دورية أكاديمية

INPP4B is an oncogenic regulator in human colon cancer.

التفاصيل البيبلوغرافية
العنوان: INPP4B is an oncogenic regulator in human colon cancer.
المؤلفون: Guo ST; Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Shanxi, China., Chi MN; School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia., Yang RH; Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Shanxi, China., Guo XY; Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Shanxi, China., Zan LK; Department of Pathology, Shanxi Cancer Hospital and Institute, Shanxi, China., Wang CY; Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Shanxi, China., Xi YF; Department of Pathology, Shanxi Cancer Hospital and Institute, Shanxi, China., Jin L; School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia., Croft A; Department of Medical Oncology, Calvary Mater Newcastle Hospital, Newcastle, New South Wales, Australia., Tseng HY; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia., Yan XG; School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia., Farrelly M; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia., Wang FH; Department of Molecular Biology, Shanxi Cancer Hospital and Institute, Affiliated Hospital of Shanxi Medical University, Shanxi, China., Lai F; School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia., Wang JF; Department of Pathology, Shanxi Cancer Hospital and Institute, Shanxi, China., Li YP; Department of Colorectal Surgery, Shanxi Cancer Hospital and Institute, Shanxi, China., Ackland S; Department of Medical Oncology, Calvary Mater Newcastle Hospital, Newcastle, New South Wales, Australia., Scott R; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia., Agoulnik IU; Department of Cellular Biology and Pharmacology, Herbert Wertheim College of Medicine, Miami, FL, USA., Hondermarck H; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia., Thorne RF; School of Environmental and Life Sciences, University of Newcastle, Callaghan, New South Wales, Australia., Liu T; Children's Cancer Institute Australia for Medical Research, University of New South Wales, Sydney, New South Wales, Australia., Zhang XD; School of Biomedical Sciences and Pharmacy, University of Newcastle, Newcastle, New South Wales, Australia., Jiang CC; School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.
المصدر: Oncogene [Oncogene] 2016 Jun 09; Vol. 35 (23), pp. 3049-61. Date of Electronic Publication: 2015 Sep 28.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8711562 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5594 (Electronic) Linking ISSN: 09509232 NLM ISO Abbreviation: Oncogene Subsets: MEDLINE
أسماء مطبوعة: Publication: <2002->: Basingstoke : Nature Publishing Group
Original Publication: Basingstoke, Hampshire, UK : Scientific & Medical Division, MacMillan Press, c1987-
مواضيع طبية MeSH: Colonic Neoplasms/*genetics , Phosphoric Monoester Hydrolases/*genetics, Cell Line, Tumor ; Cell Proliferation/genetics ; Colonic Neoplasms/metabolism ; Colonic Neoplasms/pathology ; Humans ; Immunohistochemistry ; Phosphoric Monoester Hydrolases/metabolism
مستخلص: Inositol polyphosphate 4-phosphatase type II (INPP4B) negatively regulates phosphatidylinositol 3-kinase signaling and is a tumor suppressor in some types of cancers. However, we have found that it is frequently upregulated in human colon cancer cells. Here we show that silencing of INPP4B blocks activation of Akt and serum- and glucocorticoid-regulated kinase 3 (SGK3), inhibits colon cancer cell proliferation and retards colon cancer xenograft growth. Conversely, overexpression of INPP4B increases proliferation and triggers anchorage-independent growth of normal colon epithelial cells. Moreover, we demonstrate that the effect of INPP4B on Akt and SGK3 is associated with inactivation of phosphate and tensin homolog through its protein phosphatase activity and that the increase in INPP4B is due to Ets-1-mediated transcriptional upregulation in colon cancer cells. Collectively, these results suggest that INPP4B may function as an oncogenic driver in colon cancer, with potential implications for targeting INPP4B as a novel approach to treat this disease.
References: Am J Surg. 2008 Jun;195(6):719-25. (PMID: 18440486)
J Cell Sci. 2008 Dec 15;121(Pt 24):4124-33. (PMID: 19033389)
J Biol Chem. 2002 Mar 15;277(11):9027-35. (PMID: 11781306)
J Biol Chem. 2002 Feb 22;277(8):6266-72. (PMID: 11706019)
Breast Cancer Res. 2012 Sep 12;14(5):R125. (PMID: 22971289)
Cell Cycle. 2003 Jul-Aug;2(4):339-45. (PMID: 12851486)
Biochem J. 2013 Jun 15;452(3):e11-3. (PMID: 23725458)
Nat Rev Clin Oncol. 2010 Jul;7(7):367-80. (PMID: 20551944)
FEBS Lett. 2000 Jun 23;475(3):213-7. (PMID: 10869559)
Science. 1997 Jan 31;275(5300):665-8. (PMID: 9005852)
Oncogene. 2013 Apr 11;32(15):1910-20. (PMID: 22710713)
J Clin Oncol. 2010 Feb 20;28(6):1075-83. (PMID: 20085938)
Blood. 2009 Nov 26;114(23):4897-906. (PMID: 19789387)
Mod Pathol. 2001 May;14(5):415-22. (PMID: 11353051)
Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):15840-5. (PMID: 21896753)
J Clin Oncol. 2006 Sep 10;24(26):4340-6. (PMID: 16908931)
Anticancer Res. 2002 May-Jun;22(3):1581-4. (PMID: 12168840)
Mol Cell. 2014 Nov 20;56(4):595-607. (PMID: 25458846)
Blood. 2015 Apr 30;125(18):2815-24. (PMID: 25736313)
Cancer Cell. 2009 Aug 4;16(2):115-25. (PMID: 19647222)
Biochem Biophys Res Commun. 2013 Oct 18;440(2):277-82. (PMID: 24070612)
Science. 1996 Nov 8;274(5289):998-1001. (PMID: 8875945)
Cell Signal. 2008 Apr;20(4):684-94. (PMID: 18249092)
Cancer Res. 2011 Feb 1;71(3):629-33. (PMID: 21266353)
Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22231-6. (PMID: 21127264)
Nat Commun. 2013;4:1508. (PMID: 23443536)
J Biol Chem. 2001 Feb 16;276(7):4781-7. (PMID: 11087761)
Nature. 2006 May 11;441(7090):227-30. (PMID: 16688177)
Oncogene. 2001 Jul 5;20(30):3949-58. (PMID: 11494123)
J Biol Chem. 1999 Apr 16;274(16):10669-72. (PMID: 10196133)
J Virol. 1998 Nov;72(11):8463-71. (PMID: 9765382)
Growth Factors. 2010 Dec;28(6):394-408. (PMID: 20919962)
Mol Biol Cell. 2006 Feb;17 (2):607-22. (PMID: 16280363)
Leukemia. 2015 Jul;29(7):1485-95. (PMID: 25736236)
Cancer Res. 2011 Jan 15;71(2):572-82. (PMID: 21224358)
Trends Biochem Sci. 2014 Apr;39(4):183-90. (PMID: 24656806)
Science. 1997 Nov 21;278(5342):1481,1483. (PMID: 9411767)
Cancer Res. 2015 Apr 1;75(7):1399-412. (PMID: 25712345)
معلومات مُعتمدة: R15 CA179287 United States CA NCI NIH HHS
المشرفين على المادة: EC 3.1.3.2 (Phosphoric Monoester Hydrolases)
EC 3.1.3.66 (phosphatidylinositol-3,4-bisphosphate 4-phosphatase)
تواريخ الأحداث: Date Created: 20150929 Date Completed: 20170925 Latest Revision: 20181113
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC4908438
DOI: 10.1038/onc.2015.361
PMID: 26411369
قاعدة البيانات: MEDLINE
الوصف
تدمد:1476-5594
DOI:10.1038/onc.2015.361