Upregulation of sestrin 2 expression via JNK pathway activation contributes to autophagy induction in cancer cells.

Abstract:

:JNK signaling functions to induce defense mechanisms that protect organisms against a variety of different situations. The sestrin 2 gene, a p53-regulated member of the sestrins family, which lead to AMPK-dependent inhibition of TOR signaling, emerges as a novel player in autophagy induction. However, the relationship between JNK pathway, autophagy induction and sestrin 2 expression remains elusive. In the present study, we identify JNK as a regulator of autophagy in nasopharyngeal carcinoma cell lines CNE1 and CNE2 exposed to excisanin A or serum deprivation and demonstrate that activation of JNK can cause upregulation of sestrin 2 expression, which could be blocked by specific siRNAs directed against JNK1/2 or c-Jun. Chromatin immunoprecipitation and luciferase reporter analysis revealed that c-Jun was transcriptionally involved in the regulation of sestrin 2. Furthermore, knockdown of sestrin 2 by siRNAs similarly inhibited autophagy induction. Moreover, silencing the expression of autophagy related gene ATG5 or sestrin 2 significantly decreases cell death induced by excisanin A. Our results therefore identify JNK as a novel mediator of sestrin 2 expression, which plays a key role in autophagy induction following anticancer therapies in cancers.

journal_name

Cell Signal

journal_title

Cellular signalling

authors

Zhang XY,Wu XQ,Deng R,Sun T,Feng GK,Zhu XF

doi

10.1016/j.cellsig.2012.09.004

subject

Has Abstract

pub_date

2013-01-01 00:00:00

pages

150-8

issue

1

eissn

0898-6568

issn

1873-3913

pii

S0898-6568(12)00246-X

journal_volume

25

pub_type

杂志文章
  • JIP4 is a PLK1 binding protein that regulates p38MAPK activity in G2 phase.

    abstract::Cell cycle progression from G2 phase into mitosis is regulated by a complex network of mechanisms, all of which finally control the timing of Cyclin B/CDK1 activation. PLK1 regulates a network of events that contribute to regulating G2/M phase progression. Here we have used a proteomics approach to identify proteins t...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2015.08.009

    authors: Pinder A,Loo D,Harrington B,Oakes V,Hill MM,Gabrielli B

    更新日期:2015-11-01 00:00:00

  • The effect of oxidized low density lipoprotein (oxLDL)-induced heme oxygenase-1 on LPS-induced inflammation in RAW 264.7 macrophage cells.

    abstract::Macrophages take up oxidized low density lipoprotein (oxLDL) after being exposed to it in the blood vessels. oxLDL transforms macrophages into foam cells, which are a hallmark of atherosclerosis. The effects that oxLDL have on the inflammatory responses of foam cells are not clear. Here, we investigated how oxLDL modu...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2012.02.001

    authors: Min KJ,Cho KH,Kwon TK

    更新日期:2012-06-01 00:00:00

  • Both EGFR kinase and Src-related tyrosine kinases regulate human ether-à-go-go-related gene potassium channels.

    abstract::Human ether-à-go-go-related gene (hERG or Kv11.1) encodes the rapidly activated delayed rectifier K(+) current (I(Kr)) in the human heart. Potential regulation of hERG channel by protein tyrosine kinases (PTKs) is not understood. The present study was designed to investigate whether this channel is modulated by PTKs u...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2008.06.006

    authors: Zhang DY,Wang Y,Lau CP,Tse HF,Li GR

    更新日期:2008-10-01 00:00:00

  • Structural determinants governing β-arrestin2 interaction with PDZ proteins and recruitment to CRFR1.

    abstract::β-Arrestins are multifunctional adaptor proteins best know for their vital role in regulating G protein coupled receptor (GPCR) trafficking and signaling. β-arrestin2 recruitment and receptor internalization of corticotropin-releasing factor receptor 1 (CRFR1), a GPCR whose antagonists have been shown to demonstrate b...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2019.109361

    authors: Gupta S,Abd-Elrahman KS,Albaker A,Dunn HA,Ferguson SSG

    更新日期:2019-11-01 00:00:00

  • Involvement of proteinase-activated receptor-2 in mast cell tryptase-induced barrier dysfunction in bovine aortic endothelial cells.

    abstract::We report here a direct modulation by mast cell tryptase of endothelial barrier function through activation of proteinase-activated receptor-2 (PAR-2). In cultured bovine aortic endothelial cells (BAECs), tryptase, trypsin and PAR-2 activating peptide impaired the barrier function as determined by the permeability of ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(03)00014-7

    authors: Sendo T,Sumimura T,Itoh Y,Goromaru T,Aki K,Yano T,Oike M,Ito Y,Mori S,Nishibori M,Oishi R

    更新日期:2003-08-01 00:00:00

  • Downstream signalling events regulated by phosphatidylinositol 3-kinase activity.

    abstract::The phosphatidylinositol (PI) 3-kinase family of enzymes is now known to be regulated by several different upstream pathways in response to virtually all growth factors and cytokines. In the past few years, the phosphoinositides phosphorylated at the 3-OH position of the inositol ring have been shown to be lipid secon...

    journal_title:Cellular signalling

    pub_type: 杂志文章,评审

    doi:10.1016/s0898-6568(97)00129-0

    authors: Duronio V,Scheid MP,Ettinger S

    更新日期:1998-04-01 00:00:00

  • Angiotensin II induces nephrin dephosphorylation and podocyte injury: role of caveolin-1.

    abstract::Nephrin, an important structural and signal molecule of podocyte slit-diaphragm (SD), has been suggested to contribute to the angiotensin II (Ang II)-induced podocyte injury. Caveolin-1 has been demonstrated to play a crucial role in signaling transduction. In the present study, we evaluated the role of caveolin-1 in ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2011.09.022

    authors: Ren Z,Liang W,Chen C,Yang H,Singhal PC,Ding G

    更新日期:2012-02-01 00:00:00

  • Reduced phosphorylation of Stat3 at Ser-727 mediated by casein kinase 2 - protein phosphatase 2A enhances Stat3 Tyr-705 induced tumorigenic potential of glioma cells.

    abstract::Signal transducer and activator of transcription 3 (Stat3) is a transcription factor that is involved in cell survival and proliferation and has been found to be persistently activated in most human cancers mainly through its phosphorylation at Tyr-705. However, the role and regulation of Stat3 Ser-727 phosphorylation...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2014.04.003

    authors: Mandal T,Bhowmik A,Chatterjee A,Chatterjee U,Chatterjee S,Ghosh MK

    更新日期:2014-08-01 00:00:00

  • The monoamine oxidase-A inhibitor clorgyline promotes a mesenchymal-to-epithelial transition in the MDA-MB-231 breast cancer cell line.

    abstract::Monoamine oxidase-A (MAO-A) dysfunction has been historically associated with depression. Recently, depression as well as altered MAO-A expression have both been associated with a poor prognosis in cancers, although the mechanism involved remains ambiguous. For example, MAO-A mRNA is repressed across cancers, yet MAO-...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2014.08.005

    authors: Satram-Maharaj T,Nyarko JN,Kuski K,Fehr K,Pennington PR,Truitt L,Freywald A,Lukong KE,Anderson DH,Mousseau DD

    更新日期:2014-12-01 00:00:00

  • LncRNA TP73-AS1/miR-539/MMP-8 axis modulates M2 macrophage polarization in hepatocellular carcinoma via TGF-β1 signaling.

    abstract:PURPOSE:Our study aimed to study the role of lncRNA TP73-AS1/miR-539/MMP-8 axis in modulating M2 macrophage polarization in hepatocellular carcinoma (HCC). METHODS:The gene expression levels of TP73-AS1, miR-539 and MMP-8 were modified by transfection with the overexpression or knockdown vectors. The patient survival ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2020.109738

    authors: Chen J,Huang ZB,Liao CJ,Hu XW,Li SL,Qi M,Fan XG,Huang Y

    更新日期:2020-11-01 00:00:00

  • Leptin upregulates VEGF in breast cancer via canonic and non-canonical signalling pathways and NFkappaB/HIF-1alpha activation.

    abstract::High levels of VEGF and leptin are strongly linked to worse prognosis of breast cancer. Leptin signalling upregulates VEGF in human and mouse mammary tumor cells (MT), but the specific molecular mechanisms are largely unknown. Pharmacologic and genetic approaches were used to dissect the mechanism of leptin regulation...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2010.05.003

    authors: Gonzalez-Perez RR,Xu Y,Guo S,Watters A,Zhou W,Leibovich SJ

    更新日期:2010-09-01 00:00:00

  • In addition to the SH3 binding region, multiple regions within the N-terminal noncatalytic portion of the cAMP-specific phosphodiesterase, PDE4A5, contribute to its intracellular targeting.

    abstract::The long cyclic AMP (cAMP)-specific phosphodiesterase isoform, PDE4A5 (PDE4A subfamily isoform variant 5), when transiently expressed in COS-7 cells, was shown in subcellular fractionation studies to be associated with both membrane and cytosol fractions, with immunofluorescence analyses identifying PDE4A5 as associat...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(01)00264-9

    authors: Beard MB,Huston E,Campbell L,Gall I,McPhee I,Yarwood S,Scotland G,Houslay MD

    更新日期:2002-05-01 00:00:00

  • Protein kinase C-alpha and -beta play antagonistic roles in the differentiation process of THP-1 cells.

    abstract::The roles of protein kinase C (PKC) isoenzymes in the differentiation process of THP-1 cells are investigated. Inhibition of PKC by RO 31-8220 reduces the phagocytosis of latex particles and the release of superoxide, prostaglandin E(2) (PGE(2)), and tumour necrosis factor (TNF)-alpha. The proliferation of THP-1 cells...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(00)00069-3

    authors: Dieter P,Schwende H

    更新日期:2000-05-01 00:00:00

  • Differential effect of TPA on PGE2 and cicaprost-induced cAMP synthesis in UMR-106 cells.

    abstract::PGE2 and prostacyclin each enhance cAMP synthesis in the osteoblast-like cell line UMR-106. The amount of cAMP induced by PGE2 was 5-7-fold greater than the amount induced by cicaprost or iloprost, stable prostacyclin analogues. Both PGE2 and the two prostacyclin analogues enhanced cAMP synthesis with similar time dep...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(98)00052-7

    authors: Khanin M,Liel Y,Rimon G

    更新日期:1999-03-01 00:00:00

  • A novel role for TPX2 as a scaffold and co-activator protein of the Chromosomal Passenger Complex.

    abstract::Aurora B kinase forms the enzymatic core of the Chromosomal Passenger Complex (CPC) and is a master regulator of mitosis. Understanding the regulation of Aurora B is critical to illuminate its role in mitosis. INCENP, Survivin and Borealin have all been known to promote Aurora B activation. In this study, we have iden...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2012.04.014

    authors: Iyer J,Tsai MY

    更新日期:2012-08-01 00:00:00

  • cGMP-dependent protein kinase anchoring by IRAG regulates its nuclear translocation and transcriptional activity.

    abstract::Type I cGMP-dependent protein kinases (PKGs) translocate to the nucleus to regulate gene expression in some, but not all cell types; we hypothesized that nuclear translocation of PKG may be regulated by extra-nuclear anchoring proteins. The inositol 1,4,5-triphosphate (IP(3)) receptor-associated cGMP kinase substrate ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2008.03.009

    authors: Casteel DE,Zhang T,Zhuang S,Pilz RB

    更新日期:2008-07-01 00:00:00

  • Starvation of a clonal osteoblast-like cell line, MOB 3-4-F2, down-regulates prostaglandin E2 receptors but increases cAMP response to prostaglandin E2.

    abstract::Prostaglandin E2 (PGE2) stimulated cAMP production in the MOB 3-4-F2 cell line, a subclone of the osteoblast-like MOB 3-4 cell line. After being cultured in alpha-minimum essential medium supplemented with 10% heat-inactivated foetal calf serum (HIFCS), cells responded to PGE2 (greater than or equal to 50 ng/ml) with ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(91)90022-m

    authors: Kawase T,Orikasa M,Suzuki A

    更新日期:1991-01-01 00:00:00

  • Differential regulation and role of interleukin-1 receptor associated kinase-M in innate immunity signaling.

    abstract::Toll-like-receptor mediated signaling is finely regulated by a complex intracellular protein network including the interleukin-1 receptor associate kinases (IRAKs). IRAK-4, 1, and 2 may positively regulate innate immunity signaling through the activation of various downstream kinases such as MAPKs. In contrast, IRAK-M...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2007.02.009

    authors: Su J,Xie Q,Wilson I,Li L

    更新日期:2007-07-01 00:00:00

  • Identification of a basolateral sorting signal within the cytoplasmic domain of the interleukin-6 signal transducer gp130.

    abstract::Interleukin-6-type cytokine receptors are expressed in polarized cells such as hepatocytes and intestinal cells. For the interleukin-6-receptor gp80 and its signal transducer gp130, a preferential basolateral localization was demonstrated in Madin-Darby canine kidney (MDCK) cells and two basolateral sorting signals we...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2005.09.006

    authors: Doumanov JA,Daubrawa M,Unden H,Graeve L

    更新日期:2006-08-01 00:00:00

  • Redox control of p53 in the transcriptional regulation of TGF-β1 target genes through SMAD cooperativity.

    abstract::Transforming growth factor-β1 (TGF-β1) regulates the tissue response to injury and is the principal driver of excessive scarring leading to fibrosis and eventual organ failure. The TGF-β1 effectors SMAD3 and p53 are major contributors to disease progression. While SMAD3 is an established pro-fibrotic factor, the role ...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2014.02.017

    authors: Overstreet JM,Samarakoon R,Meldrum KK,Higgins PJ

    更新日期:2014-07-01 00:00:00

  • Molecular insights into connective tissue growth factor action in rat pancreatic stellate cells.

    abstract::Pancreatic fibrosis, a key feature of chronic pancreatitis and pancreatic cancer, is mediated by activated pancreatic stellate cells (PSC). Connective tissue growth factor (CTGF) has been suggested to play a major role in fibrogenesis by enhancing PSC activation after binding to alpha5beta1 integrin. Here, we have foc...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2008.06.016

    authors: Karger A,Fitzner B,Brock P,Sparmann G,Emmrich J,Liebe S,Jaster R

    更新日期:2008-10-01 00:00:00

  • Prostaglandin E2 can bimodally inhibit and stimulate the epididymal adipocyte adenylyl cyclase activity.

    abstract::Measurements of prostaglandin E2 (PGE2)-induced adenylyl cyclase activity in membranes isolated from epididymal rat adipocytes revealed inhibition of cAMP production at low concentrations of PGE2 (less than 10 mM) and stimulation at higher concentrations. This biphasic effect of PGE2 was obtained when adenylyl cyclase...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(92)90073-h

    authors: Cohen-Luria R,Rimon G

    更新日期:1992-05-01 00:00:00

  • Effects of retinoic acid on signalling by prostaglandin E2 in osteoblast-like cells.

    abstract::We investigated the effects of retinoic acid (RA) on the signalling pathways by prostaglandin E2 (PGE2) in osteoblast-like MC3T3-E1 cells. The pretreatment with RA significantly inhibited the formation of inositol phosphates induced by 10 microM PGE2 in a dose-dependent manner in the range between 0.1 nM and 0.1 micro...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(93)90080-6

    authors: Kotoyori J,Tokuda H,Oiso Y,Kozawa O

    更新日期:1993-07-01 00:00:00

  • Cycloheximide-induced cPLA(2) activation is via the MKP-1 down-regulation and ERK activation.

    abstract::Extracellular signal-regulated kinase (ERK)-dependent phosphorylation is an important regulator for cytosolic phospholipase A(2) (cPLA(2)). In this study, we found that the protein synthesis inhibitor cycloheximide can potentiate thapsigargin-induced arachidonic acid (AA) release concomitant with ERK phosphorylation f...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/s0898-6568(00)00090-5

    authors: Lin WW,Hsu YW

    更新日期:2000-07-01 00:00:00

  • A small molecule PAI-1 functional inhibitor attenuates neointimal hyperplasia and vascular smooth muscle cell survival by promoting PAI-1 cleavage.

    abstract::Plasminogen activator inhibitor-1 (PAI-1), the primary inhibitor of urokinase-and tissue-type plasminogen activators (uPA and tPA), is an injury-response gene implicated in the development of tissue fibrosis and cardiovascular disease. PAI-1 mRNA and protein levels were elevated in the balloon catheter-injured carotid...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2015.01.009

    authors: Simone TM,Higgins SP,Archambeault J,Higgins CE,Ginnan RG,Singer H,Higgins PJ

    更新日期:2015-05-01 00:00:00

  • Phosphorylation of serine 323 of ASB2α is pivotal for the targeting of filamin A to degradation.

    abstract::ASB proteins are the specificity subunits of cullin5-RING E3 ubiquitin ligases (CRL5) that play roles in ubiquitin-mediated protein degradation. However, how their activity is regulated remains poorly understood. Here, we unravel a novel mechanism of regulation of a CRL5 through phosphorylation of its specificity subu...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2013.09.011

    authors: Zakaria R,Lamsoul I,Uttenweiler-Joseph S,Erard M,Monsarrat B,Burlet-Schiltz O,Moog-Lutz C,Lutz PG

    更新日期:2013-12-01 00:00:00

  • p130Cas: a key signalling node in health and disease.

    abstract::p130Cas/breast cancer anti-oestrogen resistance 1 (BCAR1) is a member of the Cas (Crk-associated substrate) family of adaptor proteins, which have emerged as key signalling nodes capable of interactions with multiple proteins, with important regulatory roles in normal and pathological cell function. The Cas family of ...

    journal_title:Cellular signalling

    pub_type: 杂志文章,评审

    doi:10.1016/j.cellsig.2012.12.019

    authors: Barrett A,Pellet-Many C,Zachary IC,Evans IM,Frankel P

    更新日期:2013-04-01 00:00:00

  • Cyclic AMP modulates interleukin-1 action in a cytotoxic T-cell hybridoma.

    abstract::The induction of cytolytic activity in PC60, a murine T-cell hybridoma, is paralleled by a rise in the level of BLT-esterase (N-alpha-benzyloxycarbonyl-L-lysine thiobenzyl esterase), a serine esterase specific for activated T-cells. Both interleukin-1 (IL-1) and dibutyryl cAMP were albe to increase the esterase activi...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/0898-6568(90)90045-c

    authors: Schlegel-Haueter SE,Aebischer F

    更新日期:1990-01-01 00:00:00

  • Regulation of innate immune response by MAP kinase phosphatase-1.

    abstract::Mitogen-activated protein (MAP) kinase cascades are signal transduction pathways that play pivotal regulatory roles in the biosynthesis of pro-inflammatory cytokines. MAP kinase phosphatase (MKP)-1, an archetypal member of the MKP family, is essential for the dephosphorylation/deactivation of MAP kinases p38 and JNK. ...

    journal_title:Cellular signalling

    pub_type: 杂志文章,评审

    doi:10.1016/j.cellsig.2007.03.013

    authors: Wang X,Liu Y

    更新日期:2007-07-01 00:00:00

  • Role of CYP3A4 in the regulation of the aryl hydrocarbon receptor by omeprazole sulphide.

    abstract::Cross-talk between nuclear receptors involved in the control of drug metabolism is being increasingly recognised as a source of drug side effects. Omeprazole is a well known activator of the aryl hydrocarbon receptor (AhR). We investigated the regulation of AhR by omeprazole-sulphide, a degradation metabolite of omepr...

    journal_title:Cellular signalling

    pub_type: 杂志文章

    doi:10.1016/j.cellsig.2005.07.007

    authors: Gerbal-Chaloin S,Pichard-Garcia L,Fabre JM,Sa-Cunha A,Poellinger L,Maurel P,Daujat-Chavanieu M

    更新日期:2006-05-01 00:00:00