Publication: Plasma Metabolomic Changes following PI3K Inhibition as Pharmacodynamic Biomarkers: Preclinical Discovery to Phase I Trial Evaluation
| dc.contributor.author | Ang, Joo Ern | |
| dc.contributor.author | Pandher, Rupinder | |
| dc.contributor.author | Ang, Joo Chew | |
| dc.contributor.author | Asad, Yasmin J | |
| dc.contributor.author | Henley, Alan T | |
| dc.contributor.author | Valenti, Melanie | |
| dc.contributor.author | Box, Gary | |
| dc.contributor.author | de, Haven Brandon Alexis | |
| dc.contributor.author | Baird, Richard | |
| dc.contributor.author | Friedman, Lori | |
| dc.contributor.author | Derynck, Mika | |
| dc.contributor.author | Vanhaesebroeck, Bart | |
| dc.contributor.author | Eccles, Suzanne A | |
| dc.contributor.author | Kaye, Stan B | |
| dc.contributor.author | Workman, Paul | |
| dc.contributor.author | de, Bono Johann S | |
| dc.contributor.author | Raynaud, Florence I | |
| dc.contributor.other | Antwerp X-ray Analysis, Electrochemistry and Speciation (AXES) | |
| dc.date.accessioned | 2019-04-26T08:57:05Z | |
| dc.date.available | 2019-04-26T08:57:05Z | |
| dc.date.issued | 05/04/16 | |
| dc.description | PI3K plays a key role in cellular metabolism and cancer. Using a mass spectrometry-based metabolomics platform, we discovered that plasma concentrations of 26 metabolites, including amino acids, acylcarnitines, and phosphatidylcholines, were decreased in mice bearing PTEN-deficient tumors compared with non-tumor-bearing controls and in addition were increased following dosing with class I PI3K inhibitor pictilisib (GDC-0941). These candidate metabolomics biomarkers were evaluated in a phase I dose-escalation clinical trial of pictilisib. Time- and dose-dependent effects were observed in patients for 22 plasma metabolites. The changes exceeded baseline variability, resolved after drug washout, and were recapitulated on continuous dosing. Our study provides a link between modulation of the PI3K pathway and changes in the plasma metabolome and demonstrates that plasma metabolomics is a feasible and promising strategy for biomarker evaluation. Also, our findings provide additional support for an association between insulin resistance, branched-chain amino acids, and related metabolites following PI3K inhibition. | |
| dc.identifier.uri | https://demo7.dspace.org/handle/123456789/449 | |
| dc.language | en | |
| dc.publisher | American Association for Cancer Research | |
| dc.title | Plasma Metabolomic Changes following PI3K Inhibition as Pharmacodynamic Biomarkers: Preclinical Discovery to Phase I Trial Evaluation | |
| dspace.entity.type | Publication | |
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