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环状 RNA circSKA3 通过结合整合素 β1 诱导侵袭伪足形成从而增强乳腺癌侵袭。

The Circular RNA circSKA3 Binds Integrin β1 to Induce Invadopodium Formation Enhancing Breast Cancer Invasion.

机构信息

Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada.

Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.

出版信息

Mol Ther. 2020 May 6;28(5):1287-1298. doi: 10.1016/j.ymthe.2020.03.002. Epub 2020 Mar 10.

Abstract

Metastatic cancer cells invade surrounding tissues by forming dynamic actin-based invadopodia, which degrade the surrounding extracellular matrix and allow cancer cell invasion. Regulatory RNAs, including circular RNA, have been implicated in this process. By microarray, we found that the circular RNA circSKA3 was highly expressed in breast cancer cells and human breast cancer tissues. We further found that the invasive capacity of breast cancer cells was positively correlated with circSKA3 expression, through the formation of invadopodia. Mechanistically, we identified Tks5 and integrin β1 as circSKA3 binding partners in these tumor-derived invadopodia. Ectopic circSKA3 expression conferred increased tumor invasiveness in vitro and in vivo. We further identified the RNA-protein binding sites between circSKA3, Tks5 and integrin β1. In tumor formation assays, we found that circSKA3 expression promoted tumor progression and invadopodium formation. Mutation of the circSKA3 binding sites or transfection with blocking oligos abrogated the observed effects. Thus, we provide evidence that the circular RNA circSKA3 promotes tumor progression by complexing with Tks5 and integrin β1, inducing invadopodium formation.

摘要

转移性癌细胞通过形成动态肌动蛋白基侵袭伪足来侵袭周围组织,降解周围细胞外基质并允许癌细胞侵袭。调节 RNA,包括环状 RNA,已被牵涉到这个过程中。通过微阵列,我们发现环状 RNA circSKA3 在乳腺癌细胞和人乳腺癌组织中高度表达。我们进一步发现,乳腺癌细胞的侵袭能力与 circSKA3 的表达呈正相关,通过侵袭伪足的形成。在机制上,我们确定了 Tks5 和整合素 β1 是这些肿瘤衍生侵袭伪足中 circSKA3 的结合伙伴。外源性 circSKA3 表达赋予了体外和体内更高的肿瘤侵袭性。我们进一步确定了 circSKA3、Tks5 和整合素 β1 之间的 RNA-蛋白质结合位点。在肿瘤形成实验中,我们发现 circSKA3 的表达促进了肿瘤的进展和侵袭伪足的形成。circSKA3 结合位点的突变或阻断寡核苷酸的转染消除了观察到的效果。因此,我们提供的证据表明,环状 RNA circSKA3 通过与 Tks5 和整合素 β1 复合,诱导侵袭伪足形成,从而促进肿瘤的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/510c/7210749/b1f67b674bf0/fx1.jpg

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