The PGC-1/ERR signaling axis in cancer.

Abstract:

:Proliferating cells need to produce a large amount of energy and, at the same time, need to maintain a constant supply of biosynthetic precursors of macromolecules that are used as building blocks for generating new cells. Indeed, many cancer cells undergo a switch from mitochondrial to glycolytic metabolism and display a truncated tricarboxylic acid cycle to match these specific metabolic requirements of proliferation. Understanding the mechanisms by which cancer cells reprogram various metabolic pathways to satisfy their unique bioenergetic requirements has become an active field of research. Concomitantly, it has emerged that members of a family of orphan nuclear receptors known as the estrogen-related receptors (ERRs), working in concert with members of the PPARγ coactivator (PGC)-1 family, act as central transcriptional regulators of metabolic gene networks involved in maintaining energy homeostasis in normal cells. Recent studies have suggested that the PGC-1/ERR transcriptional axis is also important in the metabolic reprogramming of cancer cells. This review focuses on the functional integration of the PGC-1/ERR axis with known oncogenes and the observation that modulation of the activity of this axis can have both pro- and anti-proliferative properties.

journal_name

Oncogene

journal_title

Oncogene

authors

Deblois G,St-Pierre J,Giguère V

doi

10.1038/onc.2012.529

subject

Has Abstract

pub_date

2013-07-25 00:00:00

pages

3483-90

issue

30

eissn

0950-9232

issn

1476-5594

pii

onc2012529

journal_volume

32

pub_type

杂志文章,评审

相关文献

ONCOGENE文献大全
  • TBX3 promotes proliferation of papillary thyroid carcinoma cells through facilitating PRC2-mediated p57KIP2 repression.

    abstract::The T-box transcription factor TBX3 has been implicated in the patterning and differentiation of a number of tissues during embryonic development, and is overexpressed in a variety of cancers; however, the precise function of TBX3 in papillary thyroid carcinoma (PTC) development remains to be determined. In the curren...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-017-0090-2

    authors: Li X,Ruan X,Zhang P,Yu Y,Gao M,Yuan S,Zhao Z,Yang J,Zhao L

    更新日期:2018-05-01 00:00:00

  • MHC class I dysfunction of glioma stem cells escapes from CTL-mediated immune response via activation of Wnt/β-catenin signaling pathway.

    abstract::Glioma stem cells (GSCs) decrease T cells cognition and evade systemic immunosurveillance via downregulations or defects of major histocompatibility complex class I (MHC-I) molecule and antigen-processing machinery (APM) components. Improvement of tumor surface antigens of GSCs may be effective strategy to trigger an ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-019-1045-6

    authors: Yang W,Li Y,Gao R,Xiu Z,Sun T

    更新日期:2020-01-01 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

  • Discovery of a novel dual-target inhibitor against RSK1 and MSK2 to suppress growth of human colon cancer.

    abstract::Colon cancer is the most aggressive tumor in both men and women globally. As many the chemotherapeutic regimens have adverse side effects and contribute to the resistance and recurrence, therefore, finding novel therapeutic targets and developing effective agents are urgent. Based on the TCGA and GTEx database analysi...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-020-01467-w

    authors: Jin G,Yan M,Liu K,Yao K,Chen H,Zhang C,Yi Y,Reddy K,Gorja DR,Laster KV,Guo Z,Dong Z

    更新日期:2020-10-01 00:00:00

  • TGF-beta1 up-regulates paxillin protein expression in malignant astrocytoma cells: requirement for a fibronectin substrate.

    abstract::Cytokines can influence the interactions between members of the integrin cell adhesion receptor family and the extracellular matrix thereby potentially affecting cell function and promoting cell adhesion, growth and migration of malignant astrocytoma tumor cells. As malignant astrocytoma cells synthesize TGF-beta1 in ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204996

    authors: Han X,Stewart JE Jr,Bellis SL,Benveniste EN,Ding Q,Tachibana K,Grammer JR,Gladson CL

    更新日期:2001-11-29 00:00:00

  • GASDERMIN, suppressed frequently in gastric cancer, is a target of LMO1 in TGF-beta-dependent apoptotic signalling.

    abstract::Defining apoptosis-regulatory cascades of the epithelium is important for understanding carcinogenesis, since cancer cells are considered to arise as a result of the collapse of the cascades. We previously reported that a novel gene GASDERMIN (GSDM) is expressed in the stomach but suppressed in gastric cancer cell lin...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1210475

    authors: Saeki N,Kim DH,Usui T,Aoyagi K,Tatsuta T,Aoki K,Yanagihara K,Tamura M,Mizushima H,Sakamoto H,Ogawa K,Ohki M,Shiroishi T,Yoshida T,Sasaki H

    更新日期:2007-10-04 00:00:00

  • Identification of two translational products for c-myb.

    abstract::The c-myb gene is the normal cellular homolog of v-myb, the oncogenic component of Avian Myeloblastosis Virus (AMV). The c-myb gene has previously been shown to code for a single protein species of about 75 kd. However, accumulating evidence indicates that this gene could code for multiple mRNAs as a result of differe...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Dudek H,Reddy EP

    更新日期:1989-09-01 00:00:00

  • Apc and p53 interaction in DNA damage and genomic instability in hepatocytes.

    abstract::Disruption of Apc (adenomatous polyposis coli) within hepatocytes activates Wnt signalling, perturbs differentiation and ultimately leads to neoplasia. Apc negatively regulates Wnt signalling but is also involved in organizing the cytoskeleton and may have a role in chromosome segregation. In vitro studies have implic...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2014.342

    authors: Méniel V,Megges M,Young MA,Cole A,Sansom OJ,Clarke AR

    更新日期:2015-07-30 00:00:00

  • Differential effects of the widely expressed dMax splice variant of Max on E-box vs initiator element-mediated regulation by c-Myc.

    abstract::dMax, a naturally occurring splice variant of the Myc binding protein Max, lacks the DNA binding basic region and helix 1 of the Helix-Loop-Helix domain; dMax interacts with c-Myc in vitro and in vivo, and inhibits E-box Myc site driven transcription in transient transfection assays. Here we have investigated the expr...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202611

    authors: FitzGerald MJ,Arsura M,Bellas RE,Yang W,Wu M,Chin L,Mann KK,DePinho RA,Sonenshein GE

    更新日期:1999-04-15 00:00:00

  • ELAS1-mediated inhibition of the cyclin G1-B'γ interaction promotes cancer cell apoptosis via stabilization and activation of p53.

    abstract::Radiation therapy (RT) is useful for selectively killing cancer cells. However, because high levels of ionizing radiation (IR) are toxic to normal cells, RT cannot be applied repeatedly to cancer patients. Therefore, novel chemicals that enhance the efficacy of chemoradiotherapy (CRT) would be valuable. Here, we repor...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2015.47

    authors: Ohno S,Naito Y,Mukai S,Yabuta N,Nojima H

    更新日期:2015-12-03 00:00:00

  • A novel protein, RTN-XS, interacts with both Bcl-XL and Bcl-2 on endoplasmic reticulum and reduces their anti-apoptotic activity.

    abstract::Bcl-2 and Bcl-XL serve as critical inhibitors of apoptosis triggered by a broad range of stimuli, mainly acting on the mitochondria. We identified two members of the reticulon (RTN) family as Bcl-XL binding proteins, i.e., NSP-C (RTN1-C) and a new family member, RTN-XS, both of which did not belong to the Bcl-2 family...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203948

    authors: Tagami S,Eguchi Y,Kinoshita M,Takeda M,Tsujimoto Y

    更新日期:2000-11-23 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

  • 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

  • Over expression of endoglin in human prostate cancer suppresses cell detachment, migration and invasion.

    abstract::The regulation of cell adhesion and motility in human prostate is not well understood. We have previously shown that the endoglin gene is differently expressed during changes in prostate cell adhesion. Endoglin is a transmembrane transforming growth factor beta binding protein typically expressed by endothelial cells....

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1206117

    authors: Liu Y,Jovanovic B,Pins M,Lee C,Bergan RC

    更新日期:2002-11-28 00:00:00

  • AP-1--Introductory remarks.

    abstract::This issue attempts to give a 'state of the art' overview of the AP-1 transcription factor family, a fundamental class of transcriptional regulators. The AP-1 family consists of several bZIP (basic region leucine zipper) domain proteins, the Jun, the Fos, and the ATF subfamilies, which all have to dimerize before they...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1204416

    authors: Wagner EF

    更新日期:2001-04-30 00:00:00

  • T antigens' role in polyomavirus transformation: c-myc but not c-fos or c-jun expression is a target for middle T.

    abstract::Polyoma virus (Py) causes neoplastic transformation in vitro and multiple tumors in vivo. The role played by large and middle T antigens (LT, MT) and their mechanisms of action are focused here. Py-transformed Balb-3T3 cells become independent of platelet-derived growth factor (PDGF) for growth. JE, c-fos, c-jun and c...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Rameh LE,Armelin MC

    更新日期:1991-06-01 00:00:00

  • Opposing roles of angiomotin-like-1 and zona occludens-2 on pro-apoptotic function of YAP.

    abstract::YAP (Yes-associated protein) oncogene has been found to form a stable complex with members of the Angiomotin (Amot) family of proteins, which bind WW domains of YAP and sequester the protein in the cytoplasm and junctional complexes. The Amot-mediated retention of YAP in the cytoplasm results in the inhibition of its ...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2011.216

    authors: Oka T,Schmitt AP,Sudol M

    更新日期:2012-01-05 00:00:00

  • Aurora-A-mediated phosphorylation of LKB1 compromises LKB1/AMPK signaling axis to facilitate NSCLC growth and migration.

    abstract::Deletion or loss-of-function mutation of LKB1, frequently occurring in non-small cell lung cancers (NSCLCs), is a predominant caution of NSCLC initiation and progression. However, the upstream signaling pathways governing LKB1 activation are largely unknown. Here, we report that LKB1 undergoes Aurora kinase A (AURKA)-...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2017.354

    authors: Zheng X,Chi J,Zhi J,Zhang H,Yue D,Zhao J,Li D,Li Y,Gao M,Guo J

    更新日期:2018-01-25 00:00:00

  • Non-canonical activation of hedgehog in prostate cancer cells mediated by the interaction of transcriptionally active androgen receptor proteins with Gli3.

    abstract::Hedgehog (Hh) is an oncogenic signaling pathway that regulates the activity of Gli transcription factors. Canonical Hh is a Smoothened- (Smo-) driven process that alters the post-translational processing of Gli2/Gli3 proteins. Though evidence supports a role for Gli action in prostate cancer (PCa) cell growth and prog...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-017-0098-7

    authors: Li N,Truong S,Nouri M,Moore J,Al Nakouzi N,Lubik AA,Buttyan R

    更新日期:2018-04-01 00:00:00

  • Mechanisms involved in the activation of C/EBPα by small activating RNA in hepatocellular carcinoma.

    abstract::Hepatocellular carcinoma (HCC) is generally accompanied by high mortality and low cure rate. CCAAT enhancer-binding proteins (CEBPs) are transcriptional regulators that play a key role in maintaining liver function. Altered expression of C/EBPα and C/EBPβ occurs in many tumours including HCC. saRNAs are small double-s...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0665-6

    authors: Zhao X,Reebye V,Hitchen P,Fan J,Jiang H,Sætrom P,Rossi J,Habib NA,Huang KW

    更新日期:2019-05-01 00:00:00

  • Establishment of an inducible expression system of chimeric MLL-LTG9 protein and inhibition of Hox a7, Hox b7 and Hox c9 expression by MLL-LTG9 in 32Dcl3 cells.

    abstract::The MLL (HRX/ALL-1 gene is frequently disrupted in infantile leukemias and therapy-related leukemias and fused to various translocation partner genes. We previously showed that chimeric MLL proteins localize in the nuclei in a fashion similar to that of MLL protein even if the partner gene encodes a cytoplasmic protei...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1202400

    authors: Joh T,Hosokawa Y,Suzuki R,Takahashi T,Seto M

    更新日期:1999-01-28 00:00:00

  • CD4 and p56lck can stably associate when co-expressed in NIH3T3 cells.

    abstract::The CD4 T-cell surface antigen and the lymphocyte-specific tyrosine-protein kinase p56lck form a stable noncovalent complex in CD4+ T-lymphocytes. In this report, we demonstrate that these two gene products can also associate when co-expressed in NIH3T3 fibroblasts, therefore implying that other lymphoid specific comp...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Simpson SC,Bolen JB,Veillette A

    更新日期:1989-09-01 00:00:00

  • Retrovirus-mediated gene transfer of a human c-fos cDNA into mouse bone marrow stromal cells.

    abstract::A cDNA encoding a complete human c-fos protein was isolated and inserted into two different murine MoMuLV-derived recombinant retroviruses allowing expression of c-fos protein in different cell types. One c-fos-expressing retrovirus, chosen for its ability to express high levels of proteins in fibroblast-like cells, w...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Roux P,Verrier B,Klein B,Niccolino M,Marty L,Alexandre C,Piechaczyk M

    更新日期:1991-11-01 00:00:00

  • Search for in vivo somatic mutations in the mitotic checkpoint gene, hMAD1, in human lung cancers.

    abstract::We previously reported the presence of mitotic check-point impairment in about 40% of lung cancer cell lines. To gain an insight into the molecular basis of this impairment, we examined 49 lung cancer specimens for alterations in the hMAD1 mitotic checkpoint gene and identified a somatic, non-conservative missense mut...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1203141

    authors: Nomoto S,Haruki N,Takahashi T,Masuda A,Koshikawa T,Takahashi T,Fujii Y,Osada H,Takahashi T

    更新日期:1999-11-25 00:00:00

  • CtBP promotes metastasis of breast cancer through repressing cholesterol and activating TGF-β signaling.

    abstract::Metastasis is the process through which the primary cancer cells spread beyond the primary tumor and disseminate to other organs. Most cancer patients die of metastatic disease. EMT is proposed to be the initial event associated with cancer metastasis and how it occurred is still a mystery. CtBP is known as a co-repre...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/s41388-018-0570-z

    authors: Zhao Z,Hao D,Wang L,Li J,Meng Y,Li P,Wang Y,Zhang C,Zhou H,Gardner K,Di LJ

    更新日期:2019-03-01 00:00:00

  • Selective loss of endogenous p21waf1/cip1 induction underlies the G1 checkpoint defect of monomeric p53 proteins.

    abstract::Wild-type p53 protein displays a spectrum of activities including the ability to suppress transformed cell growth to direct apoptotic cell death and to mediate G1 checkpoint in response to cellular DNA damage. Earlier work showed that a self-association defective p53 protein retained transformation suppressor activity...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Tarunina M,Grimaldi M,Ruaro E,Pavlenko M,Schneider C,Jenkins JR

    更新日期:1996-08-01 00:00:00

  • Rad54 and Mus81 cooperation promotes DNA damage repair and restrains chromosome missegregation.

    abstract::Rad54 and Mus81 mammalian proteins physically interact and are important for the homologous recombination DNA repair pathway; however, their functional interactions in vivo are poorly defined. Here, we show that combinatorial loss of Rad54 and Mus81 results in hypersensitivity to DNA-damaging agents, defects on both t...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/onc.2016.16

    authors: Ghamrasni SE,Cardoso R,Li L,Guturi KK,Bjerregaard VA,Liu Y,Venkatesan S,Hande MP,Henderson JT,Sanchez O,Hickson ID,Hakem A,Hakem R

    更新日期:2016-09-15 00:00:00

  • Regulation of TRAIL-induced apoptosis by XIAP in pancreatic carcinoma cells.

    abstract::Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a promising candidate for cancer therapy because of its relative tumor selectivity. However, many cancers including pancreatic cancer remain resistant towards TRAIL. To develop TRAIL for cancer therapy of pancreatic carcinoma, it will therefore b...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:10.1038/sj.onc.1209776

    authors: Vogler M,Dürr K,Jovanovic M,Debatin KM,Fulda S

    更新日期:2007-01-11 00:00:00

  • Analysis of mammalian fibroblast transformation by normal and mutated human EGF receptors.

    abstract::Activation of the EGF receptor (c-erbB) tyrosine kinase has been implicated in tumorigenesis, either by overexpression of the normal receptor in the presence of EGF, or through expression of a truncated receptor lacking the EGF binding domain as in the viral oncogene v-erbB. Here, normal and truncated human EGF recept...

    journal_title:Oncogene

    pub_type: 杂志文章

    doi:

    authors: Haley JD,Hsuan JJ,Waterfield MD

    更新日期:1989-03-01 00:00:00

  • How do glycolytic enzymes favour cancer cell proliferation by nonmetabolic functions?

    abstract::Cancer cells enhance their glycolysis, producing lactate, even in the presence of oxygen. Glycolysis is a series of ten metabolic reactions catalysed by enzymes whose expression is most often increased in tumour cells. HKII and phosphoglucose isomerase (PGI) have mainly an antiapoptotic effect; PGI and glyceraldehyde-...

    journal_title:Oncogene

    pub_type: 杂志文章,评审

    doi:10.1038/onc.2014.320

    authors: Lincet H,Icard P

    更新日期:2015-07-01 00:00:00