CARMA3 Promotes Colorectal Cancer Cell Motility and Cancer Stemness via YAP-Mediated NF-κB Activation.
Ting-Yu ChangCheng-Tien WuMeei-Ling SheuRong-Sen YangShing-Hwa LiuPublished in: Cancers (2021)
CARD-recruited membrane-associated protein 3 (CARMA3) is overexpressed in various cancers and is associated with cancer cell proliferation, metastasis, and tumor progression; however, the underlying mechanisms of CARMA3 in colorectal cancer (CRC) metastasis remain unclear. Here, we found that higher CARMA3 expression was correlated with poor overall survival and metastasis in CRC patients from the TNMplot database and Human Tissue Microarray staining. Elevating CARMA3 expression promoted cell proliferation, epithelial-mesenchymal transition (EMT) induction, migration/invasion abilities, sphere formation, and cancer stem cell markers expression. Knockdown of CARMA3 decreased these processes via the EMT-related transcription factor Slug. Moreover, CARMA3 depletion significantly reduced tumor growth in mice that were consistent with the in vitro results. CRC migration/invasion could be regulated by CARMA3/YAP/Slug signaling axis using genetic inhibition of Yes-associated protein (YAP). Interestingly, CARMA3 induced activation of nuclear factor (NF)-κB through YAP expression, contributing to upregulation of Slug. YAP expression positively correlated with CARMA3, NF-κB, and Slug gene expression and poor clinical outcomes in CRC patients. Our findings demonstrate for the first time that CARMA3 plays an important role in CRC progression, which may serve as a potential diagnostic biomarker and candidate therapeutic target for CRC treatment.
Keyphrases
- epithelial mesenchymal transition
- poor prognosis
- signaling pathway
- nuclear factor
- cell proliferation
- gene expression
- transforming growth factor
- end stage renal disease
- ejection fraction
- transcription factor
- pi k akt
- newly diagnosed
- long non coding rna
- toll like receptor
- oxidative stress
- prognostic factors
- lps induced
- endothelial cells
- chronic kidney disease
- adipose tissue
- binding protein
- cancer stem cells
- squamous cell carcinoma
- type diabetes
- papillary thyroid
- immune response
- metabolic syndrome
- inflammatory response
- biofilm formation
- electronic health record
- combination therapy
- staphylococcus aureus
- squamous cell
- copy number
- cell migration
- patient reported outcomes
- diabetic rats
- pseudomonas aeruginosa
- young adults
- free survival
- high glucose
- induced pluripotent stem cells
- insulin resistance