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Article

Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1

  • Authors:
    • Zhiyuan Hu
    • Pengjun Zhao
    • Huifang Xu
  • View Affiliations / Copyright

    Affiliations: Department of Cardio‑Thoracic Surgery, Zhuji People's Hospital, Zhuji, Zhejiang 311800, P.R. China, Department of Radiotherapy, Hangzhou Cancer Hospital, Hangzhou, Zhejiang 310002, P.R. China, Department of Oncology, Zhejiang Hospital, Hangzhou, Zhejiang 310013, P.R. China
  • Pages: 617-624
    |
    Published online on: December 18, 2019
       https://doi.org/10.3892/or.2019.7440
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Abstract

Acquired epidermal growth factor receptor (EGFR) T790M mutation is the most common mechanism that accounts for EGFR‑TKI (tyrosine kinase inhibitor) resistance of non‑small cell lung cancer (NSCLC). High expense and acquired resistance weaken support for the use of osimertinib for T790M‑positive NSCLC treatment, and limit the efficacy and application of this drug. Hyperoside, a flavonol glycoside compound, extracted from Hypericum perforatum, has been reported to inhibit the growth of a variety of tumors. The present study aimed to investigate the role of hyperoside in treating NSCLC with T790M mutations, and to elucidate the underlying molecular mechanisms. Cell viability assays, apoptosis analysis, reverse transcription‑quantitative PCR, western blot analysis, animal experiments and immunohistochemistry were performed to examine the anticancer activity of hyperoside. Hyperoside inhibited the proliferation and induced the apoptosis of T790M‑positive NSCLC cells. Hyperoside upregulated forkhead box protein O1 (FoxO1) expression and downregulated the level of long non‑coding RNA (lncRNA) colon cancer associated transcript 1 (CCAT1) in T790M‑positive NSCLC cells. In the in vivo study, hyperoside inhibited the growth of T790M‑positive NSCLC xenografts. In conclusion, hyperoside inhibited proliferation and induced apoptosis by upregulating FoxO1 via CCAT1 in T790M‑positive NSCLC both in vitro and in vivo, suggesting that hyperoside is a novel candidate for T790M‑positive NSCLC treatment.
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Copy and paste a formatted citation
Spandidos Publications style
Hu Z, Zhao P and Xu H: Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1. Oncol Rep 43: 617-624, 2020.
APA
Hu, Z., Zhao, P., & Xu, H. (2020). Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1. Oncology Reports, 43, 617-624. https://doi.org/10.3892/or.2019.7440
MLA
Hu, Z., Zhao, P., Xu, H."Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1". Oncology Reports 43.2 (2020): 617-624.
Chicago
Hu, Z., Zhao, P., Xu, H."Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1". Oncology Reports 43, no. 2 (2020): 617-624. https://doi.org/10.3892/or.2019.7440
Copy and paste a formatted citation
x
Spandidos Publications style
Hu Z, Zhao P and Xu H: Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1. Oncol Rep 43: 617-624, 2020.
APA
Hu, Z., Zhao, P., & Xu, H. (2020). Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1. Oncology Reports, 43, 617-624. https://doi.org/10.3892/or.2019.7440
MLA
Hu, Z., Zhao, P., Xu, H."Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1". Oncology Reports 43.2 (2020): 617-624.
Chicago
Hu, Z., Zhao, P., Xu, H."Hyperoside exhibits anticancer activity in non‑small cell lung cancer cells with T790M mutations by upregulating FoxO1 via CCAT1". Oncology Reports 43, no. 2 (2020): 617-624. https://doi.org/10.3892/or.2019.7440
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