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Expression profiling of human pluripotent stem cell-derived cardiomyocytes exposed to doxorubicin - integration and visualization of multi omics data
Högskolan i Skövde, Institutionen för biovetenskap. Högskolan i Skövde, Forskningscentrum för Systembiologi. Department of Clinical Chemistry and Transfusion Medicine, Institute of Biomedicine, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden / Takara Bio Europe AB, Gothenburg, Sweden. (Bioinformatik)ORCID-id: 0000-0002-0402-1437
Högskolan i Skövde, Institutionen för biovetenskap. Högskolan i Skövde, Forskningscentrum för Systembiologi. AstraZeneca Gothenburg, CVMD GMed, GMD, Mölndal, Sweden. (Bioinformatik)
Takara Bio Europe AB, Gothenburg, Sweden.
Department of Clinical Chemistry and Transfusion Medicine, Institute of Biomedicine, University of Gothenburg, Sahlgrenska University Hospital, Gothenburg, Sweden.
Vise andre og tillknytning
2018 (engelsk)Inngår i: Toxicological Sciences, ISSN 1096-6080, E-ISSN 1096-0929, Vol. 163, nr 1, s. 182-195Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Anthracyclines, such as doxorubicin, are highly efficient chemotherapeutic agents against a variety of cancers. However, anthracyclines are also among the most cardiotoxic therapeutic drugs presently on the market. Chemotherapeutic-induced cardiomyopathy is one of the leading causes of disease and mortality in cancer survivors. The exact mechanisms responsible for doxorubicin-induced cardiomyopathy are not completely known, but the fact that the cardiotoxicity is dose-dependent and that there is a variation in time-to-onset of toxicity, and gender- and age differences suggests that several mechanisms may be involved.In the present study, we investigated doxorubicin-induced cardiotoxicity in human pluripotent stem cell-derived cardiomyocytes using proteomics. In addition, different sources of omics data (protein, mRNA, and microRNA) from the same experimental setup were further combined and analyzed using newly developed methods to identify differential expression in data of various origin and types. Subsequently, the results were integrated in order to generate a combined visualization of the findings.In our experimental model system, we exposed cardiomyocytes derived from human pluripotent stem cells to doxorubicin for up to two days, followed by a wash-out period of additionally 12 days. Besides an effect on the cell morphology and cardiomyocyte functionality, the data show a strong effect of doxorubicin on all molecular levels investigated. Differential expression patterns that show a linkage between the proteome, transcriptome, and the regulatory microRNA network, were identified. These findings help to increase the understanding of the mechanisms behind anthracycline-induced cardiotoxicity and suggest putative biomarkers for this condition.

sted, utgiver, år, opplag, sider
2018. Vol. 163, nr 1, s. 182-195
Emneord [en]
Human pluripotent stem cells, cardiomyocytes, doxorubicin, multi-omics data, proteomics, toxicity
HSV kategori
Forskningsprogram
Bioinformatik; INF502 Biomarkörer; INF501 Integrering av -omicsdata
Identifikatorer
URN: urn:nbn:se:his:diva-14745DOI: 10.1093/toxsci/kfy012ISI: 000432299900018PubMedID: 29385562Scopus ID: 2-s2.0-85046994085OAI: oai:DiVA.org:his-14745DiVA, id: diva2:1182877
Tilgjengelig fra: 2018-02-14 Laget: 2018-02-14 Sist oppdatert: 2019-02-14bibliografisk kontrollert

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