MicroRNA regulation of proteoglycan function in cancer.
Ibrahim S, Hassan H, Götte M
Forschungsartikel (Zeitschrift) | Peer reviewedZusammenfassung
MicroRNAs are small noncoding RNAs acting as physiological regulators of gene expression at the post-transcriptional level. In cancer, the expression of microRNAs is dysregulated compared to healthy tissue, suggesting a mechanistic role in disease progression. Recent experimental evidence supports the important molecular role of proteoglycans as microRNA targets in this process. Misexpression of specific microRNAs results in aberrant expression patterns of proteoglycans, as well as their biosynthetic enzymes. Consequently, cell proliferation and apoptosis, adhesion, migration, invasiveness, epithelial-to-mesenchymal transition and cancer stem cell properties are affected as a result of the multifunctional properties of proteoglycans. A pharmacological targeting of the microRNA-proteoglycan axis emerges as a new therapeutic concept in cancer.
Details zur Publikation
Fachzeitschrift: The FEBS Journal (FEBS J)
Jahrgang / Bandnr. / Volume: 281
Ausgabe / Heftnr. / Issue: 22
Seitenbereich: 5009-22
Status: Veröffentlicht
Veröffentlichungsjahr: 2014
Sprache, in der die Publikation verfasst ist: Englisch
Stichwörter: microRNA; HEPATOCELLULAR-CARCINOMA; heparanase; BREAST-CANCER; decorin; TARGETING; cancer; heparan; cancer stem cells; GLYPICAN-3; ceRNA; EXTRACELLULAR-MATRIX; sulfate; glypican; syndecan; OVARIAN-CANCER; SYNDECAN-1 CD138; POTENTIAL BIOMARKER; HUMAN; post-transcriptional regulation; CARCINOMA CELL-PROLIFERATION; TUMOR MICROENVIRONMENT; HEPARAN-SULFATE PROTEOGLYCANS; post-transcriptional regulation; heparan sulfate; syndecan; Glypican; Tumor Microenvironment; Cancer stem cells; Heparanase; MicroRNA; CERNA; CANCER; OVARIAN-CANCER; DECORIN; TARGETING GLYPICAN-3; HEPATOCELLULAR-CARCINOMA; HEPARAN-SULFATE PROTEOGLYCANS; POTENTIAL BIOMARKER; SYNDECAN-1 CD138; CARCINOMA CELL-PROLIFERATION; EXTRACELLULAR-MATRIX; HUMAN BREAST-CANCER
Autor*innen der Universität Münster
Projekte, aus denen die Publikation entstanden ist
Laufzeit: 01.01.2015 - 31.12.2015 Gefördert durch: Deutscher Akademischer Austauschdienst Art des Projekts: Beteiligung in sonstigen Verbundvorhaben |