Faculty of Life Sciences, Toyo University, Itakura, Oura, Gunma 374-0193, Japan.
Oncol Rep. 2012 Nov;28(5):1889-93. doi: 10.3892/or.2012.2010. Epub 2012 Sep 3.
The constitutive activation of the Src family kinases (SFKs) has been established as a poor prognostic factor in malignant mesothelioma (MM), however, the family member(s) which contribute to the malignancy have not been defined. This study aimed to identify the SFK member(s) contributing to cell growth using RNA interference in various MM cell lines. Silencing of Yes but not of c-Src or Fyn in MM cells leads to cell growth suppression. This suppressive effect caused by Yes silencing mainly depends on G1 cell cycle arrest and partly the induction of apoptosis. Also, the knockout of Yes induces the inactivation of β-catenin signaling and subsequently decreases the levels of cyclin D necessary for G1-S transition in the cell cycle. In addition, Yes knockout has less effect on cell growth suppression in β-catenin-deficient H28 MM cells compared to other MM cells which express the catenin. Overall, we conclude that Yes is a central mediator for MM cell growth that is not shared with other SFKs such as c-Src.
Src 家族激酶(SFKs)的组成性激活已被确定为恶性间皮瘤(MM)的预后不良因素,但导致恶性的家族成员尚未确定。本研究旨在使用 RNA 干扰鉴定各种 MM 细胞系中促进细胞生长的 SFK 成员。Yes 的沉默而非 c-Src 或 Fyn 的沉默导致 MM 细胞生长受到抑制。Yes 沉默引起的这种抑制作用主要取决于 G1 细胞周期停滞,部分原因是诱导细胞凋亡。此外,Yes 的敲除诱导β-连环蛋白信号失活,随后降低细胞周期中 G1-S 转换所需的细胞周期蛋白 D 的水平。此外,与其他表达连接蛋白的 MM 细胞相比,Yes 敲除对β-连接蛋白缺陷型 H28 MM 细胞生长抑制的影响较小。总的来说,我们得出结论,Yes 是 MM 细胞生长的中央介质,与其他 SFKs(如 c-Src)不同。