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C6orf15通过WNT/β-连环蛋白信号通路促进结直肠癌肝转移。

C6orf15 promotes liver metastasis via WNT/β-catenin signalling in colorectal cancer.

作者信息

Yu Jiankang, Sun Jian, Tang Jingtong, Xu Jiayu, Qian Guanru, Zhou Jianping

机构信息

Department of Gastrointestinal Surgery & Hernia and Abdominal Wall Surgery, The First Hospital, China Medical University, Shenyang, 110001, China.

Shenyang Medical Nutrition Clinical Medical Research Center, Shenyang, China.

出版信息

Cancer Cell Int. 2024 Apr 23;24(1):146. doi: 10.1186/s12935-024-03324-2.

Abstract

BACKGROUND

Colon cancer ranks third among global tumours and second in cancer-related mortality, prompting an urgent need to explore new therapeutic targets. C6orf15 is a novel gene that has been reported only in Sjogren's syndrome and systemic lupus erythematosus patients. We found a close correlation between increased C6orf15 expression and the occurrence of colon cancer. The aim of this study was to explore the potential of C6orf15 as a therapeutic target for colorectal cancer.

METHOD

RNA-seq differential expression analysis of the TCGA database was performed using the R package 'limma.' The correlation between target genes and survival as well as tumour analysis was analysed using GEPIA. Western blot and PCR were used to assess C6orf15 expression in colorectal cancer tissue samples. Immunofluorescence and immunohistochemistry were used to assess C6orf15 subcellular localization and tissue expression. The role of C6orf15 in liver metastasis progression was investigated via a mouse spleen infection liver metastasis model. The association of C6orf15 with signalling pathways was assessed using the GSEA-Hallmark database. Immunohistochemistry (IHC), qPCR and western blotting were performed to assess the expression of related mRNAs or proteins. Biological characteristics were evaluated through cell migration assays, MTT assays, and Seahorse XF96 analysis to monitor fatty acid metabolism.

RESULTS

C6orf15 was significantly associated with liver metastasis and survival in CRC patients as determined by the bioinformatic analysis and further verified by immunohistochemistry (IHC), qPCR and western blot results. The upregulation of C6orf15 expression in CRC cells can promote the nuclear translocation of β-catenin and cause an increase in downstream transcription. This leads to changes in the epithelial-mesenchymal transition (EMT) and alterations in fatty acid metabolism, which together promote liver metastasis of CRC.

CONCLUSION

Our study identified C6orf15 as a marker of liver metastasis in CRC. C6orf15 can activate the WNT/β-catenin signalling pathway to promote EMT and fatty acid metabolism in CRC.

摘要

背景

结肠癌在全球肿瘤中位列第三,在癌症相关死亡率中位居第二,这促使人们迫切需要探索新的治疗靶点。C6orf15是一个仅在干燥综合征和系统性红斑狼疮患者中被报道过的新基因。我们发现C6orf15表达增加与结肠癌的发生密切相关。本研究的目的是探索C6orf15作为结直肠癌治疗靶点的潜力。

方法

使用R包“limma”对TCGA数据库进行RNA测序差异表达分析。使用GEPIA分析目标基因与生存以及肿瘤之间的相关性。采用蛋白质免疫印迹法和聚合酶链反应评估结直肠癌组织样本中C6orf15的表达。利用免疫荧光和免疫组织化学评估C6orf15的亚细胞定位和组织表达。通过小鼠脾脏感染肝转移模型研究C6orf15在肝转移进展中的作用。使用GSEA-Hallmark数据库评估C6orf15与信号通路的关联。进行免疫组织化学(IHC)、定量聚合酶链反应和蛋白质免疫印迹法以评估相关mRNA或蛋白质的表达。通过细胞迁移试验、MTT试验和海马XF96分析监测脂肪酸代谢来评估生物学特性。

结果

生物信息学分析确定C6orf15与结直肠癌患者的肝转移和生存显著相关,免疫组织化学(IHC)、定量聚合酶链反应和蛋白质免疫印迹结果进一步验证了这一点。结直肠癌细胞中C6orf15表达上调可促进β-连环蛋白的核转位并导致下游转录增加。这导致上皮-间质转化(EMT)改变和脂肪酸代谢变化,共同促进结直肠癌的肝转移。

结论

我们的研究确定C6orf15为结直肠癌肝转移的标志物。C6orf15可激活WNT/β-连环蛋白信号通路,促进结直肠癌中的EMT和脂肪酸代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0e/11040941/ad0aa82c35e2/12935_2024_3324_Fig1_HTML.jpg

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