Knockdown of death receptor 5 antisense long noncoding RNA and cisplatin treatment modulate similar macromolecular and metabolic changes in HeLa cells

dc.contributor.author Gürer, Dilek Cansu
dc.contributor.author Erdoğan Vatansever, İpek
dc.contributor.author Ceylan, Çağatay
dc.contributor.author Akgül, Bünyamin
dc.date.accessioned 2026-01-23T10:54:40Z
dc.date.available 2026-01-23T10:54:40Z
dc.date.issued 2022-12
dc.description You can access the datasets of the publication. https://aperta.ulakbim.gov.tr/records/252114
dc.description The registration includes data sets.
dc.description.abstract Background/aim: Despite great progress in complex gene regulatory mechanisms in the dynamic tumor microenvironment, the potential contribution of long noncoding RNAs (lncRNAs) to cancer cell metabolism is poorly understood. Death receptor 5 antisense (DR5-AS) is a cisplatin inducible lncRNA whose knockdown modulates cell morphology. However, its effect on cell metabolism is unknown. The aim of this study is to examine metabolic changes modulated by cisplatin and DR5-AS lncRNA in HeLa cells. Materials and methods: We used cisplatin as a universal cancer therapeutic drug to modulate metabolic changes in HeLa cervix cancer cells. We then examined the extent of metabolic changes by Fourier transform infrared spectroscopy (FTIR). We also performed transcriptomics analyses by generating new RNA-seq data with total RNAs isolated from cisplatin-treated HeLa cells. Then, we compared cisplatin-mediated transcriptomics and macromolecular changes with those mediated by DR5-AS knockdown. Results: Cisplatin treatment caused changes in the unsaturated fatty acid and lipid-to-protein ratios and the glycogen content. These observations in altered cellular metabolism were supported by transcriptomics analyses. FTIR spectroscopy analyses have revealed that DR5-AS knockdown causes a 20.9% elevation in the lipid/protein ratio and a 76.6% decrease in lipid peroxidation. Furthermore, we detected a 3.42% increase in the chain length of the aliphatic lipids, a higher content of RNA, and a lower amount of glycogen indicating relatively lower metabolic activity in the DR5-AS knockdown HeLa cells. Interestingly, we observed a similar gene expression pattern under cisplatin treatment and DR5-AS knockdown HeLa cells. Conclusion: These results suggest that DR5-AS lncRNA appears to account for a fraction of cisplatin-mediated macromolecular and metabolic changes in HeLa cervix cancer cells. Turkish Journal of Biology dergisine gönderilmiş "Knockdown of death receptor 5 antisense long noncoding RNA and cisplatin treatment modulate similar macromolecular and metabolic changes in HeLa cells" isimli makalenin supplementary data dosyalarını içerir. 117Z243 no'lu TÜBİTAK projesinin yürütücüsü Prof. Dr. Bünyamin AKGÜL'dür.
dc.description.sponsorship TÜBİTAK
dc.identifier.doi 10.55730/1300-0152.2634
dc.identifier.issn 1300-0152
dc.identifier.uri https://doi.org/10.55730/1300-0152.2634
dc.identifier.uri https://aperta.ulakbim.gov.tr/records/252114
dc.identifier.uri https://hdl.handle.net/11147/18829
dc.language.iso en_US
dc.publisher TÜBİTAK
dc.rights info:eu-repo/semantics/openAccess
dc.subject Cisplatin
dc.subject Cancer
dc.subject HeLa cells
dc.subject Transcriptomics
dc.subject Metabolism
dc.title Knockdown of death receptor 5 antisense long noncoding RNA and cisplatin treatment modulate similar macromolecular and metabolic changes in HeLa cells
dc.type Dataset
dspace.entity.type Publication
gdc.author.id 0000-0001-5558-8575
gdc.author.id 0000-0001-6415-7654
gdc.author.id 0009-0000-3090-3989
gdc.author.id 0000-0001-9877-9689
gdc.coar.access open access
gdc.coar.type dataset
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Molecular Biology and Genetics
gdc.description.department İzmir Institute of Technology. Food Engineering
gdc.description.publicationcategory Diğer
gdc.identifier.openalex W4313207786
gdc.openalex.collaboration National
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gdc.openalex.normalizedpercentile 0.19
gdc.opencitations.count 0
gdc.plumx.mendeley 5
gdc.plumx.scopuscites 0
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