Centre of Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
Cholangiocarcinoma Research Institute, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Cancer Genomics Proteomics. 2022 Jan-Feb;19(1):35-49. doi: 10.21873/cgp.20302.
BACKGROUND/AIM: We previously demonstrated that a mitochondrial protein, apoptosis-inducing factor, mitochondrion-associated 3 (AIFM3) is over-expressed in cholangiocarcinoma (CCA) and its serum levels can be a prognostic biomarker for CCA. To elucidate the functional roles of AIFM3 in CCA progression, we aimed to determine the signaling pathways of AIFM3 in CCA.
AIFM3 gene in CCA cells was silenced and AIFM3-related proteins were identified using mass spectrometry and bioinformatics tools. The relationships between AIFM3 and 441 related proteins were explored. To validate the functions of AIFM3, transwell migration/invasion assays were used.
Bioinformatic analyses predicted that AIFM3 interacts with formin-like protein 3 (FMNL3) and is involved in tumor cell motilities. Online database analysis revealed higher AIFM3 mRNA expression levels in CCA, particularly with lymph node metastasis. After AIFM3 gene silencing, CCA cell migration/invasion was significantly decreased (p<0.001). Furthermore, AIFM3 expression levels were significantly associated with lymph node metastasis (p=0.0009) and shorter survival time (p=0.020).
The AIFM3 signaling pathway is mediated via FMNL3 and involved in metastasis, suggesting that AIFM3 might be a molecular target to prevent CCA metastasis.
背景/目的:我们之前的研究表明,线粒体蛋白凋亡诱导因子,线粒体相关 3(AIFM3)在胆管癌(CCA)中过度表达,其血清水平可以作为 CCA 的预后生物标志物。为了阐明 AIFM3 在 CCA 进展中的功能作用,我们旨在确定 AIFM3 在 CCA 中的信号通路。
使用质谱和生物信息学工具沉默 CCA 细胞中的 AIFM3 基因,并鉴定 AIFM3 相关蛋白。探索 AIFM3 与 441 种相关蛋白之间的关系。为了验证 AIFM3 的功能,使用 Transwell 迁移/侵袭测定法。
生物信息学分析预测 AIFM3 与formin-like protein 3(FMNL3)相互作用,参与肿瘤细胞迁移。在线数据库分析显示,CCA 中 AIFM3 mRNA 表达水平较高,尤其是伴有淋巴结转移。AIFM3 基因沉默后,CCA 细胞迁移/侵袭明显减少(p<0.001)。此外,AIFM3 的表达水平与淋巴结转移显著相关(p=0.0009),生存时间较短(p=0.020)。
AIFM3 信号通路通过 FMNL3 介导,参与转移,提示 AIFM3 可能是预防 CCA 转移的分子靶点。