Journal Article

Epigenome-wide analysis across the development span of pediatric acute lymphoblastic leukemia: backtracking to birth

Casement, John, Håberg, Siri Eldevik, Novoloaca, Alexei, Wiemels, Joseph Leo, Krali, Olga, Pearce, Mark S., Strathdee, Gordon, Hansen, Helen M., Roy, Ritu, de Smith, Adam J., Munthe-Kaas, Monica Cheng, Herceg, Zdenko, Cahais, Vincent, McKay, Jill A., Dwyer, Terence, Spitz, Natalia, Li, Shaobo, Nusslé, Semira Gonseth, Caron, Maxime, Lee, Hwi-Ho, Magnus, Per, Lee, Yong Sun, Cuenin, Cyrille, Lam, Dilys, Ghantous, Akram, Sinnett, Daniel, Nickels, Eric, Fransquet, Peter Daniel, Nordlund, Jessica, Saffery, Richard, Nassar, Farah J.

2024

Overview

Background Cancer is the leading cause of disease-related mortality in children. Causes of leukemia, the most common form, are largely unknown. Growing evidence points to an origin in-utero , when global redistribution of DNA methylation occurs driving tissue differentiation. Methods Epigenome-wide DNA methylation was profiled in surrogate (blood) and target (bone marrow) tissues at birth, diagnosis, remission and relapse of pediatric pre-B acute lymphoblastic leukemia (pre-B ALL) patients. Double-blinded analyses was performed between prospective cohorts extending from birth to diagnosis and retrospective studies backtracking from clinical disease to birth. Validation was carried out using independent technologies and populations. Results The imprinted and immuno-modulating VTRNA2-1 was hypermethylated (FDR<0.05) at birth in nested cases relative to controls in all tested populations (totaling 317 cases and 483 controls), including European and Hispanic ancestries. VTRNA2-1 methylation was stable over follow-up years after birth and across surrogate, target and other tissues ( n =5,023 tissues; 30 types). When profiled in leukemic tissues from two clinical cohorts (totaling 644 cases), VTRNA2-1 methylation exhibited higher levels at diagnosis relative to controls, it reset back to normal levels at remission, and then re-increased to above control levels at relapse. Hypermethylation was significantly associated with worse pre-B ALL patient survival and with reduced VTRNA2-1 expression ( n =2,294 tissues; 26 types), supporting a functional and translational role for VTRNA2-1 methylation. Conclusion This study provides proof-of-concept to detect at birth epigenetic precursors of pediatric pre-B ALL. These alterations were reproducible with different technologies, in three continents and in two ethnicities, and can offer biomarkers for early detection and prognosis as well as actionable targets for therapy. Key points • Precursors of pediatric acute lymphoblastic leukemia may be of epigenetic origin, detectable since birth and affecting patient prognosis. • These epigenetic precursors can be robust over several years and across several populations, ethnicities and surrogate and target tissues.

• Publisher: BioMed Central,BioMed Central Ltd,BMC
• Subject: Acute lymphocytic leukemia / Adolescent / Analysis / Biomarkers, Tumor - genetics / Biomedical and Life Sciences / Biomedicine / Birth cohort / Cancer Research / Case-Control Studies / Child / Child, Preschool / Correspondence / DNA Methylation / drug resistance / Epigenesis, Genetic / Epigenetic inheritance / Epigenetics / Epigenome / Female / Humans / Infant / Infant, Newborn / Latest Correspondence on Biomarkers for Cancer diagnosis / Male / Medical research / Medicine, Experimental / Methylation / Neonatal blood spots / Oncology / Pediatric leukemia / Pediatrics / Precursor Cell Lymphoblastic Leukemia-Lymphoma - diagnosis / Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics / Precursor Cell Lymphoblastic Leukemia-Lymphoma - mortality / Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology / Prognosis / VTRNA2-1