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STAT5a和SH2B3新突变在一名三阴性原发性骨髓纤维化患者中显示出恶性作用。

STAT5a and SH2B3 novel mutations display malignancy roles in a triple-negative primary myelofibrosis patient.

作者信息

Zhang Shubing, Yan Jinhua, He Lan, Jiang Zhiping, Jiang Hao

机构信息

Department of Cell Biology, School of Life Sciences, Central South University, 410013, Changsha, Hunan, P. R. China.

Hunan Key Laboratory of Animal Models for Human Diseases, Central South University, 410013, Changsha, Hunan, P. R. China.

出版信息

Cancer Gene Ther. 2024 Mar;31(3):484-494. doi: 10.1038/s41417-023-00719-7. Epub 2023 Dec 22.

DOI:10.1038/s41417-023-00719-7
PMID:38135698
Abstract

Primary myelofibrosis (PMF) patients frequently have JAK2 (V617F), CALR (exon 9), or MPL (W515 or exon 10) strong driver gene mutation, which triggers abnormal activation of the JAK2-STATs signaling pathway that plays a complex role in the occurrence of PMF. However, about 10-15% of PMF patients have no above typical mutations in these strong driver genes, known as being "triple-negative", which are associated with poor prognosis. In this paper, we reported a unique secondary acute myeloid leukemia (sAML) case transformed from triple-negative PMF combined with lung cancer and erythroderma occurrence at the same time, which has not been reported so far. Through whole blood exome sequencing, four novel noncanonical mutations were detected in key regulatory genes SH2B3 (Q748 and S710) and STAT5a (C350 and K354). Meanwhile, STAT5a-S710 and SH2B3-K354 noncanonical mutations gained strong malignant biofunction on promoting cell growth and tumorigenesis by accelerating the G1/S transition. In the mechanistic study, these pernicious phenotypes driven by noncanonical mutations might be initial PMF by activating p-STAT5a/c-Myc/CyclinD1 and p-STAT3/p-AKT/p-ERK1/2 signaling axes. Therefore, our study explored the deleterious roles of novel noncanonical mutations in STAT5a and SH2B3, which may serve as susceptibility genes and display the oncogenic biofunction in the progression of PMF to acute myeloid leukemia-M2a (AML-M2a).

摘要

原发性骨髓纤维化(PMF)患者经常发生JAK2(V617F)、CALR(第9外显子)或MPL(W515或第10外显子)强驱动基因突变,这些突变会触发JAK2-STATs信号通路的异常激活,该信号通路在PMF的发生中起复杂作用。然而,约10%-15%的PMF患者在这些强驱动基因中没有上述典型突变,即所谓的“三阴性”,其预后较差。在本文中,我们报告了一例独特的继发性急性髓系白血病(sAML)病例,该病例由三阴性PMF转化而来,同时合并肺癌和红皮病,目前尚未见报道。通过全血外显子测序,在关键调控基因SH2B3(Q748和S710)和STAT5a(C350和K354)中检测到四个新的非经典突变。同时,STAT5a-S710和SH2B3-K354非经典突变通过加速G1/S期转换在促进细胞生长和肿瘤发生方面获得了强大的恶性生物学功能。在机制研究中,这些由非经典突变驱动的有害表型可能通过激活p-STAT5a/c-Myc/CyclinD1和p-STAT3/p-AKT/p-ERK1/2信号轴引发原发性PMF。因此,我们的研究探讨了STAT5a和SH2B3中新的非经典突变的有害作用,这些突变可能作为易感基因,并在PMF进展为急性髓系白血病-M2a(AML-M2a)过程中发挥致癌生物学功能。

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Am J Hematol. 2023 May;98(5):801-821. doi: 10.1002/ajh.26857. Epub 2023 Feb 6.
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Novel Molecular Insights into Leukemic Evolution of Myeloproliferative Neoplasms: A Single Cell Perspective.从单细胞角度看骨髓增殖性肿瘤向白血病演变的新分子认识。
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