Identification of RCC1-LCK as a novel fusion gene in pediatric erythroid sarcoma

被引:1
|
作者
Oya, Satoru [1 ]
Osone, Shinya [1 ]
Yoshida, Masanori [2 ]
Nishimoto, Sota [1 ]
Taura, Yoshihiro [1 ]
Yoshida, Hideki [1 ]
Miyachi, Mitsuru [1 ]
Inaba, Tohru [3 ]
Konishi, Eiichi [4 ]
Kato, Motohiro [2 ,5 ]
Imamura, Toshihiko [1 ]
Iehara, Tomoko [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Pediat, Kyoto, Japan
[2] Natl Ctr Child Hlth & Dev, Dept Pediat Hematol & Oncol Res, Res Inst, Tokyo, Japan
[3] Kyoto Prefectural Univ Med, Dept Infect Control & Lab Med, Kyoto, Japan
[4] Kyoto Prefectural Univ Med, Dept Surg Pathol, Kyoto, Japan
[5] Univ Tokyo, Dept Pediat, Tokyo, Japan
关键词
erythroid sarcoma; fusion gene; LCK; leukemogenesis; myeloid sarcoma; ACUTE MYELOID-LEUKEMIA; CELL; HETEROGENEITY; MUTATIONS; PROTEIN; INFANT; LCK;
D O I
10.1002/pbc.29848
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Erythroid sarcoma is a very rare subtype of myeloid sarcoma with undetermined biological features. Here, we present an infant with a multifocal erythroid sarcoma, diagnosed because the tumor cells were positive for glycophorin A. After acute myeloid leukemia-oriented chemotherapy and surgical resection followed by cord blood transplantation, he has successfully maintained complete remission without any late effects. Total transcriptome analysis of the tumor identified a novel fusion gene, RCC1-LCK, and high LCK expression levels, suggesting that LCK overexpression was involved in leukemogenesis in this case.
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页数:5
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