Breast Cancer Cells in 3D Model Alters Their Sensitivity to Hormonal and Growth Factors

被引:1
作者
Nushtaeva A.A. [1 ]
Savinkova M.M. [1 ,2 ]
Ermakov M.S. [1 ]
Varlamov M.E. [1 ,2 ]
Novak D.D. [1 ,2 ]
Richter V.A. [1 ]
Koval O.A. [1 ,2 ]
机构
[1] Institute of Chemical Biology and Fundamental Medicine, Siberian Branch, Russian Academy of Sciences, Novosibirsk
[2] Novosibirsk State University, Novosibirsk
基金
俄罗斯科学基金会;
关键词
17-β; estradiol; 3D cell cultures; breast cancer; cell lines; epidermal growth-factor receptor type 2 (HER2); fibroblasts; transforming growth factor β; tumor cells;
D O I
10.1134/S1990519X22060050
中图分类号
学科分类号
摘要
Abstract: The purpose of this work was to study the formation and growth of mono- (3D) and heterogeneous (3D-2) spheroids composed of stromal and tumor cells that mimic three types of breast cancer: ER+/PR+, HER2+, and ER-/PR-/HER2 when spheroids are exposed to 17-β estradiol (E2) and TGF-β. Breast cancer cell lines MCF7, MDA-MB-231, SK-BR-3 and non-transformed BN120f fibroblasts were used to generate 3D and 3D-2 heterogeneous cultures. Uniform conditions for 3D culturing of all three breast-cancer cell lines are proposed that results in, proliferating spheroids. When tumor cells and healthy fibroblasts were mixed in a ratio of 1 : 4, the inner core of 3D-2 structures contained fibroblasts and the epithelial tumor cells formed outer layer of spheroids. The morphological analysis of spheroids showed that such co-cultivation of tumor and stromal cells in the 3D-2 model, produced more rounded and well-structured spheroids that is typical for self-organization into microtissue in comparison with 3D tumor cell model. It was found that E2 stimulated tumor cell proliferation in 3D and 3D-2 spheroids, regardless of that breast-cancer type these cells imitate. , while in 2D model, MDA-MB-231 cells were resistant to E2. In 3D models MDA-MB-231 cells lost, and SK-BR-3 cells acquired sensitivity to the pro-proliferative effect of TGF-β. Thus, it has been shown that 3D and 3D-2 cell models of breast cancer are an important tool to study the tumor progression and for testing new antitumor approaches, despite the existing 2D models. © 2022, Pleiades Publishing, Ltd.
引用
收藏
页码:555 / 567
页数:12
相关论文
共 40 条
[1]  
Acconcia F., Marino M., The effects of 17β-estradiol in cancer are mediated by estrogen receptor signaling at the plasma membrane, Front. Physiol., 2, (2011)
[2]  
Antoni D., Burckel H., Josset E., Noel G., Three-dimensional cell culture: a breakthrough in vivo, Int. J. Mol. Sci, 16, (2015)
[3]  
Batlle E., Massague J., Transforming growth factor-β signaling in immunity and cancer, Immunity, 50, pp. 924-940, (2019)
[4]  
Boyer J.Z., Phillips G.D.L., Nitta H., Garsha K., Admire B., Kraft R., Dennis E., Vela E., Towne P., Activity of trastuzumab emtansine (T-DM1) in 3D cell culture, Breast Cancer Res Treat, 188, (2021)
[5]  
Brockhoff G., Hei P., Schlegel J., Hofstaedter F., Knuechel R., Epidermal growth factor receptor, c-erbB2 and c-erbB3 receptor interaction, and related cell cycle kinetics of SK-BR-3 and BT474 breast carcinoma cells, Cytometry, 44, (2001)
[6]  
Chen W., Wong C., Vosburgh E., Levine A.J., Foran D.J., an Xu E.Y., High-throughput image analysis of tumor spheroids: a user-friendly software application to measure the size of spheroids automatically and accurately, J. Vis. Exp, 89, (2014)
[7]  
Costa E.C., Moreira A.F., de Melo-Diogo D., Gaspar V.M., Carvalho M.P., Correia I.J., 3D tumor spheroids: an overview on the tools and techniques used for their analysis, Biotechnol. Adv, 34, (2016)
[8]  
Ferlay J., Colombet M., Soerjomataram I., Parkin D.M., Pineros M., Znaor A., Bray F., Cancer statistics for the year 2020: an overview, Int. J. Cancer, 149, (2021)
[9]  
Fernando R.I., Wimalasena J., Estradiol abrogates apoptosis in breast cancer cells through inactivation of BAD: Ras-dependent nongenomic pathways requiring signaling through ERK and Akt, Mol. Biol. Cell, 15, (2004)
[10]  
Ferreira L.P., Gaspar V.M., Mano J.F., Design of spherically structured 3D in vitro tumor models—advances and prospects, Acta Biomat, 75, (2018)