Glucose impacts onto the reciprocal reprogramming between mammary adipocytes and cancer cells.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
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

24674

Subventions

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

Auteurs

Maria Rosaria Ambrosio (MR)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy. mariarosaria.ambrosio@cnr.it.

Michiel Adriaens (M)

Maastricht Center for Systems Biology (MaCSBio), Maastricht University, Maastricht, The Netherlands.

Kasper Derks (K)

Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.

Teresa Migliaccio (T)

Department of Translational Medicine (DiSMeT), University of Naples "Federico II", Naples, Italy.

Valerio Costa (V)

Institute of Genetics and Biophysics "A. Buzzati Traverso", National Council of Research (IGB-CNR), Naples, Italy.

Domenico Liguoro (D)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy.

Simona Cataldi (S)

Institute of Genetics and Biophysics "A. Buzzati Traverso", National Council of Research (IGB-CNR), Naples, Italy.

Vittoria D'Esposito (V)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy.

Giovanni Maneli (G)

Department of Translational Medicine (DiSMeT), University of Naples "Federico II", Naples, Italy.

Rita Bassolino (R)

Department of Translational Medicine (DiSMeT), University of Naples "Federico II", Naples, Italy.

Simone Di Paola (S)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy.

Marinella Pirozzi (M)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy.

Fabrizio Schonauer (F)

Department of Public Health, University of Naples "Federico II", Naples, Italy.

Francesco D'Andrea (F)

Department of Public Health, University of Naples "Federico II", Naples, Italy.

Francesco Beguinot (F)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy.
Department of Translational Medicine (DiSMeT), University of Naples "Federico II", Naples, Italy.

Ilja Arts (I)

Maastricht Center for Systems Biology (MaCSBio), Maastricht University, Maastricht, The Netherlands.

Pietro Formisano (P)

Institute of Experimental Endocrinology and Oncology "G. Salvatore", National Council of Research (IEOS-CNR), Naples, Italy. fpietro@unina.it.
Department of Translational Medicine (DiSMeT), University of Naples "Federico II", Naples, Italy. fpietro@unina.it.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH