Autophagy Modulation in Human Thyroid Cancer Cells following Aloperine Treatment

Aloperine, an alkaloid isolated from Sophora alopecuroides, exhibits multiple pharmacological activities including anti-inflammatory, antioxidant, antiallergic, antinociceptive, antipathogenic, and antitumor effects. Furthermore, it exerts protective effects against renal and neuronal injuries. Seve...

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Published inInternational journal of molecular sciences Vol. 20; no. 21; p. 5315
Main Authors Yu, Hui-I, Shen, Hui-Ching, Chen, Shu-Hsin, Lim, Yun-Ping, Chuang, Hsiang-Hsun, Tai, Tsai-Sung, Kung, Fang-Ping, Lu, Chieh-Hsiang, Hou, Chia-Yi, Lee, Ying-Ray
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 25.10.2019
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Summary:Aloperine, an alkaloid isolated from Sophora alopecuroides, exhibits multiple pharmacological activities including anti-inflammatory, antioxidant, antiallergic, antinociceptive, antipathogenic, and antitumor effects. Furthermore, it exerts protective effects against renal and neuronal injuries. Several studies have reported antitumor effects of aloperine against various human cancers, including multiple myeloma; colon, breast, and prostate cancers; and osteosarcoma. Cell cycle arrest, apoptosis induction, and tumorigenesis suppression have been demonstrated following aloperine treatment. In a previous study, we demonstrated antitumor effects of aloperine on human thyroid cancer cells through anti-tumorigenesis and caspase-dependent apoptosis induction via the Akt signaling pathway. In the present study, we demonstrated the modulation of the autophagy mechanism following the incubation of multidrug-resistant papillary and anaplastic human thyroid cancer cells with aloperine; we also illustrate the underlying mechanisms, including AMPK, Erk, JNK, p38, and Akt signaling pathways. Further investigation revealed the involvement of the Akt signaling pathway in aloperine-modulated autophagy in human thyroid cancer cells. These results indicate a previously unappreciated function of aloperine in autophagy modulation in human thyroid cancer cells.
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These authors contributed equally to this work.
Hsiang-Hsun Chuang had passed away.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms20215315