Prognostic value of metastin expression in human pancreatic cancer.
Nagai. Kazuyuki K; Doi. Ryuichiro R; Katagiri. Fumihiko F; Ito. Tatsuo T; Kida. Atsushi A; Koizumi. Masayuki M; Masui. Toshihiko T; Kawaguchi. Yoshiya Y; Tomita. Kenji K; Oishi. Shinya S; Fujii. Nobutaka N; Uemoto. Shinji S
Key Findings
- Strong metastin expression was present in about 25% of pancreatic cancers and was associated with better outcomes.
- Tumors lacking both metastin and its receptor were larger and more aggressive.
- High plasma metastin levels after surgery correlated with 100% short‑term survival in the small group studied.
Practical Outcomes
- For most biohackers, this research is not directly actionable because it deals with tumor biology and prognosis rather than a supplement or protocol you can use. It suggests that measuring blood metastin could help doctors assess pancreatic cancer risk, but there’s no guidance on how to safely raise metastin levels for health benefits.
Summary
The study found that higher levels of the protein metastin (kisspeptin-10) and its receptor GPR54 in pancreatic tumors are linked to smaller tumors, lower recurrence, and longer survival after surgery. Patients with high blood levels of metastin after removal of the tumor all survived during the follow‑up period.
Abstract
KiSS-1 was identified as a metastasis-suppressing gene in melanoma cells. The KiSS-1 gene product (metastin) was isolated from human placenta as the ligand of GPR54, a G-protein-coupled receptor. The role of metastin and GPR54 in tumor progression is not fully understood. We investigated the clinical significance of metastin and GPR54 expression in pancreatic cancer. We evaluated immunohistochemical expression of metastin and GPR54 in pancreatic ductal adenocarcinoma tissues obtained from 53 consecutive patients who underwent resection between July 2003 and May 2007 at Kyoto University Hospital. In 23 consecutive patients, the plasma metastin level was measured before surgery by enzyme immunoassay. Strong immunohistochemical expression of metastin was detected in 13 tumors (24.5%), while strong expression of GPR54 was detected in 30 tumors (56.6%). Tumors that were negative for both metastin and GPR54 expression were significantly larger than tumors that were positive for either metastin or GPR54 (p = 0.047). Recurrence was less frequent in patients who had metastin-positive tumors compared with those who had metastin-negative tumors (38.5% versus 70.0%, p = 0.04). Strong expression of metastin and GPR54 was significantly correlated with longer survival (p = 0.02). Metastin expression by pancreatic cancer was an independent prognostic factor for longer survival (hazard ratio, 2.1; 95% confidence interval, 1.1-4.7; p = 0.03), and the patients with a high plasma metastin level (n = 6) did not die after surgical resection. Strong expression of metastin and GPR54 by pancreatic cancer is associated with longer survival. Metastin expression is an independent prognostic factor for the survival of pancreatic cancer patients. The plasma metastin level could become a noninvasive prognostic factor for the assessment of pancreatic cancer.
Study Information
pubmed
2009
2009-01-21T00:00:00.000Z
10.1186/1756-9966-28-9
54
39