Osteopontin splice variant as a potential marker for metastatic disease in pancreatic adenocarcinoma.
Osteopontin splice variant as a potential marker for metastatic disease in pancreatic adenocarcinoma.
复制标题
骨桥蛋白剪接变体作为胰腺腺癌转移性疾病的潜在标志物。
DOI：
10.1111/jgh.12561
复制
发表时间：
2014
影响因子：
4.1
通讯作者：
Arafat,HwydaA
中科院分区：
文献类型：
--
作者：
Siddiqui,AliA;Jones,Elizabeth;Andrade,Darren;Shah,Apeksha;Kowalski,ThomasE;Loren,DavidE;Chipitsyna,Galina;Arafat,HwydaA
Background and AimOsteopontin (OPN) is a phosphoprotein that activates pathways that induce cancer cell survival and metastasis. Our aim was to examine the expression pattern of OPN splice variants a, b, and c in fine‐needle aspirates and to determine their correlation with stage‐adjusted pancreatic ductal adenocarcinoma (PDA) survival.MethodsEndoscopic ultrasound‐guided fine‐needle aspiration (EUS‐FNA) was performed in patients with solid pancreatic masses. The tissue was collected and analyzed for the expression of OPN isoforms by reverse transcription–polymerase chain reaction. Survival curves of stages and overexpression of OPN splice variants (a, b, c) were estimated according to the Kaplan–Meier and the log‐rank test.ResultsEUS‐FNA was performed in 46 patients with solid pancreatic lesions (40 PDA and 6 chronic pancreatitis). OPNa was highly expressed in 39/40 (98%), OPNb in 24/40 (60%), while OPNc was present in 10/40 (25%) of PDA samples. The median survival was lower in patients whose fine‐needle aspiration (FNA) samples expressed OPNb than those without (406 daysvs749 days,P= 0.049). There was no significant difference in survival in patients with OPNc. Cox proportional hazard model demonstrated that OPNb expression had a trend toward decrease overall survival (P= 0.06), with these patients having a hazard of death three times higher than those without. OPNc was found to significantly correlate with metastatic disease (P= 0.009) in PDA patients.ConclusionsOur data show for the first time that in FNA samples, there is a strong association between OPNc and presence of metastasis in PDA, and OPNb and poor survival.
