肥大细胞在结直肠癌中的推测功能及预后分子标志物。

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY
Jiani Guo, Jie Chen, Yiting Wang, Xiaoming Bai, Haimei Feng, Siqi Sheng, Hongyu Wang, Ke Xu, Mengxi Huang, Zengjie Lei, Xiaoyuan Chu
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引用次数: 0

摘要

背景:对结直肠癌(CRC)标志物需求的增加凸显了研究参与结直肠癌进展的免疫细胞的重要性。本研究旨在解剖CRC中的肥大细胞,表征肥大细胞在CRC发生发展中的作用,协调肥大细胞与恶性细胞之间的分子通讯,构建并验证基于肥大细胞标志物的预后分类模型。方法:从GSE146771中提取结直肠癌患者的单细胞转录组数据,进行细胞分类和注释。用copykat识别恶性细胞,用CellChat分析肥大细胞与恶性细胞之间的通讯。在TCGA-COAD队列中,对肥大细胞标记物进行LASSO回归分析和Cox回归分析,构建预后分类模型。采用qRT-PCR检测P815和MC-9细胞中分类模型分子的mRNA表达情况。在12孔transwell皿中进行MC38与P815细胞共培养实验。采用伤口愈合试验和Transwell试验检测细胞迁移和侵袭。结果:GSE146771的10186个优质细胞被标注为9种细胞类型。选择肥大细胞中的6个标记(HDC、GATA2、ASAH1、BTBD19、TIMP1、FAM110A)构建分类模型。高风险评分定义为免疫抑制细胞的高浸润,包括内皮细胞、CAFs、Tregs和高血管生成和上皮间充质转化(EMT)活性。在模型中,HDC在P815细胞中异常低表达,而BTBD19、FAM110A、GATA2、ASAH1、TIMP1在P815细胞中异常高表达。在P815和MC38细胞共培养系统中,敲低GATA2可阻断细胞迁移和侵袭。结论:本研究明确了结直肠癌内部的细胞类型,阐述了肥大细胞在结直肠癌发生发展中的细胞功能及其分子通讯协调恶性细胞,突出了构成有希望的预后分类模型的分子成分和生物学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Putative function and prognostic molecular marker of mast cells in colorectal cancer.

Background: The increased demand for markers for colorectal cancer (CRC) highlights the importance of investigating immune cells involved in CRC progression. This study aims to dissect the mast cells in CRC, characterize the role of mast cells in CRC development, coordinate molecular communication between mast cells and malignant cells, and construct and validate a prognostic classification model based on mast cell markers.

Methods: Single-cell transcriptome data of CRC patients were extracted from GSE146771 for cell classification and annotation. The malignant cells were identified by copykat and the communication between mast cells and malignant cells was analyzed by CellChat. Least absolute shrinkage and selection operator (LASSO) regression analysis and Cox regression analysis of mast cell markers were performed in the TCGA-COAD cohort to construct a prognostic classification model. qRT-PCR was performed to detect the mRNA expression of the molecules in the classification model in P815 and MC-9 cells. The co-culture experiment of MC38 and P815 cells were performed in 12-well transwell dish. Wound healing assay and Transwell assay were performed to detect cell migration and invasion.

Results: 10,186 high-quality cells in GSE146771 were annotated to 9 cell types. Six markers in mast cells (HDC, GATA2, ASAH1, BTBD19, TIMP1, FAM110A) were selected to construct a classification model. The high-risk score defined showed high infiltration of immunosuppressive cells, including endothelial cells, CAFs, Tregs and high angiogenesis and epithelial-mesenchymal transition (EMT) activities. In the model, HDC were abnormally low expressed in P815 cells, while BTBD19, FAM110A, GATA2, ASAH1 and TIMP1 showed excessive expression in P815 cells. Knockdown of GATA2 in the co-culture system of P815 and MC38 cells blocked cell migration and invasion.

Conclusion: This study identified the cell types within CRC, elaborated the cellular functions of mast cells in CRC development and their molecular communication to coordinate malignant cells, and highlighted the molecular components and biological features that constitute promising prognostic classification model.

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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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