Development and characterisation of a novel 3D in vitro model of obesity-associated breast cancer as a tool for drug testing

被引:0
作者
Blyth, Rhianna R. R. [1 ]
Laversin, Stephanie A. [1 ]
Foxall, Russell B. [1 ]
Savva, Constantinos [1 ]
Copson, Ellen [2 ,3 ]
Cutress, Ramsey I. [2 ,3 ]
Birts, Charles N. [1 ,4 ,5 ]
Beers, Stephen A. [1 ,5 ]
机构
[1] Univ Southampton, Sch Canc Sci, Antibody & Vaccine Grp, Ctr Canc Immunol,Fac Med, Southampton SO16 6YD, England
[2] Univ Southampton, Fac Med, Sch Canc Sci, Southampton SO16 6YD, England
[3] Univ Hosp Southampton NHS Fdn Trust, NIHR Southampton Biomed Res Ctr, Southampton SO16 6YD, England
[4] Univ Southampton, Fac Environm & Life Sci, Sch Biol Sci, Southampton SO17 1BJ, England
[5] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, England
关键词
ADIPOSE-TISSUE; MYOEPITHELIAL CELLS; NEOADJUVANT CHEMOTHERAPY; TUMOR PROGRESSION; ADIPOCYTE DEATH; FAT-CELLS; EXPRESSION; WOMEN; INFLAMMATION; CONTRIBUTE;
D O I
10.1038/s41523-025-00766-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Obesity is associated with worse breast cancer outcomes and decreased therapeutic efficacy. However, the mechanisms driving obesity-associated therapy resistance remain unclear; in part due to a lack of suitable models that recapitulate the obese tumour microenvironment. To address this, we developed a 3D in vitro model of obesity-associated breast cancer, to investigate biological mechanisms and to use as a drug testing tool. A penta-culture system was developed by co-culturing adipocyte spheroids with breast tumour cells, myoepithelial cells, macrophages, and fibroblasts in a collagen matrix. Tumour cells and macrophages infiltrated adipocyte spheroids, replicating the inflamed-adipose border typical of obese patients. This model was then assessed as a drug testing platform. Obese cultures exhibited increased sensitivity to metformin and, conversely, resistance to paclitaxel, compared to non-obese cultures. This 3D organotypic model effectively recapitulates key features of the obese adipose tumour microenvironment, providing a useful tool to interrogate mechanisms underpinning obesity-related therapy resistance.
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页数:16
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