Analysis of Yes-Associated Protein-1 (YAP1) Target Gene Signature to Predict Progressive Breast Cancer

被引:2
作者
Venkatasubramanian, Gomathi [1 ]
Kelkar, Devaki A. [1 ,2 ]
Mandal, Susmita [3 ]
Jolly, Mohit Kumar [3 ]
Kulkarni, Madhura [1 ,2 ]
机构
[1] Ctr Translat Canc Res, Pune 411016, Maharashtra, India
[2] Prashanti Canc Care Mission, 1-2 Kapil Vastu,Senapati Bapat Rd, Pune 411016, Maharashtra, India
[3] Indian Inst Sci, Ctr BioSyst Sci & Engn, Bangalore 560012, Karnataka, India
关键词
yes-associated protein-1; breast cancer; cancer prognosis; gene signatures; HIPPO SIGNALING PATHWAY; POOR-PROGNOSIS; 70-GENE SIGNATURE; YAP/TAZ; EXPRESSION; TUMOR; OVEREXPRESSION;
D O I
10.3390/jcm11071947
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Breast cancers are treated according to the ER/PR or HER2 expression and show better survival outcomes with targeted therapy. Triple-negative breast cancers (TNBCs) with a lack of expression of ER/PR and HER2 are treated with systemic therapy with unpredictable responses and outcomes. It is essential to investigate novel markers to identify targeted therapies for TNBC. One such marker is YAP1, a transcription co-activator protein that shows association with poor prognosis of breast cancer. YAP1 transcriptionally regulates the expression of genes that drive the oncogenic phenotypes. Here, we assess a potential YAP target gene signature to predict a progressive subset of breast tumors from METABRIC and TCGA datasets. YAP1 target genes were shortlisted based on expression correlation and concordance with YAP1 expression and significant association with survival outcomes of patients. Hierarchical clustering was performed for the shortlisted genes. The utility of the clustered genes was assessed by survival analysis to identify a recurring subset. Expression of the shortlisted target genes showed significant association with survival outcomes of HER2-positive and TNBC subset in both datasets. The shortlisted genes were verified using an independent dataset. Further validation using IHC can prove the utility of this potential prognostic signature to identify a recurrent subset of HER2-positive and TNBC subtypes.
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页数:25
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