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The role of CEMIP in cancers and its transcriptional and post-transcriptional regulation.
Guo, Song; Guo, Yunfei; Chen, Yuanyuan; Cui, Shuaishuai; Zhang, Chunmei; Chen, Dahu.
Affiliation
  • Guo S; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
  • Guo Y; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
  • Chen Y; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
  • Cui S; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
  • Zhang C; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
  • Chen D; Shandong University of Technology, School of Life Sciences and Medicine, Zibo, Shandong, China.
PeerJ ; 12: e16930, 2024.
Article in En | MEDLINE | ID: mdl-38390387
ABSTRACT
CEMIP is a protein known for inducing cell migration and binding to hyaluronic acid. Functioning as a hyaluronidase, CEMIP primarily facilitates the breakdown of the extracellular matrix component, hyaluronic acid, thereby regulating various signaling pathways. Recent evidence has highlighted the significant role of CEMIP in different cancers, associating it with diverse pathological states. While identified as a biomarker for several diseases, CEMIP's mechanism in cancer seems distinct. Accumulating data suggests that CEMIP expression is triggered by chemical modifications to itself and other influencing factors. Transcriptionally, chemical alterations to the CEMIP promoter and involvement of transcription factors such as AP-1, HIF, and NF-κB regulate CEMIP levels. Similarly, specific miRNAs have been found to post-transcriptionally regulate CEMIP. This review provides a comprehensive summary of CEMIP's role in various cancers and explores how both transcriptional and post-transcriptional mechanisms control its expression.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: MicroRNAs / Neoplasms Language: En Journal: PeerJ Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: MicroRNAs / Neoplasms Language: En Journal: PeerJ Year: 2024 Document type: Article Affiliation country: China