Lysophosphatidic Acid is a Biomarker for Peritoneal Carcinomatosis of Gastric Cancer and Correlates with Poor Prognosis

溶血磷脂酸 腹水 医学 胃肠病学 内科学 癌症 腹膜癌病 生物标志物 肝硬化 化疗 结直肠癌 生物 生物化学 受体
作者
Ruolan Zeng,Bin Li,Junhui Huang,Meizuo Zhong,Li Li,Chaojun Duan,Shan Zeng,Jin Huang,Wei Liu,Jingchen Lu,Youhong Tang,Lingming Zhou,Yiping Liu,Jianhuang Li,Zhengxi He,Quan Wang,Youyi Dai
出处
期刊:Genetic Testing and Molecular Biomarkers [Mary Ann Liebert]
卷期号:21 (11): 641-648 被引量:28
标识
DOI:10.1089/gtmb.2017.0060
摘要

Background: Peritoneal carcinomatosis (PC) is an important cause of morbidity and mortality among patients with gastric cancer. Thus, it is important to identify an ideal biomarker for PC. Methods: Plasma and ascites samples were collected from gastric cancer patients with PC and a control group. Lysophosphatidic acid (LPA) levels were tested and analyzed. Results: The plasma LPA levels of gastric cancer patients with PC were significantly higher than those in gastric cancer patients after radical resection (p = 0.046) and healthy volunteers (p < 0.001). Besides, plasma LPA levels were statistically lower after chemotherapy in gastric cancer patients with PC (p = 0.028). Furthermore, the ascites LPA levels were significantly higher in gastric cancer patients with peritoneal carcinomatosis than those in liver cirrhosis patients (p < 0.001). Moreover, ascites LPA levels were statistically lower after intraperitoneal chemotherapy injection than before (p < 0.001). In addition, the plasma LPA levels were significantly associated with serum CA125 levels (p = 0.032) and TNM stage in gastric cancer patients (p = 0.009). Individuals with plasma LPA levels >20,000 ng/mL had significantly worse overall survival (OS) than those with plasma LPA levels <20,000 ng/mL group (p = 0.006). In addition the group with ascites LPA levels >24,000 ng/mL showed significantly worse progression-free survival (PFS) and OS (p < 0.001 in PFS and OS). Conclusions: This study demonstrated that LPA levels in plasma and ascites may be useful diagnostic biomarkers for PC of gastric cancer and that higher levels are associated with poor prognosis.
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