Crosstalk of SPINK4 Expression With Patient Mortality, Immunotherapy and Metastasis in Pan-Cancer Based on Integrated Multi-Omics Analyses.

IF 2.7 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
OncoTargets and therapy Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.2147/OTT.S487126
Xiuhua Cao, Na Luo, Xiaoyan Liu, Kan Guo, Mingming Deng, Chaoxiang Lv
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引用次数: 0

Abstract

Background: Cancer remains a major global health challenge, with early detection and prompt treatment being crucial for reducing mortality rates. The SPINK4 has been linked to the development of several tumors, and there is growing evidence of its involvement. However, its specific functions and effects in different cancer types remain unclear.

Methods: The association between SPINK4 expression levels and tumor progression was investigated and confirmed using the TCGA dataset. Kaplan-Meier curves were utilized to examine the correlation between SPINK4 expression with survival outcomes in pan-cancer patients. The Pearson method was employed to investigate the association of SPINK4 expression with the tumor microenvironment, stemness score, immunoinfiltrating subtype, and chemotherapy sensitivity in human different cancer types. Wound healing and Transwell assays were performed to confirm the roles of the model gene in colon adenocarcinoma cells.

Results: The expression of SPINK4 shows heterogeneity across pan-cancer tissues, and is closely associated with poor prognosis, immune cell invasion, tumor cell resistance, and tumor metastasis in a various human cancer. Mutation of SPINK4 hold significant predictive value for poor prognosis of pan-cancer patients. In addition, SPINK4 expression was significantly correlated with the tumor microenvironment (stromal cells and immune cells) and stemness score (DNAss and RNAss) in human pan-cancer tissues, particularly in BLCA and COAD. Single-cell sequencing analysis showed that SPINK4 is mainly expressed in endothelial cells in BLCA and in malignant cells in COAD. Drug resistance analysis showed a significant association between SPINK4 expression and sensitivity to several cancer chemotherapy drugs. Importantly, overexpression of SPINK4 promoted the metastasis of colon cancer cell lines (HCT116 and RKO), whereas SPINK4 knockout markedly inhibited their metastasis.

Conclusion: These findings reveal the crucial role of SPINK4 in the pan-cancer process and may have significant implications for the diagnosis and treatment of cancer in the future.

基于综合多组学分析的SPINK4表达与泛癌患者死亡率、免疫治疗和转移的串扰
背景:癌症仍然是一项重大的全球健康挑战,早期发现和及时治疗对于降低死亡率至关重要。SPINK4与几种肿瘤的发展有关,并且有越来越多的证据表明它与肿瘤有关。然而,其在不同癌症类型中的具体功能和作用尚不清楚。方法:使用TCGA数据集研究并证实SPINK4表达水平与肿瘤进展之间的关系。利用Kaplan-Meier曲线检验SPINK4表达与泛癌患者生存结局的相关性。采用Pearson法研究SPINK4表达与人不同癌型肿瘤微环境、干性评分、免疫浸润亚型及化疗敏感性的关系。通过伤口愈合和Transwell实验来证实模型基因在结肠腺癌细胞中的作用。结果:SPINK4在泛癌组织中的表达具有异质性,与多种人类癌症的预后不良、免疫细胞侵袭、肿瘤细胞耐药、肿瘤转移密切相关。SPINK4突变对泛癌患者预后不良具有重要的预测价值。此外,SPINK4的表达与人泛癌组织中肿瘤微环境(基质细胞和免疫细胞)和干性评分(dna和rna)显著相关,尤其是在BLCA和COAD中。单细胞测序分析显示,SPINK4在BLCA中主要表达于内皮细胞,在COAD中主要表达于恶性细胞。耐药分析显示,SPINK4表达与对几种肿瘤化疗药物的敏感性有显著相关性。重要的是,过表达SPINK4促进结肠癌细胞系(HCT116和RKO)的转移,而敲除SPINK4则显著抑制其转移。结论:这些发现揭示了SPINK4在泛癌过程中的重要作用,可能对未来癌症的诊断和治疗具有重要意义。
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来源期刊
OncoTargets and therapy
OncoTargets and therapy BIOTECHNOLOGY & APPLIED MICROBIOLOGY-ONCOLOGY
CiteScore
9.70
自引率
0.00%
发文量
221
审稿时长
1 months
期刊介绍: OncoTargets and Therapy is an international, peer-reviewed journal focusing on molecular aspects of cancer research, that is, the molecular diagnosis of and targeted molecular or precision therapy for all types of cancer. The journal is characterized by the rapid reporting of high-quality original research, basic science, reviews and evaluations, expert opinion and commentary that shed novel insight on a cancer or cancer subtype. Specific topics covered by the journal include: -Novel therapeutic targets and innovative agents -Novel therapeutic regimens for improved benefit and/or decreased side effects -Early stage clinical trials Further considerations when submitting to OncoTargets and Therapy: -Studies containing in vivo animal model data will be considered favorably. -Tissue microarray analyses will not be considered except in cases where they are supported by comprehensive biological studies involving multiple cell lines. -Biomarker association studies will be considered only when validated by comprehensive in vitro data and analysis of human tissue samples. -Studies utilizing publicly available data (e.g. GWAS/TCGA/GEO etc.) should add to the body of knowledge about a specific disease or relevant phenotype and must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Bioinformatics studies must be validated using the authors’ own data through replication in an independent sample set and functional follow-up. -Single nucleotide polymorphism (SNP) studies will not be considered.
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