Aloperine executes antitumor effects through the induction of apoptosis and cell cycle arrest in prostate cancer in vitro and in vivo

• Main Authors: Ling Z, Guan H, You Z, Wang C, Hu L, Zhang L, Wang Y, Chen S, Xu B, Chen M
• Format: Article
• Language: English
• Published: Dove Medical Press 2018-05-01
• Series: OncoTargets and Therapy
• Subjects: Aloperine; Prostate cancer; Proliferation; Apoptosis; Cell cycle
• Online Access: https://www.dovepress.com/aloperine-executes-antitumor-effects-through-the-induction-of-apoptosi-peer-reviewed-article-OTT

Zhixin Ling,1,2,* Han Guan,3,* Zonghao You,1,2,* Can Wang,1,2 Ling Hu,4 Lei Zhang,1,2 Yiduo Wang,1,2 Shuqiu Chen,1,2 Bin Xu,1,2 Ming Chen1,2 1Department of Urology, Affiliated Zhongda Hospital of Southeast University, Nanjing, People’s Republic of China; 2Surgical Research Center, Institute of Urology, Medical School of Southeast University, Nanjing, People’s Republic of China; 3Department of Urology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, People’s Republic of China; 4Department of Nephrology, People’s Hospital of Wuxi City, Wuxi, People’s Republic of China *These authors contributed equally to this work Background: Prostate cancer (PCa) is one of the most common malignant diseases among male patients. Although androgen deprivation therapy remains the main treatment for PCa, most patients would inevitably progress to castration-resistant PCa, which is the main cause of cancer-related deaths. Thus, novel antitumor agents are urgently needed. Recent studies demonstrated that aloperine (ALO) as a natural alkaloid showed antitumor effects in other cancer types. However, the biological function and underlying mechanisms of ALO in PCa have not been investigated. Methods: PCa cell lines including LNCaP, PC3 and DU145 were cultured and treated with ALO. Cell Counting Kit-8 assay, colony formation assay, apoptosis assay and cell cycle assay were conducted to assess the biological role of ALO. In addition, a PCa subcutaneous xenograft mouse model was established to evaluate the role of ALO in terms of proliferation and apoptosis in vivo. We further measured the protein expression levels of p-Akt/Akt, p-ERK/ERK, c-Myc, cleaved caspase 3, p21, p53, Bcl-2 and Bax using the Western blot 48 h after ALO treatment of PCa cells. Results: ALO effectively inhibited the cell viability of PCa by inducing cell cycle arrest via the activation of the p53/p21 pathway and triggering apoptosis in vitro and in vivo. ALO also inhibited phosphorylation of Akt and ERK protein kinases and activated cleaved caspase 3 while exerting antiproliferation function through inducing apoptosis and cell cycle arrest in PCa cells. Conclusion: Based on our findings, we conclude that ALO could suppress the tumor growth and promote cell apoptosis and cell cycle arrest in PCa cells, which indicated that ALO could act as a novel therapeutic agent in treatment of human PCa. Keywords: aloperine, prostate cancer, proliferation, apoptosis, cell cycle