α-Terthienyl induces prostate cancer cell death through inhibiting androgen receptor expression

LNCaP公司 前列腺癌 雄激素受体 癌症研究 雄激素 癌细胞 癌症 细胞生长 前列腺 生物 蛋白激酶B 信号转导 内科学 化学 内分泌学 医学 细胞生物学 生物化学 激素
作者
Xia Gan,Hailing Huang,Jing Wen,Kai Liu,Yuting Yang,Xiaoning Li,Gang Fang,Wen-Jun Li,Wang Xueni
出处
期刊:Biomedicine & Pharmacotherapy [Elsevier]
卷期号:152: 113266-113266 被引量:1
标识
DOI:10.1016/j.biopha.2022.113266
摘要

Prostate cancer is a disease that often occurs in elderly men. Androgen receptor signaling pathway runs through the occurrence and development of prostate cancer. Thereby, targeting androgen receptor is a crucial strategy for the treatment of prostate cancer. α-Terthienyl, which has been used as photosensitive activator and insecticide, is a natural compound rich in marigold. In the present study, we found α- terthienyl could inhibit the cell viability of four prostate cancer cell lines, especially on LNCaP and 22Rv1 cells which endogenously express androgen receptor. Then we proved that it could inhibit the proliferation of prostate cancer cells and induce apoptosis of prostate cancer cells by plate clone formation assay and flow cytometry respectively. Furthermore, we found α-terthienyl could inhibit androgen receptor nuclear translocation, reduce androgen receptor expression, reduce the mRNA and protein expression of androgen receptor target genes (KLK3, TMPRSS2, PCA3) and nuclear proliferation antigen Ki67 and PCNA. In addition, it inhibited the expression and phosphorylation of Akt protein while increasing the expression of tumor suppressor p27. Besides, we constructed a mouse xenograft prostate cancer model and confirmed that α-terthienyl also inhibited the growth of prostate cancer in vivo. In conclusively, α-terthienyl played an anti-prostate cancer role by inhibiting both the expression of androgen receptor and the transduction of its signal pathway, suggesting that it is a promising natural small molecule for the treatment of prostate cancer.
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