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Coupled expression of dipeptidyl peptidase-IV and fibroblast activation protein-α in transformed astrocytic cells
E. Balaziova, P. Busek, J. Stremenova, L. Sromova, E. Krepela, L. Lizcova, A. Sedo
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
ProQuest Central
from 1997-01-01 to 1 year ago
Medline Complete (EBSCOhost)
from 2011-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 1997-01-01 to 1 year ago
- MeSH
- Cell Differentiation MeSH
- Cell Extracts chemistry MeSH
- Cell Culture Techniques MeSH
- Dipeptidyl Peptidase 4 genetics metabolism MeSH
- Enzyme Assays MeSH
- Transcription, Genetic MeSH
- Humans MeSH
- Membrane Proteins genetics metabolism MeSH
- RNA, Messenger genetics metabolism MeSH
- Neuroglia enzymology metabolism MeSH
- Recombinant Proteins genetics metabolism MeSH
- Serine Endopeptidases genetics metabolism MeSH
- Cell Line, Transformed MeSH
- Gelatinases genetics metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Dipeptidyl peptidase-IV (DPP-IV) and fibroblast activation protein-α (FAP) are speculated to participate in the regulation of multiple biological processes, because of their unique enzymatic activity, as well as by non-hydrolytic molecular interactions. At present, the role of DPP-IV and FAP in the development and progression of various types of tumors, including glioblastoma, is intensively studied, and their functional crosstalk is hypothesized. In this article, we describe the correlative expression of DPP-IV and FAP mRNA in primary cell cultures derived from human glioblastoma and associated expression dynamics of both molecules in astrocytoma cell lines depending on culture conditions. Although the molecular mechanisms of DPP-IV and FAP co-regulations remain unclear, uncoupled expression of transgenic DPP-IV and the endogenous FAP suggests that it occurs rather at the transcriptional than at the posttranscriptional level. Understanding of the expressional and functional coordinations of DPP-IV and FAP may help clarify the mechanisms of biological roles of both molecules in transformed astrocytic cells.
References provided by Crossref.org
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