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     CircRNA Drives Cancer Metastasis Via TGF-β Signaling

Fig. 1. TGF-β activation upregulates circRNA CDR1as, which interacts with IGF2BP1 protein to stabilize m6A modified Slug mRNA. The increased Slug, a key factor in epithelial-to-mesenchymal transition (EMT), causes cancer metastasis [1].


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Using Arraystar circRNA Microarray, the circRNA expression was profiled with TGF-β agonist treatment in cancer cells. CDR1as was found to be the top differentially expressed circRNA [1].
Further, CDR1as facilitates IGF2BP1 to stabilize m6A modified Slug mRNA, a key EMT factor. Additionally, CDR1as activates other TGF-β signaling factors known to promote EMT, including P-Smad2 and P-Smad3. Thus, CDR1as promotes cervical cancer metastasis and shortens cancer survival.

Reference

[1] Zhong G. et al (2023) TGF-β signaling promotes cervical cancer metastasis via CDR1as. Mol Cancer 22(1):66 [PMID:37004067]


 

Arraystar CircRNA Arrays

• The effective and practical platform for highly sensitive and specific circular RNA profiling.

• Circular junction-specific probes, linear RNA removal and efficient circRNA labeling ensure the most specific, accurate and reliable circRNA expression profiling.

• Detailed annotation specific to circRNA biology, e.g. miRNA binding sites, miRSVR scores and conservation status, to unravel functional roles as miRNA sponges.

• The preferred choice over RNA-sequencing, due to the particular properties of circular RNAs.


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Latest Publications

Circular RNA
• Yuan Q, et al. (2023)
   Signal Transduction &Targeted Therapy
   [PMID: 36882410]
• Zhong GL, et al. (2023)
   Molecular Cancer
   [PMID: 37004067]

RNA Modification
• Yan W, et al. (2023)
   International Journal of Oral Science
   [PMID: 36631441]


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