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Erschienen in: Pathology & Oncology Research 3/2017

20.10.2016 | Original Article

Strong Correlation between the Expression Levels of HDAC4 and SIRT6 in Hematological Malignancies of the Adults

verfasst von: Zsuzsanna Gaál, Éva Oláh, László Rejtő, Ferenc Erdődi, László Csernoch

Erschienen in: Pathology & Oncology Research | Ausgabe 3/2017

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Abstract

Histone deacetylase enzymes, confirmed to have important role in the pathogenesis of leukemia, are promising targets of epigenetic treatment. However, in acute myeloid leukemia, our knowledge on their expression levels is limited, and controversial data have been published about their potential oncogenic or tumorsuppressor properties in solid tumors. In our study, the expression levels of HDAC4 and SIRT6 were evaluated via Western blot analysis in 45 bone marrow samples (2 uninfiltrated and 43 concerned by different kinds of hematological malignancies), including 32 specimens obtained from patients with newly diagnosed AML. Significantly higher HDAC4 level was detected in case of FLT3-ITD mutation compared to the group of patients without carrying this mutation (p < 0.05). Compared to the non-infiltrated samples, the expression level of HDAC4 in AML M5 patients has been proved to be significantly higher (p < 0.05). Decreasing expression levels of both HDAC4 and SIRT6 were observed during the induction treatment of FAB M5 type AML. Strong correlation has been proved between the expression levels of HDAC4 and SIRT6 (r = 0.722 in full cohort and r = 0.794 in AML), that confirms the recently suggested cooperation between NAD+-independent and NAD+-dependent HDAC enzymes in leukemia.
Literatur
1.
Zurück zum Zitat Haberland M, Montgomery RL, Olson EN (2009) The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat Rev Genet 10:32–42CrossRefPubMedPubMedCentral Haberland M, Montgomery RL, Olson EN (2009) The many roles of histone deacetylases in development and physiology: implications for disease and therapy. Nat Rev Genet 10:32–42CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Linggi BE, Brandt SJ, Sun ZW, Hiebert SW (2005) Translating the histone code into leukemia. J Cell Biochem 96(5):938–950CrossRefPubMed Linggi BE, Brandt SJ, Sun ZW, Hiebert SW (2005) Translating the histone code into leukemia. J Cell Biochem 96(5):938–950CrossRefPubMed
3.
Zurück zum Zitat Delcuve GP, Khan DH, Davie JR (2012) Roles of histone deacetylases in epigenetic regulation: emerging paradigms from studies with inhibitors. Clin Epigenetics 4(1):5CrossRefPubMedPubMedCentral Delcuve GP, Khan DH, Davie JR (2012) Roles of histone deacetylases in epigenetic regulation: emerging paradigms from studies with inhibitors. Clin Epigenetics 4(1):5CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat de Ruijter AJ, van Gennip AH, Caron HN, Kemp S, van Kuilenburg AB (2003) Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J 370(Pt3):737–749CrossRefPubMedPubMedCentral de Ruijter AJ, van Gennip AH, Caron HN, Kemp S, van Kuilenburg AB (2003) Histone deacetylases (HDACs): characterization of the classical HDAC family. Biochem J 370(Pt3):737–749CrossRefPubMedPubMedCentral
5.
Zurück zum Zitat Marks PA (2010) Histone deacetylase inhibitors: a chemical genetics approach to understanding cellular functions. Biochim Biophys Acta 1799(10–12):717–725CrossRefPubMedPubMedCentral Marks PA (2010) Histone deacetylase inhibitors: a chemical genetics approach to understanding cellular functions. Biochim Biophys Acta 1799(10–12):717–725CrossRefPubMedPubMedCentral
6.
Zurück zum Zitat Yang XJ, Seto E (2008) The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men. Nat Rev Mol Cell Biol 9(3):206–218CrossRefPubMedPubMedCentral Yang XJ, Seto E (2008) The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men. Nat Rev Mol Cell Biol 9(3):206–218CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Verdin E, Dequiedt F, Kasler HG (2003) Class II histone deacetylases: versatile regulators. Trends Genet 19(5):286–293CrossRefPubMed Verdin E, Dequiedt F, Kasler HG (2003) Class II histone deacetylases: versatile regulators. Trends Genet 19(5):286–293CrossRefPubMed
8.
10.
Zurück zum Zitat Saunders LR, Verdin E (2007) Sirtuins: critical regulators at the crossroads between cancer and aging. Oncogene 26(37):5489–5504CrossRefPubMed Saunders LR, Verdin E (2007) Sirtuins: critical regulators at the crossroads between cancer and aging. Oncogene 26(37):5489–5504CrossRefPubMed
11.
Zurück zum Zitat Liu H, Hu Q, D'Ercole AJ, Ye P (2009) Histone deacetylase regulates 11. Oligodendrocyte-specific gene expression and cell development in OL-1 oligodendroglia cells. Glia 57(1):1–12CrossRefPubMedPubMedCentral Liu H, Hu Q, D'Ercole AJ, Ye P (2009) Histone deacetylase regulates 11. Oligodendrocyte-specific gene expression and cell development in OL-1 oligodendroglia cells. Glia 57(1):1–12CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Villagra A, Cheng F, Wang HW, Suarez I, Glozak M, Maurin M et al (2009) The histone deacetylase HDAC11 regulates the expression of interleukin 10 and immune tolerance. Nat Immunol 10(1):92–100CrossRefPubMed Villagra A, Cheng F, Wang HW, Suarez I, Glozak M, Maurin M et al (2009) The histone deacetylase HDAC11 regulates the expression of interleukin 10 and immune tolerance. Nat Immunol 10(1):92–100CrossRefPubMed
13.
Zurück zum Zitat Smith KT, Workman JL (2009) Histone deacetylase inhibitors: anticancer compounds. Int J Biochem Cell Biol 41(1):21–25CrossRefPubMed Smith KT, Workman JL (2009) Histone deacetylase inhibitors: anticancer compounds. Int J Biochem Cell Biol 41(1):21–25CrossRefPubMed
14.
Zurück zum Zitat Bantscheff M, Hopf C, Savitski MM, Dittmann A, Grandi P, Michon AM (2011) Chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes. Nat Biotechnol 29(3):255–265CrossRefPubMed Bantscheff M, Hopf C, Savitski MM, Dittmann A, Grandi P, Michon AM (2011) Chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes. Nat Biotechnol 29(3):255–265CrossRefPubMed
15.
Zurück zum Zitat Khan O, La Thangue NB (2012) HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications. Immunol Cell Biol 90(1):85–94CrossRefPubMed Khan O, La Thangue NB (2012) HDAC inhibitors in cancer biology: emerging mechanisms and clinical applications. Immunol Cell Biol 90(1):85–94CrossRefPubMed
16.
Zurück zum Zitat Witt O, Deubzer HE, Milde T, Oehme I (2009) HDAC family: what are the cancer relevant targets? Cancer Lett 277(1):8–21CrossRefPubMed Witt O, Deubzer HE, Milde T, Oehme I (2009) HDAC family: what are the cancer relevant targets? Cancer Lett 277(1):8–21CrossRefPubMed
17.
Zurück zum Zitat Tabe Y, Jin L, Contractor R, Gold D, Ruvolo P, Radke S et al (2007) Novel role of HDAC inhibitors in AML1/ETO AML cells: activation of apoptosis and phagocytosis through induction of annexin A1. Cell Death Differ 14(8):1443–1456CrossRefPubMed Tabe Y, Jin L, Contractor R, Gold D, Ruvolo P, Radke S et al (2007) Novel role of HDAC inhibitors in AML1/ETO AML cells: activation of apoptosis and phagocytosis through induction of annexin A1. Cell Death Differ 14(8):1443–1456CrossRefPubMed
18.
Zurück zum Zitat Holmlund T, Lindberg MJ, Grander D, Wallberg AE (2013) GCN5 acetylates and regulates the stability of the oncoprotein E2A-PBX1 in acute lymphoblastic leukemia. Leukemia 27(3):578–585CrossRefPubMed Holmlund T, Lindberg MJ, Grander D, Wallberg AE (2013) GCN5 acetylates and regulates the stability of the oncoprotein E2A-PBX1 in acute lymphoblastic leukemia. Leukemia 27(3):578–585CrossRefPubMed
19.
Zurück zum Zitat Di Croce L (2005) Chromatin modifying activity of leukemia associated fusion proteins. Hum Mol Genet 14(Review Issue 1):R77–R84CrossRefPubMed Di Croce L (2005) Chromatin modifying activity of leukemia associated fusion proteins. Hum Mol Genet 14(Review Issue 1):R77–R84CrossRefPubMed
20.
Zurück zum Zitat Hackanson B, Rimmele L, Benkißer M, Abdelkarim M, Fliegauf M, Jung M et al (2012) HDAC6 as a target for antileukemic drugs in acute myeloid leukemia. Leuk Res 36(8):1055–1062CrossRefPubMed Hackanson B, Rimmele L, Benkißer M, Abdelkarim M, Fliegauf M, Jung M et al (2012) HDAC6 as a target for antileukemic drugs in acute myeloid leukemia. Leuk Res 36(8):1055–1062CrossRefPubMed
21.
Zurück zum Zitat Novotny-Diermayr V, Hart S, Goh KC, Cheong A, Ong LC, Hentze H et al (2012) The oral HDAC inhibitor pracinostat (SB939) is efficacious and synergistic with the JAK2 inhibitor pacritinib(SB1518) in preclinical models of AML. Blood Cancer J 2(5):e69CrossRefPubMedPubMedCentral Novotny-Diermayr V, Hart S, Goh KC, Cheong A, Ong LC, Hentze H et al (2012) The oral HDAC inhibitor pracinostat (SB939) is efficacious and synergistic with the JAK2 inhibitor pacritinib(SB1518) in preclinical models of AML. Blood Cancer J 2(5):e69CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat Zhou L, Ruvolo VR, McQueen T, Chen W, Samudio IJ, Conneely O et al (2013) HDAC inhibition by SNDX-275 (Entinostat) restores expression of silenced leukemia-associated transcription factors Nur77 and Nor1 and of key pro-apoptotic proteins in AML. Leukemia 27(6):1358–1368CrossRefPubMed Zhou L, Ruvolo VR, McQueen T, Chen W, Samudio IJ, Conneely O et al (2013) HDAC inhibition by SNDX-275 (Entinostat) restores expression of silenced leukemia-associated transcription factors Nur77 and Nor1 and of key pro-apoptotic proteins in AML. Leukemia 27(6):1358–1368CrossRefPubMed
23.
Zurück zum Zitat Tran HT, Kim HN, Lee IK, Nguyen-Pham TN, Ahn JS, Kim YK et al (2013) Improved therapeutic effect against leukemia by a combination of the histone methyltransferase inhibitor chaetocin and the histone deacetylase inhibitor trichostatin a. J Korean Med Sci 28(2):237–246CrossRefPubMedPubMedCentral Tran HT, Kim HN, Lee IK, Nguyen-Pham TN, Ahn JS, Kim YK et al (2013) Improved therapeutic effect against leukemia by a combination of the histone methyltransferase inhibitor chaetocin and the histone deacetylase inhibitor trichostatin a. J Korean Med Sci 28(2):237–246CrossRefPubMedPubMedCentral
24.
Zurück zum Zitat Cea M, Soncini D, Fruscione F, Raffaghello L, Garuti A, Emionite L et al (2011) Synergistic interactions between HDAC and Sirtuin inhibitors in human leukemia cells. PLoS ONE 6(7):e22739CrossRefPubMedPubMedCentral Cea M, Soncini D, Fruscione F, Raffaghello L, Garuti A, Emionite L et al (2011) Synergistic interactions between HDAC and Sirtuin inhibitors in human leukemia cells. PLoS ONE 6(7):e22739CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Van Damme M, Crompot E, Meuleman N, Mineur P, Bron D, Lagneaux L et al (2012) HDAC isoenzyme expression is deregulated in chronic lymphocytic leukemia B-cells and has a complex prognostic significance. Epigenetics 7(12):1403–1412CrossRefPubMedPubMedCentral Van Damme M, Crompot E, Meuleman N, Mineur P, Bron D, Lagneaux L et al (2012) HDAC isoenzyme expression is deregulated in chronic lymphocytic leukemia B-cells and has a complex prognostic significance. Epigenetics 7(12):1403–1412CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Yu SL, Lee DC, Son JW, Park CG, Lee HY, Kang J (2013) Histone deacetylase 4 mediates SMAD family member 4 deacetylation and induces 5-fluorouracil resistance in breast cancer cells. Oncol Rep 30(3):1293–1300PubMed Yu SL, Lee DC, Son JW, Park CG, Lee HY, Kang J (2013) Histone deacetylase 4 mediates SMAD family member 4 deacetylation and induces 5-fluorouracil resistance in breast cancer cells. Oncol Rep 30(3):1293–1300PubMed
27.
Zurück zum Zitat Wilson AJ, Byun DS, Nasser S, Murray LB, Ayyanar K, Arango D et al (2008) HDAC4 promotes growth of colon cancer cells via repression of p21. Mol Biol Cell 19(10):4062–4075CrossRefPubMedPubMedCentral Wilson AJ, Byun DS, Nasser S, Murray LB, Ayyanar K, Arango D et al (2008) HDAC4 promotes growth of colon cancer cells via repression of p21. Mol Biol Cell 19(10):4062–4075CrossRefPubMedPubMedCentral
28.
Zurück zum Zitat Zhu L, Yang J, Zhao L, Yu X, Wang L, Wang F et al (2015) Expression of hMOF, but not HDAC4, is responsible for the global histone H4K16 acetylation in gastric carcinoma. Int J Oncol 46(6):2535–2545PubMed Zhu L, Yang J, Zhao L, Yu X, Wang L, Wang F et al (2015) Expression of hMOF, but not HDAC4, is responsible for the global histone H4K16 acetylation in gastric carcinoma. Int J Oncol 46(6):2535–2545PubMed
29.
Zurück zum Zitat Niegisch G, Knievel J, Koch A, Hader C, Fischer U, Albers P et al (2013) Changes in histone deacetylase (HDAC) expression patterns and activity of HDAC inhibitors in urothelial cancers. Urol Oncol 31(8):1770–1779CrossRefPubMed Niegisch G, Knievel J, Koch A, Hader C, Fischer U, Albers P et al (2013) Changes in histone deacetylase (HDAC) expression patterns and activity of HDAC inhibitors in urothelial cancers. Urol Oncol 31(8):1770–1779CrossRefPubMed
30.
Zurück zum Zitat Gruhn B, Naumann T, Gruner D, Walther M, Wittig S, Becker S et al (2013) The expression of histone deacetylase 4 is associated with prednisone poor-response in childhood acute lymphoblastic leukemia. Leuk Res 37(10):1200–1207CrossRefPubMed Gruhn B, Naumann T, Gruner D, Walther M, Wittig S, Becker S et al (2013) The expression of histone deacetylase 4 is associated with prednisone poor-response in childhood acute lymphoblastic leukemia. Leuk Res 37(10):1200–1207CrossRefPubMed
31.
Zurück zum Zitat Sebastián C, Zwaans BM, Silberman DM, Gymrek M, Goren A, Zhong L et al (2012) The histone deacetylase SIRT6 is a tumor suppressor that controls cancer metabolism. Cell 151(6):1185–1199CrossRefPubMedPubMedCentral Sebastián C, Zwaans BM, Silberman DM, Gymrek M, Goren A, Zhong L et al (2012) The histone deacetylase SIRT6 is a tumor suppressor that controls cancer metabolism. Cell 151(6):1185–1199CrossRefPubMedPubMedCentral
32.
Zurück zum Zitat Khongkow M, Olmos Y, Gong C, Gomes AR, Monteiro LJ, Yagüe E et al (2013) SIRT6 modulates paclitaxel and epirubicin resistance and survival in breast cancer. Carcinogenesis 34(7):1476–1486CrossRefPubMed Khongkow M, Olmos Y, Gong C, Gomes AR, Monteiro LJ, Yagüe E et al (2013) SIRT6 modulates paclitaxel and epirubicin resistance and survival in breast cancer. Carcinogenesis 34(7):1476–1486CrossRefPubMed
33.
Zurück zum Zitat Chen X, Hao B, Liu Y, Dai D, Han G, Li Y et al (2014) The histone deacetylase SIRT6 suppresses the expression of the RNA-binding protein PCBP2 in glioma. Biochem Biophys Res Commun 446(1):364–369CrossRefPubMed Chen X, Hao B, Liu Y, Dai D, Han G, Li Y et al (2014) The histone deacetylase SIRT6 suppresses the expression of the RNA-binding protein PCBP2 in glioma. Biochem Biophys Res Commun 446(1):364–369CrossRefPubMed
34.
Zurück zum Zitat Fukuda T, Wada-Hiraike O, Oda K, Tanikawa M, Makii C, Inaba K et al (2015) Putative tumor suppression function of SIRT6 in endometrial cancer. FEBS Lett 589(17):2274–2281CrossRefPubMed Fukuda T, Wada-Hiraike O, Oda K, Tanikawa M, Makii C, Inaba K et al (2015) Putative tumor suppression function of SIRT6 in endometrial cancer. FEBS Lett 589(17):2274–2281CrossRefPubMed
35.
Zurück zum Zitat Zhang ZG, Qin CY (2014) Sirt6 suppresses hepatocellular carcinoma cell growth via inhibiting the extracellular signal-regulated kinase signaling pathway. Mol Med Rep 9(3):882–888PubMed Zhang ZG, Qin CY (2014) Sirt6 suppresses hepatocellular carcinoma cell growth via inhibiting the extracellular signal-regulated kinase signaling pathway. Mol Med Rep 9(3):882–888PubMed
36.
Zurück zum Zitat Zhang J, Yin XJ, Xu CJ, Ning YX, Chen M, Zhang H et al (2015) The histone deacetylase SIRT6 inhibits ovarian cancer cell proliferation via down-regulation of notch 3 expression. Eur Rev Med Pharmacol Sci 19(5):818–824PubMed Zhang J, Yin XJ, Xu CJ, Ning YX, Chen M, Zhang H et al (2015) The histone deacetylase SIRT6 inhibits ovarian cancer cell proliferation via down-regulation of notch 3 expression. Eur Rev Med Pharmacol Sci 19(5):818–824PubMed
37.
Zurück zum Zitat Wang JC, Kafeel MI, Avezbakiyev B, Chen C, Sun Y, Rathnasabapathy C et al (2011) Histone deacetylase in chronic lymphocytic leukemia. Oncology 81(5–6):325–329CrossRefPubMed Wang JC, Kafeel MI, Avezbakiyev B, Chen C, Sun Y, Rathnasabapathy C et al (2011) Histone deacetylase in chronic lymphocytic leukemia. Oncology 81(5–6):325–329CrossRefPubMed
38.
Zurück zum Zitat Zhou J, Bi C, Chng WJ, Cheong LL, Liu SC, Mahara S et al (2011) PRL-3, a metastasis associated tyrosine phosphatase, is involved in FLT3-ITD signaling and implicated in anti-AML therapy. PLoS ONE 6(5):e19798CrossRefPubMedPubMedCentral Zhou J, Bi C, Chng WJ, Cheong LL, Liu SC, Mahara S et al (2011) PRL-3, a metastasis associated tyrosine phosphatase, is involved in FLT3-ITD signaling and implicated in anti-AML therapy. PLoS ONE 6(5):e19798CrossRefPubMedPubMedCentral
Metadaten
Titel
Strong Correlation between the Expression Levels of HDAC4 and SIRT6 in Hematological Malignancies of the Adults
verfasst von
Zsuzsanna Gaál
Éva Oláh
László Rejtő
Ferenc Erdődi
László Csernoch
Publikationsdatum
20.10.2016
Verlag
Springer Netherlands
Erschienen in
Pathology & Oncology Research / Ausgabe 3/2017
Print ISSN: 1219-4956
Elektronische ISSN: 1532-2807
DOI
https://doi.org/10.1007/s12253-016-0139-5

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