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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
2003 pubmed

Tumor suppressor role of KiSS-1 in bladder cancer: loss of KiSS-1 expression is associated with bladder cancer progression and clinical outcome.

Sanchez-Carbayo. Marta M; Capodieci. Paola P; Cordon-Cardo. Carlos C

Key Findings

  • KiSS-1 expression is lower in bladder cancer cells from advanced tumors.
  • Complete loss of KiSS-1 is seen in invasive bladder tumors compared to normal bladder tissue.
  • Patients with low KiSS-1 levels have worse overall survival, indicating a potential tumor‑suppressor role.

Practical Outcomes

  • The findings are primarily of clinical interest for cancer diagnosis and prognosis and do not provide any actionable guidance for self‑directed health optimization, supplementation, or performance enhancement.

Summary

The study shows that the protein made from the KiSS-1 gene (kisspeptin) is often missing in aggressive bladder cancers, and patients whose tumors lack KiSS-1 tend to have poorer survival. This suggests KiSS-1 may help keep bladder cells from turning cancerous, but the research does not test taking kisspeptin as a supplement or therapy.

Abstract

The expression profiles of nine bladder cancer cell lines were compared against a pool containing equal total RNA quantities of each of them. Lower expression of KiSS-1 was revealed in cells derived from the most advanced bladder tumors. When comparing 15 primary bladder tumors versus a pool of four bladder cancer cell lines, lower transcript levels of KiSS-1 were observed in the invasive bladder carcinomas as compared to superficial tumors. KiSS-1 expression ratios provided prognostic information. The expression pattern of KiSS-1 transcripts was analyzed using in situ hybridization in nine bladder cancer cells, paired normal urothelium and bladder tumor samples (n = 25), and tissue microarrays of bladder tumors (n = 173). We observed complete loss of KiSS-1 in all invasive tumors under study as compared to their respective normal urothelium. The expression of KiSS-1 was found to be significantly associated with histopathological stage. Patients with lower KiSS-1 expression showed a direct correlation with overall survival in a subset of bladder tumors whose follow-up was available (n = 69). We did not observe any significant differential KiSS-1 expression along cell cycle by sorting analysis. A potential tumor suppressor role in bladder cancer was revealed for KiSS-1. Moreover, it showed predictive value by identifying patients with poor outcome.

Study Information

Provider

pubmed

Year

2003

DOI

10.1016/s0002-9440(10)63854-0