Vertaisarvioitu alkuperäisartikkeli tai data-artikkeli tieteellisessä aikakauslehdessä (A1)
The PIM1 kinase promotes prostate cancer cell migration and adhesion via multiple signalling pathways
Julkaisun tekijät: Niina M. Santio, Maria Salmela, Heidi Arola, Sini K.Eerola, Jyrki Heino, Eeva-Marja Rainio, Päivi J.Koskinen
Kustantaja: Academic Press
Julkaisuvuosi: 2016
Journal: Experimental Cell Research
Tietokannassa oleva lehden nimi: EXPERIMENTAL CELL RESEARCH
Lehden akronyymi: EXP CELL RES
Volyymi: 342
Julkaisunumero: 2
Aloitussivu: 113
Lopetussivun numero: 124
Sivujen määrä: 12
ISSN: 0014-4827
eISSN: 1090-2422
DOI: http://dx.doi.org/10.1016/j.yexcr.2016.02.018
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/2933532
The ability of cells to migrate and form metastases is one of the fatal hallmarks of cancer that can be conquered only with better understanding of the molecules and regulatory mechanisms involved. The oncogenic PIM kinases have been shown to support cancer cell survival and motility, but the PIM-regulated pathways stimulating cell migration and invasion are less well characterized than those affecting cell survival. Here we have identified the glycogen synthase kinase 3 beta (GSK3B) and the forkhead box P3 (FOXP3) transcription factor as direct PIM targets, whose tumour-suppressive effects in prostate cancer cells are inhibited by PIM-induced phosphorylation, resulting in increased cell migration. Targeting GSK3B is also essential for the observed PIM-enhanced expression of the prostaglandin-endoperoxide synthase 2 (PTGS2), which is an important regulator of both cell migration and adhesion. Accordingly, selective inhibition of PIM activity not only reduces cell migration, but also affects integrin-mediated cell adhesion. Taken together, these data provide novel mechanistic insights on how and why patients with metastatic prostate cancer may benefit from therapies targeting PIM kinases, and how such approaches may also be applicable to inflammatory conditions
Ladattava julkaisu This is an electronic reprint of the original article. |