Skip to main content
Erschienen in: Strahlentherapie und Onkologie 2/2012

01.02.2012 | Original article

Suberoylanilide hydroxamic acid affects γH2AX expression in osteosarcoma, atypical teratoid rhabdoid tumor and normal tissue cell lines after irradiation

verfasst von: C. Blattmann, M.D., S. Oertel, M. Thiemann, K.J. Weber, P. Schmezer, O. Zelezny, R. Lopez Perez, A.E. Kulozik, J. Debus, V. Ehemann

Erschienen in: Strahlentherapie und Onkologie | Ausgabe 2/2012

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Osteosarcoma and atypical teratoid rhabdoid tumors are tumor entities with varying response to common standard therapy protocols. Histone acetylation affects chromatin structure and gene expression which are considered to influence radiation sensitivity. The aim of this study was to investigate the effect of the combination therapy with the histone deacetylase inhibitor suberoylanilide hydroxamic acid (SAHA) and irradiation on atypical teratoid rhabdoid tumors and osteosarcoma compared to normal tissue cell lines.

Methods

Clonogenic assay was used to determine cell survival. DNA double-strand breaks (DSB) were examined by pulsed-field electrophoresis (PFGE) as well as by γH2AX immunostaining involving flow cytometry, fluorescence microscopy, and immunoblot analysis.

Results

SAHA lead to an increased radiosensitivity in tumor but not in normal tissue cell lines. γH2AX expression as an indicator for DSB was significantly increased when SAHA was applied 24 h before irradiation to the sarcoma cell cultures. In contrast, γH2AX expression in the normal tissue cell lines was significantly reduced when irradiation was combined with SAHA. Analysis of initial DNA fragmentation and fragment rejoining by PFGE, however, did not reveal differences in response to the SAHA pretreatment for either cell type.

Conclusion

SAHA increases radiosensitivity in tumor but not normal tissue cell lines. The increased H2AX phosphorylation status of the SAHA-treated tumor cells post irradiation likely reflects its delayed dephosphorylation within the DNA damage signal decay rather than chromatin acetylation-dependent differences in the overall efficacy of DSB induction and rejoining. The results support the hypothesis that combining SAHA with irradiation may provide a promising strategy in the treatment of solid tumors.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Baschnagel A, Russo A, Burgan WE et al (2009) Vorinostat enhances the radiosensitivity of a breast cancer brain metastatic cell line grown in vitro and as intracranial xenografts. Mol Cancer Ther 8:1589–1595PubMedCrossRef Baschnagel A, Russo A, Burgan WE et al (2009) Vorinostat enhances the radiosensitivity of a breast cancer brain metastatic cell line grown in vitro and as intracranial xenografts. Mol Cancer Ther 8:1589–1595PubMedCrossRef
2.
Zurück zum Zitat Biade S, Stobbe CC, Boyd JT et al (2001) Chemical agents that promote chromatin compaction radiosensitize tumour cells. Int J Radiat Biol 77:1033–1042PubMedCrossRef Biade S, Stobbe CC, Boyd JT et al (2001) Chemical agents that promote chromatin compaction radiosensitize tumour cells. Int J Radiat Biol 77:1033–1042PubMedCrossRef
3.
Zurück zum Zitat Blattmann C, Oertel S, Ehemann V et al (2010) Enhancement of radiation response in osteosarcoma and rhabdomyosarcoma cell lines by histone deacetylase inhibition. Int J Radiat Oncol Biol Phys 78:237–245PubMedCrossRef Blattmann C, Oertel S, Ehemann V et al (2010) Enhancement of radiation response in osteosarcoma and rhabdomyosarcoma cell lines by histone deacetylase inhibition. Int J Radiat Oncol Biol Phys 78:237–245PubMedCrossRef
4.
Zurück zum Zitat Camphausen K, Burgan W, Cerra M et al (2004) Enhanced radiation-induced cell killing and prolongation of γH2AX foci expression by the histone deacetylase inhibitor MS-275. Cancer Res 64:316–321PubMedCrossRef Camphausen K, Burgan W, Cerra M et al (2004) Enhanced radiation-induced cell killing and prolongation of γH2AX foci expression by the histone deacetylase inhibitor MS-275. Cancer Res 64:316–321PubMedCrossRef
5.
Zurück zum Zitat Chen X, Wong J, Wong P et al (2011) Low dose valproic acid enhances radiosensitivity of prostate cancer through acetylated p53-dependent modulation of mitochondrial membrane potential and apoptosis. Mol Cancer Res 9:448–461PubMedCrossRef Chen X, Wong J, Wong P et al (2011) Low dose valproic acid enhances radiosensitivity of prostate cancer through acetylated p53-dependent modulation of mitochondrial membrane potential and apoptosis. Mol Cancer Res 9:448–461PubMedCrossRef
6.
Zurück zum Zitat Chinnaiyan P, Vallabhaneni G, Armstrong E et al (2005) Modulation of radiation response by histone deacetylase inhibition. Int J Radiat Oncol Biol Phys 62:223–229PubMedCrossRef Chinnaiyan P, Vallabhaneni G, Armstrong E et al (2005) Modulation of radiation response by histone deacetylase inhibition. Int J Radiat Oncol Biol Phys 62:223–229PubMedCrossRef
7.
Zurück zum Zitat Chung YL, Lee MY, Pui NN (2009) Epigenetic therapy using the histone deacetylase inhibitor for increasing therapeutic gain in oral cancer: prevention of radiation-induced oral mucositis and inhibition of chemical-induced oral carcinogenesis. Carcinogenesis 30:1387–1397PubMedCrossRef Chung YL, Lee MY, Pui NN (2009) Epigenetic therapy using the histone deacetylase inhibitor for increasing therapeutic gain in oral cancer: prevention of radiation-induced oral mucositis and inhibition of chemical-induced oral carcinogenesis. Carcinogenesis 30:1387–1397PubMedCrossRef
8.
Zurück zum Zitat Furchert SE, Lanvers-Kaminsky C, Jürgens H et al (2007) Inhibitors of histone deacetylases as potential therapeutic tools for high-risk embryonal tumors of the nervous system of childhood. Int J Cancer 120:1787–1794PubMedCrossRef Furchert SE, Lanvers-Kaminsky C, Jürgens H et al (2007) Inhibitors of histone deacetylases as potential therapeutic tools for high-risk embryonal tumors of the nervous system of childhood. Int J Cancer 120:1787–1794PubMedCrossRef
9.
Zurück zum Zitat Huang X, Darzynkiewicz Z (2006) Cytometric assessment of histone H2AX phosphorylation. Methods Mol Biol 314:73–80PubMedCrossRef Huang X, Darzynkiewicz Z (2006) Cytometric assessment of histone H2AX phosphorylation. Methods Mol Biol 314:73–80PubMedCrossRef
10.
Zurück zum Zitat Jeggo PA (1998) Identification of genes involved in repair of DNA double-strand breaks in mammalian cells. Radiat Res 150:80–91CrossRef Jeggo PA (1998) Identification of genes involved in repair of DNA double-strand breaks in mammalian cells. Radiat Res 150:80–91CrossRef
11.
Zurück zum Zitat Kaatsch P, Debling D, Blettner M et al (2009) Second malignant neoplasms after childhood cancer in Germany—results from the long-term follow-up of the German childhood cancer registry. Strahlenther Onkol 185:8–10PubMedCrossRef Kaatsch P, Debling D, Blettner M et al (2009) Second malignant neoplasms after childhood cancer in Germany—results from the long-term follow-up of the German childhood cancer registry. Strahlenther Onkol 185:8–10PubMedCrossRef
12.
Zurück zum Zitat Kappler M, Taubert H, Bartel F et al (2005) Radiosensitization after a combined treatment of survivin siRNA and irradiation, is correlated with the activation of caspases 3 and 7 in a wt-p53 sarcoma cell line, but not in a mt-p53 sarcoma cell line. Oncol Rep 13:167–172PubMed Kappler M, Taubert H, Bartel F et al (2005) Radiosensitization after a combined treatment of survivin siRNA and irradiation, is correlated with the activation of caspases 3 and 7 in a wt-p53 sarcoma cell line, but not in a mt-p53 sarcoma cell line. Oncol Rep 13:167–172PubMed
13.
Zurück zum Zitat Karagiannis TC, Kn H, El-Osta A (2006) The epigenetic modifier, valproic acid, enhances radiation sensitivity. Epigenetics 1:131–137PubMedCrossRef Karagiannis TC, Kn H, El-Osta A (2006) The epigenetic modifier, valproic acid, enhances radiation sensitivity. Epigenetics 1:131–137PubMedCrossRef
14.
Zurück zum Zitat Khanna KK, Jackson SP (2001) DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet 27:247–254PubMedCrossRef Khanna KK, Jackson SP (2001) DNA double-strand breaks: signaling, repair and the cancer connection. Nat Genet 27:247–254PubMedCrossRef
15.
Zurück zum Zitat Klenke FM, Abdollahi A, Bischof M et al (2011) Celecoxib enhances radiation response of secondary bone tumors of a human non-small cell lung cancer via antiangiogenesis in vivo. Strahlenther Onkol 187:45–51PubMedCrossRef Klenke FM, Abdollahi A, Bischof M et al (2011) Celecoxib enhances radiation response of secondary bone tumors of a human non-small cell lung cancer via antiangiogenesis in vivo. Strahlenther Onkol 187:45–51PubMedCrossRef
16.
Zurück zum Zitat Lee M-J, Kim YS, Kummar S et al (2008) Histone deacetylase inhibitors in cancer therapy. Curr Opin Oncol 20:639–649PubMedCrossRef Lee M-J, Kim YS, Kummar S et al (2008) Histone deacetylase inhibitors in cancer therapy. Curr Opin Oncol 20:639–649PubMedCrossRef
17.
Zurück zum Zitat Levesque AA, Fanous AA, Poh A et al (2008) Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest. Mol Cancer Ther 7:252–262PubMedCrossRef Levesque AA, Fanous AA, Poh A et al (2008) Defective p53 signaling in p53 wild-type tumors attenuates p21waf1 induction and cyclin B repression rendering them sensitive to Chk1 inhibitors that abrogate DNA damage-induced S and G2 arrest. Mol Cancer Ther 7:252–262PubMedCrossRef
18.
Zurück zum Zitat MacPhail SH, Banath JP, Yu Y et al (2003) Cell cycle-dependent expression of phosphorylated histone H2AX: reduced expression in unirradiated but not X-irradiated G1-phase cells. Radiat Res 159:759–767PubMedCrossRef MacPhail SH, Banath JP, Yu Y et al (2003) Cell cycle-dependent expression of phosphorylated histone H2AX: reduced expression in unirradiated but not X-irradiated G1-phase cells. Radiat Res 159:759–767PubMedCrossRef
19.
Zurück zum Zitat Marks PA, Richon VM, Rifkind RA (2000) Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer Inst 92:1210–1216PubMedCrossRef Marks PA, Richon VM, Rifkind RA (2000) Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer Inst 92:1210–1216PubMedCrossRef
20.
Zurück zum Zitat Minucci S, Pelicci P (2006) Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 6:38–51PubMedCrossRef Minucci S, Pelicci P (2006) Histone deacetylase inhibitors and the promise of epigenetic (and more) treatments for cancer. Nat Rev Cancer 6:38–51PubMedCrossRef
21.
Zurück zum Zitat Munshi A, Tanaka T, Hobbs ML et al (2006) Vorinostat, a histone deacetylase inhibitor, enhances the response of human tumor cells to ionizing radiation through prolongation of gamma-H2AX foci. Mol Cancer Ther 5:1967–1974PubMedCrossRef Munshi A, Tanaka T, Hobbs ML et al (2006) Vorinostat, a histone deacetylase inhibitor, enhances the response of human tumor cells to ionizing radiation through prolongation of gamma-H2AX foci. Mol Cancer Ther 5:1967–1974PubMedCrossRef
22.
Zurück zum Zitat Niermann KJ, Moretti L, Giacalone NJ (2011) Enhanced radiosensitivity of androgen-resistant prostate cancer: AZD1152-mediated aurora kinase B inhibition. Radiat Res 175:444–451PubMedCrossRef Niermann KJ, Moretti L, Giacalone NJ (2011) Enhanced radiosensitivity of androgen-resistant prostate cancer: AZD1152-mediated aurora kinase B inhibition. Radiat Res 175:444–451PubMedCrossRef
23.
Zurück zum Zitat O’Connor OA, Heaney ML, Schwartz L et al (2006) Clinical experience with intravenous and oral formulations of the novel histone deacetylase inhibitor suberoylanilide hydroxamic acid in patients with advanced hematologic malignancies. J Clin Oncol 24:166–173CrossRef O’Connor OA, Heaney ML, Schwartz L et al (2006) Clinical experience with intravenous and oral formulations of the novel histone deacetylase inhibitor suberoylanilide hydroxamic acid in patients with advanced hematologic malignancies. J Clin Oncol 24:166–173CrossRef
24.
Zurück zum Zitat Patties I, Jahns J, Hildebrandt G et al (2009) Additive effects of 5-aza-2’-deoxycytidine and irradiation on clonogenic survival of human medulloblastoma cell lines. Strahlenther Onkol 185:331–338PubMedCrossRef Patties I, Jahns J, Hildebrandt G et al (2009) Additive effects of 5-aza-2’-deoxycytidine and irradiation on clonogenic survival of human medulloblastoma cell lines. Strahlenther Onkol 185:331–338PubMedCrossRef
25.
Zurück zum Zitat Paull TT, Rogakou EP, Yamazaki V et al (2000) A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage. Curr Biol 10:886–895PubMedCrossRef Paull TT, Rogakou EP, Yamazaki V et al (2000) A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage. Curr Biol 10:886–895PubMedCrossRef
26.
Zurück zum Zitat Pawlik TM, Keyomarsi K (2004) Role of cell cycle in mediating sensitivity to radiotherapy. Int J Radiat Oncol Biol Phys 59:928–942PubMedCrossRef Pawlik TM, Keyomarsi K (2004) Role of cell cycle in mediating sensitivity to radiotherapy. Int J Radiat Oncol Biol Phys 59:928–942PubMedCrossRef
27.
Zurück zum Zitat Purrucker JC, Fricke A, Ong MF et al (2010) HDAC inhibition radiosensitizes human normal tissue cells and reduces DNA Double-Strand Break repair capacity. Oncol Rep 23:263–269PubMed Purrucker JC, Fricke A, Ong MF et al (2010) HDAC inhibition radiosensitizes human normal tissue cells and reduces DNA Double-Strand Break repair capacity. Oncol Rep 23:263–269PubMed
28.
Zurück zum Zitat Rudat V, Bachmann N, Kuepper JH et al (2001) Overexpression of the DNA-binding domain of poly (ADP-ribose) polymerase inhibits rejoining of ionizing radiation-induced DNA-double-strand breaks. Int J Radiat Biol 77:303–307PubMedCrossRef Rudat V, Bachmann N, Kuepper JH et al (2001) Overexpression of the DNA-binding domain of poly (ADP-ribose) polymerase inhibits rejoining of ionizing radiation-induced DNA-double-strand breaks. Int J Radiat Biol 77:303–307PubMedCrossRef
29.
Zurück zum Zitat Weiss C, Grabenbauer GG, Sauer R et al (2003) Significant increase in residual DNA damage as a possible mechanism of radiosensitization by gemcitabine. Strahlenther Onkol 179:93–98PubMedCrossRef Weiss C, Grabenbauer GG, Sauer R et al (2003) Significant increase in residual DNA damage as a possible mechanism of radiosensitization by gemcitabine. Strahlenther Onkol 179:93–98PubMedCrossRef
30.
Zurück zum Zitat Welte B, Suhr P, Bootke D et al (2010) Second malignancies in high-dose areas of previous tumor radiotherapy. Strahlenther Onkol 186:174–179PubMedCrossRef Welte B, Suhr P, Bootke D et al (2010) Second malignancies in high-dose areas of previous tumor radiotherapy. Strahlenther Onkol 186:174–179PubMedCrossRef
31.
Zurück zum Zitat Wolff HA, Hennies S, Herrmann MK et al (2011) Comparison of the micronucleus and chromosome aberration techniques for the documentation of cytogenetic damage in radiochemotherapy-treated patients with rectal cancer. Strahlenther Onkol 187:52–58PubMedCrossRef Wolff HA, Hennies S, Herrmann MK et al (2011) Comparison of the micronucleus and chromosome aberration techniques for the documentation of cytogenetic damage in radiochemotherapy-treated patients with rectal cancer. Strahlenther Onkol 187:52–58PubMedCrossRef
32.
Zurück zum Zitat Zhang Y, Jung M, Dritschilo A et al (2005) Enhancement of radiation sensitivity of human squamous cells by histone deacetylase inhibition. Radiat Res 163:488–493CrossRef Zhang Y, Jung M, Dritschilo A et al (2005) Enhancement of radiation sensitivity of human squamous cells by histone deacetylase inhibition. Radiat Res 163:488–493CrossRef
Metadaten
Titel
Suberoylanilide hydroxamic acid affects γH2AX expression in osteosarcoma, atypical teratoid rhabdoid tumor and normal tissue cell lines after irradiation
verfasst von
C. Blattmann, M.D.
S. Oertel
M. Thiemann
K.J. Weber
P. Schmezer
O. Zelezny
R. Lopez Perez
A.E. Kulozik
J. Debus
V. Ehemann
Publikationsdatum
01.02.2012
Verlag
Springer Berlin Heidelberg
Erschienen in
Strahlentherapie und Onkologie / Ausgabe 2/2012
Print ISSN: 0179-7158
Elektronische ISSN: 1439-099X
DOI
https://doi.org/10.1007/s00066-011-0028-5

Weitere Artikel der Ausgabe 2/2012

Strahlentherapie und Onkologie 2/2012 Zur Ausgabe

Mitteilungen der Fachgesellschaften

Adressen, Personalia, Preisausschreibung, Tagungen

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.