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放射性诱导性脑胶质瘤是 H3-/IDH 野生型儿童脑胶质瘤,具有复发性 PDGFRA 扩增和 CDKN2A/B 缺失。

Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B.

机构信息

Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg University Hospital and German Cancer Resarch Center (DKFZ), Heidelberg, Germany.

Division of Pediatric Glioma Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Nat Commun. 2021 Sep 20;12(1):5530. doi: 10.1038/s41467-021-25708-y.

Abstract

Long-term complications such as radiation-induced second malignancies occur in a subset of patients following radiation-therapy, particularly relevant in pediatric patients due to the long follow-up period in case of survival. Radiation-induced gliomas (RIGs) have been reported in patients after treatment with cranial irradiation for various primary malignancies such as acute lymphoblastic leukemia (ALL) and medulloblastoma (MB). We perform comprehensive (epi-) genetic and expression profiling of RIGs arising after cranial irradiation for MB (n = 23) and ALL (n = 9). Our study reveals a unifying molecular signature for the majority of RIGs, with recurrent PDGFRA amplification and loss of CDKN2A/B and an absence of somatic hotspot mutations in genes encoding histone 3 variants or IDH1/2, uncovering diagnostic markers and potentially actionable targets.

摘要

长期并发症,如放射诱导的第二恶性肿瘤,发生在放射治疗后的患者亚组中,在儿科患者中尤为相关,因为在存活的情况下需要长期随访。放射诱导的胶质瘤(RIG)已在接受颅照射治疗各种原发性恶性肿瘤(如急性淋巴细胞白血病(ALL)和髓母细胞瘤(MB))的患者中报告。我们对颅照射治疗 MB(n=23)和 ALL(n=9)后发生的 RIG 进行了全面的(表观)遗传和表达谱分析。我们的研究揭示了大多数 RIG 的统一分子特征,包括 PDGFRA 扩增和 CDKN2A/B 缺失,以及编码组蛋白 3 变体或 IDH1/2 的基因中不存在体细胞热点突变,揭示了诊断标志物和潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8087/8452680/4915a695f032/41467_2021_25708_Fig1_HTML.jpg

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