Autotaxin is induced by TSA through HDAC3 and HDAC7 inhibition and antagonizes the TSA-induced cell apoptosis
2011

Autotaxin Induction by TSA and Its Role in Cancer Cell Survival

publication Evidence: moderate

Author Information

Author(s): Li Song, Wang Baolu, Xu Yan, Zhang Junjie

Primary Institution: The Key Laboratory for Cell Proliferation and Regulation Biology of Ministry of Education, College of Life Sciences, Beijing Normal University, Beijing, China

Hypothesis

The study investigates how trichostatin A (TSA) induces autotaxin (ATX) expression in cancer cells and its role in apoptosis resistance.

Conclusion

ATX is induced by TSA through the inhibition of HDAC3 and HDAC7, which helps cancer cells resist apoptosis.

Supporting Evidence

  • TSA treatment significantly induced ATX expression in SW480 and other cancer cells.
  • Down-regulation of HDAC3 and HDAC7 led to increased ATX expression.
  • ATX induction by TSA protected cancer cells from apoptosis by producing LPA.

Takeaway

When cancer cells are treated with a drug called TSA, they make more of a protein called autotaxin that helps them survive instead of dying.

Methodology

The study used various cancer cell lines to assess the effects of TSA on ATX expression and its role in apoptosis.

Limitations

The study does not explore the effects of ATX induction in all cancer cell types, as some cell lines did not respond to TSA.

Statistical Information

P-Value

p<0.001

Statistical Significance

p<0.001

Digital Object Identifier (DOI)

10.1186/1476-4598-10-18

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