Abstract
Malignant tumors of childhood represent a rather heterogeneous group of neoplasms originating from virtually any anatomical structure. Despite major improvements in the clinical management including timely diagnosis, advanced supportive care and refined multimodality treatment, prognosis remains grim for certain risk groups. Aberrant epigenetic regulation, i.e. changes in gene transcription not due to DNA sequence alterations, is now increasingly recognized as a fundamental process in malignant transformation, tumor progression and drug resistance. The molecular mechanisms involve aberrant activity of enzymes controlling the packaging and transcriptional regulation of the genome. Two major protein families are involved in this process, DNA methyltransferases and histone deacetylases. With the availability of small molecule inhibitors targeting the aberrant epigenetic machinery in cancer cells, these compounds are evaluated in several clinical trials.
Zusammenfassung
Trotz großer Fortschritte in der Diagnostik und Therapie von Krebserkrankungen im Kindes- und Jugendalter ist die Prognose insbesondere von fortgeschrittenen Tumoren weiterhin ungünstig. In den letzten Jahren hat sich gezeigt, dass fehlgesteuerte epigenetische Regulationsmechanismen eine fundamentale Rolle in der malignen Transformation, Progression und Therapieresistenz von Tumoren spielen. Unter „Epigenetik” versteht man den erblichen Aktivitätszustand von Genen, dessen Information unabhängig von der Basensequenz der DNA ist. Hierbei spielen die DNA-Methyltransferasen und die Histon-Deacetylasen eine zentrale Rolle. Sie regulieren den „Verpackungszustand” des menschlichen Genoms und sind an der Kontrolle des Expressionsprofils von Genen in einer Zelle beteiligt. In malignen Geweben sind diese Enzymfamilien pathologisch aktiv. Durch kleinmolekulare Inhibitoren können DNA-Methyltransferasen und Histon-Deacetylasen gehemmt werden und dadurch anti-tumorale Wirkungen entfalten.
Key words
epigenetics - DNMT - HDAC - inhibitors - pediatric oncology
Schlüsselwörter
Epigenetik - DNMT - HDAC - Inhibitoren - pädiatrische Onkologie
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HDAC family: what are the cancer relevant targets?.
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Induction of fetal hemoglobin expression by the histone deacetylase inhibitor apicidin.
Blood.
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Butyrate-induced erythroid differentiation of human K562 leukemia cells involves inhibition of ERK and activation of p38 MAP kinase pathways.
Blood.
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95
2391-2396
131
Witt O, Schweigerer L, Driever PH. et al .
Valproic acid treatment of glioblastoma multiforme in a child.
Pediatr Blood Cancer.
2004;
43
181
132
Yoon JH, Smith LE, Feng Z. et al .
Methylated CpG dinucleotides are the preferential targets for G-to-T transversion mutations induced by benzo[a]pyrene diol epoxide in mammalian cells: similarities with the p53 mutation spectrum in smoking-associated lung cancers.
Cancer Res.
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61
7110-7117
Correspondence
Prof. Dr. Dr. Michael C. Frühwald
University Children's Hospital Muenster, Department of Pediatric Hematology and Oncology, Münster
Albert-Schweitzer-Str. 33
48149 Münster
Germany
Phone: +49/251/83 45 644
Fax: +49/251/83 47 828
Email: Michael.Fruehwald@ukmuenster.de
Prof. Dr. Olaf Witt
Clinical Cooperation Unit Pediatric Oncology, German Cancer
Research Centre, Heidelberg
Germany and Clinic for Pediatric Oncology, Haematology,
Immunology and Pneumonology, University Children's Hospital Heidelberg
Phone: +49/6221/42 3570
Fax: +49/6221/42 3277
Email: o.witt@dkfz.de