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Epigenomic machinery regulating pediatric AML: Clonal expansion mechanisms, therapies, and future perspectives.
Chianese, Ugo; Papulino, Chiara; Megchelenbrink, Wout; Tambaro, Francesco Paolo; Ciardiello, Fortunato; Benedetti, Rosaria; Altucci, Lucia.
Affiliation
  • Chianese U; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
  • Papulino C; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
  • Megchelenbrink W; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy; Princess Máxima Center, Heidelberglaan 25, 3584 CS, Utrecht, the Netherlands.
  • Tambaro FP; Bone Marrow Transplant Unit, Pediatric Oncology Department AORN Santobono Pausilipon, 80129 Naples, Italy.
  • Ciardiello F; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
  • Benedetti R; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy. Electronic address: rosaria.benedetti@unicampania.it.
  • Altucci L; Department of Precision Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy; Biogem Institute of Molecular and Genetic Biology, 83031 Ariano Irpino, Italy; IEOS, Institute for Endocrinology and Oncology "Gaetano Salvatore" (IEOS), 80131 Naples, Italy. Electronic address: lucia.a
Semin Cancer Biol ; 92: 84-101, 2023 07.
Article in En | MEDLINE | ID: mdl-37003397
ABSTRACT
Acute myeloid leukemia (AML) is a heterogeneous disease with a genetic, epigenetic, and transcriptional etiology mainly presenting somatic and germline abnormalities. AML incidence rises with age but can also occur during childhood. Pediatric AML (pAML) accounts for 15-20% of all pediatric leukemias and differs considerably from adult AML. Next-generation sequencing technologies have enabled the research community to "paint" the genomic and epigenomic landscape in order to identify pathology-associated mutations and other prognostic biomarkers in pAML. Although current treatments have improved the prognosis for pAML, chemoresistance, recurrence, and refractory disease remain major challenges. In particular, pAML relapse is commonly caused by leukemia stem cells that resist therapy. Marked patient-to-patient heterogeneity is likely the primary reason why the same treatment is successful for some patients but, at best, only partially effective for others. Accumulating evidence indicates that patient-specific clonal composition impinges significantly on cellular processes, such as gene regulation and metabolism. Although our understanding of metabolism in pAML is still in its infancy, greater insights into these processes and their (epigenetic) modulation may pave the way toward novel treatment options. In this review, we summarize current knowledge on the function of genetic and epigenetic (mis)regulation in pAML, including metabolic features observed in the disease. Specifically, we describe how (epi)genetic machinery can affect chromatin status during hematopoiesis, leading to an altered metabolic profile, and focus on the potential value of targeting epigenetic abnormalities in precision and combination therapy for pAML. We also discuss the possibility of using alternative epidrug-based therapeutic approaches that are already in clinical practice, either alone as adjuvant treatments and/or in combination with other drugs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Epigenomics Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Myeloid, Acute / Epigenomics Type of study: Prognostic_studies Limits: Child / Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country: Italy