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Fascin激活β-连环蛋白信号通路并主要通过粘着斑激酶(FAK)促进乳腺癌干细胞功能:与疾病进展的关系

Fascin Activates β-Catenin Signaling and Promotes Breast Cancer Stem Cell Function Mainly Through Focal Adhesion Kinase (FAK): Relation With Disease Progression.

作者信息

Barnawi Rayanah, Al-Khaldi Samiyah, Bakheet Tala, Fallatah Mohannad, Alaiya Ayodele, Ghebeh Hazem, Al-Alwan Monther

机构信息

Stem Cell and Tissue Re-Engineering Program, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

National Center for Stem Cells, Life Science and Environment Research Institute, King Abdulaziz City for Sciences and Technology, Riyadh, Saudi Arabia.

出版信息

Front Oncol. 2020 Apr 21;10:440. doi: 10.3389/fonc.2020.00440. eCollection 2020.

Abstract

Cancer stem cells (CSCs), a rare population of tumor cells with high self-renewability potential, have gained increasing attention due to their contribution to chemoresistance and metastasis. We have previously demonstrated a critical role for the actin-bundling protein (fascin) in mediating breast cancer chemoresistance through activation of focal adhesion kinase (FAK). The latter is known to trigger the β-catenin signaling pathway. Whether fascin activation of FAK would ultimately trigger β-catenin signaling pathway has not been elucidated. Here, we assessed the effect of fascin manipulation in breast cancer cells on triggering β-catenin downstream targets and its dependence on FAK. Gain and loss of fascin expression showed its direct effect on the constitutive expression of β-catenin downstream targets and enhancement of self-renewability. In addition, fascin was essential for glycogen synthase kinase 3β inhibitor-mediated inducible expression and function of the β-catenin downstream targets. Importantly, fascin-mediated constitutive and inducible expression of β-catenin downstream targets, as well as its subsequent effect on CSC function, was at least partially FAK dependent. To assess the clinical relevance of the findings, we evaluated the consequence of fascin, FAK, and β-catenin downstream target coexpression on the outcome of breast cancer patient survival. Patients with coexpression of fascin and FAK or high β-catenin downstream targets showed the worst survival outcome, whereas in fascin, patient coexpression of FAK or high β-catenin targets had less significant effect on the survival. Altogether, our data demonstrated the critical role of fascin-mediated β-catenin activation and its dependence on intact FAK signaling to promote breast CSC function. These findings suggest that targeting of fascin-FAK-β-catenin axis may provide a novel therapeutic approach for eradication of breast cancer from the root.

摘要

癌症干细胞(CSCs)是一群具有高自我更新潜能的罕见肿瘤细胞,因其对化疗耐药性和转移的作用而受到越来越多的关注。我们之前已经证明肌动蛋白捆绑蛋白(fascin)在通过激活粘着斑激酶(FAK)介导乳腺癌化疗耐药性中起关键作用。已知后者会触发β-连环蛋白信号通路。fascin对FAK的激活是否最终会触发β-连环蛋白信号通路尚未阐明。在此,我们评估了在乳腺癌细胞中操纵fascin对触发β-连环蛋白下游靶点的影响及其对FAK的依赖性。fascin表达的增加和减少显示了其对β-连环蛋白下游靶点组成性表达的直接影响以及自我更新能力的增强。此外,fascin对于糖原合酶激酶3β抑制剂介导的β-连环蛋白下游靶点的诱导性表达和功能至关重要。重要的是,fascin介导的β-连环蛋白下游靶点的组成性和诱导性表达,以及其随后对CSC功能的影响,至少部分依赖于FAK。为了评估这些发现的临床相关性,我们评估了fascin、FAK和β-连环蛋白下游靶点共表达对乳腺癌患者生存结果的影响。fascin和FAK共表达或β-连环蛋白下游靶点高表达的患者显示出最差的生存结果,而在fascin、FAK或β-连环蛋白靶点共表达的患者中,对生存的影响较小。总之,我们的数据证明了fascin介导的β-连环蛋白激活的关键作用及其对完整FAK信号传导的依赖性,以促进乳腺CSC功能。这些发现表明,靶向fascin-FAK-β-连环蛋白轴可能为从根本上根除乳腺癌提供一种新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67b/7186340/8269b98a0505/fonc-10-00440-g0001.jpg

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