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Cyanidin Curtails Renal Cell Carcinoma Tumorigenesis

Authors :
Zhenxing Yang
Yaxing Hao
Xin Liu
Jie Xu
Qingqing Wang
Jing Luo
Yuqi Wu
Tao Zhou
Xing Luo
Qian Liu
Longkun Li
Dangling Zhang
Xiaobing Liu
Bishao Sun
Source :
Cellular Physiology and Biochemistry, Vol 46, Iss 6, Pp 2517-2531 (2018)
Publication Year :
2018
Publisher :
S. Karger AG, 2018.

Abstract

Background/Aims: Cyanidin is an anthocyanin found in many foods. Although its variable antioxidant levels are well-documented, little is known about its effects on renal cell carcinoma (RCC) tumorigenesis. This study, therefore, investigated the effects of cyanidin on the proliferation, migration, and invasion of renal cell carcinoma lines and demonstrated, for the first time, significant inhibitory effects of cyanidin on RCC tumorigenesis. Methods: RCC cells were treated with different doses of cyanidin and the effects were tested by Cell Counting Kit-8 reagent, clone formation assay, transwell assay, and flow cytometry. Moreover, the cyanidin-mediated mechanism that curtailed tumorigenesis was analyzed by RNA sequencing (RNA-seq). Sequencing data from The Cancer Genome Atlas (TCGA) were used to compare the expression of both early growth response protein 1 (EGR1) and selenoprotein W (SEPW1) in RCC and tumor-free adjacent normal tissue samples. Real-time PCR (RT-PCR) and/or western blot were used to assess the expression of E-cadherin, cleaved-caspase3, Bcl2, p62, and ATG4. Results: We found significantly greater induction of cell-cycle arrest, apoptosis, and suppression of RCC cell invasion and migration at concentrations of 25 µM and 100 µM than at a concentration of 50 µM. It was also discovered, first through RNA-seq then confirmed by RT-PCR, that cyanidin (100 µM) inhibited RCC carcinogenesis through EGR1 and SEPW1. TCGA data indicated that the expression level of EGR1 was lower and that of SEPW1 was higher in RCC tumor tissue than in normal tissues. Moreover, western blot and/or RT-PCR indicated that cleaved-caspase3 was enhanced and E-cadherin was inhibited by cyanidin treatment. Furthermore, western blot and RT-PCR also showed regulation of p62 and ATG4, which are associated with autophagy. Cyanidin in vivo significantly inhibited the growth of xenografts in nude mice. Conclusions: The results of this study showed the therapeutic potential of cyanidin for the treatment of RCC and the prevention of recurrence and metastasis.

Details

ISSN :
14219778 and 10158987
Volume :
46
Database :
OpenAIRE
Journal :
Cellular Physiology and Biochemistry
Accession number :
edsair.doi.dedup.....c52c1ca5658cb3ff2bfb08e1cf3c7e9f
Full Text :
https://doi.org/10.1159/000489658