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Morphomechanical Alterations Induced by Transforming Growth Factor-β1 in Epithelial Breast Cancer Cells

机译:转化生长因子-β1在上皮性乳腺癌细胞中诱导的形态力学改变

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The Epithelial to mesenchymal transition (EMT) is the process that drives epithelial tumor cells to acquire an invasive phenotype. The role of transforming growth factor-β1 (TGF-β1) in EMT is still debated. We used confocal laser scanning microscopy and scanning force spectroscopy to perform a morphomechanical analysis on epithelial breast cancer cells (MCF-7), comparing them before and after TGF-β1 exogenous stimulation (5 ng/mL for 48 h). After TGF-β1 treatment, loss of cell–cell adherence (mainly due to the reduction of E-cadherin expression of about 24%) and disaggregation of actin cortical fibers were observed in treated MCF-7. In addition, TGF-β1 induced an alteration of MCF-7 nuclei morphology as well as a decrease in the Young’s modulus, owing to a rearrangement that involved the cytoskeletal networks and the nuclear region. These relevant variations in morphological features and mechanical properties, elicited by TGF-β1, suggested an increased capacity of MCF-7 to migrate, which was confirmed by a wound healing assay. By means of our biophysical approach, we highlighted the malignant progression of breast cancer cells induced by TGF-β1 exposure. We are confirming TGF-β1’s role in EMT by means of morphomechanical evidence that could represent a turning point in understanding the molecular mechanisms involved in cancer progression.
机译:上皮向间质转化(EMT)是驱动上皮肿瘤细胞获得侵袭性表型的过程。转化生长因子-β1(TGF-β1)在EMT中的作用仍存在争议。我们使用共聚焦激光扫描显微镜和扫描力光谱法对上皮性乳腺癌细胞(MCF-7)进行了形态力学分析,比较了TGF-β1外源刺激(5 ng / mL,持续48 h)之前和之后。 TGF-β1处理后,在处理过的MCF-7中观察到细胞间粘附力的丧失(主要是由于E-钙粘蛋白表达降低约24%)和肌动蛋白皮质纤维的分解。此外,由于涉及细胞骨架网络和核区域的重排,TGF-β1诱导了MCF-7核形态的改变以及杨氏模量的降低。由TGF-β1引起的形态学特征和机械性能的这些相关变化表明,MCF-7迁移的能力增强,这一点已通过伤口愈合试验得以证实。通过我们的生物物理方法,我们强调了TGF-β1暴露诱导的乳腺癌细胞的恶性进展。我们正在通过形态力学证据来证实TGF-β1在EMT中的作用,这可能是理解癌症发展所涉及的分子机制的转折点。

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