MacAulay C,Lam S,Lam WL

    更新日期:2005-07-14 00:00:00

  • Apoptin is modified by SUMO conjugation and targeted to promyelocytic leukemia protein nuclear bodies.

    abstract::Apoptin, a protein of the chicken anemia virus (CAV), represents a novel potential anticancer therapeutic, because it induces apoptotic death specifically in tumor but not normal cells. The cellular localization appears to be crucial for apoptin's selective toxicity. In normal cells apoptin remains in the cytoplasm, w...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209923

    authors: Janssen K,Hofmann TG,Jans DA,Hay RT,Schulze-Osthoff K,Fischer U

    更新日期:2007-03-08 00:00:00