| Literature DB >> 34736136 |
Huan Zhu1, Ou Dai2, Fei Zhou1, Lian Yang3, Fei Liu1, Yu Liu3, Yu-Lin He3, Lan Bu1, Li Guo4, Cheng Peng5, Liang Xiong6.
Abstract
Lung cancer is one of the most malignant tumors with the highest mortality and morbidity. The tubers of Bletilla striata are known as "an excellent medicine for lung diseases" in traditional Chinese medicine. This study performed a targeted study to explore compounds with anti-lung cancer activity and the molecular mechanisms using A549 cells. Eighteen bibenzyl derivatives, including four new compounds (13, 14, 16, and 18), were isolated from the tubers of B. striata. Analysis of the structure-activity relationship indicated that the cytotoxicity of the bibenzyls against A549 cells increased gradually as the number of the benzyl groups in the structures increased. Bletillain (18), an unusual benzyl polymer, was found to be the most active compound. Further flow cytometric analysis, dual-luciferase assays, real-time PCR assays, and western blot assays revealed that bletillain induced autophagy in A549 cells by regulating the Akt/GSK-3β/β-catenin signaling pathway. Beclin 1, LC3, and p62 are downstream autophagy factors of Akt, and Beclin 1 was the key autophagy factor. These results suggested that bibenzyls of B. striata play important roles in the treatment of lung cancer and provided scientific evidence illustrating why the tubers of B. striata are a suitable medicine for the treatment of lung cancer in traditional Chinese medicine.Entities:
Keywords: A549 lung cancer cells; Akt/GSK-3β/β-catenin pathway; Autophagy-inducing effect; Bibenzyl derivatives; Bletilla striata; Bletillain
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Year: 2021 PMID: 34736136 DOI: 10.1016/j.bioorg.2021.105449
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275