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建立具有17号染色体短臂异常的新型人类巨核母细胞系CMY。

Establishment of a new human megakaryoblastic cell line, CMY, with chromosome 17p abnormalities.

作者信息

Miura N, Sato T, Fuse A, Okimoto Y, Kinugawa N, Horie H, Ota S, Kakuda H, Yokoe H, Miya T, Suzuki N, Niimi H

机构信息

Department of Pediatrics, School of Medicine, Chiba University, Chuo-ku, Chiba 260, Japan.

出版信息

Int J Mol Med. 1998 Mar;1(3):559-63. doi: 10.3892/ijmm.1.3.559.

Abstract

A new megakaryoblastic cell line CMY was established from a Down's syndrome patient suffering from acute megakaryoblastic leukemia. The karyotypes of CMY showed deletion of chromosome 17 or the translocation of 17p, whereas the blasts of the patient did not reveal these abnormalities of chromosome 17 by conventional karyotype analysis. Blasts of the patient failed to respond to chemotherapy and complete remission could not be attained. The abnormalities of 17p became progressively predominant in the patient. These results suggest that the blasts of a minor clone which had the abnormalities of chromosome 17p might have existed in the patient from the beginning and CMY was established from the minor clone. Investigation of p53 gene by PCR-SSCP analysis revealed that blasts of the patient showed normal patterns, while CMY showed an abnormally migrating band in exon 5 alone. This result suggests that another novel oncogenic factor(s) besides p53 might be present on chromosome 17p and other tumor suppresser genes need to be studied.

摘要

从一名患有急性巨核细胞白血病的唐氏综合征患者中建立了一种新的巨核母细胞系CMY。CMY的核型显示17号染色体缺失或17p易位,而该患者的原始细胞通过传统核型分析未显示17号染色体的这些异常。该患者的原始细胞对化疗无反应,无法实现完全缓解。17p的异常在该患者中逐渐占主导地位。这些结果表明,该患者从一开始可能就存在具有17p染色体异常的小克隆原始细胞,而CMY是从小克隆中建立的。通过PCR-SSCP分析对p53基因进行研究发现,该患者的原始细胞显示正常模式,而CMY仅在外显子5中显示异常迁移带。这一结果表明,除p53外,17p染色体上可能还存在另一种新的致癌因子,需要对其他肿瘤抑制基因进行研究。

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