The role of TXNDC5 in castration-resistant prostate cancer-involvement of androgen receptor signaling pathway.

Abstract:

:Castration-resistant prostate cancer (CRPC) continues to be a major clinical problem and the mechanisms behind it remain unclear. Thioredoxin domain-containing protein 5 (TXNDC5) is involved in protein folding and chaperone activity, and its overexpression has been reported in multiple malignancies. In the current study, we demonstrated that TXNDC5 is up-regulated following long-term androgen-deprivation treatment (ADT) and is highly overexpressed in CRPC tumors compared with hormone-naive prostate cancer (PCa) cases. Functionally, in vitro and in vivo studies demonstrated that TXNDC5 overexpression promotes the growth of both androgen-dependent and castration-resistant PCa xenografts. Mechanistically, TXNDC5 directly interacts with the AR protein to increase its stability and thus enhances its transcriptional activity. TXDNC5-mediated CRPC growth can be fully abolished by AR inhibition, suggesting TXDNC5 up-regulation as an escape pathway for aberrant AR re-activation and CRPC growth in the milieu of low androgen. Indeed, we found that TXNDC5 is increased by ADT-induced hypoxia through HIF-1α in an miR-200b-dependent manner. Overall, we defined an important role of TXNDC5 in CRPC and further investigations are needed to screen TXNDC5 antagonists as a novel therapeutic approaches to treat PCa patients with CRPC.

journal_name

Oncogene

journal_title

Oncogene

authors

Wang L,Song G,Chang X,Tan W,Pan J,Zhu X,Liu Z,Qi M,Yu J,Han B

doi

10.1038/onc.2014.401

subject

Has Abstract

pub_date

2015-09-03 00:00:00

pages

4735-45

issue

36

eissn

0950-9232

issn

1476-5594

pii

onc2014401

journal_volume

34

pub_type

杂志文章

相关文献

ONCOGENE文献大全
  • Dysregulation of BMI1 and microRNA-16 collaborate to enhance an anti-apoptotic potential in the side population of refractory mantle cell lymphoma.

    abstract::The proto-oncogene BMI1 and its product, Bmi1, is overexpressed in various types of tumors, particularly in aggressive tumors and tumors resistant to conventional chemotherapy. BMI1/Bmi1 is also crucially involved in cancer-initiating cell maintenance, and is recurrently upregulated in mantle cell lymphoma (MCL), espe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.177

    authors: Teshima K,Nara M,Watanabe A,Ito M,Ikeda S,Hatano Y,Oshima K,Seto M,Sawada K,Tagawa H

    更新日期:2014-04-24 00:00:00

  • Loss of IGFBP7 expression and persistent AKT activation contribute to SMARCB1/Snf5-mediated tumorigenesis.

    abstract::SMARCB1 (Snf5/Ini1/Baf47) is a potent tumor suppressor, the loss of which serves as the diagnostic feature in malignant rhabdoid tumors (MRT) and atypical teratoid/rhabdoid tumors (AT/RT), two highly aggressive forms of pediatric neoplasms. SMARCB1 is a core subunit of Swi/Snf chromatin remodeling complexes, and loss ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2013.261

    authors: Darr J,Klochendler A,Isaac S,Eden A

    更新日期:2014-06-05 00:00:00

  • Utilizing somatic mutation data from numerous studies for cancer research: proof of concept and applications.

    abstract::Large cancer projects measure somatic mutations in thousands of samples, gradually assembling a catalog of recurring mutations in cancer. Many methods analyze these data jointly with auxiliary information with the aim of identifying subtype-specific results. Here, we show that somatic gene mutations alone can reliably...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2016.489

    authors: Amar D,Izraeli S,Shamir R

    更新日期:2017-06-15 00:00:00

  • Correction: FGFR1-ERK1/2-SOX2 axis promotes cell proliferation, epithelial-mesenchymal transition, and metastasis in FGFR1-amplified lung cancer.

    abstract::An amendment to this paper has been published and can be accessed via a link at the top of the paper. ...

    journal_title:Oncogene

    pub_type: 已发布勘误

    doi:10.1038/s41388-020-01441-6

    authors: Wang K,Ji W,Yu Y,Li Z,Niu X,Xia W,Lu S

    更新日期:2020-10-01 00:00:00

  • MKL1 potentiates lung cancer cell migration and invasion by epigenetically activating MMP9 transcription.

    abstract::Malignant tumors are exemplified by excessive proliferation and aggressive migration/invasion contributing to increased mortality of cancer patients. Matrix metalloproteinase 9 (MMP9) expression is positively correlated with lung cancer malignancy. The mechanism underlying an elevated MMP9 expression is not clearly de...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.14

    authors: Cheng X,Yang Y,Fan Z,Yu L,Bai H,Zhou B,Wu X,Xu H,Fang M,Shen A,Chen Q,Xu Y

    更新日期:2015-10-29 00:00:00

  • Adenosine A1 receptor, a target and regulator of estrogen receptoralpha action, mediates the proliferative effects of estradiol in breast cancer.

    abstract::Estrogen receptor-alpha (ERalpha) and its ligand estradiol (E2) has critical roles in breast cancer growth and are key therapeutic targets. In this study, we report a novel dual role of the adenosine A1 receptor (Adora1) as an E2/ERalpha target and a regulator of ERalpha transcriptional activity. In ERalpha-positive b...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2009.409

    authors: Lin Z,Yin P,Reierstad S,O'Halloran M,Coon VJ,Pearson EK,Mutlu GM,Bulun SE

    更新日期:2010-02-25 00:00:00

  • Polymorphism of the human c-abl gene: relation to incidence and course of chronic myelogenous leukemia.

    abstract::Abnormalities in structure and expression of the proto-oncogene c-abl have been implicated in the genesis of chronic myelogenous leukemia (CML). We studied leukemic cell DNA from 42 CML patients for evidence of rearrangement and/or amplification of c-abl analogous to that described in the CML cell line K562. Using the...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Daniel L,Ahmed CM,Bloodgood RS,Kidd JR,Castiglione CM,Duttagupta S,Lebowitz P

    更新日期:1987-05-01 00:00:00

  • Nrh, a human homologue of Nr-13 associates with Bcl-Xs and is an inhibitor of apoptosis.

    abstract::In search of human homologues of the anti-apoptotic protein Nr-13, we have characterized a human EST clone that potentially encodes a protein, which is the closest homologue of Nr-13 among the Bcl-2 family members, to date known, in humans. Phylogenetic analyses suggest Human nrh, Mouse diva/boo and Quail nr-13 to be ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204740

    authors: Aouacheria A,Arnaud E,Venet S,Lalle P,Gouy M,Rigal D,Gillet G

    更新日期:2001-09-13 00:00:00

  • Characterization of p53 oligomerization domain mutations isolated from Li-Fraumeni and Li-Fraumeni like family members.

    abstract::p53 is a tumour suppressor gene which functions as a transcription factor to upregulate genes for growth arrest and apoptosis following DNA damage. p53 mutations are associated with Li-Fraumeni and Li-Fraumeni like syndromes. Recently mutations of the oligomerization domain have been isolated from an LFS and an LFL fa...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201974

    authors: Lomax ME,Barnes DM,Hupp TR,Picksley SM,Camplejohn RS

    更新日期:1998-08-06 00:00:00

  • Interferon-gamma suppresses transforming growth factor-beta-induced invasion of gastric carcinoma cells through cross-talk of Smad pathway in a three-dimensional culture model.

    abstract::We reconstituted a three-dimensional gastric carcinoma model similar to invasive gastric carcinoma tissue. This model consists of a human gastric carcinoma cell line, GCTM-1, a human fibroblast cell line, TIG-1-20, and transforming growth factor-beta (TGF-beta)-containing type I collagen gel. Using this model, we were...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1207046

    authors: Kuga H,Morisaki T,Nakamura K,Onishi H,Noshiro H,Uchiyama A,Tanaka M,Katano M

    更新日期:2003-10-30 00:00:00

  • In vitro differentiation of epithelial cells from cervical neoplasias resembles in vivo lesions.

    abstract::Cell lines derived from cervical neoplasias, as well as cells from normal cervix and neonatal foreskin were examined in an in vitro culture system (raft system) that allows for stratification and differentiation of epithelial cells at an air-liquid interface. Epithelial cells from human foreskin and ectocervix were ob...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Rader JS,Golub TR,Hudson JB,Patel D,Bedell MA,Laimins LA

    更新日期:1990-04-01 00:00:00

  • The E5 protein of BPV-4 interacts with the heavy chain of MHC class I and irreversibly retains the MHC complex in the Golgi apparatus.

    abstract::BPV-4 E5 inhibits transcription of the bovine MHC class I heavy chain (HC) gene, increases degradation of HC and downregulates surface expression of MHC class I by retaining the complex in the Golgi apparatus (GA). Here we report that transcription inhibition can be alleviated by interferon treatment and the degradati...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209245

    authors: Marchetti B,Ashrafi GH,Dornan ES,Araibi EH,Ellis SA,Campo MS

    更新日期:2006-04-06 00:00:00

  • DNA binding and selective gene induction by different forms of the p53 protein.

    abstract::P53 is a tumor suppressor gene that plays a crucial role in suppressing tumorigenesis by inducing either cell cycle arrest or apoptosis in cells with DNA damage. In more than 50% of tumors p53 is inactivated by gene mutations. However, there have also been reports of tumor cells in which p53 remains wild type and is p...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210110

    authors: Mayelzadeh F,Martinez JD

    更新日期:2007-05-10 00:00:00

  • Nuclear DLC1 exerts oncogenic function through association with FOXK1 for cooperative activation of MMP9 expression in melanoma.

    abstract::A Rho GTPase-activating protein (RhoGAP), deleted in liver cancer 1 (DLC1), is known to function as a tumor suppressor in various cancer types; however, whether DLC1 is a tumor-suppressor gene or an oncogene in melanoma remains to be clarified. Here we revealed that high DLC1 expression was detected in most of the mel...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-1274-8

    authors: Yang X,Hu F,Liu JA,Yu S,Cheung MPL,Liu X,Ng IO,Guan XY,Wong KKW,Sharma R,Lung HL,Jiao Y,Lee LTO,Cheung M

    更新日期:2020-05-01 00:00:00

  • Murine WNT11 is a secreted glycoprotein that morphologically transforms mammary epithelial cells.

    abstract::Wnt genes encode a set of structurally related cell surface glycoproteins that appear to have roles in cell-cell signalling. The ectopic expression of several murine Wnt genes has been implicated in the transformation of mammary epithelial and the onset of mammary tumours. Wnt11 is expressed in the developing embryo i...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Christiansen JH,Monkley SJ,Wainwright BJ

    更新日期:1996-06-20 00:00:00

  • The lncRNA BORG facilitates the survival and chemoresistance of triple-negative breast cancers.

    abstract::Disseminated breast cancer cells employ adaptive molecular responses following cytotoxic therapeutic insult which promotes their survival and subsequent outgrowth. Here we demonstrate that expression of the pro-metastatic lncRNA BORG (BMP/OP-Responsive Gene) is greatly induced within triple-negative breast cancer (TNB...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0586-4

    authors: Gooding AJ,Zhang B,Gunawardane L,Beard A,Valadkhan S,Schiemann WP

    更新日期:2019-03-01 00:00:00

  • Platelet-activating factor activates mitogen-activated protein kinases, inhibits proliferation, induces differentiation and suppresses the malignant phenotype of human colon carcinoma cells.

    abstract::Recent studies suggest that the action of platelet-activating factor (PAF), a potent phospholipid modulator of allergic and inflammatory reactions, is diverse and functions as a modulator of a variety of physiological and pathological events in many cell types and tissues. Its role (if any) in modulating the prolifera...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206348

    authors: Wang H,Chakrabarty S

    更新日期:2003-04-10 00:00:00

  • Mouse Sin3A interacts with and can functionally substitute for the amino-terminal repression of the Myc antagonist Mxi1.

    abstract::Mxi1 is a basic region helix-loop-helix leucine zipper (bHLH/LZ) protein that, in association with Max, antagonizes Myc oncogenic activities. A possible mechanistic basis for Mxi1-mediated repression was provided by the recent demonstration that the repressive potential of Mxi1 correlates with its ability to physicall...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Rao G,Alland L,Guida P,Schreiber-Agus N,Chen K,Chin L,Rochelle JM,Seldin MF,Skoultchi AI,DePinho RA

    更新日期:1996-03-07 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

  • Triggering of p73-dependent apoptosis in osteosarcoma is under the control of E2Fs-pRb2/p130 complexes.

    abstract::Mechanisms underlying multidrug resistance (MDR), one of the major causes of cancer treatment failure, are still poorly understood. We selected the osteosarcoma MDR HosDXR150 cell line by culturing Hos cells in the presence of increasing doxorubicin doses and showed that it is crossresistant to vinblastine. Similarly ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206487

    authors: La Sala D,Macaluso M,Trimarchi C,Giordano A,Cinti C

    更新日期:2003-06-05 00:00:00

  • miR-34a functions as a tumor suppressor modulating EGFR in glioblastoma multiforme.

    abstract::Chromosome 1p36.23 is frequently deleted in glioblastoma multiforme (GBM). miR-34a localizes in this region. Our experiments found that miR-34a was often deleted and epidermal growth factor receptor (EGFR) was frequently amplified in genomic DNA of 55 GBMs using single-nucleotide polymorphism DNA microarray. Notably, ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2012.132

    authors: Yin D,Ogawa S,Kawamata N,Leiter A,Ham M,Li D,Doan NB,Said JW,Black KL,Phillip Koeffler H

    更新日期:2013-02-28 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

  • Effects of methylation on expression of TMS1/ASC in human breast cancer cells.

    abstract::Gene silencing associated with aberrant methylation of promoter region CpG islands is one mechanism in which tumor suppressor genes are inactivated in human cancers. Recently, we identified a novel gene, Target of Methylation-associated Silencing-1 (TMS1) (also called ASC), which is aberrantly methylated and silenced ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206430

    authors: Levine JJ,Stimson-Crider KM,Vertino PM

    更新日期:2003-05-29 00:00:00

  • ETO-2, a new member of the ETO-family of nuclear proteins.

    abstract::The t(8;21) is associated with 12-15% of acute myelogenous leukemias of the M2 subtype. The translocation results in the fusion of two genes, AML1 (CBFA2) on chromosome 21 and ETO (MTG8) on chromosome 8. AML1 encodes a DNA binding factor; the ETO protein product is less well characterized, but is thought to be a trans...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202412

    authors: Davis JN,Williams BJ,Herron JT,Galiano FJ,Meyers S

    更新日期:1999-02-11 00:00:00

  • Characterization of the mouse Ron/Stk receptor tyrosine kinase gene.

    abstract::In an effort to understand the mechanisms governing the regulation of the mouse Ron receptor gene, a mouse genomic library was screened and overlapping clones coding for the Ron gene and flanking DNA were identified. Continuous DNA sequence was obtained for approximately 16.4 kilobases. The gene, from the initiator me...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1201508

    authors: Waltz SE,Toms CL,McDowell SA,Clay LA,Muraoka RS,Air EL,Sun WY,Thomas MB,Degen SJ

    更新日期:1998-01-08 00:00:00

  • Cytoplasmic localization of NPM in myeloid leukemias is dictated by gain-of-function mutations that create a functional nuclear export signal.

    abstract::Nucleophosmin (NPM) is a nucleus-cytoplasmic shuttling protein that is implicated in centrosome duplication, cell cycle progression and stress response. At the steady state, NPM localizes mainly in the nucleolus, where it forms a complex with different cellular proteins. One-third of acute myeloid leukemias (AML) are ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209453

    authors: Mariano AR,Colombo E,Luzi L,Martinelli P,Volorio S,Bernard L,Meani N,Bergomas R,Alcalay M,Pelicci PG

    更新日期:2006-07-20 00:00:00

  • Inhibition of AP-1 transcription factor causes blockade of multiple signal transduction pathways and inhibits breast cancer growth.

    abstract::AP-1 transcription factors play a critical role in signal transduction pathways in many cells. We have investigated the role of AP-1 in controlling proliferative signals in breast cells, and have previously shown that AP-1 complexes are activated by peptide and steroid growth factors in both normal and malignant breas...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1205883

    authors: Liu Y,Ludes-Meyers J,Zhang Y,Munoz-Medellin D,Kim HT,Lu C,Ge G,Schiff R,Hilsenbeck SG,Osborne CK,Brown PH

    更新日期:2002-10-31 00:00:00

  • Neurotrophin-induced melanoma cell migration is mediated through the actin-bundling protein fascin.

    abstract::Expression of the p75 neurotrophin receptor (p75(NTR)) in primary melanomas is associated with deeply invasive lesions. In turn, there is expression of high levels of neurotrophins at the invasion front of normal tissue adjacent to brain metastases, thus implicating this growth factor-receptor system in melanoma tumor...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206561

    authors: Shonukan O,Bagayogo I,McCrea P,Chao M,Hempstead B

    更新日期:2003-06-05 00:00:00

  • CD44 cleavage induced by a membrane-associated metalloprotease plays a critical role in tumor cell migration.

    abstract::CD44 is a cell surface receptor for hyaluronate, a component of the extracellular matrix (ECM). Although CD44 has been implicated in tumor invasion and metastasis, the molecular mechanisms remain to be elucidated. Here we find that CD44 expressed in cancer cells is cleaved at the membrane-proximal region of the ectodo...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202447

    authors: Okamoto I,Kawano Y,Tsuiki H,Sasaki J,Nakao M,Matsumoto M,Suga M,Ando M,Nakajima M,Saya H

    更新日期:1999-02-18 00:00:00

  • Mel-CAM-specific genetic suppressor elements inhibit melanoma growth and invasion through loss of gap junctional communication.

    abstract::Normal human melanocytes are interspersed singly among keratinocytes along the basement membrane of the epidermis, whereas melanoma cells readily adhere to each other during invasion of the dermis or distant organs. The tumorigenic and metastatic phenotype of melanoma cells often correlates with increased expression o...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204616

    authors: Satyamoorthy K,Muyrers J,Meier F,Patel D,Herlyn M

    更新日期:2001-08-02 00:00:00