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Multi-omics characterization of lymphedema-induced adipose tissue resulting from breast cancer-related surgery
Wihuri Res Inst, Haartmaninkatu 8, FI- 00290 Helsinki, Finland.;Univ Helsinki, Fac Med, Translat Canc Med Res Program, Helsinki, Finland.;Univ Helsinki, Fac Med, Individualized Drug Therapy Res Program, Helsinki, Finland..ORCID iD: 0000-0002-0719-1773
Wihuri Res Inst, Haartmaninkatu 8, FI- 00290 Helsinki, Finland.;Univ Jyvaskyla, Fac Sport & Hlth Sci, Jyvaskyla, Finland..
KTH, Centres, Science for Life Laboratory, SciLifeLab. KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Protein Science, Systems Biology.ORCID iD: 0000-0002-3721-8586
Univ Helsinki, Res Programs Unit, Clin & Mol Metab, Helsinki, Finland..ORCID iD: 0000-0002-6229-3588
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2024 (English)In: The FASEB Journal, ISSN 0892-6638, E-ISSN 1530-6860, Vol. 38, no 20, article id e70097Article in journal (Refereed) Published
Abstract [en]

Secondary 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. This study analyzes adipose tissue changes using RNA sequencing, metabolomics, and lipidomics in lymphedema after breast cancer-related surgery. Transcriptomics analyses revealed increased inflammation, new blood vessel formation, and reduced skin cell and nerve growth in lymphedema adipose tissue. Compared to obesity, only a few genes were similarly affected. Additionally, lower levels of the amino acid valine and its transporter were observed in lymphedema adipose tissue, while lipid composition remained similar in both swollen and nonswollen arms.image

Place, publisher, year, edition, pages
Wiley , 2024. Vol. 38, no 20, article id e70097
Keywords [en]
adipose-deposition, lipidomics, liposuction, lymphedema, metabolomics, transcriptomics
National Category
Endocrinology and Diabetes Cancer and Oncology
Identifiers
URN: urn:nbn:se:kth:diva-355358DOI: 10.1096/fj.202400498RRISI: 001330093000001PubMedID: 39394863Scopus ID: 2-s2.0-85206123255OAI: oai:DiVA.org:kth-355358DiVA, id: diva2:1909621
Note

QC 20241031

Available from: 2024-10-31 Created: 2024-10-31 Last updated: 2024-10-31Bibliographically approved

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Zhang, ChengMardinoglu, Adil

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Karaman, SinemZhang, ChengTaskinen, Marja-RiittaMardinoglu, AdilBrorson, Hakan
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