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染色体畸变在预测乳腺癌风险中的应用。

The use of chromosome aberrations in predicting breast cancer risk.

作者信息

Kolusayin Ozar M O, Orta T

机构信息

Dept. of Biology, Faculty of Science, Istanbul University, Istanbul, Turkey.

出版信息

J Exp Clin Cancer Res. 2005 Jun;24(2):217-22.

Abstract

In order to assess the usefulness of chromosome aberrations in predicting breast cancer risk, 10 patients with breast cancer diagnosis and appropriately matching 10 healthy controls were chosen. Spontaneous and radiation induced unstable chromosome aberrations in peripheral blood lymphocytes were compared in the two groups. When the spontaneous aberration frequencies were compared, acentric chromosome frequency, scored in the group of patients was significantly higher than that found in the control group (p<0.01). Absolute aberration frequencies as a determinant of radiosensitivity were calculated by subtracting spontaneous aberration frequencies from the frequencies that were obtained following 2 Gy of Co-60 gamma irradiation. Absolute dicentric chromosome frequency significantly increased in the patients1 group (p<0.01) as compared to that observed in the control group. Increases in either spontaneous acentric chromosome frequency or dicentric chromosome frequency as a determinant of an enhanced radiosensitivity in the group of patients may be valuable in predicting breast cancer risk. The studies involving unstable chromosome aberrations can be easily performed and can facilitate cancer diagnosis with minor effort and low cost.

摘要

为了评估染色体畸变在预测乳腺癌风险方面的作用,选取了10例经乳腺癌诊断的患者,并适当匹配了10名健康对照。比较了两组外周血淋巴细胞中自发的和辐射诱导的不稳定染色体畸变。比较自发畸变频率时,患者组中无着丝粒染色体频率显著高于对照组(p<0.01)。通过从2 Gy的钴-60γ射线照射后获得的频率中减去自发畸变频率来计算作为放射敏感性决定因素的绝对畸变频率。与对照组相比,患者组的绝对双着丝粒染色体频率显著增加(p<0.01)。患者组中自发无着丝粒染色体频率或双着丝粒染色体频率的增加作为放射敏感性增强的决定因素,可能在预测乳腺癌风险方面具有价值。涉及不稳定染色体畸变的研究易于进行,且只需付出少量努力和低成本就能促进癌症诊断。

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