1. Academic Validation
  2. Disruption of SHH signaling cascade by SBE attenuates lung cancer progression and sensitizes DDP treatment

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

  • Sci Rep. 2017 May 15;7(1):1899. doi: 10.1038/s41598-017-02063-x.
Jing Du 1 Weiwei Chen 1 Lijuan Yang 1 Juanjuan Dai 1 Jiwei Guo 1 Yan Wu 1 Kaikai Gong 1 Jian Zhang 2 Ning Yu 3 Zhen Xie 4 Sichuan Xi 5
Affiliations

Affiliations

  • 1 Cancer Research Institute, Binzhou Medical University hospital, 256600, Binzhou, P.R. China.
  • 2 Department of Pathology, Binzhou City People's Hospital, 256610, Binzhou, P.R. China.
  • 3 Department of Pathology, Binzhou Medical University Hospital, 256600, Binzhou, P.R. China.
  • 4 Department of Thoracic Surgery, Binzhou Medical University Hospital, 256600, Binzhou, P.R. China.
  • 5 Cancer Research Institute, Binzhou Medical University hospital, 256600, Binzhou, P.R. China. [email protected].
Abstract

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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