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急性非淋巴细胞白血病体外培养模式与Q带核型的相关性

Correlation of in vitro culture pattern and Q-banded karyotype in acute nonlymphocytic leukemia.

作者信息

Richman C M, Rowley J D

出版信息

Am J Hematol. 1983 Feb;14(1):37-47. doi: 10.1002/ajh.2830140105.

Abstract

Both cytogenetic abnormalities and in vitro growth patterns of leukemic cells have prognostic significance in acute nonlymphocytic leukemia (ANLL). The present study was undertaken to analyze the interrelationship between these two factors and response to therapy. Blast cells from 43 patients with de novo ANLL, four patients with secondary ANLL, and two patients with ANLL following a preleukemic phase were studied using both in vitro culture in methylcellulose and quinacrine chromosome banding techniques. In 19 patients with de novo ANLL, minimal growth in culture (less than or equal to 5 colonies without prominence of small clusters) was noted (Pattern I). Blast cells from the remaining 24 patients formed numerous abnormal clusters and colonies in a continuum distribution (Pattern II). Sixty-three percent of Pattern I patients had completely normal karyotypes (NN). Only 29% of Pattern II patients were NN. No Pattern I patient had only abnormal karyotypes (AA), while 25% of Pattern II patients were AA (p less than 0.05). All six patients with secondary leukemia or leukemia following a preleukemic phase demonstrated both Pattern II growth and cytogenetic abnormalities. Fifty-six percent of Pattern I patients with de novo ANLL responded to chemotherapy, 35% of Pattern II patients responded, and 0% of patients with secondary or post-preleukemic ANLL responded. The correlation between the presence of cytogenetic abnormalities in leukemic cells and a pattern of excessive, abnormal growth in vitro coupled with the trend toward poor prognosis in these patients suggests that cytogenetically abnormal cells may have a proliferative advantage both in vitro and in vivo.

摘要

细胞遗传学异常和白血病细胞的体外生长模式在急性非淋巴细胞白血病(ANLL)中均具有预后意义。本研究旨在分析这两个因素之间的相互关系以及对治疗的反应。采用甲基纤维素体外培养和喹吖因染色体显带技术,对43例初发ANLL患者、4例继发ANLL患者和2例白血病前期后发生ANLL的患者的原始细胞进行了研究。在19例初发ANLL患者中,观察到培养中生长极少(小于或等于5个集落且无小集落突出)(模式I)。其余24例患者的原始细胞形成了大量呈连续分布的异常集落和簇(模式II)。模式I患者中有63%的核型完全正常(NN)。模式II患者中只有29%为NN。模式I患者中没有仅具有异常核型(AA)的,而模式II患者中有25%为AA(p<0.05)。所有6例继发白血病或白血病前期后发生白血病的患者均表现出模式II生长和细胞遗传学异常。初发ANLL的模式I患者中有56%对化疗有反应,模式II患者中有35%有反应,继发或白血病前期后ANLL患者中有0%有反应。白血病细胞中细胞遗传学异常的存在与体外过度异常生长模式之间的相关性以及这些患者预后不良的趋势表明,细胞遗传学异常的细胞在体外和体内可能都具有增殖优势。

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