Kindlin-3在癌症中的新功能

S. Mourah, Farah Khayati, Ibtissem Djaafri, J. Delyon, C. R. D. Moura, J. Tost, C. Lebbé, S. Ménashi
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摘要

Kindlin-3 (FERMT-3)是一种重要的整合素激活蛋白,属于Kindlin家族,包括三个成员Kindlin-1、2和3。Kindlins可以直接结合各类整合素并参与其活化,在细胞-基质粘附调节中起关键作用。已知Kindlin-3在止血和血栓形成的控制中起中心作用,因为它的缺乏会破坏血小板聚集并导致白细胞粘附缺乏症。到目前为止,它的表达只在造血细胞中被描述,最近在内皮细胞中被描述。目前的手稿强调了我们最近研究的关键发现,描述了Kindlin-3作为肿瘤抑制因子在癌症中的新作用。我们提供的数据显示,kindin -3的表达比以前认为的更为普遍,并且通过基因失活机制,其表达在几种人类实体癌病变中显着降低。沉默Kindlin-3表达后,肿瘤细胞的恶性特性增加,Kindlin-3与肿瘤启动子EMMPRIN/CD147的逆表达证实了Kindlin-3的抑瘤作用。基于我们的研究数据,提出了一个描述Kindlin-3在肿瘤细胞中的作用模式的示意图模型。
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A novel function of Kindlin-3 in cancer
Kindlin-3 (FERMT-3) is a key integrin activating protein belonging to the Kindlin family which includes three members Kindlin-1, 2 and 3. Kindlins can directly bind to various classes of integrins and participate in their activation, thus playing a key role in the regulation of cell-matrix adhesions. Kindlin-3 has been known to be central in the control of hemostasis and thrombosis as its deficiency disrupts platelet aggregation and causes Leukocyte Adhesion Deficiency disease. Its expression has so far been only described in hematopoietic cells, and more recently in endothelial cells. The current manuscript highlights key findings from our recent research describing a novel role of Kindlin-3 as a tumor suppressor in cancer. We present data showing that Kindlin-3 is expressed more ubiquitously than previously thought, and that through gene inactivation mechanisms, its expression is significantly reduced in several human solid cancer lesions. The increase in the malignant properties of tumor cells when Kindlin-3 expression is silenced and the inverse expression of Kindlin-3 with the tumor promoter EMMPRIN/CD147 corroborate the tumor suppressor role of Kindlin-3. A schematic model based on our research data describing Kindlin-3 mode of action in tumor cells is presented.
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