Wei Jun-Dong, Jang Jae-Hyun, Kim Jae-Hong
School of Life Sciences and Biotechnology, Korea University, 5-1 Anam-dong, Sungbuk-gu, Seoul, 02841, South Korea.
School of Life Sciences and Biotechnology, Korea University, 5-1 Anam-dong, Sungbuk-gu, Seoul, 02841, South Korea.
Biochem Biophys Res Commun. 2017 Jan 29;483(1):305-311. doi: 10.1016/j.bbrc.2016.12.147. Epub 2016 Dec 25.
RanBPM is a scaffolding protein that regulates several cellular processes by interacting with various proteins. Previously, we reported that RanBPM acts as a negative regulator of BLT2, a low-affinity leukotriene B receptor; thus, it interferes with BLT2-mediated cell motility. In the present study, we observed that the expression levels of RanBPM were markedly reduced in the highly aggressive MDA-MB-435 and MDA-MB-231 human breast cancer cell lines compared with those in non-invasive MCF-7 cells. Additionally, we found that the restoration of RanBPM levels suppressed the invasiveness of these aggressive breast cancer cells in a manner dependent on BLT2 activation. In contrast, the knockdown of endogenous RanBPM by shRNA strongly promoted invasiveness in non-invasive MCF-7 cells. We also observed that RanBPM suppressed the invasiveness of aggressive breast cancer cells by inhibiting BLT2-mediated reactive oxygen species (ROS) generation and IL-8 production. Taken together, our results suggest that RanBPM acts as a negative regulator of BLT2, thus attenuating the invasiveness of aggressive breast cancer cells.
RanBPM是一种支架蛋白,通过与多种蛋白质相互作用来调节多种细胞过程。此前,我们报道RanBPM作为低亲和力白三烯B受体BLT2的负调节因子;因此,它会干扰BLT2介导的细胞运动。在本研究中,我们观察到,与非侵袭性MCF-7细胞相比,高侵袭性的MDA-MB-435和MDA-MB-231人乳腺癌细胞系中RanBPM的表达水平显著降低。此外,我们发现恢复RanBPM水平以依赖BLT2激活的方式抑制了这些侵袭性乳腺癌细胞的侵袭性。相反,通过shRNA敲低内源性RanBPM强烈促进了非侵袭性MCF-7细胞的侵袭性。我们还观察到RanBPM通过抑制BLT2介导的活性氧(ROS)生成和IL-8产生来抑制侵袭性乳腺癌细胞的侵袭性。综上所述,我们的结果表明RanBPM作为BLT2的负调节因子,从而减弱侵袭性乳腺癌细胞的侵袭性。