胶质瘤中FHL1蛋白的下调通过PI3K/AKT信号通路抑制肿瘤生长。
Downregulation of FHL1 protein in glioma inhibits tumor growth through PI3K/AKT signaling.
作者信息
Li San-Zhong, Hu Yi-Yang, Zhao Jun-Long, Zang Jian, Fei Zhou, Han Hua, Qin Hong-Yan
机构信息
Department of Neurosurgery, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China.
Department of Medical Genetics and Developmental Biology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710032, P.R. China.
出版信息
Oncol Lett. 2020 Jun;19(6):3781-3788. doi: 10.3892/ol.2020.11476. Epub 2020 Mar 27.
Human four-and-a-half LIM domains protein 1 (FHL1) is a member of the FHL protein family, which serves an important role in multiple cellular events by interacting with transcription factors using its cysteine-rich zinc finger motifs. A previous study indicated that FHL1 was downregulated in several types of human cancer and served a role as a tumor suppressive gene. The overexpression of FHL1 inhibited tumor cell proliferation. However, to the best of our knowledge, there is no evidence to confirm whether FHL1 affected glioma growth, and the molecular mechanisms through which FHL1 represses tumor development remain unclear. In the present study, the expression level of FHL1 was determined using immunohistochemical staining in 114 tumor specimens from patients with glioma. The results indicated that FHL1 expression was negatively associated with the pathological grade of gliomas. Furthermore, Kaplan-Meier survival curves demonstrated that the patients with an increased FHL1 expression exhibited a significantly longer survival time, suggesting that FHL1 may be a prognostic marker for glioma. The protein level of FHL1 was relatively increased in the U251 glioma cell line compared with that in the U87 cell line. Therefore, FHL1 was knocked down in U251 by siRNA and overexpressed in U87, and it was identified that FHL1 significantly decreased the activation of PI3K/AKT signaling by interacting with AKT. Further experiments verified that FHL1 inhibited the growth of gliomas by modulating PI3K/AKT signaling. In conclusion, the results of the present study demonstrated that FHL1 suppressed glioma development through PI3K/AKT signaling.
人类四半LIM结构域蛋白1(FHL1)是FHL蛋白家族的成员,它通过其富含半胱氨酸的锌指基序与转录因子相互作用,在多种细胞事件中发挥重要作用。先前的一项研究表明,FHL1在几种类型的人类癌症中表达下调,并作为一种肿瘤抑制基因发挥作用。FHL1的过表达抑制肿瘤细胞增殖。然而,据我们所知,尚无证据证实FHL1是否影响神经胶质瘤的生长,并且FHL1抑制肿瘤发展的分子机制仍不清楚。在本研究中,使用免疫组织化学染色法测定了114例神经胶质瘤患者肿瘤标本中FHL1的表达水平。结果表明,FHL1表达与神经胶质瘤的病理分级呈负相关。此外,Kaplan-Meier生存曲线表明,FHL1表达增加的患者生存时间显著延长,这表明FHL1可能是神经胶质瘤的一个预后标志物。与U87细胞系相比,U251神经胶质瘤细胞系中FHL1的蛋白水平相对增加。因此,通过siRNA在U251中敲低FHL1,并在U87中过表达FHL1,结果发现FHL1通过与AKT相互作用显著降低PI3K/AKT信号的激活。进一步的实验证实,FHL1通过调节PI3K/AKT信号抑制神经胶质瘤的生长。总之,本研究结果表明,FHL1通过PI3K/AKT信号抑制神经胶质瘤的发展。