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pmid:31078528

Adaptation of Human iPSC-Derived Cardiomyocytes to Tyrosine Kinase Inhibitors Reduces Acute Cardiotoxicity via Metabolic Reprogramming.

Huan Wang · Robert P Sheehan · Adam C Palmer · Robert A Everley · Sarah A Boswell · Noga Ron-Harel · Alison E Ringel · Kristina M Holton · Connor A Jacobson · Alison R Erickson · Laura Maliszewski · Marcia C Haigis · Peter K Sorger

Cell systems · 2019 doi:10.1016/j.cels.2019.03.009

Paper

complete

Experiment

complete

Data

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title
Adaptation of Human iPSC-Derived Cardiomyocytes to Tyrosine Kinase Inhibitors Reduces Acute Cardiotoxicity via Metabolic Reprogramming.
doi
10.1016/j.cels.2019.03.009
pmid
31078528
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[0]
Huan Wang
[1]
Robert P Sheehan
[2]
Adam C Palmer
[3]
Robert A Everley
[4]
Sarah A Boswell
[5]
Noga Ron-Harel
[6]
Alison E Ringel
[7]
Kristina M Holton
[8]
Connor A Jacobson
[9]
Alison R Erickson
[10]
Laura Maliszewski
[11]
Marcia C Haigis
[12]
Peter K Sorger
journal
Cell systems
year
2019
abstract
Tyrosine kinase inhibitors (TKIs) are widely used to treat solid tumors but can be cardiotoxic. The molecular basis for this toxicity and its relationship to therapeutic mechanisms remain unclear; we therefore undertook a systems-level analysis of human cardiomyocytes (CMs) exposed to four TKIs. CMs differentiated from human induced pluripotent stem cells (hiPSCs) were exposed to sunitinib, sorafenib, lapatinib, or erlotinib, and responses were assessed by functional assays, microscopy, RNA sequencing, and mass spectrometry (GEO: GSE114686; PRIDE: PXD012043). TKIs have diverse effects on hiPSC-CMs distinct from inhibition of tyrosine-kinase-mediated signal transduction; cardiac metabolism is particularly sensitive. Following sorafenib treatment, oxidative phosphorylation is downregulated, resulting in a profound defect in mitochondrial energetics. Cells adapt by upregulating aerobic glycolysis. Adaptation makes cells less acutely sensitive to sorafenib but may have long-term negative consequences. Thus, CMs exhibit adaptive responses to anti-cancer drugs conceptually similar to those previously shown in tumors to mediate drug resistance.
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In Figure 7B, media were collected from 1–3 replicate wells per experiment and from 3 independent experiments. Student’s t test was used to compare drug treatment and control at the same times points (n=3).
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Following Sorafenib treatment, oxidative phosphorylation is down-regulated, resulting in a profound defect in mitochondrial energetics.
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