Disruption of SHH signaling cascade by SBE attenuates lung cancer progression and sensitizes DDP treatment

被引:18
作者
Du, Jing [1 ]
Chen, Weiwei [1 ]
Yang, Lijuan [1 ]
Dai, Juanjuan [1 ]
Guo, Jiwei [1 ]
Wu, Yan [1 ]
Gong, Kaikai [1 ]
Zhang, Jian [2 ]
Yu, Ning [3 ]
Xie, Zhen [4 ]
Xi, Sichuan [1 ]
机构
[1] Binzhou Med Univ Hosp, Canc Res Inst, Binzhou 256600, Peoples R China
[2] Binzhou City Peoples Hosp, Dept Pathol, Binzhou 256610, Peoples R China
[3] Binzhou Med Univ Hosp, Dept Pathol, Binzhou 256600, Peoples R China
[4] Binzhou Med Univ Hosp, Dept Thorac Surg, Binzhou 256600, Peoples R China
关键词
BARBATA D. DON; HEDGEHOG PATHWAY; CELLS; RESISTANCE; MECHANISMS; THERAPIES; TRIAL; REQUIREMENT; COMBINATION; INHIBITION;
D O I
10.1038/s41598-017-02063-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Deregulated Sonic Hedgehog (SHH) pathway facilitates the initiation, progression, and metastasis of Non-small cell lung cancer (NSCLC), confers drug resistance and renders a therapeutic interference option to lung cancer patients with poor prognosis. In this study, we screened and evaluated the specificity of a Chinese herb Scutellariabarbata D. Don extraction (SBE) in repressing SHH signaling pathway to block NSCLC progression. Our study confirmed that aberrant activation of the SHH signal pathway conferred more proliferative and invasive phenotypes to human lung cancer cells. This study revealed that SBE specifically repressed SHH signaling pathway to interfere the SHH-mediated NSCLC progression and metastasis via arresting cell cycle progression. We also found that SBE significantly sensitized lung cancer cells to chemotherapeutic agent DDP via repressing SHH components in vitro and in vivo. Mechanistic investigations indicated that SBE transcriptionally and specifically downregulated SMO and consequently attenuated the activities of GLI1 and its downstream targets in SHH signaling pathway, which interacted with cell cycle checkpoint enzymes to arrest cell cycle progression and lead to cellular growth inhibition and migration blockade. Collectively, our results suggest SBE as a novel drug candidate for NSCLC which specifically and sensitively targets SHH signaling pathway.
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页数:12
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