Zhang Xiaohui, Zhang Lingmin, Cui Manli, Ji Shiyu, Zhang Yanan, Li Qian, Zhang Mingxin
Xi'an No.3 Hospital, The Affiliated Hospital of Northwest University, Xi'an, 710021, Shaanxi, China.
The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Eur J Med Res. 2024 Dec 19;29(1):596. doi: 10.1186/s40001-024-02182-y.
Sperm-associated antigen 5 (SPAG5) is a mitotic spindle protein crucial for coordinating the separation of sister chromatids into daughter cells. Increasing evidence suggests that SPAG5 is overexpressed in various malignancies, functioning as an oncogene. However, research specifically examining SPAG5 in esophageal cancer remains limited.
In this research, we leveraged bioinformatics techniques to evaluate the expression and prognostic significance of SPAG5 in a variety of cancer types. We conducted Gene Set Enrichment Analysis (GSEA) to elucidate the relationship between SPAG5 and cancer characteristics. Additionally, we investigated the correlation between SPAG5 expression and immune cell infiltration utilizing the TIMER2.0 platform. The TIDE platform was used to assess the impact of SPAG5 on the effectiveness of immunotherapy and to screen for potential therapeutic drugs. We employed qRT-PCR and immunohistochemistry staining to ascertain the expression of SPAG5 in esophageal cancer tissue. Through cellular functional experiments, we examined the influence of SPAG5 expression on the proliferation, apoptosis, invasion, and migration of esophageal cancer cells. The Pathscan Stress Signaling Antibody Array was utilized to probe the potential molecular mechanisms of SPAG5.
SPAG5 exhibits high levels of expression in various cancers, encompassing esophageal cancer, and its presence indicates an unfavorable prognosis. SPAG5 is primarily enriched in pathways associated with cellular proliferation and demonstrates a correlation with immune gene expression as well as the infiltration of immune cells. Suppression of SPAG5 expression in esophageal cancer cells not only inhibits cell proliferation, but also attenuates cell invasion and migration while inducing cellular apoptosis. The depletion of SPAG5 results in a decline in the levels of critical signaling proteins.
SPAG5 plays a pivotal role in esophageal cancer cell proliferation, apoptosis, and metastasis within the tumor microenvironment, making it a promising therapeutic target.
精子相关抗原5(SPAG5)是一种有丝分裂纺锤体蛋白,对协调姐妹染色单体分离到子细胞中至关重要。越来越多的证据表明,SPAG5在各种恶性肿瘤中过度表达,发挥癌基因的作用。然而,专门研究食管癌中SPAG5的研究仍然有限。
在本研究中,我们利用生物信息学技术评估SPAG5在多种癌症类型中的表达及预后意义。我们进行基因集富集分析(GSEA)以阐明SPAG5与癌症特征之间的关系。此外,我们利用TIMER2.0平台研究SPAG5表达与免疫细胞浸润之间的相关性。TIDE平台用于评估SPAG5对免疫治疗效果的影响并筛选潜在治疗药物。我们采用qRT-PCR和免疫组织化学染色来确定SPAG5在食管癌组织中的表达。通过细胞功能实验,我们研究了SPAG5表达对食管癌细胞增殖、凋亡、侵袭和迁移的影响。利用Pathscan应激信号抗体芯片探究SPAG5的潜在分子机制。
SPAG5在包括食管癌在内的各种癌症中均表现出高表达水平,其存在预示着不良预后。SPAG5主要富集于与细胞增殖相关的通路,并与免疫基因表达以及免疫细胞浸润相关。抑制食管癌细胞中SPAG5的表达不仅抑制细胞增殖,还减弱细胞侵袭和迁移,同时诱导细胞凋亡。SPAG5的缺失导致关键信号蛋白水平下降。
SPAG5在肿瘤微环境中的食管癌细胞增殖、凋亡和转移中起关键作用,使其成为一个有前景的治疗靶点。