%0 Journal Article
%T Ginsenosides synergize with mitomycin C in combating human non-small cell lung cancer by repressing Rad51-mediated DNA repair
%A Chang Shao
%A Dan-dan Wang
%A Hai-ping Hao
%A Li-juan Cao
%A Meng-qiu Wu
%A Min Zhao
%A Qing-ran Li
%A Yuan Che
%A Yun Wang
%J Archive of "Acta Pharmacologica Sinica".
%D 2018
%R 10.1038/aps.2017.53
%X The use of ginseng extract as an adjuvant for cancer treatment has been reported in both animal models and clinical applications, but its molecular mechanisms have not been fully elucidated. Mitomycin C (MMC), an anticancer antibiotic used as a first- or second-line regimen in the treatment for non-small cell lung carcinoma (NSCLC), causes serious adverse reactions when used alone. Here, by using both in vitro and in vivo experiments, we provide evidence for an optimal therapy for NSCLC with total ginsenosides extract (TGS), which significantly enhanced the MMC-induced cytotoxicity against NSCLC A549 and PC-9 cells in vitro when used in combination with relatively low concentrations of MMC. A NSCLC xenograft mouse model was used to confirm the in vivo synergistic effects of the combination of TGS with MMC. Further investigation revealed that TGS could significantly reverse MMC-induced S-phase cell cycle arrest and inhibit Rad51-mediated DNA damage repair, which was evidenced by the inhibitory effects of TGS on the levels of phospho-MEK1/2, phospho-ERK1/2 and Rad51 protein and the translocation of Rad51 from the cytoplasm to the nucleus in response to MMC. In summary, our results demonstrate that TGS could effectively enhance the cytotoxicity of MMC against NSCLC cells in vitro and in vivo, thereby revealing a novel adjuvant anticancer mechanism of TGS. Combined treatment with TGS and MMC can significantly lower the required concentration of MMC and can further reduce the risk of side effects, suggesting a better treatment option for NSCLC patients
%K non-small cell lung carcinoma
%K total ginsenosides extract
%K mitomycin C
%K synergistic effect
%K cell cycle arrest
%K DNA damage repair
%K MEK1/2
%K ERK1/2
%K Rad51
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843838/