Cancer cells activate p53 in response to 10-formyltetrahydrofolate dehydrogenase expression.

Abstract

A folate enzyme, FDH (10-formyltetrahydrofolate dehydrogenase; EC 1.5.1.6), is not a typical tumour suppressor, but it has two basic characteristics of one, i.e. it is down-regulated in tumours and its expression is selectively cytotoxic to cancer cells. We have recently shown that ectopic expression of FDH in A549 lung cancer cells induces G1 arrest and apoptosis that was accompanied by elevation of p53 and its downstream target, p21. It was not known, however, whether FDH-induced apoptosis is p53-dependent or not. In the present study, we report that FDH-induced suppressor effects are strictly p53-dependent in A549 cells. Both knockdown of p53 using an RNAi (RNA interference) approach and disabling of p53 function by dominant-negative inhibition with R175H mutant p53 prevented FDH-induced cytotoxicity in these cells. Ablation of the FDH-suppressor effect is associated with an inability to activate apoptosis in the absence of functional p53. We have also shown that FDH elevation results in p53 phosphorylation at Ser-6 and Ser-20 in the p53 transactivation domain, and Ser-392 in the C-terminal domain, but only Ser-6 is strictly required to mediate FDH effects. Also, translocation of p53 to the nuclei and expression of the pro-apoptotic protein PUMA (Bcl2 binding component 3) was observed after induction of FDH expression. Elevation of FDH in p53 functional HCT116 cells induced strong growth inhibition, while growth of p53-deficient HCT116 cells was unaffected. This implies that activation of p53-dependent pathways is a general downstream mechanism in response to induction of FDH expression in p53 functional cancer cells.

• Authors: Natalia V Oleinik, Natalia I Krupenko, David G Priest, Sergey A Krupenko
• Journal: The Biochemical journal (Biochem J) Vol. 391 Issue Pt 3 Pg. 503-11 (Nov 01 2005) ISSN: 1470-8728 [Electronic] England
• PMID: 16014005 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Apoptosis Regulatory Proteins
• Tumor Suppressor Protein p53
• Serine
• Guanosine Triphosphate
• Adenosine Triphosphate
• Oxidoreductases Acting on CH-NH Group Donors
• formyltetrahydrofolate dehydrogenase

Topics

• Adenosine Triphosphate (metabolism)
• Apoptosis
• Apoptosis Regulatory Proteins (metabolism)
• Cell Line, Tumor
• Gene Expression
• Gene Expression Regulation, Neoplastic
• Guanosine Triphosphate (metabolism)
• Humans
• Lung Neoplasms (enzymology, metabolism)
• Mutagenesis, Site-Directed
• Oxidoreductases Acting on CH-NH Group Donors (genetics, metabolism)
• Phosphorylation
• Protein Transport
• RNA Interference
• Serine (genetics, metabolism)
• Tumor Suppressor Protein p53 (genetics, metabolism)