PuSH - Publikationsserver des Helmholtz Zentrums München

Zieker, D.* ; Königsrainer, I.* ; Traub, F.* ; Nieselt, K.* ; Knapp, B.* ; Schillinger, C.* ; Stirnkorb, C.* ; Fend, F.* ; Northoff, H.* ; Kupka, S.* ; Brücher, B.L.* ; Königsrainer, A.*

PGK1 a potential marker for peritoneal dissemination in gastric cancer.

Cell. Physiol. Biochem. 21, 429-436 (2008)
Verlagsversion DOI
Open Access Gold
BACKGROUND/AIMS: Peritoneal carcinomatosis, which is caused by the dissemination of cancer cells into the abdominal cavity is a frequent finding in patients with primary gastric cancer, and it is associated with a poor prognosis. The mechanisms that mediate peritoneal carcinomatosis in diffuse primary gastric tumours require definition. METHODS: We therefore compared the gene expression profile in diffuse primary gastric cancer patients with and without peritoneal carcinomatosis (n=13). Human specimens from consecutive gastric cancer patients with and without peritoneal carcinomatosis were investigated using oligonucleotide microarrays. Differentially expressed genes of interest were further evaluated using quantitative real-time polymerase chain reaction (qRT-PCR). RESULTS: The results reveal a significant overexpression of phosphoglycerate kinase 1 (PGK1), the chemokine CXCR4 and its ligand CXCL12 in specimens from diffuse gastric cancer patients with peritoneal carcinomatosis. Overexpression of PGK1 is known to increase the expression of CXCR4. CXCR4 on its part can increase CXCL12 expression. Elevated levels of CXCR4 and CXCL12 are associated with an increase in the metastatic rate and play an important role in the metastatic homing of malignant cells. CONCLUSION: The overexpression of PGK1 and its signalling targets may be a expression-pathway in diffuse primary gastric carcinomas promoting peritoneal dissemination and may function as prognostic markers and/or be potential therapeutic targets to prevent the migration of gastric carcinoma cells into the peritoneum.
Weitere Metriken?
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1015-8987
e-ISSN 1421-9778
Quellenangaben Band: 21, Heft: 5-6, Seiten: 429-436 Artikelnummer: , Supplement: ,
Verlag Karger
Begutachtungsstatus Peer reviewed