Comprehensive characterization of adipogenesis-related genes in colorectal cancer for clinical significance and immunogenomic landscape analyses

被引:1
作者
Han, Jing [1 ]
Li, Shangshang [1 ]
Zhan, Qiong [1 ]
Hu, Yuchao [1 ]
Zhong, Chaoxiang [1 ]
Yang, Jie [1 ]
Qiu, Zhengcai [1 ]
机构
[1] Shuyang Hosp TCM, Dept Gen Surg, Suqian, Jiangsu, Peoples R China
关键词
DISCOVERY;
D O I
10.1186/s12944-023-01942-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
ObjectiveColorectal cancer (CRC) is a major global health concern, necessitating the identification of biomarkers and molecular subtypes for improved clinical management. This study aims to evaluate the clinical value of adipogenesis-related genes and molecular subtypes in CRC.MethodsA comprehensive analysis of adipogenesis-related genes in CRC was performed using publicly available datasets (TCGA and GEO database) and bioinformatics tools. Unsupervised cluster analysis was employed to identify the molecular subtypes of CRC, while LASSO regression analysis was utilized to develop a risk prognostic model. The immunogenomic patterns and immunotherapy analysis were used to predict patient response to immunotherapy. Furthermore, qPCR analysis was conducted to confirm the expression of the identified key genes in vitro.ResultsThrough the analysis of RNAseq data from normal and tumor tissues, we identified 50 differentially expressed genes. Unsupervised cluster analysis identified two subtypes (Cluster A and Cluster B) with significantly different survival outcomes. Cluster A and B displayed differential immune cell compositions and enrichment in specific biological pathways, providing insights into potential therapeutic targets. A risk-scoring model was developed using five ARGs, which successfully classified patients into high and low-risk groups, showing distinct survival outcomes. The model was validated and showed robust predictive performance. High-risk patients exhibited altered immune cell proportions and gene expression patterns compared to low-risk patients. In qPCR validation, four out of the five key genes were consistent with the results of bioinformatics analysis.ConclusionOverall, the findings of our investigation offer valuable understanding regarding the clinical relevance of ARGs and molecular subtypes in CRC, laying the groundwork for improved precision medicine applications and personalized treatment modalities.
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页数:13
相关论文
共 32 条
[11]   affy -: analysis of Affymetrix GeneChip data at the probe level [J].
Gautier, L ;
Cope, L ;
Bolstad, BM ;
Irizarry, RA .
BIOINFORMATICS, 2004, 20 (03) :307-315
[12]   GSVA: gene set variation analysis for microarray and RNA-Seq data [J].
Haenzelmann, Sonja ;
Castelo, Robert ;
Guinney, Justin .
BMC BIOINFORMATICS, 2013, 14
[13]   Mutations in lysine methyltransferase 2C and PEG3 are associated with tumor mutation burden, prognosis, and antitumor immunity in pancreatic adenocarcinoma patients [J].
Huang, Yili ;
Liu, Jinsong ;
Zhu, Xiaole .
DIGITAL HEALTH, 2022, 8
[14]   The evolving role of diet in prostate cancer risk and progression [J].
Kaiser, Adeel ;
Haskins, Christopher ;
Siddiqui, Mohummad M. ;
Hussain, Arif ;
D'Adamo, Christopher .
CURRENT OPINION IN ONCOLOGY, 2019, 31 (03) :222-229
[15]   Bioinformatics for cancer management in the post-genome era [J].
Katoh, M ;
Katoh, M .
TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2006, 5 (02) :169-175
[16]   Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2 [J].
Love, Michael I. ;
Huber, Wolfgang ;
Anders, Simon .
GENOME BIOLOGY, 2014, 15 (12)
[17]   The adipocyte microenvironment and cancer [J].
Mukherjee, Abir ;
Bilecz, Agnes J. ;
Lengyel, Ernst .
CANCER AND METASTASIS REVIEWS, 2022, 41 (03) :575-587
[18]   Adipocytes promote ovarian cancer metastasis and provide energy for rapid tumor growth [J].
Nieman, Kristin M. ;
Kenny, Hilary A. ;
Penicka, Carla V. ;
Ladanyi, Andras ;
Buell-Gutbrod, Rebecca ;
Zillhardt, Marion R. ;
Romero, Iris L. ;
Carey, Mark S. ;
Mills, Gordon B. ;
Hotamisligil, Goekhan S. ;
Yamada, S. Diane ;
Peter, Marcus E. ;
Gwin, Katja ;
Lengyel, Ernst .
NATURE MEDICINE, 2011, 17 (11) :1498-U207
[19]  
Perry M., 2016, R Package Version, V1
[20]   limma powers differential expression analyses for RNA-sequencing and microarray studies [J].
Ritchie, Matthew E. ;
Phipson, Belinda ;
Wu, Di ;
Hu, Yifang ;
Law, Charity W. ;
Shi, Wei ;
Smyth, Gordon K. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (07) :e47