Shared chromatin remodeling mutations drive concurrent rhabdomyosarcoma and leukemia in a pediatric patient

Abstract The co-occurrence of rhabdomyosarcoma (RMS) and B-cell acute lymphoblastic leukemia (B-ALL) has been rarely reported, and the shared molecular drivers remain unidentified. This case report describes a pediatric patient diagnosed with both malignancies simultaneously. Whole exome sequencing...

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Bibliographic Details
Main Authors: Ji’ou Zhao, Huimin Li, Yongren Wang, Xiaoyan Sun, Yongjun Fang, Yao Xue
Format: Article
Language:English
Published: Springer 2025-06-01
Series:Discover Oncology
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Online Access:https://doi.org/10.1007/s12672-025-02967-5
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Summary:Abstract The co-occurrence of rhabdomyosarcoma (RMS) and B-cell acute lymphoblastic leukemia (B-ALL) has been rarely reported, and the shared molecular drivers remain unidentified. This case report describes a pediatric patient diagnosed with both malignancies simultaneously. Whole exome sequencing of RMS and B-ALL samples from this patient identified 91 shared somatic mutations. Subsequent principal component analysis (PCA) of the GSE240287, GSE140556, and GSE26713 datasets, combined with cancer driver gene identification using the IntOGen database, revealed five key drivers: ARID1A, CTCF, SUZ12, CREBBP, and ARID2. These genes may collectively drive tumorigenesis in both malignancies through their involvement in chromatin remodeling pathways.
ISSN:2730-6011