Näytä suppeat kuvailutiedot

dc.contributor.authorKaraman, Sinem
dc.contributor.authorLehti, Satu
dc.contributor.authorZhang, Cheng
dc.contributor.authorTaskinen, Marja‐Riitta
dc.contributor.authorKäkelä, Reijo
dc.contributor.authorMardinoglu, Adil
dc.contributor.authorBrorson, Håkan
dc.contributor.authorAlitalo, Kari
dc.contributor.authorKivelä, Riikka
dc.date.accessioned2024-10-28T12:51:52Z
dc.date.available2024-10-28T12:51:52Z
dc.date.issued2024
dc.identifier.citationKaraman, S., Lehti, S., Zhang, C., Taskinen, M., Käkelä, R., Mardinoglu, A., Brorson, H., Alitalo, K., & Kivelä, R. (2024). Multi‐omics characterization of lymphedema‐induced adipose tissue resulting from breast cancer‐related surgery. <i>Faseb Journal</i>, <i>38</i>(20), Article e70097. <a href="https://doi.org/10.1096/fj.202400498RR" target="_blank">https://doi.org/10.1096/fj.202400498RR</a>
dc.identifier.otherCONVID_243484722
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/97759
dc.description.abstractSecondary lymphedema (LE) following breast cancer-related surgery is a life-long complication, which currently has no cure. LE induces significant regional adipose tissue deposition, requiring liposuction as a treatment. Here, we aimed to elucidate the transcriptional, metabolomic, and lipidomic signature of the adipose tissue developed due to the surgery-induced LE in short- and long-term LE patients and compared the transcriptomic landscape of LE adipose tissue to the obesity-induced adipose tissue. Adipose tissue biopsies were obtained from breast cancer-operated females with LE from the affected and non-affected arms (n = 20 patients). To decipher the molecular properties of the LE adipose tissue, we performed RNA sequencing, metabolomics, and lipidomics combined with bioinformatics analyses. Differential gene expression data from a cohort of lean and obese patients without LE was used for comparisons. Integrative analysis of functional genomics revealed that inflammatory response, cell chemotaxis, and angiogenesis were upregulated biological processes in the LE arm, indicating a sustained inflammation in the edematous adipose tissue; whereas, epidermal differentiation, cell–cell junction organization, water homeostasis, and neurogenesis were downregulated in the LE arm. Surprisingly, only a few genes were found to be the same in the LE-induced and the obesity-induced adipose tissue expansion, indicating a different type of adipose tissue development in these two conditions. In metabolomics analysis, we found reduced levels of a branched-chain amino acid valine in the LE arm and downregulation of the mRNA levels of its transporter SLC6A15. Lipidomics analyses did not show any significant differences between the LE and non-LE arms, suggesting that other factors affect the lipid composition of the adipose tissue more than the LE in these patients. Our results provide a detailed molecular characterization of adipose tissue in secondary LE after breast cancer-related surgery. We also show distinct differences in transcriptomic signatures between LE-induced adipose tissue and obesity-induced adipose tissue, but only minor differences in metabolome and lipidome between the LE and the non-LE arm.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesFaseb Journal
dc.rightsCC BY 4.0
dc.subject.otheradipose-deposition
dc.subject.otherlipidomics
dc.subject.otherliposuction
dc.subject.otherlymphedema
dc.subject.othermetabolomics
dc.subject.othertranscriptomics
dc.titleMulti‐omics characterization of lymphedema‐induced adipose tissue resulting from breast cancer‐related surgery
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202410286613
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0892-6638
dc.relation.numberinseries20
dc.relation.volume38
dc.type.versionpublishedVersion
dc.rights.copyright© 2024 The Author(s). The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.
dc.rights.accesslevelopenAccessfi
dc.subject.ysorintasyöpä
dc.subject.ysometabolomiikka
dc.subject.ysogeeniekspressio
dc.subject.ysorasvakudokset
dc.subject.ysoleikkaushoito
dc.subject.ysotranskriptomi
dc.subject.ysolymfedeema
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p20019
jyx.subject.urihttp://www.yso.fi/onto/yso/p40121
jyx.subject.urihttp://www.yso.fi/onto/yso/p25831
jyx.subject.urihttp://www.yso.fi/onto/yso/p24382
jyx.subject.urihttp://www.yso.fi/onto/yso/p842
jyx.subject.urihttp://www.yso.fi/onto/yso/p38915
jyx.subject.urihttp://www.yso.fi/onto/yso/p27942
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1096/fj.202400498RR
jyx.fundinginformationThis work was funded by the Leducq Foundation Transatlantic Network of Excellence Lymph Vessels in Obesity and Cardiovascular Disease (grant 11CVD03 to K.A.), Jenni and Antti Wihuri Foundation, and the Novo Nordisk Foundation (NNF16OC0023554). S.K. was supported by the Swiss National Science Foundation (Advanced Postdoc. Mobility grant number: P300PB_164732), Orion Research Foundation, Finnish Foundation for Cardiovascular Research, Maud Kuistila Memorial Foundation, Academy of Finland (330053), the Sigrid Juselius Foundation and University of Helsinki. R. Kivelä. was supported by the Academy of Finland (297245), the Sigrid Jusélius Foundation, and the Finnish Foundation for Cardiovascular Research. H.B. was funded by the Swedish Cancer Society, Stockholm (CAN 2016/639, CAN 2013/505) and Skåne County Council's Research, and Development Foundation (REGSKANE-454091, REGSKANE-626131, REGSKANE-816751, Project 2020-0460).
dc.type.okmA1


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