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结直肠腺瘤-癌发生过程中 4 个差异表达 LIM 基因的生物信息学分析及实验验证

Bioinformatics Profiling and Experimental Validation of 4 Differentially-Expressed LIM Genes in the Course of Colorectal-Adenoma-Carcinoma.

机构信息

Central Laboratory, The First Affliated Hospital of Huzhou University, Huzhou, Zhejiang, China (mainland).

Huzhou Key Laboratory of Translational Medicine, The First Affiliated Hospital of Huzhou University, Huzhou, Zhejiang, China (mainland).

出版信息

Med Sci Monit. 2022 Jul 20;28:e937081. doi: 10.12659/MSM.937081.

Abstract

BACKGROUND LIM domain proteins play crucial roles in tumors by interacting with diverse proteins. However, their roles in the course of colorectal mucosa-adenoma-carcinoma remain unclear. This study aimed to depict their dynamic expression profiles and elucidate their potential functions in this transition course. MATERIAL AND METHODS Differentially-expressed LIM proteins (DELGs) in paired adenomas, carcinomas, and mucosae were identified using the GEO dataset (GSE 117606) and validated by immunohistochemistry using our tissue microarray. Kaplan-Meier survival analysis, WGCNA, module-trait analysis, and KEGG enrichment were conducted. The correlation of DELGs expression levels with immune infiltration was assessed using the ESTIMATE package and TISCH database. The role of DELGs of interest was validated using cell proliferation, migration, and invasion assays. RESULTS Four DELGs were identified - LMO3, FHL1, NEBL, and TGFB1I1 - all of which were of significance in prognosis. Module-trait correlation and KEGG enrichment revealed their involvement in cancer-related signaling. Immunohistochemistry showed gradual downregulation of LMO3 but upregulation of NEBL in the mucosa-adenoma-carcinoma sequence. The opposite expression patterns were observed for FHL1 and TGFB1I1 in tumor epithelium and mesenchyme. High expression levels of the DELGs were correlated with increased infiltration of NK, NKT, and macrophages, except for NEBL. Importantly, LMO3 inhibited proliferation, migration, and invasion of colon epithelial cells. CONCLUSIONS This study identified 4 differentially-expressed LIM genes - LMO3, FHL1, TGFB1I1, and NEBL - and revealed they were involved in the mucosa-adenoma-carcinoma sequence via regulating cancer-related pathways, influencing epigenetic field, or affecting immune infiltration. Our findings provide new insights into the roles of LIM proteins in the course of mucosa-adenoma-carcinoma.

摘要

背景

LIM 结构域蛋白通过与多种蛋白相互作用,在肿瘤中发挥着关键作用。然而,它们在结直肠黏膜-腺瘤-癌的过程中的作用尚不清楚。本研究旨在描绘它们的动态表达谱,并阐明它们在这一转变过程中的潜在功能。

材料和方法

使用 GEO 数据集(GSE117606)识别配对腺瘤、癌和黏膜中差异表达的 LIM 蛋白(DELGs),并使用我们的组织微阵列进行免疫组织化学验证。进行 Kaplan-Meier 生存分析、WGCNA、模块特征分析和 KEGG 富集。使用 ESTIMATE 包和 TISCH 数据库评估 DELGs 表达水平与免疫浸润的相关性。使用细胞增殖、迁移和侵袭实验验证感兴趣的 DELGs 的作用。

结果

鉴定出 4 个 DELGs,即 LMO3、FHL1、NEBL 和 TGFB1I1,它们在预后方面均有意义。模块特征相关性和 KEGG 富集显示它们参与了癌症相关信号。免疫组织化学显示 LMO3 在黏膜-腺瘤-癌序列中逐渐下调,而 NEBL 则上调。FHL1 和 TGFB1I1 在肿瘤上皮和间质中的表达模式相反。DELGS 的高表达水平与 NK、NKT 和巨噬细胞浸润增加相关,除了 NEBL。重要的是,LMO3 抑制了结肠上皮细胞的增殖、迁移和侵袭。

结论

本研究鉴定出 4 个差异表达的 LIM 基因,即 LMO3、FHL1、TGFB1I1 和 NEBL,并揭示它们通过调节癌症相关途径、影响表观遗传场或影响免疫浸润,参与黏膜-腺瘤-癌序列。我们的研究结果为 LIM 蛋白在黏膜-腺瘤-癌过程中的作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f971/9310551/0cd2bf7f83b8/medscimonit-28-e937081-g001.jpg

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