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来曲唑使乳腺癌细胞对电离辐射敏感。

Letrozole sensitizes breast cancer cells to ionizing radiation.

作者信息

Azria David, Larbouret Christel, Cunat Severine, Ozsahin Mahmut, Gourgou Sophie, Martineau Pierre, Evans Dean B, Romieu Gilles, Pujol Pascal, Pèlegrin Andre

机构信息

Department of Radiation Oncology, CRLC Val d'Aurelle, Montpellier, France.

出版信息

Breast Cancer Res. 2005;7(1):R156-63. doi: 10.1186/bcr969. Epub 2004 Dec 7.

Abstract

INTRODUCTION

Radiotherapy (RT) is considered a standard treatment option after surgery for breast cancer. Letrozole, an aromatase inhibitor, is being evaluated in the adjuvant setting. We determined the effects of the combination of RT and letrozole in the aromatase-expressing breast tumour cell line MCF-7CA, stably transfected with the CYP19 gene.

METHODS

Irradiations were performed using a cobalt-60 source with doses ranging from 0 to 4 Gy. Cells were incubated with androstenedione in the presence or absence of letrozole. Effects of treatment were evaluated using clonogenic assays, tetrazolium salt colorimetric (MTT) assays, and cell number determinations. Cell-cycle analyses were conducted using flow cytometry.

RESULTS

The survival fraction at 2 Gy was 0.66 for RT alone and was 0.44 for RT plus letrozole (P = 0.02). Growth of MCF-7CA cells as measured by the cell number 6 days after radiotherapy (2 and 4 Gy) was decreased by 76% in those cells treated additionally with letrozole (0.7 microM) compared with those receiving radiotherapy alone (P = 0.009). Growth inhibition, assessed either by cell number (P = 0.009) or by the MTT assay (P = 0.02), was increased after 12 days of the combination treatment. Compared with radiation alone, the combination of radiation and letrozole produced a significant decrease in radiation-induced G2 phase arrest and a decrease of cells in the S phase, with cell redistribution in the G1 phase.

CONCLUSIONS

These radiobiological results may form the basis for concurrent use of letrozole and radiation as postsurgical adjuvant therapy for breast cancer.

摘要

引言

放射治疗(RT)被认为是乳腺癌手术后的标准治疗选择。芳香化酶抑制剂来曲唑正在辅助治疗环境中进行评估。我们确定了RT与来曲唑联合应用于稳定转染CYP19基因的表达芳香化酶的乳腺癌细胞系MCF-7CA中的效果。

方法

使用钴-60源进行照射,剂量范围为0至4 Gy。在存在或不存在来曲唑的情况下,将细胞与雄烯二酮一起孵育。使用克隆形成试验、四唑盐比色法(MTT)试验和细胞计数来评估治疗效果。使用流式细胞术进行细胞周期分析。

结果

单独RT时2 Gy的存活分数为0.66,RT加来曲唑时为0.44(P = 0.02)。与单独接受放疗的细胞相比,在放疗后6天(2和4 Gy),额外接受来曲唑(0.7 microM)治疗的细胞中,通过细胞计数测量的MCF-7CA细胞生长减少了76%(P = 0.009)。联合治疗12天后,通过细胞计数(P = 0.009)或MTT试验(P = 0.02)评估的生长抑制作用增强。与单独放疗相比,放疗与来曲唑联合应用显著减少了辐射诱导的G2期阻滞,并使S期细胞减少,细胞重新分布到G1期。

结论

这些放射生物学结果可能为来曲唑与放疗同时作为乳腺癌术后辅助治疗的应用提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/101a/1064115/4c276bad3c99/bcr969-1.jpg

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