B型核心结合因子β/平滑肌肌球蛋白重链融合转录物在慢性髓性白血病髓母细胞期:与融合蛋白的核和细胞质定位的相关性

C. Cameron Yin , Dan Jones , Jorge E. Cortés , Hagop Kantarjian , Mihai Merzianu , L. Jeffrey Medeiros , Carlos E. Bueso-Ramos
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引用次数: 3

摘要

dinv (16)(p13q22)或罕见的t(16;16)(p13;q22)是M4Eo型急性髓系白血病的特征,导致16q22的核心结合因子β基因(CBFB)与16p13的平滑肌肌球蛋白重链基因(MYH11)融合。融合转录物CBFB/MYH11在白血病发生中起重要作用。这种融合转录物的许多变体已被报道,其中A型最常见,发生在>85%的病例。患者和方法我们用inv(16)(p13q22)研究了4例骨髓母细胞期慢性髓性白血病的融合转录本。结果4例患者中3例检测到B型融合转录物。免疫组织化学显示融合蛋白的核和细胞质染色。尽管这一发现的生物学意义尚不清楚,但一种不寻常类型的融合转录物在原细胞期慢性髓性白血病病例中的高频率,其中inv(16)(p13q22)在原细胞转化时首次出现,表明B型转录物可能在疾病进展中发挥作用。B型融合中额外的平滑肌肌球蛋白重链序列对蛋白产物亚细胞定位的影响也被提出。
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Type B Core Binding Factor β/Smooth Muscle Myosin Heavy Chain Fusion Transcript in Myeloid Blast Phase of Chronic Myeloid Leukemia: Correlation with Nuclear and Cytoplasmic Localization of the Fusion Protein

Background

Inv(16)(p13q22) or the rare t(16;16)(p13;q22) is characteristic of the M4Eo type of acute myeloid leukemia and results in the fusion of the core binding factor β gene (CBFB) at 16q22 with the smooth muscle myosin heavy chain gene (MYH11) at 16p13. The fusion transcript CBFB/MYH11 plays an important role in leukemogenesis. Many variations of this fusion transcript have been reported, with type A being most common and occurring in > 85% of cases.

Patients and Methods

We studied the fusion transcripts in 4 cases of chronic myelogenous leukemia in myeloid blast phase with inv(16)(p13q22).

Results

Sequencing analysis revealed type B fusion transcript in 3 of the 4 cases. Immunohistochemistry demonstrated both nuclear and cytoplasmic staining for the fusion protein.

Conclusion

Although the biologic significance of this finding is unknown, the high frequency of an unusual type of fusion transcript in the chronic myelogenous leukemia cases in blast phase in which inv(16)(p13q22) first occurred at the time of blast transformation suggests that the type B transcript might play a role in disease progression. The effect of the additional smooth muscle myosin heavy chain sequences in the type B fusion on subcellular localization of the protein product is also suggested.

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