Suppr超能文献

视网膜母细胞瘤患者细胞对G2期X射线照射的细胞遗传学反应。

Cytogenetic responses to G2 phase x-irradiation of cells from retinoblastoma patients.

作者信息

Sanford K K, Parshad R, Price F M, Tarone R E, Benedict W F

机构信息

Laboratory of Cellular and Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892, USA.

出版信息

Cancer Genet Cytogenet. 1996 May;88(1):43-8. doi: 10.1016/0165-4608(95)00279-0.

Abstract

Fibroblast cell lines from 20 retinoblastoma (RB) patients with the hereditary bilateral form of disease compared with 16 lines from normal donors had a significantly higher chromatid aberration frequency (CAF), and more displaced and nondisplaced breaks per 100 metaphase cells after x-irradiation during the G2 phase of the cell cycle. The mean CAF was 39 +/- 1.0, range 30-46, for cells from normal subjects, compared to a mean of 245.6, range 101-506, for cells from hereditary RB patients (p < 10(-6). Of fibroblast lines from eight patients with unilateral RB, four had a CAF comparable to that of lines from normal donors (< 60) and four had a high CAF (> 130), resembling that of hereditary forms; two of the latter four lines were from patients with familial or deletion 13 forms of RB. Furthermore, in two families, PHA-stimulated blood lymphocytes from RB patients, one bilateral and one unilateral, and from certain unaffected first-degree relatives after G2 phase X-irradiation had a high CAF (> or = 110) compared to a CAF (> or = 53) of cells from three normal donors sampled at the same time. These results were shown not to be related to differences in cell cycle progression or initial extent of chromatid damage. The results suggest that the high frequency of chromatid aberrations in the cells from hereditary RB patients results from a genetic deficiency in DNA repair.

摘要

与来自16名正常供体的成纤维细胞系相比,20名患有遗传性双侧视网膜母细胞瘤(RB)患者的成纤维细胞系在细胞周期的G2期经X射线照射后,具有显著更高的染色单体畸变频率(CAF),且每100个中期细胞中有更多的移位和非移位断裂。正常受试者细胞的平均CAF为39±1.0,范围为30 - 46,而遗传性RB患者细胞的平均CAF为245.6,范围为101 - 506(p < 10⁻⁶)。在8名单侧RB患者的成纤维细胞系中,4个的CAF与正常供体的细胞系相当(< 60),4个具有高CAF(> 130),类似于遗传性RB;后4个细胞系中的2个来自患有家族性或13号染色体缺失型RB的患者。此外,在两个家族中,经G2期X射线照射后,来自RB患者(一名双侧和一名单侧)以及某些未受影响的一级亲属的PHA刺激的血液淋巴细胞具有高CAF(≥110),而同时采样的来自三名正常供体的细胞CAF(≥53)。这些结果表明与细胞周期进程或染色单体损伤的初始程度差异无关。结果提示,遗传性RB患者细胞中染色单体畸变的高频率是由DNA修复的遗传缺陷导致的。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验