Bayasgalan Tuvshin, Kanda Mitsuro, Sato Yusuke, Zhu Haote, Hamrah Mohammad Hussain, Martinez Flor Esther Garza, Shinozuka Takahiro, Ito Yuki, Sasahara Masahiro, Shimizu Dai, Umeda Shinichi, Inokawa Yoshikuni, Hattori Norifumi, Hayashi Masamichi, Tanaka Chie, Kodera Yasuhiro
Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan;
Cancer Genomics Proteomics. 2025 Mar-Apr;22(2):306-325. doi: 10.21873/cgp.20503.
BACKGROUND/AIM: Comprehensive transcriptome analysis has revealed SPOC Domain Containing 1 (SPOCD1) as a potential biomarker for esophageal squamous cell carcinoma (ESCC). However, the expression and oncological roles of SPOCD1 in ESCC remains underexplored. We aimed to evaluate the role of SPOCD1 in oncogenesis and prognosis of ESCC and Materials and Methods: The Cancer Cell Line Encyclopedia (CCLE) database was utilized to evaluate correlations between SPOCD1 expression and oncogenes in ESCC. mRNA and protein levels were measured by qRT-PCR and Simple Western assays, respectively. siRNA-mediated knockdown and overexpression experiments assessed the effects of SPOCD1 expression on proliferation, migration, and invasion of ESCC cell lines. , siRNA knockdown effects on tumor growth were tested in mouse xenograft models. SPOCD1 mRNA levels in 164 resected tissues were correlated with clinicopathological parameters and survival, while a cohort of 177 patients was analyzed for protein expression and survival.
SPOCD1 mRNA expression varied widely among ESCC cell lines and correlated with epithelial-mesenchymal transition-related genes. Knockdown significantly suppressed proliferation, migration, and invasion (<0.001), while overexpression increased proliferation (<0.001). , siRNA knockdown reduced tumor growth compared to both si-control (=0.005) and untransfected groups (<0.001). High SPOCD1 mRNA expression was linked to poor disease-specific survival (=0.009, HR=1.965, 95% CI=1.187-3.252) and disease-free survival (=0.047, HR=1.602, 95% CI=1.007-2.549). Similarly, elevated protein levels were associated with unfavorable disease-specific (=0.013, HR=1.860, 95% CI=1.137-3.041) and disease-free survival (=0.032, HR=1.618, 95% CI=1.042-2.513).
SPOCD1 expression correlates with the aggressiveness of ESCC cells, and its expression levels in tumor tissues may serve as a prognostic factor for ESCC patients.
背景/目的:综合转录组分析已揭示含SPOC结构域蛋白1(SPOCD1)作为食管鳞状细胞癌(ESCC)的潜在生物标志物。然而,SPOCD1在ESCC中的表达及肿瘤学作用仍未得到充分研究。我们旨在评估SPOCD1在ESCC发生发展及预后中的作用。材料与方法:利用癌细胞系百科全书(CCLE)数据库评估ESCC中SPOCD1表达与癌基因之间的相关性。分别通过qRT-PCR和Simple Western检测法测量mRNA和蛋白质水平。siRNA介导的敲低和过表达实验评估SPOCD1表达对ESCC细胞系增殖、迁移和侵袭的影响。在小鼠异种移植模型中测试siRNA敲低对肿瘤生长的影响。分析164例切除组织中SPOCD1 mRNA水平与临床病理参数及生存情况的相关性,同时分析177例患者队列的蛋白质表达及生存情况。
SPOCD1 mRNA表达在ESCC细胞系中差异很大,且与上皮-间质转化相关基因相关。敲低显著抑制增殖、迁移和侵袭(<0.001),而过表达则增加增殖(<0.001)。与si对照(=0.005)组和未转染组相比(<0.001),siRNA敲低降低了肿瘤生长。高SPOCD1 mRNA表达与较差的疾病特异性生存(=0.009,HR=1.965,95%CI=1.187 - 3.252)和无病生存(=0.047,HR=1.602,95%CI=1.007 - 2.549)相关。同样,蛋白水平升高与不良的疾病特异性生存(=0.013,HR=1.860,95%CI=1.137 - 3.041)和无病生存(=0.032,HR=1.618,95%CI=1.042 - 2.513)相关。
SPOCD1表达与ESCC细胞的侵袭性相关,其在肿瘤组织中的表达水平可能作为ESCC患者的预后因素。