Transcription Factor HOXA9 is Linked to the Calcification and Invasion of Papillary Thyroid Carcinoma.
Yilan JinHyeung Kyoo KimJeonghun LeeEuy Young SohJang-Hee KimInsun SongYoon-Sok ChungYong Jun ChoiPublished in: Scientific reports (2019)
Calcification is important for the diagnosis of papillary thyroid carcinoma (PTC). Runt-related transcription factor 2 (RUNX2), a master transcription factor associated with osteogenic differentiation, is reportedly related to PTC calcification and invasiveness. However, its regulatory role in this process is somewhat uncharacterized. Here, we attempted to identify genes that regulate RUNX2 and clarify its function in PTC carcinogenesis and calcification. The expression of RUNX2-upstream genes was evaluated by real-time PCR in Nthy-Ori 3-1 normal thyroid cells and TPC1 and BHP10-3 PTC cell lines. Luciferase and chromatin immunoprecipitation assays were performed with candidate genes after cloning the RUNX2 promoter. We found that RUNX2 promoter activity was enhanced by homeobox family A9 (HOXA9). Over-expression of HOXA9 was found to enhance alkaline phosphatase activity, mineralization, and in vitro tumour cell migration and invasion, whereas downregulation had the opposite effects. These results indicate that HOXA9, a positive regulator of RUNX2, can enhance calcification, migration, and invasion in PTC. Our data improve the understanding of the molecular mechanisms of microcalcification in PTC as well as tumorigenesis.
Keyphrases
- transcription factor
- genome wide identification
- chronic kidney disease
- long non coding rna
- dna binding
- poor prognosis
- long noncoding rna
- lymph node
- real time pcr
- genome wide
- lymph node metastasis
- induced apoptosis
- mesenchymal stem cells
- cell proliferation
- gene expression
- dna methylation
- single cell
- squamous cell carcinoma
- binding protein
- cell cycle arrest
- cell therapy
- big data
- oxidative stress
- signaling pathway
- cell death
- endoplasmic reticulum stress
- machine learning
- artificial intelligence