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Erschienen in: Journal of Neuro-Oncology 1/2010

01.05.2010 | Clinical Study - Patient Study

Clinical and biological significance of forkhead class box O 3a expression in glioma: mediation of glioma malignancy by transcriptional regulation of p27kip1

verfasst von: Jinlong Shi, Li Zhang, Aiguo Shen, Jianguo Zhang, Yuchan Wang, Yueming Zhao, Lin Zou, Qing Ke, Fei He, Ping Wang, Chun Cheng, Gongshen Shi

Erschienen in: Journal of Neuro-Oncology | Ausgabe 1/2010

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Abstract

Forkhead box class O 3a (FOXO3a) is an important direct target of the phosphatidylinositol 3-kinase (PI3K)/protein B(Akt) pathway, mediating signal transduction in regulating cell survival and cell-cycle progression. Recent reports have shown that FOXO3a inhibits cell-cycle progression at the G1/S transition by controlling transcription of the cyclin-dependent kinase inhibitor p27kip1, which is frequently down-regulated in human cancers, including human glioma. In this study we investigated the status of FOXO3a expression and related signaling in human glioma in order to test its potential value as a therapeutic target for this disease. Immunohistochemistry, western blot, RT-PCR, and immunofluorescence staining analysis were performed on specimens from 70 cases of human glioma and on U87MG and T98G glioma cells. Our data showed FOXO3a expression is directly correlated with the malignant grade of glioma. More importantly, low expression of FOXO3a was associated with poor patient outcome. In vitro, FOXO3a modulated the cell cycle by transcriptional regulation of p27kip1. Administration of the PI3K pharmacological inhibitor LY294002 abrogated this effect by regulating FOXO3a expression and subcellular localization. Our results suggested that FOXO3a may be a favorable independent prognostic indicator of glioma. Gene therapeutic approaches aimed at PI3K or at pharmacological inhibitors of PI3K to down-regulate P-FOXO3a expression could be developed for management of glioma.
Literatur
1.
Zurück zum Zitat Jemal A, Murray T, Ward E, Samuels A, Tiwari RC et al (2005) Cancer statistics. CA Cancer J Clin 55:10–30CrossRefPubMed Jemal A, Murray T, Ward E, Samuels A, Tiwari RC et al (2005) Cancer statistics. CA Cancer J Clin 55:10–30CrossRefPubMed
2.
Zurück zum Zitat Surawicz TS, Davis F, Freels S et al (1998) Brain tumor survival: results from the national cancer data base. J Neurooncol 40:151–160CrossRefPubMed Surawicz TS, Davis F, Freels S et al (1998) Brain tumor survival: results from the national cancer data base. J Neurooncol 40:151–160CrossRefPubMed
3.
Zurück zum Zitat Das A, Banik NL, Patel SJ, Ray SK (2004) Dexamethasone protected human glioblastoma U87MG cells from temozolomide induced apoptosis by maintaining Bax: Bcl-2 ratio and preventing proteolytic activities. Mol Cancer 3:36CrossRefPubMed Das A, Banik NL, Patel SJ, Ray SK (2004) Dexamethasone protected human glioblastoma U87MG cells from temozolomide induced apoptosis by maintaining Bax: Bcl-2 ratio and preventing proteolytic activities. Mol Cancer 3:36CrossRefPubMed
4.
Zurück zum Zitat Choi JW, Lee MM, Kim IA, Kim JH et al (2008) The outcomes of concomitant chemoradiotherapy followed by adjuvant chemotherapy with temozolomide for newly diagnosed high grade gliomas: the preliminary results of single center prospective study. J Korean Neurosurg Soc 44:222–227CrossRefPubMed Choi JW, Lee MM, Kim IA, Kim JH et al (2008) The outcomes of concomitant chemoradiotherapy followed by adjuvant chemotherapy with temozolomide for newly diagnosed high grade gliomas: the preliminary results of single center prospective study. J Korean Neurosurg Soc 44:222–227CrossRefPubMed
5.
Zurück zum Zitat Accili D, Arden KC (2004) FoxOs at the crossroads of cellular metabolism, differentiation, and transformation. Cell 117:421–426CrossRefPubMed Accili D, Arden KC (2004) FoxOs at the crossroads of cellular metabolism, differentiation, and transformation. Cell 117:421–426CrossRefPubMed
6.
Zurück zum Zitat Burgering BM, Kops GJ (2002) Cell cycle and death control: long live forkheads. Trends Biochem Sci 27:352–360CrossRefPubMed Burgering BM, Kops GJ (2002) Cell cycle and death control: long live forkheads. Trends Biochem Sci 27:352–360CrossRefPubMed
7.
Zurück zum Zitat Tran H, Brunet A, Griffith EC, Greenberg ME (2003) The many forks in FOXO’s road. Sci STKE 2003: RE5 Tran H, Brunet A, Griffith EC, Greenberg ME (2003) The many forks in FOXO’s road. Sci STKE 2003: RE5
8.
Zurück zum Zitat Van Der Heide LP, Hoekman MF, Smidt MP (2004) The ins and outs of FoxO shuttling: mechanisms of FoxO translocation and transcriptional regulation. Biochem J 380:297–309CrossRef Van Der Heide LP, Hoekman MF, Smidt MP (2004) The ins and outs of FoxO shuttling: mechanisms of FoxO translocation and transcriptional regulation. Biochem J 380:297–309CrossRef
9.
Zurück zum Zitat Brunet A, Bonni A, Zigmond MJ et al (1999) Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor. Cell 96:857–868CrossRefPubMed Brunet A, Bonni A, Zigmond MJ et al (1999) Akt promotes cell survival by phosphorylating and inhibiting a forkhead transcription factor. Cell 96:857–868CrossRefPubMed
10.
Zurück zum Zitat Polyak K, Lee MH, Erdjument-Bromage H et al (1994) Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals. Cell 78:59–66CrossRefPubMed Polyak K, Lee MH, Erdjument-Bromage H et al (1994) Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals. Cell 78:59–66CrossRefPubMed
11.
Zurück zum Zitat Toyoshima H, Hunter T (1994) p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21. Cell 78:67–74CrossRefPubMed Toyoshima H, Hunter T (1994) p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21. Cell 78:67–74CrossRefPubMed
12.
Zurück zum Zitat Kirla RM, Haapasalo HK, Kalimo H, Salminen EK (2003) Low expression of p27 indicates a poor prognosis in patients with high-grade astrocytomas. Cancer 97:644–648CrossRefPubMed Kirla RM, Haapasalo HK, Kalimo H, Salminen EK (2003) Low expression of p27 indicates a poor prognosis in patients with high-grade astrocytomas. Cancer 97:644–648CrossRefPubMed
13.
Zurück zum Zitat Choe G, Horvath S, Cloughesy TF, Crosby K et al (2003) Analysis of the phosphatidylinositol 3′-kinase signaling pathway in glioblastoma patients in vivo. Cancer Res 63:2742–2746PubMed Choe G, Horvath S, Cloughesy TF, Crosby K et al (2003) Analysis of the phosphatidylinositol 3′-kinase signaling pathway in glioblastoma patients in vivo. Cancer Res 63:2742–2746PubMed
14.
Zurück zum Zitat Dijkers PF, Medema RH, Pals C, Banerji L et al (2000) Forkhead transcription factor FKHR-L1 modulates cytokine-dependent transcriptional regulation of p27(KIP1). Mol Cell Biol 20:9138–9148CrossRefPubMed Dijkers PF, Medema RH, Pals C, Banerji L et al (2000) Forkhead transcription factor FKHR-L1 modulates cytokine-dependent transcriptional regulation of p27(KIP1). Mol Cell Biol 20:9138–9148CrossRefPubMed
15.
Zurück zum Zitat Nakamura N, Ramaswamy S, Vazquez F et al (2000) Forkhead transcription factors are critical effectors of cell death and cell cycle arrest downstream of PTEN. Mol Cell Biol 20:8969–8982CrossRefPubMed Nakamura N, Ramaswamy S, Vazquez F et al (2000) Forkhead transcription factors are critical effectors of cell death and cell cycle arrest downstream of PTEN. Mol Cell Biol 20:8969–8982CrossRefPubMed
16.
Zurück zum Zitat Stahl M, Dijkers PF, Kops GJ, Lens SM (2002) The forkhead transcription factor FoxO regulates transcription of p27Kip1 and Bim in response to IL-2. J Immunol 168:5024–5031PubMed Stahl M, Dijkers PF, Kops GJ, Lens SM (2002) The forkhead transcription factor FoxO regulates transcription of p27Kip1 and Bim in response to IL-2. J Immunol 168:5024–5031PubMed
17.
Zurück zum Zitat Medema RH, Kops GJ, Bos JL, Burgering BM (2000) AFX-like forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1. Nature 404:782–787CrossRefPubMed Medema RH, Kops GJ, Bos JL, Burgering BM (2000) AFX-like forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1. Nature 404:782–787CrossRefPubMed
18.
Zurück zum Zitat Vogt PK, Bader AG, Kang S (2006) PI 3-kinases: hidden potentials revealed. Cell Cycle 5:946–949PubMed Vogt PK, Bader AG, Kang S (2006) PI 3-kinases: hidden potentials revealed. Cell Cycle 5:946–949PubMed
19.
Zurück zum Zitat Zhao JJ, Roberts TM (2006) PI3 kinases in cancer: from oncogene artifact to leading cancer target. Sci STKE 2006: pe52 Zhao JJ, Roberts TM (2006) PI3 kinases in cancer: from oncogene artifact to leading cancer target. Sci STKE 2006: pe52
20.
Zurück zum Zitat Engelman JA, Luo J, Cantley LC (2006) The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet 7:606–619CrossRefPubMed Engelman JA, Luo J, Cantley LC (2006) The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet 7:606–619CrossRefPubMed
21.
Zurück zum Zitat Lam EW, Francis RE, Petkovic M (2006) FOXO transcription factors: key regulators of cell fate. Biochem Soc Trans 34:722–726CrossRefPubMed Lam EW, Francis RE, Petkovic M (2006) FOXO transcription factors: key regulators of cell fate. Biochem Soc Trans 34:722–726CrossRefPubMed
22.
Zurück zum Zitat Kennedy SG, Wagner AJ, Conzen SD et al (1997) The PI 3-kinase/Akt signaling pathway delivers an anti-apoptotic signal. Genes Dev 11:701–713CrossRefPubMed Kennedy SG, Wagner AJ, Conzen SD et al (1997) The PI 3-kinase/Akt signaling pathway delivers an anti-apoptotic signal. Genes Dev 11:701–713CrossRefPubMed
23.
Zurück zum Zitat Songyang Z, Baltimore D, Cantley LC et al (1997) Interleukin 3-dependent survival by the Akt protein kinase. Proc Natl Acad Sci USA 94:11345–11350CrossRefPubMed Songyang Z, Baltimore D, Cantley LC et al (1997) Interleukin 3-dependent survival by the Akt protein kinase. Proc Natl Acad Sci USA 94:11345–11350CrossRefPubMed
24.
Zurück zum Zitat Downward J (1998) Mechanisms and consequences of activation of protein kinase B/Akt. Curr Opin Cell Biol 10:262–267CrossRefPubMed Downward J (1998) Mechanisms and consequences of activation of protein kinase B/Akt. Curr Opin Cell Biol 10:262–267CrossRefPubMed
25.
Zurück zum Zitat Reed SI (1997) Control of the G1/S transition. Cancer Surv 29:7–23PubMed Reed SI (1997) Control of the G1/S transition. Cancer Surv 29:7–23PubMed
26.
Zurück zum Zitat Lloyd RV, Erickson LA, Jin L et al (1999) p27kip1: a multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers. Am J Pathol 154:313–323PubMed Lloyd RV, Erickson LA, Jin L et al (1999) p27kip1: a multifunctional cyclin-dependent kinase inhibitor with prognostic significance in human cancers. Am J Pathol 154:313–323PubMed
27.
Zurück zum Zitat Kops GJ, Burgering BM (1999) Forkhead transcription factors: new insights into protein kinase B (c-akt) signaling. J Mol Med 77:656–665CrossRefPubMed Kops GJ, Burgering BM (1999) Forkhead transcription factors: new insights into protein kinase B (c-akt) signaling. J Mol Med 77:656–665CrossRefPubMed
28.
Zurück zum Zitat Carlsson P, Mahlapuu M (2002) Forkhead transcription factors: key players in development and metabolism. Dev Biol 250:1–23CrossRefPubMed Carlsson P, Mahlapuu M (2002) Forkhead transcription factors: key players in development and metabolism. Dev Biol 250:1–23CrossRefPubMed
29.
Zurück zum Zitat Lehmann OJ, Sowden JC, Carlsson P et al (2003) Fox’s in development and disease. Trends Genet 19:339–344CrossRefPubMed Lehmann OJ, Sowden JC, Carlsson P et al (2003) Fox’s in development and disease. Trends Genet 19:339–344CrossRefPubMed
30.
Zurück zum Zitat Hu MC, Lee DF, Xia W, Golfman LS et al (2004) IkappaB kinase promotes tumorigenesis through inhibition of forkhead FOXO3a. Cell 117:225–237CrossRefPubMed Hu MC, Lee DF, Xia W, Golfman LS et al (2004) IkappaB kinase promotes tumorigenesis through inhibition of forkhead FOXO3a. Cell 117:225–237CrossRefPubMed
31.
Zurück zum Zitat Burgering BM, Medema RH (2003) Decisions on life and death: FOXO forkhead transcription factors are in command when PKB/Akt is off duty. J Leukoc Biol 73:689–701CrossRefPubMed Burgering BM, Medema RH (2003) Decisions on life and death: FOXO forkhead transcription factors are in command when PKB/Akt is off duty. J Leukoc Biol 73:689–701CrossRefPubMed
32.
Zurück zum Zitat Plas DR, Thompson CB (2003) Akt activation promotes degradation of tuberin and FOXO3a via the proteasome. J Biol Chem 278:12361–12366CrossRefPubMed Plas DR, Thompson CB (2003) Akt activation promotes degradation of tuberin and FOXO3a via the proteasome. J Biol Chem 278:12361–12366CrossRefPubMed
33.
Zurück zum Zitat Yang L, Xie S, Jamaluddin MS, Altuwaijri S et al (2005) Induction of androgen receptor expression by phosphatidylinositol 3-kinase/Akt downstream substrate, FOXO3a, and their roles in apoptosis of LNCaP prostate cancer cells. J Biol Chem 280:33558–33565CrossRefPubMed Yang L, Xie S, Jamaluddin MS, Altuwaijri S et al (2005) Induction of androgen receptor expression by phosphatidylinositol 3-kinase/Akt downstream substrate, FOXO3a, and their roles in apoptosis of LNCaP prostate cancer cells. J Biol Chem 280:33558–33565CrossRefPubMed
34.
Zurück zum Zitat Nam S, Smith DM, Dou QP (2001) Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo. J Biol Chem 276:13322–13330CrossRefPubMed Nam S, Smith DM, Dou QP (2001) Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo. J Biol Chem 276:13322–13330CrossRefPubMed
35.
Zurück zum Zitat Essafi A, Fernandez de Mattos S et al (2005) Direct transcriptional regulation of Bim by FoxO3a mediates STI571-induced apoptosis in Bcr-Abl-expressing cells. Oncogene 24:2317–2329CrossRefPubMed Essafi A, Fernandez de Mattos S et al (2005) Direct transcriptional regulation of Bim by FoxO3a mediates STI571-induced apoptosis in Bcr-Abl-expressing cells. Oncogene 24:2317–2329CrossRefPubMed
36.
Zurück zum Zitat Fernandez de Mattos S, Essafi A, Soeiro I et al (2004) FoxO3a and BCR-ABL regulate cyclin D2 transcription through a STAT5/BCL6-dependent mechanism. Mol Cell Biol 24:10058–10071CrossRefPubMed Fernandez de Mattos S, Essafi A, Soeiro I et al (2004) FoxO3a and BCR-ABL regulate cyclin D2 transcription through a STAT5/BCL6-dependent mechanism. Mol Cell Biol 24:10058–10071CrossRefPubMed
37.
Zurück zum Zitat Alexia C, Bras M, Fallot G, Vadrot N et al (2006) Pleiotropic effects of PI-3′ kinase/Akt signaling in human hepatoma cell proliferation and drug-induced apoptosis. Ann NY Acad Sci 1090:1–17CrossRefPubMed Alexia C, Bras M, Fallot G, Vadrot N et al (2006) Pleiotropic effects of PI-3′ kinase/Akt signaling in human hepatoma cell proliferation and drug-induced apoptosis. Ann NY Acad Sci 1090:1–17CrossRefPubMed
38.
Zurück zum Zitat Jin S, Pang RP, Shen JN, Huang G, Wang J, Zhou JG (2007) Grifolin induces apoptosis via inhibition of PI3K/AKT signalling pathway in human osteosarcoma cells. Apoptosis 12:1317–1326CrossRefPubMed Jin S, Pang RP, Shen JN, Huang G, Wang J, Zhou JG (2007) Grifolin induces apoptosis via inhibition of PI3K/AKT signalling pathway in human osteosarcoma cells. Apoptosis 12:1317–1326CrossRefPubMed
39.
Metadaten
Titel
Clinical and biological significance of forkhead class box O 3a expression in glioma: mediation of glioma malignancy by transcriptional regulation of p27kip1
verfasst von
Jinlong Shi
Li Zhang
Aiguo Shen
Jianguo Zhang
Yuchan Wang
Yueming Zhao
Lin Zou
Qing Ke
Fei He
Ping Wang
Chun Cheng
Gongshen Shi
Publikationsdatum
01.05.2010
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 1/2010
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-009-0045-8

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