Jiménez Maria Camila, Prieto Karol, Lasso Paola, Gutiérrez Melisa, Rodriguez-Pardo Viviana, Fiorentino Susana, Barreto Alfonso
Grupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Colombia.
Heliyon. 2023 Mar 2;9(3):e14148. doi: 10.1016/j.heliyon.2023.e14148. eCollection 2023 Mar.
Interactions in the tumor microenvironment (TME) between tumor cells and stromal cells such as cancer-associated fibroblasts (CAF) favor increased survival, progression, and transformation of cancer cells by activating mechanisms of invasion and metastasis. The design of new therapies to modulate or eliminate the CAF phenotype or functionality has been the subject of recent research including natural product-based therapies. We have previously described the generation of a standardized extract rich in polyphenols obtained from the plant (P2Et), which present antitumor activities in breast cancer and melanoma models through activities that modulate the metabolism of tumor cells or induce the development of the immune response. In this work, a model of CAF generation was initially developed from the exposure of 3T3 fibroblasts to the cytokine TGFβ1. CAF-like cells generated in this way exhibited changes in the expression of Caveolin-1 and α-SMA, and alterations in glucose metabolism and redox status, typical of CAFs isolated from tumor tissues. Then, P2Et was shown to counteract in vitro-induced CAF-like cell generation, preventing caveolin-1 loss and attenuating changes in glucose uptake and redox profile. This protective effect of P2Et translates into a decrease in the functional ability of CAFs to support colony formation and migration of 4T1 murine breast cancer tumor cells. In addition to the functional interference, the P2Et extract also decreased the expression of genes associated with the epithelial-mesenchymal transition (EMT) and functional activities related to the modulation of the cancer stem cells (CSC) population. This work is an approach to evaluate natural extracts' effect on the interaction between CAF and tumor cells in the tumor microenvironment; thus, these results open the chance to design a more profound and mechanistic analysis to explore the molecular mechanisms of P2Et multimolecular activity and extent this analysis to an perspective. In summary, we present here a standardized polymolecular natural extract that has the potential to act in the TME by interfering with CAF generation and functionality.
肿瘤细胞与基质细胞(如癌症相关成纤维细胞,CAF)之间在肿瘤微环境(TME)中的相互作用,通过激活侵袭和转移机制,有利于癌细胞的存活、进展和转化。设计新的疗法来调节或消除CAF表型或功能,一直是包括基于天然产物的疗法在内的近期研究课题。我们之前描述了从该植物中获得的富含多酚的标准化提取物(P2Et)的生成,其通过调节肿瘤细胞代谢或诱导免疫反应发展的活性,在乳腺癌和黑色素瘤模型中呈现抗肿瘤活性。在这项工作中,最初通过将3T3成纤维细胞暴露于细胞因子TGFβ1建立了CAF生成模型。以这种方式产生的CAF样细胞表现出小窝蛋白-1和α-平滑肌肌动蛋白表达的变化,以及葡萄糖代谢和氧化还原状态的改变,这是从肿瘤组织中分离出的CAF的典型特征。然后,P2Et被证明可抵消体外诱导的CAF样细胞生成,防止小窝蛋白-1丢失,并减弱葡萄糖摄取和氧化还原谱的变化。P2Et的这种保护作用转化为CAF支持4T1小鼠乳腺癌肿瘤细胞集落形成和迁移的功能能力下降。除了功能干扰外,P2Et提取物还降低了与上皮-间质转化(EMT)相关的基因表达以及与癌症干细胞(CSC)群体调节相关的功能活性。这项工作是一种评估天然提取物对肿瘤微环境中CAF与肿瘤细胞之间相互作用影响的方法;因此,这些结果为设计更深入的机制分析提供了机会,以探索P2Et多分子活性的分子机制,并将该分析扩展到体内视角。总之,我们在此展示了一种标准化的多分子天然提取物,它有可能通过干扰CAF的生成和功能在肿瘤微环境中发挥作用。