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成人新发急性粒单核细胞白血病(M4)伴t(11;17)(q23;q25)中MLL与MSF的融合

Fusion of MLL and MSF in adult de novo acute myelomonocytic leukemia (M4) with t(11;17)(q23;q25).

作者信息

Yamamoto Koh, Shibata Fumi, Yamaguchi Mitsuko, Miura Osamu

机构信息

Department of Hematology and Oncology, Tokyo Medical and Dental University, Japan.

出版信息

Int J Hematol. 2002 Jun;75(5):503-7. doi: 10.1007/BF02982114.

Abstract

The MLL gene at chromosome band 11q23 is frequently rearranged and fused to partner genes in acute leukemias. Previously, the MSF gene, also called AF17q25, has been cloned as a fusion partner of the MLL gene in therapy-related or infant acute myelogenous leukemias with t(11;17)(q23;q25). MSF belongs to the septin family of proteins, which includes other MLL fusion partners, hCDCrel1 and Septin 6, and has also been implicated in the pathogenesis of human ovarian tumor and murine T-cell lymphoma. We describe here a 64-year-old man with de novo acute myelomonocytic leukemia (French-American-British subtype M4) with t(11;17)(q23;q25). His leukemia was successfully induced into a first remission, which, however, lasted only briefly. A second remission was never attained, and the patient died of sepsis 16 months after the diagnosis of leukemia. Examination of his leukemic cells at diagnosis revealed an MLL gene rearrangement, by Southern blotting, and an MLL-MSF fusion transcript, by the reverse transcriptase polymerase chain reaction (RT-PCR) method. Sequence analysis of the RT-PCR product further revealed that MLL exon 5 was fused in-frame to MSF exon 3. Further clinical and molecular analyses of acute leukemias with the MLL-MSF transcript may shed more light on the clinical characteristics and molecular mechanisms of the MLL-septin type leukemias.

摘要

位于11q23染色体带的MLL基因在急性白血病中经常发生重排并与伙伴基因融合。此前,MSF基因(也称为AF17q25)已被克隆为治疗相关或婴儿急性髓性白血病伴t(11;17)(q23;q25)中MLL基因的融合伙伴。MSF属于septin蛋白家族,该家族包括其他MLL融合伙伴hCDCrel1和Septin 6,并且也与人类卵巢肿瘤和小鼠T细胞淋巴瘤的发病机制有关。我们在此描述一名64岁的男性,患有伴t(11;17)(q23;q25)的初发急性粒单核细胞白血病(法美英亚型M4)。他的白血病成功诱导进入首次缓解期,然而,缓解期仅持续了很短时间。从未获得第二次缓解,患者在白血病诊断后16个月死于败血症。诊断时对其白血病细胞进行检查,通过Southern印迹法发现MLL基因重排,通过逆转录酶聚合酶链反应(RT-PCR)方法发现MLL-MSF融合转录本。RT-PCR产物的序列分析进一步显示MLL外显子5与MSF外显子3框内融合。对具有MLL-MSF转录本的急性白血病进行进一步的临床和分子分析可能会更深入地了解MLL-septin型白血病的临床特征和分子机制。

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