Glucose impacts onto the reciprocal reprogramming between mammary adipocytes and cancer cells.
Adipogenesis
Breast Cancer
Glucose
Mammary Adipocytes
Transcriptional signatures
Tumor Microenvironment
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
21 Oct 2024
21 Oct 2024
Historique:
received:
13
03
2024
accepted:
15
10
2024
medline:
22
10
2024
pubmed:
22
10
2024
entrez:
21
10
2024
Statut:
epublish
Résumé
An established hallmark of cancer cells is metabolic reprogramming, largely consisting in the exacerbated glucose uptake. Adipocytes in the tumor microenvironment contribute toward breast cancer (BC) progression and are highly responsive to metabolic fluctuations. Metabolic conditions characterizing obesity and/or diabetes associate with increased BC incidence and mortality. To explore BC-adipocytes interaction and define the impact of glucose in such dialogue, Mammary Adipose-derived Mesenchymal Stem Cells (MAd-MSCs) were differentiated into adipocytes and co-cultured with ER
Identifiants
pubmed: 39433816
doi: 10.1038/s41598-024-76522-7
pii: 10.1038/s41598-024-76522-7
doi:
Substances chimiques
Glucose
IY9XDZ35W2
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
24674Subventions
Organisme : European Foundation for the Study of Diabetes
ID : EFSD/Lilly Research Fellowship Programme 2016/0052351
Organisme : Ministero dell'Università e della Ricerca
ID : PRIN 2022 - n. 2022KTJLHL
Organisme : Ministero dell'Università e della Ricerca
ID : P2022LPJM4
Organisme : Regione Campania
ID : POR FESR 2014-2020 - COEPICA
Organisme : Regione Campania
ID : POR FESR 2014-2020 - COEPICA
Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : IG2023/29378
Informations de copyright
© 2024. The Author(s).
Références
Rahman, I., Athar, M. T. & Islam, M. Type 2 diabetes, obesity, and Cancer Share some Common and critical pathways. Front. Oncol.10, 600824 (2021).
doi: 10.3389/fonc.2020.600824
pubmed: 33552973
pmcid: 7855858
Scully, T., Ettela, A., LeRoith, D., Gallagher, E. J. & Obesity Type 2 diabetes, and Cancer Risk. Front. Oncol.10, 615375 (2021).
doi: 10.3389/fonc.2020.615375
pubmed: 33604295
pmcid: 7884814
Smolarz, B., Nowak, A. Z. & Romanowicz, H. Breast Cancer-epidemiology, classification, Pathogenesis and treatment (review of literature). Cancers (Basel). 14, 2569 (2022).
doi: 10.3390/cancers14102569
pubmed: 35626173
Panigrahi, G. et al. Diabetes-associated breast cancer is molecularly distinct and shows a DNA damage repair deficiency. JCI Insight. 8, e170105 (2023).
doi: 10.1172/jci.insight.170105
pubmed: 37906280
pmcid: 10795835
Devericks, E. N., Carson, M. S., McCullough, L. E., Coleman, M. F. & Hursting, S. D. The obesity-breast cancer link: a multidisciplinary perspective. Cancer Metastasis Rev.41, 607–625 (2022).
doi: 10.1007/s10555-022-10043-5
pubmed: 35752704
pmcid: 9470704
Balaban, S. et al. Adipocyte lipolysis links obesity to breast cancer growth: adipocyte-derived fatty acids drive breast cancer cell proliferation and migration. Cancer Metab.5, 1 (2017).
doi: 10.1186/s40170-016-0163-7
pubmed: 28101337
pmcid: 5237166
Warburg, O. On the origin of cancer cells. Science. 123, 309–314 (1956).
doi: 10.1126/science.123.3191.309
pubmed: 13298683
Yang, K. et al. The role of lipid metabolic reprogramming in tumor microenvironment. Theranostics. 13, 1774–1808 (2023).
doi: 10.7150/thno.82920
pubmed: 37064872
pmcid: 10091885
Schiliro, C. & Firestein, B. L. Mechanisms of metabolic reprogramming in Cancer cells supporting enhanced growth and proliferation. Cells. 10, 1056 (2022).
doi: 10.3390/cells10051056
Hoy, A. J., Balaban, S. & Saunders, D. N. Adipocyte-tumor cell metabolic crosstalk in breast Cancer. Trends Mol. Med.23, 381–392 (2017).
doi: 10.1016/j.molmed.2017.02.009
pubmed: 28330687
Rybinska, I., Agresti, R., Trapani, A., Tagliabue, E. & Triulzi, T. Adipocytes Breast Cancer Thick Thin Cells9, 560 (2020).
pubmed: 32120856
Hanahan, D. & Weinberg, R. A. Hallmarks of cancer: the next generation. Cell. 144, 646–674 (2011).
doi: 10.1016/j.cell.2011.02.013
pubmed: 21376230
Kim, D. S., Scherer, P. E. & Obesity Diabetes, and increased Cancer progression. Diabetes Metab. J.45, 799–812 (2021).
doi: 10.4093/dmj.2021.0077
pubmed: 34847640
pmcid: 8640143
Ambrosio, M. R. et al. Glucose enhances pro-tumorigenic functions of mammary adipose-derived mesenchymal Stromal/Stem cells on breast Cancer cell lines. Cancers (Basel). 14, 5421 (2022).
doi: 10.3390/cancers14215421
pubmed: 36358839
Wu, Q. et al. Cancer-associated adipocytes: key players in breast cancer progression. J. Hematol. Oncol.12, 95 (2019).
doi: 10.1186/s13045-019-0778-6
pubmed: 31500658
pmcid: 6734503
D’Esposito, V. et al. Mammary adipose tissue control of breast Cancer progression: impact of obesity and diabetes. Front. Oncol.10, 1554 (2020).
doi: 10.3389/fonc.2020.01554
pubmed: 32850459
pmcid: 7426457
Zhao, C. et al. Cancer- associated adipocytes: emerging supporters in breast cancer. J. Exp. Clin. Cancer Res.39, 156 (2020).
doi: 10.1186/s13046-020-01666-z
pubmed: 32787888
pmcid: 7425140
Rybinska, I., Mangano, N., Tagliabue, E. & Triulzi, T. Cancer-Associated adipocytes in breast Cancer: causes and consequences. Int. J. Mol. Sci.22, 3775 (2021).
doi: 10.3390/ijms22073775
pubmed: 33917351
pmcid: 8038661
Choi, J., Cha, Y. J. & Koo, J. S. Adipocyte biology in breast cancer: from silent bystander to active facilitator. Prog Lipid Res.69, 11–20 (2018).
doi: 10.1016/j.plipres.2017.11.002
pubmed: 29175445
D’Esposito, V. et al. Adipocyte-released insulin- like growth factor-1 is regulated by glucose and fatty acids and controls breast cancer cell growth in vitro. Diabetologia. 55, 2811–2822 (2012).
doi: 10.1007/s00125-012-2629-7
pubmed: 22798065
pmcid: 3433668
D’Esposito, V. et al. Adipose microenvironment promotes triple negative breast cancer cell invasiveness and dissemination by producing CCL5. Oncotarget. 7, 24495–24509 (2016).
doi: 10.18632/oncotarget.8336
pubmed: 27027351
pmcid: 5029717
Ambrosio, M. R. et al. Glucose impairs tamoxifen responsiveness modulating connective tissue growth factor in breast cancer cells. Oncotarget. 8, 109000–109017 (2017).
doi: 10.18632/oncotarget.22552
pubmed: 29312586
pmcid: 5752499
Arneth, B. Tumor Microenvironment. Med. (Kaunas). 56, 15 (2019).
Turner, K. M., Yeo, S. K., Holm, T. M., Shaughnessy, E. & Guan, J. L. Heterogeneity within molecular subtypes of breast cancer. Am. J. Physiol. Cell. Physiol.1, C343–C354 (2021).
doi: 10.1152/ajpcell.00109.2021
Pati, S., Irfan, W., Jameel, A., Ahmed, S. & Shahid, R. K. Obesity and Cancer: a current overview of Epidemiology, Pathogenesis, outcomes, and management. Cancers (Basel). 15, 485 (2023).
doi: 10.3390/cancers15020485
pubmed: 36672434
Wang, Y. Y. et al. Mammary adipocytes stimulate breast cancer invasion through metabolic remodeling of tumor cells. JCI Insight. 2, e87489 (2017).
doi: 10.1172/jci.insight.87489
pubmed: 28239646
pmcid: 5313068
Zembroski, A. S., Andolino, C., Buhman, K. K. & Teegarden, D. Proteomic characterization of cytoplasmic lipid droplets in human metastatic breast Cancer cells. Front. Oncol.11, 576326 (2021).
doi: 10.3389/fonc.2021.576326
pubmed: 34141606
pmcid: 8204105
Tan, J., Buache, E., Chenard, M. P., Dali-Youcef, N. & Rio, M. C. Adipocyte is a non- trivial, dynamic partner of breast cancer cells. Int. J. Dev. Biol.55 (7–9), 851–859 (2011).
doi: 10.1387/ijdb.113365jt
pubmed: 21948738
Aprile, M. et al. PPARγ∆5, a naturally Occurring Dominant-negative splice isoform, impairs PPARγ function and adipocyte differentiation. Cell. Rep.25, 1577–1592e6 (2018).
doi: 10.1016/j.celrep.2018.10.035
pubmed: 30404011
Ambrosio, M. R. et al. Serotoninergic receptor ligands improve tamoxifen effectiveness on breast cancer cells. BMC Cancer. 22, 171 (2022).
doi: 10.1186/s12885-021-09147-y
pubmed: 35168555
pmcid: 8845285
Dobin, A. et al. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 29, 15–21 (2013).
doi: 10.1093/bioinformatics/bts635
pubmed: 23104886
Anders, S., Pyl, P. T. & Huber, W. HTSeq–a Python framework to work with high- throughput sequencing data. Bioinformatics. 31, 166–169 (2015).
doi: 10.1093/bioinformatics/btu638
pubmed: 25260700
Love, M. I., Huber, W. & Anders, S. Moderated estimation of Fold change and dispersion for RNA-seq data with DESeq2. Genome Biol.15, 550 (2014).
doi: 10.1186/s13059-014-0550-8
pubmed: 25516281
pmcid: 4302049