ADAMTS12作为一种新的预后生物标志物,促进胃癌的增殖和侵袭。

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Discover. Oncology Pub Date : 2024-12-25 DOI:10.1007/s12672-024-01724-4
Ruimei Gao, Yalan Hu, Qiuxiang Yuan
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引用次数: 0

摘要

胃癌(GC)仍然是一种普遍和侵袭性的恶性肿瘤,预后不良。本研究旨在确定诊断和预后生物标志物,同时探索其在GC中的潜在功能。GC患者共鉴定出598个上调基因和506个下调基因。其中,与生存相关的差异表达基因(DEGs),包括ADAMTS12、F5和VCAN被突出显示。泛癌症分析揭示了它们在多种肿瘤类型中的失调。一种新的预后指标,结合ADAMTS12和F5,有效地将GC患者分为低风险组和高风险组,显示出总生存期的显着差异和强大的预测性能。ADAMTS12与晚期临床阶段和不良预后密切相关,在一项独立队列研究中得到验证,显示出良好的诊断潜力。RT-PCR和western blot分析证实其在胃癌组织和细胞系中高表达。功能实验进一步证实ADAMTS12促进GC细胞增殖和侵袭。总之,这项研究为胃癌的分子结构提供了重要的见解,提供了潜在的预后工具和治疗靶点。
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ADAMTS12 serves as a novel prognostic biomarker and promotes proliferation and invasion in gastric cancer.

Gastric cancer (GC) remains a prevalent and aggressive malignancy with a poor prognosis. This study aimed to identify diagnostic and prognostic biomarkers while exploring their potential functions in GC. A total of 598 upregulated and 506 downregulated genes were identified in GC patients. Among these, survival-related differentially expressed genes (DEGs), including ADAMTS12, F5, and VCAN, were highlighted. Pan-cancer analyses revealed their dysregulation across multiple tumor types. A novel prognostic signature, incorporating ADAMTS12 and F5, effectively stratified GC patients into low- and high-risk groups, demonstrating significant differences in overall survival and robust predictive performance. ADAMTS12, strongly associated with advanced clinical stages and poor prognosis, was validated in an independent cohort and exhibited promising diagnostic potential. RT-PCR and western blot analyses confirmed its high expression in GC tissues and cell lines. Functional assays further demonstrated that ADAMTS12 promotes GC cell proliferation and invasion. In summary, this study provides critical insights into the molecular landscape of GC, offering a potential prognostic tool and therapeutic target.

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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
期刊最新文献
Correction: Identified VCAM1 as prognostic gene in gastric cancer by co-expression network analysis. Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization. To describe the subsets of malignant epithelial cells in gastric cancer, their developmental trajectories and drug resistance characteristics. AURKB affects the proliferation of clear cell renal cell carcinoma by regulating fatty acid metabolism. A panel of cancer testis antigens in squamous cell carcinoma of the lung, head and neck, and esophagus: implication for biomarkers and therapeutic targets.
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