Title:Embelin Enhances the Sensitivity of Renal Cancer Cells to Axitinib by Inhibiting HIF
Signaling Pathway
Volume: 23
Issue: 7
Author(s): Qiong Fang, Zhiying Li, Ye Xue, Xin Zong, Wenshuang Ma, Guangmin Xi, Xiao Feng Zhang and Zuowei Li*
Affiliation:
- Shandong University of Traditional Chinese Medicine, Jinan, 250000, Shandong, P.R. China
- Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250014 Shandong, P.R. China
Keywords:
Embelin, axitinib, HIF, renal cell carcinoma, apoptosis.
Abstract:
Background: Renal cell carcinoma (RCC) is a common malignant tumor of the urinary system with a high
recurrence rate and easy metastasis. Current clinical drugs for renal cell carcinoma include immunotherapies and targeted
drugs. Axitinib is a clinically targeted drug for treating renal cell carcinoma, which has shortcomings such as
unstable efficacy and easy drug resistance. Therefore, this study aims to determine whether embelin can enhance the
sensitivity of renal cancer cells to axitinib and explore its regulatory pathways.
Methods: The enhancing effect of embelin on axitinib was detected using MTT, crystal violet staining, and annexin VFITC
staining in two renal cancer cell lines. Western blot was performed to detect the expression of autophagy-related
proteins under different conditions. Bioinformatic tools were used to predict the pathways through which embelin may
act on renal cancer cells, and pharmacological methods were used to verify the results.
Results: Embelin enhanced the sensitivity of renal cancer cells to axitinib in the following aspects: enhancing the inhibition
of cell proliferation by axitinib, and the induction of cell apoptosis. HIF was a potential pathway for embelin’s
action. After IOX2 regulated the HIF-1α pathway, the enhancing effect of embelin on axitinib was weakened. Moreover,
after PT2977 regulated the HIF-2α pathway, the enhancing effect of embelin on axitinib was weakened.
Conclusions: Embelin enhanced the sensitivity of A498 and 786-O renal cancer cells to axitinib by inhibiting the HIF
pathway.