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. 2021 Apr 3;22(7):3737. doi: 10.3390/ijms22073737

Table 1.

Most recent pre-clinical studies (last 10 years) investigating the role of human lipoaspirate on BC.

Reference Study Setting AT Component BC Model Results
Almarzouqi et al. [135] In vitro Whole AT MCF-7 cells Increased BC proliferation rate; triggered expression of MMP1, integrin α2
Massa et al. [136] In vitro Whole AT; in vitro differentiated adipocytes MDA-MB-231, MCF-7, ZR-75 cells Increased BC proliferation
Rowan et al. [137] In vitro,
in vivo
ASCs MDA-MB-231 cells Stimulated BC migration; stimulated tumor growth by ASCs from BMI 18.3 patient but not BMI 25.0 patient
Kucerova et al. [138] In vitro ASCs SKBR3 cells Increased BC migration, mammosphere formation, EMT, chemosensitivity
Devarajan et al. [139] In vitro ASCs T47D, MCF-7, BT-474 cells Induced EMT; promoted PDGF-D mediated colony formation
Lin et al. [140] In vitro ASCs MCF7 cells Promoted BC migration through ASCs-EVs
Eterno et al. [141] In vitro,
in vivo
Autologous ASCs BC cells from human donors; MDA-MB-231, MCF-7 cells Enhanced aggressiveness in MDA-MB-231 and in 50% of patient-derived BC
Wu et al. [142] In vitro ASCs MDA-MB-231, MDA-MB-468, MCF-7 cells Reduced BC viability
Orecchioni et al. [143] In vitro,
in vivo
Whole AT, ASCs, endothelial progenitors MDA-MB-436, HCC1937 cells Induced EMT; increased tumor volume and lung metastases
Tsuji et al. [144] In vivo lipograft MDA-MB-231, BT-474 xenografts Reduced engraftment; decreased BC proliferation
Silva et al. [145] In vivo Whole AT MCF-7 xenograft Reduced tumor volume and Ki67
Sabol et al. [146] In vitro,
in vivo
obASCs TNBC cell lines; TNBC patient-derived xenograft Promoted metastasis through leptin signaling
Sabol et al. [147] In vitro,
in vivo
obASCs MCF7-Y537S cells; PDX models WHIM20 (Y537S mutation) and WHIM43 (D538G mutation) Promoted metastasis in BC with mutant ERα; in vitro obASCs promoted proliferation and migration of ER WT and ER MUT cells

AT, adipose tissue; ASCs, adipose-derived stromal cells; BC, breast cancer, EMT, epithelial–mesenchymal transition; EVs, extracellular vesicles; obASCs, obesity-altered adipose stem cells; WAT, white adipose tissue.