UMR-S1124, Institut national de la santé et de la recherché médicale (Inserm), T3S, Toxicologie Environnementale, Cibles thérapeutiques, Signalisation cellulaire et Biomarqueurs, Paris, France.
Service de Chirurgie Cancérologique Gynécologique et du Sein, Hôpital Européen Georges-Pompidou, Assistance Publique-Hôpitaux de Paris, France.
Environ Health Perspect. 2021 Mar;129(3):37002. doi: 10.1289/EHP7102. Epub 2021 Mar 8.
Breast cancer (BC) is a major public health concern, and its prognosis is very poor once metastasis occurs. The tumor microenvironment and chemical pollution have been suggested recently to contribute, independently, to the development of metastatic cells. The BC microenvironment consists, in part, of adipocytes and preadipocytes in which persistent organic pollutants (POPs) can be stored.
We aimed to test the hypothesis that these two factors (2,3,7,8-tetrachlorodibenzo--dioxin (TCDD), an extensively studied, toxic POP and the microenvironment) may interact to increase tumor aggressiveness.
We used a co-culture model using BC MCF-7 cells or MDA-MB-231 cells together with hMADS preadipocytes to investigate the contribution of the microenvironment and 2,3,7,8-tetrachlorodibenzo--dioxin TCDD on BC cells. Global differences were characterized using a high-throughput proteomic assay. Subsequently we measured the BC stem cell-like activity, analyzed the cell morphology, and used a zebrafish larvae model to study the metastatic potential of the BC cells.
We found that coexposure to TCDD and preadipocytes modified BC cell properties; moreover, it induced the expression of ALDH1A3, a cancer stem cell marker, and the appearance of giant cancer cells with cell-in-cell structures (CICs), which are associated with malignant metastatic progression, that we demonstrated .
The results of our study using BC cell lines co-cultured with preadipocytes and a POP and an zebrafish model of metastasis suggest that the interactions between BC cells and their microenvironment could affect their invasive or metastatic potential. https://doi.org/10.1289/EHP7102.
乳腺癌(BC)是一个重大的公共卫生问题,一旦发生转移,其预后非常差。肿瘤微环境和化学污染物最近被认为独立地促进转移细胞的发展。BC 微环境部分由脂肪细胞和前脂肪细胞组成,其中可以储存持久性有机污染物(POPs)。
我们旨在检验以下假设,即这两个因素(广泛研究的有毒 POP 2,3,7,8-四氯二苯并对二恶英(TCDD)和微环境)可能相互作用以增加肿瘤的侵袭性。
我们使用 BC MCF-7 细胞或 MDA-MB-231 细胞与 hMADS 前脂肪细胞共培养模型来研究微环境和 2,3,7,8-四氯二苯并对二恶英 TCDD 对 BC 细胞的贡献。使用高通量蛋白质组学分析方法来描述全局差异。随后,我们测量了 BC 干细胞样活性,分析了细胞形态,并使用斑马鱼幼虫模型研究了 BC 细胞的转移潜力。
我们发现,TCDD 和前脂肪细胞的共暴露改变了 BC 细胞的特性;此外,它诱导了癌症干细胞标志物 ALDH1A3 的表达,以及出现具有细胞内细胞结构(CICs)的巨大癌细胞,这与恶性转移进展有关,我们进行了证明。
我们使用与前脂肪细胞共培养的 BC 细胞系和 POP 以及斑马鱼转移模型进行的研究结果表明,BC 细胞与其微环境之间的相互作用可能会影响其侵袭或转移潜力。https://doi.org/10.1289/EHP7102.