University of Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019-UMR 9017-CIIL-Center for Infection and Immunity of Lille, F-59000 Lille, France.
University of Lille, CNRS, Inserm, CHU Lille, UMR9020-UMR1277-CANTHER-Cancer Heterogeneity, Plasticity and Resistance to Therapies, F-59000 Lille, France.
Int J Mol Sci. 2022 Dec 16;23(24):16028. doi: 10.3390/ijms232416028.
Prostate cancer is a major public health concern and one of the most prevalent forms of cancer worldwide. The definition of altered signaling pathways implicated in this complex disease is thus essential. In this context, abnormal expression of the receptor of Macrophage Colony-Stimulating Factor-1 (M-CSF or CSF-1) has been described in prostate cancer cells. Yet, outcomes of this expression remain unknown. Using mouse and human prostate cancer cell lines, this study has investigated the functionality of the wild-type CSF-1 receptor in prostate tumor cells and identified molecular mechanisms underlying its ligand-induced activation. Here, we showed that upon CSF-1 binding, the receptor autophosphorylates and activates multiple signaling pathways in prostate tumor cells. Biological experiments demonstrated that the CSF-1R/CSF-1 axis conferred significant advantages in cell growth and cell invasion in vitro. Mouse xenograft experiments showed that CSF-1R expression promoted the aggressiveness of prostate tumor cells. In particular, we demonstrated that the ligand-activated CSF-1R increased the expression of transcript encoding for osteopontin, a key player in cancer development and metastasis. Therefore, this study highlights that the CSF-1 receptor is fully functional in a prostate cancer cell and may be a potential therapeutic target for the treatment of prostate cancer.
前列腺癌是一个主要的公共卫生关注点,也是全球最常见的癌症之一。因此,明确参与这一复杂疾病的信号通路的改变定义是至关重要的。在这种情况下,已在前列腺癌细胞中描述了巨噬细胞集落刺激因子-1(M-CSF 或 CSF-1)受体的异常表达。然而,这种表达的结果尚不清楚。本研究使用小鼠和人前列腺癌细胞系,研究了野生型 CSF-1 受体在前列腺肿瘤细胞中的功能,并确定了其配体诱导激活的分子机制。在这里,我们表明,在 CSF-1 结合后,受体在前列腺肿瘤细胞中自动磷酸化并激活多种信号通路。生物学实验表明,CSF-1R/CSF-1 轴在体外细胞生长和细胞侵袭方面赋予了显著优势。小鼠异种移植实验表明,CSF-1R 表达促进了前列腺肿瘤细胞的侵袭性。特别是,我们证明了配体激活的 CSF-1R 增加了编码骨桥蛋白的 转录本的表达,骨桥蛋白是癌症发展和转移的关键参与者。因此,本研究强调 CSF-1 受体在前列腺癌细胞中具有完全功能,可能是治疗前列腺癌的潜在治疗靶点。