MicroRNA regulation of proteoglycan function in cancer.

Ibrahim S, Hassan H, Götte M

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

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

FachzeitschriftThe FEBS Journal (FEBS J)
Jahrgang / Bandnr. / Volume281
Ausgabe / Heftnr. / Issue22
Seitenbereich5009-22
StatusVeröffentlicht
Veröffentlichungsjahr2014
Sprache, in der die Publikation verfasst istEnglisch
StichwörtermicroRNA; 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

Götte, Martin

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