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Alantolactone induces cell apoptosis partially through down-regulation of testes-specific protease 50 expression. | LitMetric

Alantolactone induces cell apoptosis partially through down-regulation of testes-specific protease 50 expression.

Toxicol Lett

National Engineering Laboratory for Druggable Gene and Protein Screening, Northeast Normal University, 130024 Changchun, China; Institute of Genetics and Cytology, Northeast Normal University, Changchun 130024, China.

Published: January 2014

AI Article Synopsis

  • * Researchers created a reporter system to test natural compounds that can inhibit TSP50 expression and found that alantolactone effectively reduces TSP50 activity at both the mRNA and protein levels.
  • * Alantolactone promotes cancer cell death by altering the balance of pro-apoptotic (Bax) and anti-apoptotic (Bcl-2) proteins, enhancing apoptosis, and this effect can be mimicked by reducing TSP50 levels.

Article Abstract

Testes-specific protease 50 (TSP50) is aberrantly expressed in many cancer biopsies and plays a crucial role in tumorigenesis, which make it a potential cancer therapeutic target for drug discovery. Here, we constructed a firefly luciferase reporter driven by the TSP50 gene promoter to screen natural compounds capable of inhibiting the expression of TSP50. Then we identified alantolactone, a sesquiterpene lactone, could efficiently inhibit the promoter activity of TSP50 gene, further results revealed that alantolactone also efficiently inhibited the expression of TSP50 in both mRNA and protein levels. Moreover, we found alantolactone could increase the ratio of Bax/Bcl-2, and activate caspase-9 and caspase-3 in the cancer cells with high expression of TSP50, surprisingly, the same effects can also be observed in the same cells just by knockdown of TSP50 gene expression. Furthermore, our results suggested that overexpression of TSP50 decreased the cell sensitivity to alantolactone-induced apoptosis in those cancer cells. Taken together, these results suggest that alantolactone induces mitochondrial-dependent apoptosis at least partially via down-regulation of TSP50 expression.

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Source
http://dx.doi.org/10.1016/j.toxlet.2013.11.002DOI Listing

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