Histone deacetylases and the immunological network: implications in cancer and inflammation.

Abstract:

:The initiation, magnitude and duration of an immune response against antigens are a tightly regulated process involving a dynamic, orchestrated balance of pro- and anti-inflammatory pathways in immune cells. Such a delicate balance is critical for allowing efficient immune response against foreign antigens while preventing autoimmune attack against self-antigens. In recent years, much effort has been devoted to understanding immune evasion by cancer cells. Also, significant advances have been made in mechanistically understanding the role of pro- and anti-inflammatory cytokines in the regulation of immune responses against antigens, including those expressed by tumors. However, we still know very little about the regulation of inflammatory/anti-inflammatory genes in their natural setting, the chromatin substrate. Several mechanisms have been identified to influence chromatin flexibility and allow dynamic changes in gene expression. Among those, chromatin modifications induced by acetylation and deacetylation of histone tails have gained wide attention. In this study, we discuss the role of histone deacetylases in the transcriptional regulation of genes involved in the inflammatory response and how these enzymes coordinate the dynamic expression of these genes during an immune response. This emerging knowledge is opening new avenues to better understand epigenetic regulation of inflammatory responses and providing new molecular targets for either amplifying or ameliorating immune responses.

journal_name

Oncogene

journal_title

Oncogene

authors

Villagra A,Sotomayor EM,Seto E

doi

10.1038/onc.2009.334

subject

Has Abstract

pub_date

2010-01-14 00:00:00

pages

157-73

issue

2

eissn

0950-9232

issn

1476-5594

pii

onc2009334

journal_volume

29

pub_type

杂志文章,评审

相关文献

ONCOGENE文献大全
  • The NF-κB subunit c-Rel regulates Bach2 tumour suppressor expression in B-cell lymphoma.

    abstract::The REL gene, encoding the NF-κB subunit c-Rel, is frequently amplified in B-cell lymphoma and functions as a tumour-promoting transcription factor. Here we report the surprising result that c-rel-/- mice display significantly earlier lymphomagenesis in the c-Myc driven, Eμ-Myc model of B-cell lymphoma. c-Rel loss als...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.399

    authors: Hunter JE,Butterworth JA,Zhao B,Sellier H,Campbell KJ,Thomas HD,Bacon CM,Cockell SJ,Gewurz BE,Perkins ND

    更新日期:2016-06-30 00:00:00

  • Reexpression of epigenetically silenced AML tumor suppressor genes by SUV39H1 inhibition.

    abstract::Reexpression of hypermethylated tumor suppressor genes using DNA methyltransferase (DNMT) and histone deacetylase inhibitors occurs by a mechanism whereby promoter demethylation is the dominant event. In support of this model, we found in acute myeloid leukemia cells with hypermethylated p15INK4B and E-cadherin promot...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.361

    authors: Lakshmikuttyamma A,Scott SA,DeCoteau JF,Geyer CR

    更新日期:2010-01-28 00:00:00

  • Expression of beta-galactosidase under the control of the human c-myc promoter in transgenic mice is inhibited by mithramycin.

    abstract::In order to assess the functional contribution of the human c-myc promoter region in the expression of the c-myc gene, transgenic mouse lines containing a bacterial lac Z gene encoding beta-galactosidase under the control of the human c-myc protooncogene promoter were generated. Transgenic mouse embryos heterozygous f...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Jones DE Jr,Cui DM,Miller DM

    更新日期:1995-06-15 00:00:00

  • Correction: Epigenetic loss of AOX1 expression via EZH2 leads to metabolic deregulations and promotes bladder cancer progression.

    abstract::After publication of this Article, the Authors noticed errors in some of the Figures. In Figures 2e, 2f-g, 4a, 4j, 5a and 6b, unmatched β-actin was inadvertently used as loading control for the immunoblots. These have been corrected using repeat data from a similar set of samples and the revised Figures containing mat...

    journal_title:Oncogene

    pub_type: 已发布勘误

    doi:10.1038/s41388-020-1283-7

    authors: Vantaku V,Putluri V,Bader DA,Maity S,Ma J,Arnold JM,Rajapakshe K,Donepudi SR,von Rundstedt FC,Devarakonda V,Dubrulle J,Karanam B,McGuire SE,Stossi F,Jain AK,Coarfa C,Cao Q,Sikora AG,Villanueva H,Kavuri SM,Lotan Y

    更新日期:2020-10-01 00:00:00

  • p12(CDK2-AP1) mediates DNA damage responses induced by cisplatin.

    abstract::We examined the biological role of p12(CDK2-AP1) in cisplatin-mediated responses by using murine ES p12(CDK2-AP1) knockout clones generated by a targeted disruption of murine p12(CDK2-AP1). Homozygous knockout clones showed an increased cellular proliferation along with an increase in S and a decrease in G2/M phase po...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208222

    authors: Kim Y,McBride J,Zhang R,Zhou X,Wong DT

    更新日期:2005-01-13 00:00:00

  • Aggrus: a diagnostic marker that distinguishes seminoma from embryonal carcinoma in testicular germ cell tumors.

    abstract::Aggrus (also known as T1alpha/podoplanin) is a membrane sialoglycoprotein whose function in tumors is unknown. We recently determined that Aggrus possessed the ability of inducing platelet aggregation and that its expression was frequently upregulated in colorectal tumors. Thus, Aggrus expression might be associated w...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1207869

    authors: Kato Y,Sasagawa I,Kaneko M,Osawa M,Fujita N,Tsuruo T

    更新日期:2004-11-04 00:00:00

  • Identification of fyn-encoded proteins in normal human blood cells.

    abstract::We have previously reported that carboxyl terminal truncations of the normal human fyn gene, a member of the src subfamily, can transform immortal mouse fibroblasts to full malignancy. In search of evidence which suggests the possible activation of the human fyn gene, we have screened DNAs and RNAs from a number of hu...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Kawakami Y,Furue M,Kawakami T

    更新日期:1989-03-01 00:00:00

  • Hyperactivation of EGFR and downstream effector phospholipase D1 by oncogenic FAM83B.

    abstract::Despite the progress made in targeted anticancer therapies in recent years, challenges remain. The identification of new potential targets will ensure that the arsenal of cancer therapies continues to expand. FAM83B was recently discovered in a forward genetic screen for novel oncogenes that drive human mammary epithe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.293

    authors: Cipriano R,Bryson BL,Miskimen KL,Bartel CA,Hernandez-Sanchez W,Bruntz RC,Scott SA,Lindsley CW,Brown HA,Jackson MW

    更新日期:2014-06-19 00:00:00

  • SCP1 regulates c-Myc stability and functions through dephosphorylating c-Myc Ser62.

    abstract::Serine 62 (Ser62) phosphorylation affects the c-Myc protein stability in cancer cells. However, the mechanism for dephosphorylating c-Myc is not well understood. In this study, we identified carboxyl-terminal domain RNA polymerase II polypeptide A small phosphatase 1 (SCP1) as a novel phosphatase specifically dephosph...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.106

    authors: Wang W,Liao P,Shen M,Chen T,Chen Y,Li Y,Lin X,Ge X,Wang P

    更新日期:2016-01-28 00:00:00

  • Transcriptional upregulation of SPARC, in response to c-Jun overexpression, contributes to increased motility and invasion of MCF7 breast cancer cells.

    abstract::Overexpression of the c-Jun proto-oncogene in MCF7 breast cancer cells results in a variety of phenotype changes related to malignant progression including increased motility and invasion. Concurrent with these phenotypic effects are changes in the expression of multiple gene targets. We previously demonstrated that e...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205857

    authors: Briggs J,Chamboredon S,Castellazzi M,Kerry JA,Bos TJ

    更新日期:2002-10-10 00:00:00

  • The HIF1alpha-inducible pro-cell death gene BNIP3 is a novel target of SIM2s repression through cross-talk on the hypoxia response element.

    abstract::The short isoform of single-minded 2 (SIM2s), a basic helix-loop-helix/PAS (bHLH/PAS) transcription factor, is upregulated in pancreatic and prostate tumours; however, a mechanistic role for SIM2s in these cancers is unknown. Microarray studies in prostate DU145 cells identified the pro-cell death gene, BNIP3 (Bcl-2/a...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.228

    authors: Farrall AL,Whitelaw ML

    更新日期:2009-10-15 00:00:00

  • DAL-1/4.1B tumor suppressor interacts with protein arginine N-methyltransferase 3 (PRMT3) and inhibits its ability to methylate substrates in vitro and in vivo.

    abstract::DAL-1 (differentially expressed in adenocarcinoma of the lung)/4.1B is a tumor suppressor gene on human chromosome 18p11.3 whose expression is lost in >50% of primary non-small-cell lung carcinomas. Based on sequence similarity, DAL-1/4.1B has been assigned to the Protein 4.1 superfamily whose members interact with pl...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208057

    authors: Singh V,Miranda TB,Jiang W,Frankel A,Roemer ME,Robb VA,Gutmann DH,Herschman HR,Clarke S,Newsham IF

    更新日期:2004-10-14 00:00:00

  • Apoptotic cues from the extracellular matrix: regulators of angiogenesis.

    abstract::A variety of factors cooperate to regulate neovessel formation and persistence. Proangiogenic growth factors have remained an area of intense interest due to their capacity to promote endothelial cell (EC) proliferation and to initiate the angiogenic program. These growth factors are associated with increased cell sur...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1207110

    authors: Stupack DG,Cheresh DA

    更新日期:2003-12-08 00:00:00

  • Weak linkage at 4p16 to predisposition for human neuroblastoma.

    abstract::The most frequent genetic alterations described in neuroblastoma (NB) are amplification of MYCN oncogene and deletion of chromosome 1p, although somatic deletions have been demonstrated at other chromosomal intervals. Since loss of heterozygosity (LOH) at distal 4p has been observed in about 20-29% of neuroblastomas, ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206009

    authors: Perri P,Longo L,Cusano R,McConville CM,Rees SA,Devoto M,Conte M,Ferrara GB,Seri M,Romeo G,Tonini GP

    更新日期:2002-11-28 00:00:00

  • Differential androgen receptor signals in different cells explain why androgen-deprivation therapy of prostate cancer fails.

    abstract::Prostate cancer is one of the major causes of cancer-related death in the western world. Androgen-deprivation therapy (ADT) for the suppression of androgens binding to the androgen receptor (AR) has been the norm of prostate cancer treatment. Despite early success to suppress prostate tumor growth, ADT eventually fail...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/onc.2010.121

    authors: Niu Y,Chang TM,Yeh S,Ma WL,Wang YZ,Chang C

    更新日期:2010-06-24 00:00:00

  • Characterization of a major colon cancer susceptibility locus (Ccs3) on mouse chromosome 3.

    abstract::Treatment of mice with the carcinogen azoxymethane (AOM) induces a number of lesions in the colon, including hyperplastic lesions, as well adenomas and carcinomas in situ. Inbred strains of mice show different responses to AOM-induced carcinogenesis. A/J mice are highly susceptible and develop a greater number of hype...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.369

    authors: Meunier C,Cai J,Fortin A,Kwan T,Marquis JF,Turbide C,Van Der Kraak L,Jothy S,Beauchemin N,Gros P

    更新日期:2010-02-04 00:00:00

  • The MAPK pathway functions as a redundant survival signal that reinforces the PI3K cascade in c-Kit mutant melanoma.

    abstract::Stimulation of the c-Kit receptor tyrosine kinase has a critical role in the development and migration of melanocytes, and oncogenic c-Kit mutants contribute to the progression of some melanomas. c-Kit signalling activates the mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3-kinase (PI3K) pathways an...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2012.562

    authors: Todd JR,Scurr LL,Becker TM,Kefford RF,Rizos H

    更新日期:2014-01-09 00:00:00

  • Frequent loss of heterozygosity on chromosomes 7 and 9 in benign epithelial ovarian tumours.

    abstract::It is presently unclear if ovarian cancers arise through malignant transformation of pre-existing benign tumours. The apparent rarity of loss of heterozygosity (LOH) reported for benign tumours has led to speculation that they lack malignant potential and represent a biological entity distinct from ovarian carcinoma. ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201372

    authors: Roy WJ Jr,Watson RH,Hitchcock A,Campbell IG

    更新日期:1997-10-23 00:00:00

  • The adenovirus E1A 289R and 243R proteins inhibit the phosphorylation of p300.

    abstract::A protein of 300 kDa (p300) associates with the adenovirus E1A proteins and has been implicated in the control of cell cycle progression. In mammalian cells, p300 is actively phosphorylated in both quiescent and proliferating cells and its level of phosphorylation increases as it travels from late G1 into M phase. E1A...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Banerjee AC,Recupero AJ,Mal A,Piotrkowski AM,Wang DM,Harter ML

    更新日期:1994-06-01 00:00:00

  • Artemis is a negative regulator of p53 in response to oxidative stress.

    abstract::Artemis is a multifunctional phospho-protein with roles in V(D)J recombination, repair of double-strand breaks by nonhomologous end-joining and regulation of cell-cycle checkpoints after DNA damage. Here, we describe a new function of Artemis as a negative regulator of p53 in response to oxidative stress in both prima...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.100

    authors: Zhang X,Zhu Y,Geng L,Wang H,Legerski RJ

    更新日期:2009-06-04 00:00:00

  • Analysis of a variant Max sequence expressed in Xenopus laevis.

    abstract::Max is a small helix-loop-helix protein which forms heterodimers with members of the Myc protein family. Myc/Max heterodimers exhibit sequence-specific DNA binding with much greater affinity than Myc homodimers. The Xenopus laevis homologue of Max, XMax, is shorter than the equivalent mammalian protein. This differenc...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Tonissen KF,Krieg PA

    更新日期:1994-01-01 00:00:00

  • A novel conditional NPM-ALK-driven model of CD30+ T-cell lymphoma mediated by a translational stop cassette.

    abstract::Targeted expression of transgenes is essential for the accurate representation of human disease in in vivo models. Current approaches to generate conditional transgenic mouse models are cumbersome and not amenable to high-throughput analysis since they require de novo generation and characterization of genetically mod...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-019-1058-1

    authors: Shoumariyeh K,Schneider N,Poggio T,Veratti P,Ehrenfeld S,Redhaber DM,Khan R,Pfeifer D,Klingeberg C,Kreutmair S,Rudelius M,Quintanilla-Martinez L,Fend F,Illert AL,Duyster J,Miething C

    更新日期:2020-02-01 00:00:00

  • Structure, expression, and activity of Tyro 3, a neural adhesion-related receptor tyrosine kinase.

    abstract::We have isolated mouse cDNA clones encoding Tyro 3, a receptor protein-tyrosine kinase (PTK) of the mammalin central nervous system (CNS). Expression of the Tyro 3 gene is strongly up-regulated in neurons of the mouse neocortex, cerebellum, and hippocampus after the day of birth, during periods of active synaptogenesi...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Lai C,Gore M,Lemke G

    更新日期:1994-09-01 00:00:00

  • The deleted in colon cancer (DCC) gene is consistently expressed in colorectal cancers and metastases.

    abstract::The DCC (deleted in colorectal cancer) gene was originally identified as a candidate tumour suppressor gene in colon carcinogenesis on the basis of allelic losses in chromosome 18q.21 in 70% of colon cancers. Reverse transcriptase polymerase chain reaction (RT-PCR) of DCC mRNA suggests that DCC expression may also be ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Gotley DC,Reeder JA,Fawcett J,Walsh MD,Bates P,Simmons DL,Antalis TM

    更新日期:1996-08-15 00:00:00

  • Mutations that disrupt PHOXB interaction with the neuronal calcium sensor HPCAL1 impede cellular differentiation in neuroblastoma.

    abstract::Heterozygous germline mutations in PHOX2B, a transcriptional regulator of sympathetic neuronal differentiation, predispose to diseases of the sympathetic nervous system, including neuroblastoma and congenital central hypoventilation syndrome (CCHS). Although the PHOX2B variants in CCHS largely involve expansions of th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.290

    authors: Wang W,Zhong Q,Teng L,Bhatnagar N,Sharma B,Zhang X,Luther W 2nd,Haynes LP,Burgoyne RD,Vidal M,Volchenboum S,Hill DE,George RE

    更新日期:2014-06-19 00:00:00

  • An 80 Kb P1 clone from chromosome 3p21.3 suppresses tumor growth in vivo.

    abstract::High frequencies of allelic loss on the short arm of chromosome 3 in small cell lung cancer (SCLC) and a number of other tumors suggest the existence of a tumor suppressor gene(s) within the deleted regions. Two small cell lung cancer lines, NCI H740 and GLC20, have been described which have homozygous deletions in th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Todd MC,Xiang RH,Garcia DK,Kerbacher KE,Moore SL,Hensel CH,Liu P,Siciliano MJ,Kok K,van den Berg A,Veldhuis P,Buys CH,Killary AM,Naylor SL

    更新日期:1996-12-05 00:00:00

  • Glycine-cysteine substitution at codon 13 of the N-ras proto-oncogene in a human T cell non-Hodgkin's lymphoma.

    abstract::Tumor-derived DNA from a non-Hodgkin's (T cell) lymphoma patient, assayed by NIH3T3 transfection followed by inoculation of cells into nude mice, was found to contain an activated N-ras proto-oncogene. The mode of activation was determined by hybridization with N-ras-specific oligonucleotide probes detecting mutations...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Wodnar-Filipowicz A,Senn HP,Jiricny J,Signer E,Moroni C

    更新日期:1987-01-01 00:00:00

  • Interaction and colocalization of PGP9.5 with JAB1 and p27(Kip1).

    abstract::PGP9.5 (UCH-L1) is a member of the ubiquitin C-terminal hydrolase (UCH) family of proteins that is expressed in neuronal tissues. Our previous studies have shown that PGP9.5 was highly expressed in primary lung cancers and lung cancer cell lines. Additionally, the frequency of PGP9.5 over expression increases with tum...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205390

    authors: Caballero OL,Resto V,Patturajan M,Meerzaman D,Guo MZ,Engles J,Yochem R,Ratovitski E,Sidransky D,Jen J

    更新日期:2002-05-02 00:00:00

  • Impairment of antioxidant defense via glutathione depletion sensitizes acute lymphoblastic leukemia cells for Smac mimetic-induced cell death.

    abstract::Evasion of apoptosis in pediatric acute lymphoblastic leukemia (ALL) is linked to aberrant expression of inhibitor of apoptosis (IAP) proteins and dysregulated redox homeostasis, rendering leukemic cells vulnerable to redox-targeting therapies. Here we discover that inhibition of antioxidant defenses via glutathione (...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2014.338

    authors: Schoeneberger H,Belz K,Schenk B,Fulda S

    更新日期:2015-07-30 00:00:00

  • Pim1 cooperates with E2a-Pbx1 to facilitate the progression of thymic lymphomas in transgenic mice.

    abstract::Mice transgenic for the leukemia oncogene E2A-PBX1 invariably develop lethal, high-grade T-cell lymphomas by 5 months of age. In this study, retroviral insertional mutagenesis was employed to identify oncogenes that cooperate with the E2A-PBX1 transgene in lymphomagenesis. Neonatal retroviral infection substantially r...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201670

    authors: Feldman BJ,Reid TR,Cleary ML

    更新日期:1997-11-27 00:00:00