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细胞周期蛋白D1过表达增强了乳腺肿瘤细胞系中辐射诱导的细胞凋亡和放射敏感性。

Cyclin D1 overexpression enhances radiation-induced apoptosis and radiosensitivity in a breast tumor cell line.

作者信息

Coco Martin J M, Balkenende A, Verschoor T, Lallemand F, Michalides R

机构信息

Division of Experimental Therapy, The Netherlands Cancer Institute, Amsterdam.

出版信息

Cancer Res. 1999 Mar 1;59(5):1134-40.

Abstract

Overexpression of cyclin D1, a G1 cell cycle regulator, is often found in many different tumor types, such as breast carcinoma and squamous cell carcinoma of the head and neck. The overexpression of this protein is, in several cases, associated with a poor prognosis. In this study, the effect of cyclin D1 on radiosensitivity was investigated in a breast tumor cell line, MCF7, containing a cyclin D1 gene construct under the control of a tetracycline-sensitive regulator. MCF7 cells cultured without tetracycline resulted in a 6-fold increase in the cyclin D1 protein. Cyclin D1-overexpressing MCF7 cells were more sensitive to ionizing radiation than the nonoverexpressing counterparts. The cyclin D1-overexpressing cells also exhibited a higher induction of apoptosis. Treatment with a dose of 5 Gy resulted in a rapid increase of p53 and p21 in the cyclin D1-overexpressing cells. Nonoverexpressing cells showed a more transient expression of these proteins after ionizing radiation. A pronounced G2-M block was observed in both cell lines. The cyclin D1-overexpressing cells were, however, released earlier from the block than the control cells. These data suggest that overexpression of cyclin D1 alters sensitivity toward ionizing radiation by modulating gamma-radiation-induced G2-M transition.

摘要

细胞周期蛋白D1是一种G1期细胞周期调节因子,在许多不同类型的肿瘤中经常发现其过表达,如乳腺癌和头颈部鳞状细胞癌。在一些病例中,这种蛋白的过表达与预后不良有关。在本研究中,利用一种受四环素敏感调节因子控制的细胞周期蛋白D1基因构建体,在乳腺癌细胞系MCF7中研究了细胞周期蛋白D1对放射敏感性的影响。在无四环素条件下培养的MCF7细胞中,细胞周期蛋白D1蛋白增加了6倍。过表达细胞周期蛋白D1的MCF7细胞比未过表达的对应细胞对电离辐射更敏感。过表达细胞周期蛋白D1的细胞也表现出更高的凋亡诱导率。5 Gy剂量的处理导致过表达细胞周期蛋白D1的细胞中p53和p21迅速增加。未过表达的细胞在电离辐射后这些蛋白的表达更短暂。在两种细胞系中均观察到明显的G2-M期阻滞。然而,过表达细胞周期蛋白D1的细胞比对照细胞更早从阻滞中释放。这些数据表明,细胞周期蛋白D1的过表达通过调节γ射线诱导的G2-M期转换来改变对电离辐射的敏感性。

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