Induction of apoptosis by p75 neurotrophin receptor in human neuroblastoma cells.

Abstract:

:The low-affinity nerve growth factor receptor p75NTR belongs to a membrane receptor superfamily whose members, in certain cell types, are able to transduce an apoptotic signal. To investigate the effect of p75NTR expression in neuroblastoma cells, we transfected the p75NTR cDNA into SK-N-BE cells, a neuroblastoma cell line that lacks expression of both p75NTR and TrkA. Cell clones expressing elevated levels of p75NTR showed a high degree of cell death by apoptosis, even in serum-supplemented medium. Moreover, the level of apoptosis correlated directly with the expression level of the receptor, indicating that p75NTR could activate the cell death program by itself. Clones expressing p75NTR showed a dramatic increase of cell death when switched into serum-free medium; these cultures rapidly extinguished. This apoptotic effect was greatly inhibited by NGF treatment. Our results support the hypothesis that p75NTR, when it is not bound by NGF, may play a role in neuronal selection during embryonic development and suggest that neuroblastomas may arise from immature neuroblasts that escape programmed cell death. Therefore, the loss of p75NTR expression in developing neural crest cells might be a primary event in the genesis of neuroblastoma.

journal_name

Oncogene

journal_title

Oncogene

authors

Bunone G,Mariotti A,Compagni A,Morandi E,Della Valle G

doi

10.1038/sj.onc.1200972

subject

Has Abstract

pub_date

1997-03-27 00:00:00

pages

1463-70

issue

12

eissn

0950-9232

issn

1476-5594

journal_volume

14

pub_type

杂志文章

相关文献

ONCOGENE文献大全
  • Systems biology analysis of G protein and MAP kinase signaling in yeast.

    abstract::Approximately a third of all drugs act by binding directly to cell surface receptors coupled to G proteins. Other drugs act indirectly on these same pathways, for example, by inhibiting neurotransmitter reuptake or by blocking the inactivation of intracellular second messengers. These drugs have revolutionized the tre...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1210416

    authors: Hao N,Behar M,Elston TC,Dohlman HG

    更新日期:2007-05-14 00:00:00

  • SCF-mediated protein degradation and cell cycle control.

    abstract::The regulatory step in ubiquitin (Ub)-mediated protein degradation involves recognition and selection of the target substrate by an E3 Ub-ligase. E3 Ub-ligases evoke sophisticated mechanisms to regulate their activity temporally and spatially, including multiple post-translational modifications, combinatorial E3 Ub-li...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1208614

    authors: Ang XL,Wade Harper J

    更新日期:2005-04-18 00:00:00

  • Direct integrin alphavbeta6-ERK binding: implications for tumour growth.

    abstract::Blockade of the mitogen-activated protein (MAP) kinase pathway suppresses growth of colon cancer in vivo. Here we demonstrate a direct link between the extracellular signal-regulated kinase ERK2 and the growth-promoting cell adhesion molecule, integrin alphavbeta6, in colon cancer cells. Down-regulation of beta6 integ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205286

    authors: Ahmed N,Niu J,Dorahy DJ,Gu X,Andrews S,Meldrum CJ,Scott RJ,Baker MS,Macreadie IG,Agrez MV

    更新日期:2002-02-21 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

  • MicroRNA-520/373 family functions as a tumor suppressor in estrogen receptor negative breast cancer by targeting NF-κB and TGF-β signaling pathways.

    abstract::MicroRNAs (miRNAs) as modulators of gene expression have been described to display both tumor-promoting and tumor-suppressive functions. Although their role has been studied in different tumor types, little is known about how they regulate nuclear factor κB (NF-κB) signaling in breast cancer. Here, we performed an unb...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.571

    authors: Keklikoglou I,Koerner C,Schmidt C,Zhang JD,Heckmann D,Shavinskaya A,Allgayer H,Gückel B,Fehm T,Schneeweiss A,Sahin O,Wiemann S,Tschulena U

    更新日期:2012-09-13 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

  • Initiation of adult myelopoiesis can occur in the absence of c-Myb whereas subsequent development is strictly dependent on the transcription factor.

    abstract::The c-Myb transcriptional regulator is crucial to the development and functioning of haemopoietic cells, so much so that mouse embryos homozygous for an inactivated c-myb allele die from anaemia at about day 15 of gestation. By analysing c-myb(-/-) chimaeras we show that no mature cells of any lymphoid or myeloid line...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203660

    authors: Sumner R,Crawford A,Mucenski M,Frampton J

    更新日期:2000-07-13 00:00:00

  • Matrilysin (MMP-7) induces homotypic adhesion of human colon cancer cells and enhances their metastatic potential in nude mouse model.

    abstract::Matrilysin (MMP-7) is thought to contribute to invasive growth and metastasis of colon carcinoma and many other human cancers. The present study demonstrates that treatment of human colon carcinoma cells with active matrilysin induces cell aggregation in vitro and promotes liver metastasis in nude mice. When two kinds...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1207181

    authors: Kioi M,Yamamoto K,Higashi S,Koshikawa N,Fujita K,Miyazaki K

    更新日期:2003-11-27 00:00:00

  • The 26S proteasome system degrades the ERM transcription factor and regulates its transcription-enhancing activity.

    abstract::ERM is a member of the ETS transcription factor family. High levels of the corresponding mRNA are detected in a variety of human breast cancer cell lines, as well as in aggressive human breast tumors. As ERM protein is almost undetectable in these cells, high degradation of this transcription factor has been postulate...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209801

    authors: Baert JL,Beaudoin C,Monte D,Degerny C,Mauen S,de Launoit Y

    更新日期:2007-01-18 00:00:00

  • Copine-I represses NF-kappaB transcription by endoproteolysis of p65.

    abstract::Nuclear factor-kappaB (NF-kappaB) is a dynamic transcription factor that regulates important biological processes involved in cancer initiation and progression. Identifying regulators that control the half-life of NF-kappaB is important to understanding molecular processes that control the duration of transcriptional ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1211030

    authors: Ramsey CS,Yeung F,Stoddard PB,Li D,Creutz CE,Mayo MW

    更新日期:2008-06-05 00:00:00

  • Requirement of the histone demethylase LSD1 in Snai1-mediated transcriptional repression during epithelial-mesenchymal transition.

    abstract::Epithelial-mesenchymal transition (EMT) has pivotal roles during embryonic development and carcinoma progression. Members of the Snai1 family of zinc finger transcription factors are central mediators of EMT and induce EMT in part by directly repressing epithelial markers such as E-cadherin, a gatekeeper of the epithe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2010.234

    authors: Lin T,Ponn A,Hu X,Law BK,Lu J

    更新日期:2010-09-02 00:00:00

  • Upregulation of histamine receptor H1 promotes tumor progression and contributes to poor prognosis in hepatocellular carcinoma.

    abstract::H1 histamine receptor (H1HR) belongs to the family of rhodopsin-like G-protein-coupled receptors. Recent studies have shown that H1HR expression is increased in several types of cancer. However, its functional roles in tumor progression remain largely unknown, especially in hepatocellular carcinoma (HCC). We found tha...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-019-1093-y

    authors: Zhao J,Hou Y,Yin C,Hu J,Gao T,Huang X,Zhang X,Xing J,An J,Wan S,Li J

    更新日期:2020-02-01 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

  • miR-130a targets MET and induces TRAIL-sensitivity in NSCLC by downregulating miR-221 and 222.

    abstract::Non-small cell lung cancer (NSCLC) accounts for ∼80% of all lung cancers. Although some advances in lung cancer therapy have been made, patient survival is still quite poor. Two microRNAs, miR-221 and miR-222, upregulated by the MET proto-oncogene, have been already described to enhance cell survival and to induce TNF...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.260

    authors: Acunzo M,Visone R,Romano G,Veronese A,Lovat F,Palmieri D,Bottoni A,Garofalo M,Gasparini P,Condorelli G,Chiariello M,Croce CM

    更新日期:2012-02-02 00:00:00

  • The renin angiotensin system (RAS) mediates bifunctional growth regulation in melanoma and is a novel target for therapeutic intervention.

    abstract::Despite emergence of new systemic therapies, metastatic melanoma remains a challenging and often fatal form of skin cancer. The renin-angiotensin system (RAS) is a major physiological regulatory pathway controlling salt-water equilibrium, intravascular volume and blood pressure. Biological effects of the RAS are media...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0563-y

    authors: Renziehausen A,Wang H,Rao B,Weir L,Nigro CL,Lattanzio L,Merlano M,Vega-Rioja A,Del Carmen Fernandez-Carranco M,Hajji N,Matin R,Harwood C,Li S,Sim VR,O'Neill K,Evans A,Thompson A,Szlosarek P,Fleming C,Stebbing J,Pr

    更新日期:2019-03-01 00:00:00

  • Interaction between p53 and TGF beta 1 in control of epithelial cell proliferation.

    abstract::Although loss of sensitivity to transforming growth factor beta (TGF beta) may be a key step in the escape of epithelial tumours from normal growth control, the intracellular signals determining responsiveness remain controversial, particularly the role of p53. We have investigated this question using thyroid epitheli...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Blaydes JP,Schlumberger M,Wynford-Thomas D,Wyllie FS

    更新日期:1995-01-19 00:00:00

  • Targeting the Akt/mTOR pathway in Brca1-deficient cancers.

    abstract::The breast cancer susceptibility gene 1 (Brca1) has a key role in both hereditary and sporadic mammary tumorigenesis. However, the reasons why Brca1-deficiency leads to the development of cancer are not clearly understood. Activation of Akt kinase is one of the most common molecular alterations associated with human m...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2010.603

    authors: Xiang T,Jia Y,Sherris D,Li S,Wang H,Lu D,Yang Q

    更新日期:2011-05-26 00:00:00

  • HER2/PI-3K/Akt activation leads to a multidrug resistance in human breast adenocarcinoma cells.

    abstract::Growth factor receptor-mediated signal transduction has been implicated in conferring resistance to conventional chemotherapy on cancer cells. In this study, we delineated a pathway that involves HER2/PI-3K/Akt in mediating multidrug resistance in human breast cancer cells. We found that the cell lines that express bo...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206394

    authors: Knuefermann C,Lu Y,Liu B,Jin W,Liang K,Wu L,Schmidt M,Mills GB,Mendelsohn J,Fan Z

    更新日期:2003-05-22 00:00:00

  • Rb may act as a transcriptional co-activator in undifferentiated F9 cells.

    abstract::The reversible interaction of the retinoblastoma susceptibility gene product (Rb) with the cellular transcription factor E2F has recently been demonstrated. Activation of the adenovirus E2a promoter by the products of the viral E1a gene correlates with the ability of both early E1a proteins to sequester Rb, thereby re...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Bocco JL,Reimund B,Chatton B,Kedinger C

    更新日期:1993-11-01 00:00:00

  • ISL2 modulates angiogenesis through transcriptional regulation of ANGPT2 to promote cell proliferation and malignant transformation in oligodendroglioma.

    abstract::Oligodendroglioma is an important type of lower-grade glioma (LGG), which is a slowly progressing brain tumor. Many LGGs eventually transform into a more aggressive or malignant type. Enhanced angiogenesis is a characteristic of malignantly transformed oligodendroglioma (m-oligodendroglioma). However, the pathogenesis...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-01411-y

    authors: Qi L,Wang ZY,Shao XR,Li M,Chen SN,Liu XQ,Yan S,Zhang B,Zhang XD,Li X,Zhao W,Pan JA,Zhao B,Zhang XD

    更新日期:2020-09-01 00:00:00

  • Epstein-Barr virus U leader exon contains an internal ribosome entry site.

    abstract::Eukaryotic translation can be initiated either by a cap-dependent mechanism or by internal ribosome entry, a process by which ribosomes are directly recruited to structured regions of mRNA upstream of the initiation codon. Here we report the finding of an internal ribosome entry site (IRES) in the untranslated region ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206149

    authors: Isaksson A,Berggren M,Ricksten A

    更新日期:2003-01-30 00:00:00

  • Molecular pathology in basal cell cancer with p53 as a genetic marker.

    abstract::Human basal cell cancer (BCC) has unique growth characteristics with virtual inability to metastasize. We investigated clonality and genetic progression using p53 mutations as marker. Sampling was done through microdissection of frozen immunohistochemically stained 16 microm slices of tumors. From 11 BCC tumors 78 sam...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201435

    authors: Pontén F,Berg C,Ahmadian A,Ren ZP,Nistér M,Lundeberg J,Uhlén M,Pontén J

    更新日期:1997-08-28 00:00:00

  • Uracil in DNA--occurrence, consequences and repair.

    abstract::Uracil in DNA results from deamination of cytosine, resulting in mutagenic U : G mispairs, and misincorporation of dUMP, which gives a less harmful U : A pair. At least four different human DNA glycosylases may remove uracil and thus generate an abasic site, which is itself cytotoxic and potentially mutagenic. These e...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1205996

    authors: Krokan HE,Drabløs F,Slupphaug G

    更新日期:2002-12-16 00:00:00

  • P150c-abl is detected in mouse male germ cells by an in vitro kinase assay and is associated with stage-specific phosphoproteins in haploid cells.

    abstract::We have utilized c-abl antibodies and an in vitro kinase assay to identify the protein products of the c-abl gene in mouse testis. Although the testis contains high levels of a unique c-abl mRNA, along with lower amounts of two c-abl mRNAs common to somatic cells, we detected only a single polypeptide of approximately...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Ponzetto C,Wadewitz AG,Pendergast AM,Witte ON,Wolgemuth DJ

    更新日期:1989-06-01 00:00:00

  • High levels of the c-myc protein in cell lines of Bloom's syndrome origin.

    abstract::Lymphoblastoid cell lines derived from cancer prone Bloom's Syndrome patients differ from cell lines representative of several other disorders by exhibiting a constitutive elevation in the level of the c-myc protein. This may be a contributing factor in the strong predisposition to malignancy observed in Bloom's syndr...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Sullivan NF,Willis AE,Moore JP,Lindahl T

    更新日期:1989-12-01 00:00:00

  • c-Met-induced epithelial carcinogenesis is initiated by the serine protease matriptase.

    abstract::The progression and negative outcome of a variety of human carcinomas are intimately associated with aberrant activity of the c-Met oncogene. The underlying cause of this dysregulation, however, remains a subject of discussion, as the majority of cancer patients do not present with activating mutations in c-Met recept...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2010.586

    authors: Szabo R,Rasmussen AL,Moyer AB,Kosa P,Schafer JM,Molinolo AA,Gutkind JS,Bugge TH

    更新日期:2011-04-28 00:00:00

  • O-GlcNAcylation is involved in the transcriptional activity of EWS-FLI1 in Ewing's sarcoma.

    abstract::The oncogene EWS-FLI1 encodes a chimeric transcription factor expressed in Ewing's sarcoma family tumors (ESFTs). EWS-FLI1 target gene expression is thought to drive ESFT pathogenesis and, therefore, inhibition of EWS-FLI1 activity holds high therapeutic promise. As the activity of many transcription factors is regula...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2008.484

    authors: Bachmaier R,Aryee DN,Jug G,Kauer M,Kreppel M,Lee KA,Kovar H

    更新日期:2009-03-05 00:00:00

  • NF-κB-HOTAIR axis links DNA damage response, chemoresistance and cellular senescence in ovarian cancer.

    abstract::The transcription factor nuclear factor kappa B (NF-κB) and the long non-coding RNA (lncRNA) HOTAIR (HOX transcript antisense RNA) have diverse functional roles in cancer. In this study, we show that upregulation of HOTAIR induced platinum resistance in ovarian cancer, and increased HOTAIR levels were observed in recu...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2016.75

    authors: Özeş AR,Miller DF,Özeş ON,Fang F,Liu Y,Matei D,Huang T,Nephew KP

    更新日期:2016-10-13 00:00:00

  • Transactivation of host and viral genes by the adenovirus E1B 19K tumor antigen.

    abstract::Adenovirus contains two nuclear oncogenes, the EIA and EIB genes, which cooperatively can transform cells through mechanisms that are not understood. The transcriptional activities of the E1A gene (transactivation and repression) are well studied. Using transient expression assays, we show here that the 19,000-Da E1B ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Herrmann CH,Dery CV,Mathews MB

    更新日期:1987-01-01 00:00:00

  • BARD1 induces apoptosis by catalysing phosphorylation of p53 by DNA-damage response kinase.

    abstract::The BRCA1-associated RING domain protein BARD1 acts with BRCA1 in double-strand break repair and ubiquitination. BARD1 plays a role as mediator of apoptosis by binding to and stabilizing p53, and BARD1-repressed cells are resistant to apoptosis. We therefore investigated the mechanism by which BARD1 induces p53 stabil...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208491

    authors: Feki A,Jefford CE,Berardi P,Wu JY,Cartier L,Krause KH,Irminger-Finger I

    更新日期:2005-05-26 00:00:00