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The Expression of Melanoma-Associated Antigen D2 Both in Surgically Resected and Serum Samples Serves as Clinically Relevant Biomarker of Gastric Cancer Progression
Ist Teil von
Annals of surgical oncology, 2016-02, Vol.23 (Suppl 2), p.214-221
Ort / Verlag
Cham: Springer International Publishing
Erscheinungsjahr
2016
Link zum Volltext
Quelle
SpringerLink
Beschreibungen/Notizen
Background
Sensitive biomarkers are necessary for risk classification of patients with gastric cancer (GC), especially ones at risk of distant metastases. Melanoma-associated antigen (MAGE)-D2 has been reported to play a role in the process of cell adhesion and metastatic potential of tumor cells in colorectal cancer. The purpose of this study was to identify a novel clinically relevant biomarker of GC.
Methods
Expression analysis of
MAGE-D2
was conducted in GC cell lines and clinical samples (surgical specimen and serum) in both mRNA and protein level. Correlations between
MAGE-D2
expression status and clinicopathological factors were evaluated.
Results
MAGE-D2
mRNA expression levels were similar between GC tissues and the corresponding normal adjacent tissues and were independent of GC differentiation or subtype. In 101 (45 %) of 225 patients, the expression level of
MAGE
-
D2
mRNA was increased in GC tissues compared with the corresponding normal adjacent tissues. Increased expression of
MAGE
-
D2
mRNA in GC tissues was associated with distant metastasis and early recurrence and was an independent prognostic factor (hazard ratio 2.27, 95 % confidence interval 1.39–3.74,
P
= 0.001). There was a stepwise increase in serum
MAGE
-
D2
level going from healthy volunteers to patients with localized GC and then to those with extended GC (stage IV). Patients with preoperative serum
MAGE
-
D2
levels >130 pg/ml had a more unfavorable prognosis than those with levels ≤130 pg/ml.
Conclusion
MAGE
-
D2
was associated with metastatic potential of GC and may represent a promising biomarker, both in gastric tissues and serum samples, for malignant behavior of GC.