Department of Mechanical Engineering, McMaster University, Hamilton, ON, L8S 0A3, Canada.
Faculty of Health Sciences, McMaster University, Hamilton, ON, L8S 4K1, Canada.
Biochem Biophys Res Commun. 2019 Dec 3;520(2):263-268. doi: 10.1016/j.bbrc.2019.09.133. Epub 2019 Oct 5.
The triple-negative breast cancer (TNBC) subtype is the most aggressive form of invasive breast cancer. Although autophagy is critical to the progression of TNBC, the mechanism of autophagy in regulating the metastatic potential of TNBC still remains unclear. Recently, the effector of the Hippo signaling pathway yes-associated protein (YAP) was shown to promote autophagy. To investigate autophagy regulation in YAP signaling in the context of cancer metastasis, we performed profiling analysis of YAP signaling, YAP subcellular localization, autophagosome formation and cell invasiveness in TNBC cell lines (MDA-MB-231 and Hs 578T) versus estrogen receptor (ER) positive breast cancer cell line MCF7. Our results showed that YAP transcriptional and protein expression was significantly upregulated in TNBC. When we triggered autophagy response in TNBC, YAP translocated into the nucleus and the expression of YAP target gene ankyrin repeat domain 1 (ANKRD1) increased remarkably. The correlation between autophagy response and YAP expression in TNBC was confirmed at the single-cell level. Furthermore, the inhibition of YAP nuclear entry greatly impeded the migration and invasion of TNBC cells while it did not affect the mobility of ER positive breast cancer cells. Therefore, this research established the autophagy-YAP-metastasis axis in TNBC and sheds light on the application of targeting YAP for TNBC therapeutics.
三阴性乳腺癌(TNBC)是最具侵袭性的浸润性乳腺癌。虽然自噬对 TNBC 的进展至关重要,但自噬调节 TNBC 转移潜能的机制仍不清楚。最近,Hippo 信号通路的效应蛋白 yes 相关蛋白(YAP)被证明可以促进自噬。为了研究 Hippo 信号转导中自噬的调节在癌症转移中的作用,我们对 YAP 信号转导、YAP 亚细胞定位、自噬体形成和 TNBC 细胞系(MDA-MB-231 和 Hs 578T)与雌激素受体(ER)阳性乳腺癌细胞系 MCF7 的细胞侵袭性进行了分析。我们的结果表明,YAP 转录和蛋白表达在 TNBC 中显著上调。当我们在 TNBC 中触发自噬反应时,YAP 易位到细胞核,YAP 靶基因锚蛋白重复结构域 1(ANKRD1)的表达显著增加。在 TNBC 中,自噬反应与 YAP 表达之间的相关性在单细胞水平上得到了证实。此外,抑制 YAP 核内进入显著阻碍了 TNBC 细胞的迁移和侵袭,但不影响 ER 阳性乳腺癌细胞的迁移。因此,这项研究确立了 TNBC 中的自噬-YAP-转移轴,并为针对 YAP 的 TNBC 治疗提供了新的思路。