AI Article Synopsis

  • Tetrandrine, extracted from the root of Stephania tetrandra, has traditional uses in treating silicosis and arthritis, and shows promise as an anti-cancer agent.
  • Research indicates that tetrandrine inhibits cell growth and induces apoptosis in human lung carcinoma cells, characterized by specific cellular changes and increased apoptotic markers.
  • The study links tetrandrine's effects to the activation of certain proteins like p21 and caspase-3, suggesting it may serve as a potential cell cycle blocker and cancer preventive therapy.

Article Abstract

Tetrandrine, isolated from the root of Stephania tetrandra, has been used in Chinese medicine for the treatment of silicosis and arthritis, and it also has anti-tumor/growth activities. However, the signaling pathways of tetrandrine-induced growth arrest and apoptosis in cancer cells remain unclear. We investigated the molecular mechanisms of tetrandrine-induced apoptosis and growth arrest in human lung carcinoma cells. Upon treatment with tetrandrine, a time-dependent inhibition of cell growth was observed and cells developed many of the hallmark features of apoptosis. Flow cytometry analysis confirmed that tetrandrine increased populations of both apoptotic sub-G1 and G1 phase. Tetrandrine-induced growth inhibition was associated with induction of Cdk inhibitor p21, inhibition of cyclin D1 and activation of caspase-3. Tetrandrine also affected the expression patterns of cytoskeletons including distribution of F-actin and expression level of microtubule. These results suggest that tetrandrine merits further investigation as a cell cycle blocker as well as a cancer chemopreventive agent.

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