陈 刚, 金冶宁, 张顺康. Effect of concurrent or sequential exemestane combined with radiation on radiosensitivity of MCF-7 cells[J]. China Oncology, 2016, 26(5): 452-457.
陈 刚, 金冶宁, 张顺康. Effect of concurrent or sequential exemestane combined with radiation on radiosensitivity of MCF-7 cells[J]. China Oncology, 2016, 26(5): 452-457. DOI: 10.3969/j.issn.1007-3969.2016.05.017.
Effect of concurrent or sequential exemestane combined with radiation on radiosensitivity of MCF-7 cells
Background and purpose: Radiotherapy and endocrine therapy are both important parts of adjuvant therapy for breast cancer
yet few studies have been conducted focusing on the interaction between radiation and endocrine therapy. Up to now
no conclusion has been drawn on the timing sequence of adjuvant radiation and endocrine therapy
which is indeed crucial in clinical practice. This study intended primarily to investigate the effect of concurrent or sequential exemestane combined with radiation on radiosensitivity of MCF-7 cells and its possible mechanism
and further to provide rationale for optimal clinical treatment modality. Methods: MCF-7 cells were arranged into three trial groups: the radiation group
exemestane sequenced with radiation group and exemestane followed radiation group. Radiosensitivity was evaluated by clonogenic assay
cell proliferation was measured by MTT assay
the ability to induce cell apoptosis was evaluated by DAPI staining assay
the changes of Bcl-2 and Bax were detected by Western blot. Results: Sensitive enhancement ratios (SER) were 1.51 and 1.37 in the exemestane sequenced with radiation group and exemestane followed radiation group
respectively. Compared with the radiation group
the percentage of cellular proliferation inhibition and apoptosis increased obviously in the exemestane sequenced with radiation group and exemestane followed radiation group. Exemestane combined with radiation made the Bax protein increase obviously and the Bcl-2 protein lowered significantly. Conclusion: Exemestane can enhance the radiosensitivity of MCF-7 cells
whose mechanism might be relevant to the promotion of cellular apoptosis. However
the treatment sequence does not affect the outcome.