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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2007 pubmed 65 citations

KiSS-1 overexpression as an independent prognostic marker in hepatocellular carcinoma: an immunohistochemical study.

Schmid. Katharina K; Wang. Xiaowei X; Haitel. Andrea A; Sieghart. Wolfang W; Peck-Radosavljevic. Markus M; Bodingbauer. Martin M; Rasoul-Rockenschaub. Susanne S; Wrba. Fritz F

Key Findings

  • Only a small percentage of liver cancers (4% for KiSS-1, 8% for its receptor AXOR12) showed detectable levels of these proteins.
  • Higher KiSS-1 expression was associated with shorter disease‑free and overall survival.
  • KiSS-1 and AXOR12 levels tended to rise together and also correlated with levels in nearby normal liver tissue.

Practical Outcomes

  • For biohackers or self‑experimenters, this research does not provide a direct way to use kisspeptin‑10 for health improvement. It mainly identifies kisspeptin‑10 as a cancer biomarker, which is useful for clinicians but not actionable for longevity, metabolic health, or performance protocols.

Summary

A study looked at the protein kisspeptin-10 (produced by the KiSS-1 gene) in liver cancer tissue and found that higher levels of this protein were linked to worse survival, making it a potential marker for aggressive tumors.

Abstract

The KiSS-1 gene has been reported to play an important role as a metastasis suppressor gene in various human malignancies. However, there is little information about its possible role in hepatocellular carcinoma (HCC). In this study, we evaluated the prognostic significance of the expression of KiSS-1 and its receptor AXOR12 in 142 HCC tissue specimens by immunohistochemistry. By using a cutoff level of 50%, immunoreactivity of KiSS-1 and AXOR12 was found in 6 (4%) and 11 (8%) HCCs. The expression of KiSS-1 and AXOR12 in HCC correlated with each other (r = 0.42, p < 0.0001) and with the expression in corresponding, surrounding liver tissue (both r = 0.35, p < 0.0001). Positive AXOR12 immunoreactivity in HCC correlated with advanced pT-stage of tumors and low tumor grading (r = 0.18, p = 0.032; r = -0.18, p = 0.029). High KiSS-1 expression in HCC had a statistically significant influence on diminished disease-free and overall survival in uni- (p = 0.006 and p = 0.002) and multivariate analysis (r = 2.874, p = 0.027 and r = 2.913, p = 0.026). In this study, we report for the first time that elevated KiSS-1 expression level in HCC correlates with worsened clinical outcome, as an independent prognostic marker for the aggressiveness of HCC.

Study Information

Provider

pubmed

Year

2007

Date

2007-01-10T00:00:00.000Z

DOI

10.1007/s00428-006-0352-9

Citations

65

References

24