Zeng Z J, Li J H, Zhang Y J, Zhao S T
Department of Radiotherapy, Cancer Center, Guangdong General Hospital, Guangdong Academy of Medical Sciences, N0. 106, Zhongshan 2nd Road, 510080 Guangzhou, Guangdong Province, People's Republic of China.
Cancer Radiother. 2013 Jun;17(3):208-14. doi: 10.1016/j.canrad.2013.01.014. Epub 2013 May 7.
Breast cancer is the most common cancer in women. Radiotherapy is considered a standard treatment option after surgery and adjuvant endocrine therapy is also universally used. Tamoxifen and letrozole are the current first-line endocrine therapy drugs. However, information has been scarce about how best to sequence these therapies to maximize their effectiveness and keep toxic effects to a minimum. In this study, we observed the effect of different sequence combination of radiotherapy and endocrine drugs, tamoxifen or letrozole, to get the best treatment sequence.
The combination effect of radiotherapy and tamoxifen was observed on breast tumour cell line MCF-7, radiotherapy and letrozole on aromatase-expressing breast tumour cell line MCF-7CA. Irradiation was performed with 6Gy, except for doses ranging from 0 to 8Gy for clone formation assay. Tamoxifen or letrozole was added before or after irradiation, respectively. Radiosensitivity was evaluated by clonogenic assay, cell viability by 3-(4,-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay. To explore the potential mechanism, cell apoptosis was determined by DNA-binding dye 4',6-diamidino-2-phenylindole dihydrochloride (DAPI) assay, the change of Bcl-2 and Bax expression was by western blot.
Although no significant statistical difference was observed between different sequence, tamoxifen and letrozole both increased radiosensitivity. Furthermore, the above inhibitory effect was related with apoptosis signaling pathway, especially Bcl-2 and Bax.
Taken together, these results suggested that endocrine drugs, such as tamoxifen and letrozole, have potential application with radiotherapy.
乳腺癌是女性最常见的癌症。放疗被认为是手术后的标准治疗选择,辅助内分泌治疗也被广泛应用。他莫昔芬和来曲唑是目前的一线内分泌治疗药物。然而,关于如何最佳地安排这些治疗顺序以最大化其疗效并将毒性作用降至最低的信息却很少。在本研究中,我们观察了放疗与内分泌药物他莫昔芬或来曲唑不同顺序组合的效果,以获得最佳治疗顺序。
观察放疗与他莫昔芬对乳腺癌细胞系MCF-7的联合作用,放疗与来曲唑对表达芳香化酶的乳腺癌细胞系MCF-7CA的联合作用。除克隆形成试验采用0至8Gy剂量范围外,其余均采用6Gy进行照射。他莫昔芬或来曲唑分别在照射前或照射后添加。通过克隆形成试验评估放射敏感性,通过3-(4, -二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑内盐(MTS)试验评估细胞活力。为探索潜在机制,通过DNA结合染料4',6-二脒基-2-苯基吲哚二盐酸盐(DAPI)试验测定细胞凋亡,通过蛋白质免疫印迹法检测Bcl-2和Bax表达的变化。
尽管不同顺序之间未观察到显著的统计学差异,但他莫昔芬和来曲唑均提高了放射敏感性。此外,上述抑制作用与凋亡信号通路有关,尤其是Bcl-2和Bax。
综上所述,这些结果表明内分泌药物,如来曲唑和他莫昔芬,在放疗中有潜在应用价值。