Identification and experimental validation of prognostic genes related to cytochrome c in breast cancer
Breast cancer (BC) is one of the most prevalent malignant diseases affecting women. Cytochrome c (Cyt c) plays a critical role in various pathological processes, however, its precise mechanism in BC remains unclear. This study aimed to identify prognostic genes linked to Cyt c in BC and explore thei...
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Published in | Frontiers in genetics Vol. 16 |
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11.08.2025
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Abstract | Breast cancer (BC) is one of the most prevalent malignant diseases affecting women. Cytochrome c (Cyt c) plays a critical role in various pathological processes, however, its precise mechanism in BC remains unclear. This study aimed to identify prognostic genes linked to Cyt c in BC and explore their underlying mechanisms. Transcriptome data related to BC were initially obtained from TCGA and GEO database. Prognostic genes were identified through differential expression analysis, univariate Cox regression, and LASSO analysis. A risk model was subsequently developed and validated. Additionally, enrichment analysis, immune microenvironment analysis, and the construction of a TFs-mRNA network were conducted. Finally, the expression levels of prognostic genes were examined in both tumor and normal tissue samples, with confirmation through RT-qPCR. Eight prognostic genes ( CETP , CLEC11A , CYP2A6 , CYP2A7 , GZMB , HGF , LDHC , and PLAU ) were identified. The risk model demonstrated that low-risk individuals have significantly higher survival rates. GSEA results indicated that seven of the prognostic genes are notably enriched in the “cytokine-cytokine receptor interaction” pathway. Transcription factors, such as ATF3 and RUNX1, were found to regulate these prognostic genes. Furthermore, immune cell profiles revealed significant differences between high-risk and low-risk groups. Bioinformatics and RT-qPCR analyses confirmed that CETP and HGF are upregulated in normal tissues, while CLEC11A and PLAU showed higher expression in BC tissues. This study identified eight Cyt c-related prognostic genes and developed a risk model, offering new insights into personalized treatment and prognosis for BC. |
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AbstractList | Breast cancer (BC) is one of the most prevalent malignant diseases affecting women. Cytochrome c (Cyt c) plays a critical role in various pathological processes, however, its precise mechanism in BC remains unclear. This study aimed to identify prognostic genes linked to Cyt c in BC and explore their underlying mechanisms. Transcriptome data related to BC were initially obtained from TCGA and GEO database. Prognostic genes were identified through differential expression analysis, univariate Cox regression, and LASSO analysis. A risk model was subsequently developed and validated. Additionally, enrichment analysis, immune microenvironment analysis, and the construction of a TFs-mRNA network were conducted. Finally, the expression levels of prognostic genes were examined in both tumor and normal tissue samples, with confirmation through RT-qPCR. Eight prognostic genes ( CETP , CLEC11A , CYP2A6 , CYP2A7 , GZMB , HGF , LDHC , and PLAU ) were identified. The risk model demonstrated that low-risk individuals have significantly higher survival rates. GSEA results indicated that seven of the prognostic genes are notably enriched in the “cytokine-cytokine receptor interaction” pathway. Transcription factors, such as ATF3 and RUNX1, were found to regulate these prognostic genes. Furthermore, immune cell profiles revealed significant differences between high-risk and low-risk groups. Bioinformatics and RT-qPCR analyses confirmed that CETP and HGF are upregulated in normal tissues, while CLEC11A and PLAU showed higher expression in BC tissues. This study identified eight Cyt c-related prognostic genes and developed a risk model, offering new insights into personalized treatment and prognosis for BC. Breast cancer (BC) is one of the most prevalent malignant diseases affecting women. Cytochrome c (Cyt c) plays a critical role in various pathological processes, however, its precise mechanism in BC remains unclear. This study aimed to identify prognostic genes linked to Cyt c in BC and explore their underlying mechanisms. Transcriptome data related to BC were initially obtained from TCGA and GEO database. Prognostic genes were identified through differential expression analysis, univariate Cox regression, and LASSO analysis. A risk model was subsequently developed and validated. Additionally, enrichment analysis, immune microenvironment analysis, and the construction of a TFs-mRNA network were conducted. Finally, the expression levels of prognostic genes were examined in both tumor and normal tissue samples, with confirmation through RT-qPCR. Eight prognostic genes ( CETP , CLEC11A , CYP2A6 , CYP2A7 , GZMB , HGF , LDHC , and PLAU ) were identified. The risk model demonstrated that low-risk individuals have significantly higher survival rates. GSEA results indicated that seven of the prognostic genes are notably enriched in the “cytokine-cytokine receptor interaction” pathway. Transcription factors, such as ATF3 and RUNX1, were found to regulate these prognostic genes. Furthermore, immune cell profiles revealed significant differences between high-risk and low-risk groups. Bioinformatics and RT-qPCR analyses confirmed that CETP and HGF are upregulated in normal tissues, while CLEC11A and PLAU showed higher expression in BC tissues. This study identified eight Cyt c-related prognostic genes and developed a risk model, offering new insights into personalized treatment and prognosis for BC. |
Author | Li, Shihong Wang, Haobin Wu, Jian Yu, Huimin |
AuthorAffiliation | 1 College of Medicine , Southwest Jiaotong University , Chengdu , China 3 Department of Thyroid and Breast Surgery , The Third People’s Hospital of Chengdu , Chengdu , China 4 Department of Thyroid and Breast Surgery , The Sixth People’s Hospital of Chengdu , Chengdu , China 2 General Hospital of Western Theater Command , Chengdu , China |
AuthorAffiliation_xml | – name: 1 College of Medicine , Southwest Jiaotong University , Chengdu , China – name: 2 General Hospital of Western Theater Command , Chengdu , China – name: 3 Department of Thyroid and Breast Surgery , The Third People’s Hospital of Chengdu , Chengdu , China – name: 4 Department of Thyroid and Breast Surgery , The Sixth People’s Hospital of Chengdu , Chengdu , China |
Author_xml | – sequence: 1 givenname: Huimin surname: Yu fullname: Yu, Huimin – sequence: 2 givenname: Shihong surname: Li fullname: Li, Shihong – sequence: 3 givenname: Jian surname: Wu fullname: Wu, Jian – sequence: 4 givenname: Haobin surname: Wang fullname: Wang, Haobin |
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Notes | Edited by: Joon-Yong Chung, National Cancer Institute (NIH), United States Olivia Lee, National Cancer Institute (NIH), United States Reviewed by: Gwan Hee Han, Kyung Hee University Hospital, Republic of Korea |
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