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使用造血生长因子对非淋巴细胞性肿瘤进行细胞遗传学研究:与粒细胞集落刺激因子(G-CSF)相比,粒细胞-巨噬细胞集落刺激因子(GM-CSF)可显著增加有丝分裂并改善带型染色体的质量。

Cytogenetic studies of non-lymphocytic neoplasias using hematopoietic growth factors: GM-CSF provides pronounced mitotic increase and improvement of the quality of banded chromosomes compared to G-CSF.

作者信息

Nakamura H, Sasagawa I, Itoyama T, Mine M, Amenomori T, Sadamori N, Tomonaga M

机构信息

Department of Hematology, Nagasaki University School of Medicine, Japan.

出版信息

Leukemia. 1993 Sep;7(9):1471-5.

PMID:7690442
Abstract

Thirty patients with a variety of non-lymphocytic neoplasias were studied cytogenetically using short-term liquid cultures of bone marrow or peripheral blood cells with or without either granulocyte colony-stimulating factor (G-CSF) or granulocyte-macrophage CSF (GM-CSF). The final concentration of these growth factors was 10 ng/ml and the duration of culture was 48 h, since these provided optimal increases in mitotic index (MI). In GM-CSF-stimulated culture, 23 out of the 30 patients (77%) had a significantly (p < 0.05) higher MI than that in unstimulated culture, whereas only five (17%) did so in G-CSF-stimulated culture. The quality of banded chromosomes was considerably good in 17 out of the 30 patients (57%) with GM-CSF, whereas it was so only in two (7%) and three (10%) patients with no CSF and G-CSF, respectively. Of the 30 patients, 27 (90%) had the same chromosomal findings with G-CSF/GM-CSF as without CSF, but the remaining three (10%) showed a remarkable change after stimulation. Culture for 72 h with G-CSF or GM-CSF disclosed a minor abnormal clone which was undetected in 24 and 48 h cultures in a patient with myelofibrosis with myeloid metaplasia. Thus, compared with G-CSF, adding GM-CSF to cell culture may be useful for cytogenetic studies of non-lymphocytic neoplasias. The chromosomal findings may, however, be changed by these growth factors for some patients.

摘要

对30例患有各种非淋巴细胞性肿瘤的患者进行了细胞遗传学研究,采用骨髓或外周血细胞的短期液体培养,添加或不添加粒细胞集落刺激因子(G-CSF)或粒细胞-巨噬细胞集落刺激因子(GM-CSF)。这些生长因子的最终浓度为10 ng/ml,培养持续时间为48小时,因为这些条件能使有丝分裂指数(MI)得到最佳提升。在GM-CSF刺激的培养中,30例患者中有23例(77%)的MI显著高于未刺激培养(p < 0.05),而在G-CSF刺激的培养中只有5例(17%)如此。在使用GM-CSF的30例患者中,有17例(57%)的带型染色体质量相当好,而在未使用CSF和使用G-CSF的患者中,分别只有2例(7%)和3例(10%)如此。30例患者中,27例(90%)在使用G-CSF/GM-CSF时与未使用CSF时的染色体结果相同,但其余3例(10%)在刺激后出现了显著变化。在一名骨髓化生伴骨髓纤维化的患者中,用G-CSF或GM-CSF培养72小时发现了一个在24小时和48小时培养中未检测到的小异常克隆。因此,与G-CSF相比,在细胞培养中添加GM-CSF可能有助于非淋巴细胞性肿瘤的细胞遗传学研究。然而,这些生长因子可能会使一些患者的染色体结果发生改变。

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