Modulation of p53 dependent gene expression and cell death through thioredoxin-thioredoxin reductase by the Interferon-Retinoid combination.

Abstract:

:We have shown earlier that the IFN-beta and all-trans retinoic acid (RA) combination, but not the single agents, induces death in several tumor cell lines. Employing a genetic technique we have identified several Genes associated with Retinoid-IFN induced Mortality (GRIM). One of the GRIMs was human thioredoxin reductase (TR), a redox enzyme. Since the overexpressed TR augments IFN/RA stimulated cell death, we explored the mechanisms of TR-mediated death. Here we show that TR augments cell death by upregulating the transcriptional activity of p53 tumor suppressor. This process does not involve a physical increase in levels of p53. Using redox inactive mutants of TR and its substrate, thioredoxin (Trx), we demonstrate that IFN/RA-induced regulation of p53 dependent gene expression requires TR and Trx. In contrast-over-expression of wildtype TR or Trx augment the p53 dependent gene expression in response to IFN/RA treatment. Consistent with these results an increased DNA binding activity of p53 was noted in the presence of TR. These studies identify a novel mechanism of p53 mediated cell death regulation involving redox enzymes.

journal_name

Oncogene

journal_title

Oncogene

authors

Hu J,Ma X,Lindner DJ,Karra S,Hofmann ER,Reddy SP,Kalvakolanu DV

doi

10.1038/sj.onc.1204585

subject

Has Abstract

pub_date

2001-07-12 00:00:00

pages

4235-48

issue

31

eissn

0950-9232

issn

1476-5594

journal_volume

20

pub_type

杂志文章

相关文献

ONCOGENE文献大全
  • Comparative analysis of the structure and function of the chicken c-myc and v-myc genes: v-myc is a more potent inducer of cell proliferation and apoptosis than c-myc.

    abstract::To gain a more complete understanding of c-myc regulation in chickens, we have completed the structural characterization of the chicken c-myc gene and have begun to investigate c-myc transcription and protein expression. A comparison of c-myc structure and expression between mammals and birds presents an enigma: there...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Petropoulos CJ,Givol I,Hughes SH

    更新日期:1996-06-20 00:00:00

  • Epigenetic silencing of the dual-role signal mediator, ANGPTL4 in tumor tissues and its overexpression in the urothelial carcinoma microenvironment.

    abstract::Urothelial carcinoma (UC) carcinogenesis has been hypothesized to occur through epigenetic repression of tumor-suppressor genes (TSGs). By quantitative real-time polymerase chain reaction array, we found that one potential TSG, angiopoietin-like 4 (ANGPTL4), was expressed at very low levels in all bladder cancer cell ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2017.375

    authors: Hsieh HY,Jou YC,Tung CL,Tsai YS,Wang YH,Chi CL,Lin RI,Hung SK,Chuang YM,Wu SF,Li C,Shen CH,Chan MWY,Hsu CD

    更新日期:2018-02-01 00:00:00

  • SPSB3 targets SNAIL for degradation in GSK-3β phosphorylation-dependent manner and regulates metastasis.

    abstract::Epithelial-mesenchymal transition (EMT) is a process during which normal epithelial cells acquire mesenchymal characteristics. EMT has a critical role in various human diseases especially in cancer. EMT facilitates tumor initiation and progression by mediating cancer cell stemness and motility. Zinc finger transcripti...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2017.370

    authors: Liu Y,Zhou H,Zhu R,Ding F,Li Y,Cao X,Liu Z

    更新日期:2018-02-08 00:00:00

  • C-Jun N-terminal kinases are required for oncolytic adenovirus-mediated autophagy.

    abstract::Oncolytic adenoviruses, such as Delta-24-RGD (Δ24RGD), are replication-competent viruses that are genetically engineered to induce selective cancer cell lysis. In cancer cells, Δ24RGD induces massive autophagy, which is required for efficient cell lysis and adenoviral spread. Understanding the cellular mechanisms unde...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2014.452

    authors: Klein SR,Piya S,Lu Z,Xia Y,Alonso MM,White EJ,Wei J,Gomez-Manzano C,Jiang H,Fueyo J

    更新日期:2015-10-08 00:00:00

  • The Ste20-like kinase SLK is required for ErbB2-driven breast cancer cell motility.

    abstract::The Ste20-like kinase, SLK, is involved in the control of cell motility through its effects on actin reorganization and focal adhesion turnover. Here we investigated the role of SLK in chemotaxis downstream of the tyrosine kinase receptor, HER2/ErbB2/Neu, which is frequently overexpressed in human breast cancers. Our ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.146

    authors: Roovers K,Wagner S,Storbeck CJ,O'Reilly P,Lo V,Northey JJ,Chmielecki J,Muller WJ,Siegel PM,Sabourin LA

    更新日期:2009-08-06 00:00:00

  • Glutamine activates STAT3 to control cancer cell proliferation independently of glutamine metabolism.

    abstract::Cancer cells can use a variety of metabolic substrates to fulfill the bioenergetic and biosynthetic needs of their oncogenic program. Besides bioenergetics, cancer cell metabolism also directly influences genetic, epigenetic and signaling events associated with tumor progression. Many cancer cells are addicted to glut...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2016.364

    authors: Cacace A,Sboarina M,Vazeille T,Sonveaux P

    更新日期:2017-04-01 00:00:00

  • Tumor stroma: a complexity dictated by the hypoxic tumor microenvironment.

    abstract::A lot of effort has been done to study how cancer cells react to low-oxygen tension, a condition known as hypoxia. Indeed, abnormal and dysfunctional blood vessels in the tumor are incapable to restore oxygenation, therefore perpetuating hypoxia, which, in turn, will fuel tumor progression, metastasis and resistance t...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/onc.2013.121

    authors: Casazza A,Di Conza G,Wenes M,Finisguerra V,Deschoemaeker S,Mazzone M

    更新日期:2014-04-03 00:00:00

  • Both the helix-loop-helix and the leucine zipper motifs of c-Myc contribute to its dimerization specificity with Max.

    abstract::The oncoprotein c-Myc contains two dimerization motifs- the helix-loop-helix (HLH) and the leucine zipper (LZ) - through which c-Myc specifically dimerizes with Max. We substituted regions of the c-Myc HLH and LZ motifs with the corresponding regions of structurally related proteins that do not interact with Max. Spec...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Davis LJ,Halazonetis TD

    更新日期:1993-01-01 00:00:00

  • Cytokinesis failure due to derailed integrin traffic induces aneuploidy and oncogenic transformation in vitro and in vivo.

    abstract::Aneuploidy is frequently detected in solid tumors but the mechanisms regulating the generation of aneuploidy and their relevance in cancer initiation remain under debate and are incompletely characterized. Spatial and temporal regulation of integrin traffic is critical for cell migration and cytokinesis. Impaired inte...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.527

    authors: Högnäs G,Tuomi S,Veltel S,Mattila E,Murumägi A,Edgren H,Kallioniemi O,Ivaska J

    更新日期:2012-08-02 00:00:00

  • Screening for mutations in exon 11 of the BRCA1 gene in 70 Italian breast and ovarian cancer patients by protein truncation test.

    abstract::The most common mutations in the familial breast and ovarian cancer susceptibility gene BRCA1 are frameshift and nonsense mutations, which lead to the synthesis of truncated proteins. On this ground, we have analysed BRCA1 exon 11, which includes about 61% of coding region, in germline DNA from 70 Italian breast and/o...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: De Benedetti VM,Radice P,Mondini P,Spatti G,Conti A,Illeni MT,Caligo MA,Cipollini G,Bevilaqua G,Pilotti S,Pierotti MA

    更新日期:1996-09-19 00:00:00

  • Cleavage of Mcl-1 by caspases impaired its ability to counteract Bim-induced apoptosis.

    abstract::Mcl-1 is an antiapoptotic member of the Bcl-2 family that can promote cell viability. We report here that Mcl-1 is a new substrate for caspases during induction of apoptosis. Mcl-1 cleavage occurs after Asp127 and Asp157 and generates four fragments of 24, 19, 17 and 12 kDa in both intact cells and in vitro, an effect...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208069

    authors: Herrant M,Jacquel A,Marchetti S,Belhacène N,Colosetti P,Luciano F,Auberger P

    更新日期:2004-10-14 00:00:00

  • siRNA-mediated knockdown of Pdcd4 expression causes upregulation of p21(Waf1/Cip1) expression.

    abstract::The transformation suppressor gene, programmed cell death gene 4 (Pdcd4), inhibits tumor-promoter-mediated transformation of mouse keratinocytes and has been implicated as a tumor suppressor gene in the development of human cancer. The Pdcd4 protein interacts with translation initiation factors eIF4A and eIF4G and bin...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2008.115

    authors: Bitomsky N,Wethkamp N,Marikkannu R,Klempnauer KH

    更新日期:2008-08-14 00:00:00

  • Specific DNA binding by different classes of human p53 mutants.

    abstract::The p53 protein is a multifunctional transcription factor which orchestrates cellular responses to DNA damage, so helping to conserve genomic stability. It may also regulate genes involved in intercellular signalling, such as thrombospondin, a negative regulator of angiogenesis and metastatic spread. Activation of p53...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Rolley N,Butcher S,Milner J

    更新日期:1995-08-17 00:00:00

  • P63 regulates tubular formation via epithelial-to-mesenchymal transition.

    abstract::P63, a p53 family member, is expressed as TA and ΔN isoforms. Interestingly, both TAp63 and ΔNp63 are transcription factors, and regulate both common and distinct sets of target genes. p63 is required for survival of some epithelial cell lineages, and lack of p63 leads to loss of epidermis and other epithelia in human...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.101

    authors: Zhang Y,Yan W,Chen X

    更新日期:2014-03-20 00:00:00

  • The chromosomal translocation t(X;14)(q28;q11) in T-cell pro-lymphocytic leukaemia breaks within one gene and activates another.

    abstract::Chromosomal translocation t(X;14)(q28;q11) has been observed in patients with pro-lymphocytic T-cell leukaemia (T-PLL). In two cases of T-PLL, one of which was associated with Ataxia telangiectasia (AT), the chromosomal break occurred in two different introns of a gene c6.1A, located at the Xq28 locus. Fusion transcri...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Fisch P,Forster A,Sherrington PD,Dyer MJ,Rabbitts TH

    更新日期:1993-12-01 00:00:00

  • V-erbA generates ribosomes devoid of RPL11 and regulates translational activity in avian erythroid progenitors.

    abstract::The v-erbA oncogene transforms chicken erythrocytic progenitors (T2EC) by blocking their differentiation and freezing them in a state of self-renewal. Transcriptomes of T2EC, expressing either v-erbA or a non-transforming form of v-erbA (S61G), were compared using serial analysis of gene expression and some, but not a...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.93

    authors: Nguyen-Lefebvre AT,Leprun G,Morin V,Viñuelas J,Couté Y,Madjar JJ,Gandrillon O,Gonin-Giraud S

    更新日期:2014-03-20 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

  • Activation-dependent degradation of protein kinase C eta.

    abstract::Prolonged activation of protein kinase Cs (PKCs) by long-term treatment of cells with phorbol ester tumor promoters down-regulates the expression of many PKCs. To investigate the molecular mechanisms involved in the down-regulation of PKC eta, we expressed the novel PKCs eta and θ and various mutant forms in bab...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203779

    authors: Kang BS,French OG,Sando JJ,Hahn CS

    更新日期:2000-08-31 00:00:00

  • Genetics of melanoma predisposition.

    abstract::Predisposition to melanoma is genetically heterogeneous. Two high penetrance susceptibility genes, CDKN2A and CDK4, have so far been identified and mapping is ongoing to localize and identify others. With the advent of a catalogue of millions of potential DNA polymorphisms, attention is now also being focused on ident...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1206445

    authors: Hayward NK

    更新日期:2003-05-19 00:00:00

  • The N-methyl-D-aspartate receptor type 2A is frequently methylated in human colorectal carcinoma and suppresses cell growth.

    abstract::N-methyl-D-aspartate receptors (NMDARs) are the predominant excitatory neurotransmitter receptors in the mammalian brain. We found that among the three NMDARs examined (NMDAR1, NMDAR2A, NMDAR2B), only NMDAR2A was silenced in colorectal carcinoma (CRC) cell lines at basal line and reactivated by the demethylating agent...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210842

    authors: Kim MS,Chang X,Nagpal JK,Yamashita K,Baek JH,Dasgupta S,Wu G,Osada M,Woo JH,Westra WH,Trink B,Ratovitski EA,Moon C,Sidransky D

    更新日期:2008-03-27 00:00:00

  • Cre-loxP chromosome engineering of a targeted deletion in the mouse corresponding to the 3p21.3 region of homozygous loss in human tumours.

    abstract::Chromosomal deletions are a common feature of epithelial tumours and when further defined by homozygous deletions, are often the location of tumour suppressor genes. Deletions within the short arm of chromosome 3 occur very frequently in human carcinomas: a minimal region of loss at 3p21.3 (the Luca) region has been d...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205530

    authors: Smith AJ,Xian J,Richardson M,Johnstone KA,Rabbitts PH

    更新日期:2002-07-04 00:00:00

  • G2A is an oncogenic G protein-coupled receptor.

    abstract::G2A is a heptahelical cell surface protein that has recently been described as a potential tumor suppressor, based on its ability to counteract transformation of pre-B cells and fibroblasts by Bcr-Abl, an oncogenic tyrosine kinase. We have isolated cDNAs encoding G2A in the course of screening libraries for clones tha...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203731

    authors: Zohn IE,Klinger M,Karp X,Kirk H,Symons M,Chrzanowska-Wodnicka M,Der CJ,Kay RJ

    更新日期:2000-08-10 00:00:00

  • RET cooperates with RB/p53 inactivation in a somatic multi-step model for murine thyroid cancer.

    abstract::Mice bred to carry germline Rb and p53 null alleles are associated with a tumor spectrum that overlaps with the inherited multiple endocrine neoplasia-1 (MEN1) and MEN2 syndromes in humans, including medullary thyroid cancer (MTC). To study the genetic basis for these tumors, we microdissected MTC specimens or obtaine...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202381

    authors: Coxon AB,Ward JM,Geradts J,Otterson GA,Zajac-Kaye M,Kaye FJ

    更新日期:1998-09-24 00:00:00

  • Critical interactions between TGF-beta signaling/ELF, and E-cadherin/beta-catenin mediated tumor suppression.

    abstract::Inactivation of the transforming growth factor-beta (TGF-beta) pathway occurs often in malignancies of the gastrointestinal (GI) system. However, only a fraction of sporadic GI tumors exhibit inactivating mutations in early stages of cancer formation, suggesting that other mechanisms play a critical role in the inacti...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209211

    authors: Katuri V,Tang Y,Li C,Jogunoori W,Deng CX,Rashid A,Sidawy AN,Evans S,Reddy EP,Mishra B,Mishra L

    更新日期:2006-03-23 00:00:00

  • Ras-MAP kinase signaling by lysophosphatidic acid and other G protein-coupled receptor agonists.

    abstract::Lysophosphatidic acid (LPA) and sphingosine-1-phosphate (S1P) are extracellular lipid mediators that signal through distinct members of the Edg/LP subfamily of G protein-coupled receptors (GPCRs). LPA and S1P receptors are expressed in almost every cell type and can couple to multiple G proteins (G(i), G(q) and G(12/1...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1204187

    authors: Kranenburg O,Moolenaar WH

    更新日期:2001-03-26 00:00:00

  • The binding of transcription factor Sp1 to multiple sites is required for maximal expression from the rat transforming growth factor alpha promoter.

    abstract::Transcription from the rat transforming growth factor alpha (TGF-alpha) promoter initiates at multiple sites within a 200-bp G+C-rich region that lacks TATA and CAAT motifs but contains multiple potential binding sites for the transcription factor Sp1. In the present study, we used deletion analysis to establish the 5...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Chen X,Azizkhan JC,Lee DC

    更新日期:1992-09-01 00:00:00

  • RNH1 regulation of reactive oxygen species contributes to histone deacetylase inhibitor resistance in gastric cancer cells.

    abstract::Histone deacetylase inhibitors (HDACis) are a promising class of anticancer epigenetic drugs, however, molecular factors influencing the responses of individual tumors to HDACi therapies remain obscure. Here, we sought to identify genes associated with HDACi resistance in gastric cancer. Treating a panel of 17 gastric...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.104

    authors: Zhu Y,Das K,Wu J,Lee MH,Tan P

    更新日期:2014-03-20 00:00:00

  • Epidermal growth factor activation of NF-kappaB is mediated through IkappaBalpha degradation and intracellular free calcium.

    abstract::The transcription factor NF-kappa-B is normally sequestered in the cytoplasm by its inhibitory subunit IkappaB. Most extracellular signals activate NF-kappa-B through a mechanism involving the phosphorylation and proteasome-dependent degradation of IkappaB. EGF activates NF-kappaB in A-431 carcinoma cells, which overe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201731

    authors: Sun L,Carpenter G

    更新日期:1998-04-23 00:00:00

  • Deregulated expression of E2F-1 induces cyclin A- and E-associated kinase activities independently from cell cycle position.

    abstract::The transcription factor E2F activates genes required for S phase, such as cyclin E and cyclin A. We show that, contrary to long term effects of E2F-1 overexpression, short ectopic overexpression of this transcription factor in logarithmically growing cells does neither affect the cell cycle distribution nor the cell ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201061

    authors: Soucek T,Pusch O,Hengstschläger-Ottnad E,Adams PD,Hengstschläger M

    更新日期:1997-05-15 00:00:00

  • Cellular ITAM-containing proteins are oncoproteins in nonhematopoietic cells.

    abstract::Immunoreceptor tyrosine-based activation motifs (ITAMs) are involved in the transduction of signals necessary for activation, differentiation, and survival in hematopoietic cells. Several viruses have been shown to encode ITAM-containing transmembrane proteins. Although expression of these viral proteins has in some c...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209296

    authors: Grande SM,Katz E,Crowley JE,Bernardini MS,Ross SR,Monroe JG

    更新日期:2006-05-04 00:00:00