Intermediate filament dynamics and breast cancer: aberrant promoter methylation of the Synemin gene is associated with early tumor relapse.

Abstract:

:Synemin (SYNM) is a type IV intermediate filament that has recently been shown to interact with the LIM domain protein zyxin, thereby possibly modulating cell adhesion and cell motility. Owing to this multiplicity of potential functions relevant to cancer development, we initiated a study to decipher SYNM expression and regulation in benign human breast tissue and breast cancer. Dot blot array analysis showed significant SYNM mRNA downregulation in 86% (n=100, P<0.001) of breast cancers compared with their normal tissue counterparts, a result that was confirmed by real-time PCR analysis (n=36, P<0.0001). Immunohistochemistry analysis showed abundant SYNM protein expression in healthy myoepithelial breast cells, whereas SYNM expression loss was evident in 57% (n=37, P<0.001) of breast cancer specimens. Next, we analyzed methylation of the SYNM promoter to clarify whether the SYNM gene can be silenced by epigenetic means. Indeed, methylation-specific PCR analysis showed tumor-specific SYNM promoter methylation in 27% (n=195) of breast cancers. As expected, SYNM promoter methylation was tightly associated (P<0.0001) with SYNM expression loss. In-depth analysis of the SYNM promoter by pyrosequencing showed extensive CpG methylation of DNA elements supposed to regulate gene transcription. Demethylating treatment of SYNM methylated breast cancer cell lines with 5-aza-2-deoxycytidine clearly reestablished the SYNM expression. Statistical analysis of the patient cohort showed a close association between SYNM promoter methylation and unfavorable recurrence-free survival (hazard ratio=2.941, P=0.0282). Furthermore, SYNM methylation positively correlated with lymph node metastases (P=0.0177) and advanced tumor grade (P=0.0275), suggesting that SYNM methylation is associated with aggressive forms of breast cancer. This is the first study on the epigenetic regulation of the SYNM gene in a cancer entity. We provide first hints that SYNM could represent a novel putative breast tumor suppressor gene that is prone to epigenetic silencing. SYNM promoter methylation may become a useful predictive biomarker to stratify breast cancer patients' risk for tumor relapse.

journal_name

Oncogene

journal_title

Oncogene

authors

Noetzel E,Rose M,Sevinc E,Hilgers RD,Hartmann A,Naami A,Knüchel R,Dahl E

doi

10.1038/onc.2010.229

subject

Has Abstract

pub_date

2010-08-26 00:00:00

pages

4814-25

issue

34

eissn

0950-9232

issn

1476-5594

pii

onc2010229

journal_volume

29

pub_type

杂志文章

相关文献

ONCOGENE文献大全
  • Classifying BRAF alterations in cancer: new rational therapeutic strategies for actionable mutations.

    abstract::The RAS-RAF-MEK-ERK signaling cascade is among the most frequently mutated pathways in human cancer. Approximately 50% of melanoma patients possess a druggable hotspot V600E/K mutation in the BRAF protein kinase. FDA-approved combination therapies of BRAF and MEK inhibitors are available that provide survival benefits...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/s41388-018-0171-x

    authors: Dankner M,Rose AAN,Rajkumar S,Siegel PM,Watson IR

    更新日期:2018-06-01 00:00:00

  • Cdc25B activity is regulated by 14-3-3.

    abstract::In the G2 phase cell cycle checkpoint arrest, the cdc25-dependent activation of cyclin B/cdc2, a critical step in regulating entry into mitosis, is blocked. Studies in yeast have demonstrated that the inhibition of cdc25 function involves 14-3-3 binding to cdc25. In humans, two cdc25 isoforms have roles in G2/M progre...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204574

    authors: Forrest A,Gabrielli B

    更新日期:2001-07-19 00:00:00

  • The non-catalytic domain of ras-GAP inhibits transformation induced by G protein coupled receptors.

    abstract::We have studied the relationship between ras-GAP and G protein coupled receptors in a proliferative setting comprised of NIH3T3 expressing transfected muscarinic receptors (mAChRs). GAP expression plasmids were engineered to encode wild-type GAP, its carboxyl-terminal catalytic domain, a mutant lacking a portion of th...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Xu N,McCormick F,Gutkind JS

    更新日期:1994-02-01 00:00:00

  • A mutation in the c-myc-IRES leads to enhanced internal ribosome entry in multiple myeloma: a novel mechanism of oncogene de-regulation.

    abstract::The 5' untranslated region of the proto-oncogene c-myc contains an internal ribosome entry segment (IRES) (Nanbru et al., 1997; Stoneley et al., 1998) and thus c-myc protein synthesis can be initiated by a cap-independent as well as a cap-dependent mechanism (Stoneley et al., 2000). In cell lines derived from patients...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203791

    authors: Chappell SA,LeQuesne JP,Paulin FE,deSchoolmeester ML,Stoneley M,Soutar RL,Ralston SH,Helfrich MH,Willis AE

    更新日期:2000-09-07 00:00:00

  • Evidence for human DNA-mediated transfer of the suppressed phenotype into malignant Chinese hamster cells.

    abstract::Genetic suppression of the neoplastic phenotype has been demonstrated in somatic cell hybrids between tumor and normal cells. Suppression in whole-cell and microcell hybrids cannot, as yet, be attributed to specific elements defined at the molecular level. To identify a gene capable of suppressing the neoplastic pheno...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Schäfer R,Nirkko AC,Ambühl PM,Grzeschik KH,Schwarte-Waldhoff I

    更新日期:1991-12-01 00:00:00

  • The tyrosine kinase Abl is required for Src-transforming activity in mouse fibroblasts and human breast cancer cells.

    abstract::The cytoplasmic tyrosine kinase Src has been implicated in signal transduction induced by growth factors and integrins. Src also shows oncogenic activity when deregulated. Accumulating evidence indicates that the tyrosine kinase Abl is an important substrate for Src signalling in normal cells. Here we show that Abl is...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210543

    authors: Sirvent A,Boureux A,Simon V,Leroy C,Roche S

    更新日期:2007-11-15 00:00:00

  • HER2/Neu-mediated activation of the ETS transcription factor ER81 and its target gene MMP-1.

    abstract::In this study, we show that the ETS transcription factor ER81 directly binds to and activates the promoter of the matrix metalloproteinase gene, MMP-1. Further, the oncoprotein HER2/Neu synergizes with ER81 to stimulate MMP-1 transcription. The activation of ER81 by HER2/Neu is mediated by MAP kinases, which phosphory...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204820

    authors: Bosc DG,Goueli BS,Janknecht R

    更新日期:2001-09-27 00:00:00

  • Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancer.

    abstract::O6-methylguanine-DNA methyltransferase (MGMT) repairs the cytotoxic and mutagenic O6-alkylguanine produced by alkylating agents such as chemotherapeutic agents and mutagens. Recent studies have shown that in a subset of tumors, MGMT expression is inversely linked to hypermethylation of the CpG island in the promoter r...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1207183

    authors: Nakagawachi T,Soejima H,Urano T,Zhao W,Higashimoto K,Satoh Y,Matsukura S,Kudo S,Kitajima Y,Harada H,Furukawa K,Matsuzaki H,Emi M,Nakabeppu Y,Miyazaki K,Sekiguchi M,Mukai T

    更新日期:2003-12-04 00:00:00

  • Absence of p53 permits propagation of mutant cells following genotoxic damage.

    abstract::Much evidence has been gathered in support of a critical role for p53 in the cellular response to DNA damage. p53 dysfunction is associated with progression and poor prognosis of many human cancers and with a high incidence of tumours in p53 knockout mice. The absence of a p53-dependent G1 arrest that facilitates DNA ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1200871

    authors: Griffiths SD,Clarke AR,Healy LE,Ross G,Ford AM,Hooper ML,Wyllie AH,Greaves M

    更新日期:1997-02-06 00:00:00

  • Overexpression of cyclin D1 in rat fibroblasts causes abnormalities in growth control, cell cycle progression and gene expression.

    abstract::Cyclin D1, a putative G1 cyclin, has been implicated in cell cycle control. The human cyclin D1 gene is located on chromosome 11q13 where DNA rearrangement and amplification have been detected in several types of human cancer. Previous studies demonstrated that the cyclin D1 gene is not only rearranged or amplified bu...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Jiang W,Kahn SM,Zhou P,Zhang YJ,Cacace AM,Infante AS,Doi S,Santella RM,Weinstein IB

    更新日期:1993-12-01 00:00:00

  • The neural guidance receptor Plexin C1 delays melanoma progression.

    abstract::Plexin C1 is a type I transmembrane receptor with intrinsic R-Ras GTPase activity, which regulates cytoskeletal remodeling and adhesion in normal human melanocytes. Melanocytes are pigment-producing cells of the epidermis, precursors for melanoma, and express high levels of Plexin C1, which is lost in melanoma in vitr...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2012.511

    authors: Chen Y,Soong J,Mohanty S,Xu L,Scott G

    更新日期:2013-10-10 00:00:00

  • DNA demethylation induces SALL4 gene re-expression in subgroups of hepatocellular carcinoma associated with Hepatitis B or C virus infection.

    abstract::Sal-like protein 4 (SALL4), an embryonic stem cell transcriptional regulator, is re-expressed by an unknown mechanism in poor prognosis hepatocellular carcinoma (HCC), often associated with chronic hepatitis B virus (HBV) infection. Herein, we investigated the mechanism of SALL4 re-expression in HBV-related HCCs. We p...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2016.399

    authors: Fan H,Cui Z,Zhang H,Mani SK,Diab A,Lefrancois L,Fares N,Merle P,Andrisani O

    更新日期:2017-04-27 00:00:00

  • New insights into apoptosis signaling by Apo2L/TRAIL.

    abstract::Apoptosis ligand 2 tumor necrosis factor (TNF)-related apoptosis-inducing ligand (Apo2L/TRAIL) belongs to a small subset of proapoptotic protein ligands in the TNF superfamily. This subset, which also includes Fas ligand and TNF-alpha, can activate the extrinsic apoptotic cell death pathway on binding to cognate death...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/onc.2010.221

    authors: Gonzalvez F,Ashkenazi A

    更新日期:2010-08-26 00:00:00

  • The putative ovarian tumour marker gene HE4 (WFDC2), is expressed in normal tissues and undergoes complex alternative splicing to yield multiple protein isoforms.

    abstract::The whey acidic protein (WAP) domain is a conserved motif, containing eight cysteines found in a characteristic 4-disulphide core arrangement, that is present in a number of otherwise unrelated proteins. WAP motifs are present in SLPI and elafin, two antiproteinases located on chromosome 20q12-13, in a locus rich in p...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205363

    authors: Bingle L,Singleton V,Bingle CD

    更新日期:2002-04-18 00:00:00

  • hHR23B is required for genotoxic-specific activation of p53 and apoptosis.

    abstract::Rad23 proteins function in both DNA repair and protein stability regulation. As ubiquitinated forms of p53 are stabilized after DNA damage in concert with p53 functional activation, and human Rad23 proteins (hHR23A and B) regulate p53 stability in unstressed cells, the role of hHR23B in post-genotoxin regulation of p5...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209865

    authors: Kaur M,Pop M,Shi D,Brignone C,Grossman SR

    更新日期:2007-02-22 00:00:00

  • Mutation of the 9q34 gene TSC1 in sporadic bladder cancer.

    abstract::Deletions involving chromosome 9 occur in more than 50% of human bladder cancers of all grades and stages. Most involve loss of the whole chromosome or of an entire chromosome arm but some small deletions are found which can be used to define critical regions which may contain tumour suppressor genes. We have localize...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202854

    authors: Hornigold N,Devlin J,Davies AM,Aveyard JS,Habuchi T,Knowles MA

    更新日期:1999-04-22 00:00:00

  • Elevated Mdm2 expression induces chromosomal instability and confers a survival and growth advantage to B cells.

    abstract::Mdm2, a regulator of the p53 tumor suppressor, is frequently overexpressed in lymphomas, including lymphomas that have inactivated p53. However, the biological consequences of Mdm2 overexpression in lymphocytes are not fully resolved. Here, we report that increased expression of Mdm2 in B cells augmented proliferation...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210788

    authors: Wang P,Lushnikova T,Odvody J,Greiner TC,Jones SN,Eischen CM

    更新日期:2008-03-06 00:00:00

  • Different p53 mutations produce distinct effects on the ability of colon carcinoma cells to become blocked at the G1/S boundary after irradiation.

    abstract::The LoVo colon carcinoma cell line that presents two wild type p53 alleles was used as the recipient for a series of transfections with p53 expression vectors coding for wild-type or three different mutants (143ala, 175his or 273his). The parental cell line as well as all clones that had rearranged the plasmid with co...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Pocard M,Chevillard S,Villaudy J,Poupon MF,Dutrillaux B,Remvikos Y

    更新日期:1996-02-15 00:00:00

  • In vitro reconstruction of tumour initiation in a human epithelium.

    abstract::Knowledge of tumour initiation in human epithelia is limited by sample availability and difficulty in experimental manipulation of human cells. The thyroid is a useful model since, in addition to multiple tumour stages, it presents two distinct 'pathways' of tumorigenesis: 'follicular' tumours, in which ras oncogene m...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Bond JA,Wyllie FS,Rowson J,Radulescu A,Wynford-Thomas D

    更新日期:1994-01-01 00:00:00

  • Regulation of Pax3 transcriptional activity by SUMO-1-modified PML.

    abstract::Pax3 is an evolutionarily conserved transcription factor that plays a major role in a variety of developmental processes. Mutations in Pax3 lead to severe malformations as seen in human Waardenburg syndrome and in the Splotch mutant mice. The transcriptional activity of Pax3 was recently shown to be repressed by Daxx ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204063

    authors: Lehembre F,Müller S,Pandolfi PP,Dejean A

    更新日期:2001-01-04 00:00:00

  • Repressed expression of the HER-2/c-erbB-2 proto-oncogene by the adenovirus E1a gene products.

    abstract::The E3 region of adenovirus induces down-regulation of epidermal growth factor receptor (EGFR) through endocytosis. Here we report that an EGFR-related protein, the HER-2/c-erbB-2 gene product, p185, is also down-regulated by adenovirus, but via a different mechanism. We found that the adenovirus E1a gene is responsib...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Yan DH,Chang LS,Hung MC

    更新日期:1991-02-01 00:00:00

  • Inhibition of endogenous reverse transcriptase antagonizes human tumor growth.

    abstract::Undifferentiated cells and embryos express high levels of endogenous non-telomerase reverse transcriptase (RT) of retroposon/retroviral origin. We previously found that RT inhibitors modulate cell growth and differentiation in several cell lines. We have now sought to establish whether high levels of RT activity are d...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208562

    authors: Sciamanna I,Landriscina M,Pittoggi C,Quirino M,Mearelli C,Beraldi R,Mattei E,Serafino A,Cassano A,Sinibaldi-Vallebona P,Garaci E,Barone C,Spadafora C

    更新日期:2005-06-02 00:00:00

  • FBXL14 abolishes breast cancer progression by targeting CDCP1 for proteasomal degradation.

    abstract::Understanding the molecular mechanisms that underlie the aggressive behavior and relapse of breast cancer may help in the development of novel therapeutic interventions. CUB-domain-containing protein 1 (CDCP1), a transmembrane adaptor protein, is highly maintained and required in the context of cellular metastatic pot...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0372-3

    authors: Cui YH,Kim H,Lee M,Yi JM,Kim RK,Uddin N,Yoo KC,Kang JH,Choi MY,Cha HJ,Kwon OS,Bae IH,Kim MJ,Kaushik N,Lee SJ

    更新日期:2018-10-01 00:00:00

  • p53 represses SV40 transcription by preventing formation of transcription complexes.

    abstract::There is now much evidence to suggest that the p53 tumour suppressor protein functions to monitor the integrity of the genome. When DNA damage is detected, p53 suppresses cell growth to allow repair or directs the cell into apoptosis. The mechanism of action of p53 is as yet unclear but recent evidence has accumulated...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Perrem K,Rayner J,Voss T,Sturzbecher H,Jackson P,Braithwaite A

    更新日期:1995-10-05 00:00:00

  • Two wnt genes in Caenorhabditis elegans.

    abstract::wnt genes encode secretory glycoproteins that have been implicated in growth control and development in mice, frogs and insects. In this report we examine properties of two wnt genes recently identified in the nematode Caenorhabditis elegans. The first gene, Ce-wnt-1, was previously identified by a polymerase chain re...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Shackleford GM,Shivakumar S,Shiue L,Mason J,Kenyon C,Varmus HE

    更新日期:1993-07-01 00:00:00

  • Apoptosis and melanoma chemoresistance.

    abstract::Melanoma is the most aggressive form of skin cancer and is notoriously resistant to all current modalities of cancer therapy. A large set of genetic, functional and biochemical studies suggest that melanoma cells become 'bullet proof' against a variety of chemotherapeutic drugs by exploiting their intrinsic resistance...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/sj.onc.1206454

    authors: Soengas MS,Lowe SW

    更新日期:2003-05-19 00:00:00

  • All-trans retinoic acid treatment of Wilms tumor cells reverses expression of genes associated with high risk and relapse in vivo.

    abstract::Wilms tumor is one of the most frequent neoplasias in children. Our previous microarray screening in a large series of Wilms tumors revealed several candidate genes that are deregulated in advanced tumors and are part of the retinoic acid signaling pathway. To investigate whether retinoic acid could be employed as a n...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1208725

    authors: Zirn B,Samans B,Spangenberg C,Graf N,Eilers M,Gessler M

    更新日期:2005-08-04 00:00:00

  • Identification of ribosomal protein S25 (RPS25)-MDM2-p53 regulatory feedback loop.

    abstract::There is an increasing interest in determining the role of ribosomal proteins (RPs) in the regulation of MDM2-p53 pathway in coordinating cellular response to stress. Herein, we report a novel regulatory role of ribosomal protein S25 (RPS25) in MDM2-mediated p53 degradation and a feedback regulation of S25 by p53. We ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2012.289

    authors: Zhang X,Wang W,Wang H,Wang MH,Xu W,Zhang R

    更新日期:2013-05-30 00:00:00

  • Serum induction of the fibroblast growth factor-binding protein (FGF-BP) is mediated through ERK and p38 MAP kinase activation and C/EBP-regulated transcription.

    abstract::The fibroblast growth factor-binding protein (FGF-BP) modulates FGF activity through binding and release from the extracellular matrix. Consequently, the expression of FGF-BP in certain tumor types is a rate-limiting regulator of FGF-mediated angiogenesis. FGF-BP is upregulated in squamous cell carcinoma by treatment ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204249

    authors: Harris VK,Kagan BL,Ray R,Coticchia CM,Liaudet-Coopman ED,Wellstein A,Tate Riegel A

    更新日期:2001-03-29 00:00:00

  • The E3 ubiquitin protein ligase MDM2 dictates all-trans retinoic acid-induced osteoblastic differentiation of osteosarcoma cells by modulating the degradation of RARα.

    abstract::Retinoic acid receptor alpha (RARα) has a critical role in the differentiation process of osteosarcoma cells induced by all-trans retinoic acid (ATRA). However, degradation of RARα through ubiquitin proteasome pathway weakens the differentiation efficiency of osteosarcoma cells. In this study, we discover that murine ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.503

    authors: Ying M,Zhang L,Zhou Q,Shao X,Cao J,Zhang N,Li W,Zhu H,Yang B,He Q

    更新日期:2016-08-18 00:00:00