Department of Oncology, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100050, China.
Cancer Chemother Pharmacol. 2013 Oct;72(4):777-88. doi: 10.1007/s00280-013-2253-3. Epub 2013 Aug 23.
Capecitabine (CAP), a prodrug, needs to be converted to 5-fluorouracil by several key enzymes, including thymidine phosphorylase (TP). To improve the therapeutic index, potentiation of antitumor activity of CAP is required. In this study, we explored whether lidamycin (LDM), an enediyne anticancer antibiotic, can induce synergistic antitumor effects in combination with CAP in murine breast cancer in vitro and in vivo.
Using MTT, cell migration and invasion, siRNA knockdown, and Western blot assays, the in vitro synergistic effects of LDM plus CAP on 4T1(LUC) cells were evaluated, and the mechanism of this synergy was explored. For in vivo model of orthotopic implantation model of 4T1(LUC) cells, optical molecular imaging system was utilized to evaluate the growth of primary tumor and metastasis. To further understand the mechanism of action of the LDM/CAP combination, immunohistochemistry analysis was carried out to detect thymidine phosphorylase induction and ERK signaling.
As determined by MTT and transwell assay, LDM enhanced the inhibitory effects of CAP on cancer cell proliferation, migration, and invasion. Western blot showed that this synergistic effect was attributed to the up-regulated expression of TP induced by LDM. Knocking down TP impaired the synergistic anti-proliferative effect of LDM and CAP. Furthermore, our data suggested that LDM-induced up-regulation of TP both in vitro and in vivo is associated with ERK activation, because the inhibition of ERK activity by ERK inhibitor U0126 abrogated LDM-induced TP up-regulation. In animal models, LDM plus CAP potently inhibited primary tumor growth as well as lung metastasis compared with control or single-agent-treated group.
LDM can potentiate the antitumor effects of CAP on breast cancer line. The synergistic effects suggest that the combination of LDM and CAP is an innovative antitumor strategy for breast cancer therapy.
卡培他滨(CAP)是一种前体药物,需要几种关键酶(包括胸苷磷酸化酶(TP))将其转化为 5-氟尿嘧啶。为了提高治疗指数,需要增强 CAP 的抗肿瘤活性。在这项研究中,我们探讨了是否榄香烯(LDM),一种烯二炔类抗癌抗生素,能够在体外和体内增强 CAP 对乳腺癌的抗肿瘤协同作用。
通过 MTT、细胞迁移和侵袭、siRNA 敲低和 Western blot 检测,评估 LDM 加 CAP 对 4T1(LUC)细胞的体外协同作用,并探讨这种协同作用的机制。对于 4T1(LUC)细胞的原位植入模型,利用光学分子成像系统评估原发肿瘤和转移的生长。为了进一步了解 LDM/CAP 联合作用的机制,进行免疫组化分析以检测胸苷磷酸化酶的诱导和 ERK 信号。
MTT 和 Transwell 检测结果表明,LDM 增强了 CAP 对癌细胞增殖、迁移和侵袭的抑制作用。Western blot 显示,这种协同作用归因于 LDM 诱导的 TP 表达上调。敲低 TP 会削弱 LDM 和 CAP 的协同抗增殖作用。此外,我们的数据表明,LDM 在体外和体内诱导的 TP 上调与 ERK 激活有关,因为 ERK 抑制剂 U0126 抑制 ERK 活性会阻断 LDM 诱导的 TP 上调。在动物模型中,与对照组或单药治疗组相比,LDM 加 CAP 可强烈抑制原发肿瘤生长和肺转移。
LDM 可增强 CAP 对乳腺癌细胞系的抗肿瘤作用。协同作用表明,LDM 和 CAP 的联合是乳腺癌治疗的一种创新抗肿瘤策略。