Tsukamoto Hirohisa, Shibata Kiyosumi, Kajiyama Hiroaki, Terauchi Mikio, Nawa Akihiro, Kikkawa Fumitaka
Department of Obstetrics and Gynecology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
BMC Cancer. 2008 Mar 19;8:74. doi: 10.1186/1471-2407-8-74.
Radiotherapy can be used to treat all stages of cervical cancer. For improving local control via radiotherapy, it is important to use additional antitumor agents. Aminopeptidase N (APN)/CD13, a 150-kDa metalloproteinase, is a multifunctional cell surface aminopeptidase with ubiquitous expression. Recent studies have suggested that APN/CD13 plays an important role in tumor progression in several human malignancies.
We investigated whether the suppression of APN/CD13 using Ubenimex, an inhibitor of APN/CD13 activity, may affect tumor radiosensitivity in cervical cancer cells both in vitro and in vivo. Cell surface APN/CD13 activity in HeLa cells was calculated using alanine-p-nitroanilido as a substrate. For colony formation assays, single-dose radiation and/or Ubenimex were administered to each dish of HeLa cells, and these dishes were cultured for 14 days. Molecular changes of apoptosis were determined by Western blot. Apoptosis was evaluated by Annexin-V PI staining (flow cytometry analysis) and the Tunel method. Moreover, we investigated the effect of combining Ubenimex and low-dose radiation on tumor growth using nude mice.
We demonstrated that Ubenimex enhanced the effectiveness of radiotherapy, acting as a radiosensitizer both in vitro and in vivo. In colony formation assays, a significant decline in clonogenic survival was observed in Ubenimex-treated cells. Mice treated with a combination of radiation and Ubenimex showed a significant prolongation of the tumor-doubling time compared with the control, Ubenimex, or radiation-alone groups. We also showed that ubenimex enhanced radiation-induced apoptosis in vitro and in vivo.
Although further studies are needed, this report suggests that Ubeniemx acts as a radiosensitizer in cervical cancer treatment, and that the inhibition of APN/CD13 activity may represent a new approach for improving the therapeutic efficacy of radiotherapy for uterine cervical cancer.
放射疗法可用于治疗宫颈癌的各个阶段。为通过放射疗法改善局部控制,使用额外的抗肿瘤药物很重要。氨肽酶N(APN)/CD13是一种150 kDa的金属蛋白酶,是一种多功能细胞表面氨肽酶,表达广泛。最近的研究表明,APN/CD13在几种人类恶性肿瘤的肿瘤进展中起重要作用。
我们研究了使用APN/CD13活性抑制剂乌苯美司抑制APN/CD13是否会在体外和体内影响宫颈癌细胞的肿瘤放射敏感性。以丙氨酸-对硝基苯胺为底物计算HeLa细胞表面的APN/CD13活性。对于集落形成试验,向每皿HeLa细胞给予单剂量辐射和/或乌苯美司,然后将这些培养皿培养14天。通过蛋白质免疫印迹法测定凋亡的分子变化。通过膜联蛋白-V碘化丙啶染色(流式细胞术分析)和Tunel法评估凋亡。此外,我们使用裸鼠研究了乌苯美司与低剂量辐射联合对肿瘤生长的影响。
我们证明乌苯美司增强了放射疗法的有效性,在体外和体内均作为放射增敏剂起作用。在集落形成试验中,观察到经乌苯美司处理的细胞克隆形成存活率显著下降。与对照组、乌苯美司组或单独放疗组相比,接受放疗和乌苯美司联合治疗的小鼠肿瘤倍增时间显著延长。我们还表明,乌苯美司在体外和体内均增强了辐射诱导的凋亡。
尽管需要进一步研究,但本报告表明乌苯美司在宫颈癌治疗中作为放射增敏剂起作用,并且抑制APN/CD13活性可能代表一种提高子宫颈癌放射治疗疗效的新方法。