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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2017 pubmed 5 citations

Evaluation of Plasmatic Kisspetin-10 as a Biomarker for Malignancy and Subtype Differentiation in Small Renal Tumours.

Horstmann. Marcus M; Krause. Felix F; Steinbach. Daniel D; Twelker. Lars L; Grimm. Marc-Oliver MO

Key Findings

  • Kisspeptin‑10 levels were significantly higher in patients with small renal tumors compared to controls (10.04 vs 6.37 pmol/L).
  • The amount of kisspeptin‑10 varied by tumor subtype, highest in oncocytomas and lower in other RCC types.
  • The test could distinguish any tumor from healthy people fairly well (AUC 0.82) but was less accurate at separating malignant from benign tumors (AUC 0.671).

Practical Outcomes

  • This research is mainly about a potential diagnostic blood test for kidney tumors, not a treatment or lifestyle tweak. It doesn’t provide actionable steps for biohackers, but it may hint at future blood‑based cancer screening tools.

Summary

Researchers measured a blood molecule called kisspeptin‑10 in people with very small kidney tumors and found it was higher than in healthy folks, with levels differing between tumor types, but the study doesn’t give any tips you can use for health or performance.

Abstract

To evaluate Kisspeptin-10 (Kiss-10) in patients with small renal tumours (SRTs) and controls. Kiss-10 was measured in preoperative plasma samples in a cohort of 143 patients with unilateral renal tumours smaller than or equal to 4 cm and 40 age-matched controls by a competitive ELISA test kit. The cohort of patients included 56 patients with clear cell renal cell carcinoma (ccRCC), 43 with papillary RCC (pRCC), 12 with chromophobe RCC (chRCC) and 32 with oncocytomas. Kiss-10 was detected in all patients and controls. SRT patients revealed significantly higher Kiss-10 levels than controls (mean value 10.04 vs. 6.37 pmol/l, p < 0.001). In SRT patients, Kiss-10 was detected at significantly different concentrations between the subgroups (p = 0.021). The highest concentration was observed in those with oncocytomas (11.50 pmol/) followed by chRCC, pRCC and ccRCC patients (9.89, 10.01 and 9.25 pmol/l, respectively). Receiver operating characteristic curve analyses revealed an area under the curve (AUC) of 0.82 for the comparison of all tumours vs. controls (p < 0.001) and an AUC of 0.671 for all malignant tumours vs. oncoytomas (p = 0.003). This study shows that Kiss-10 levels are significantly altered by malignancy and tumour subtypes even in patients with SRTs. Kiss-10 therefore deserves further attention as a plasmatic biomarker for renal tumours.

Study Information

Provider

pubmed

Year

2017

Date

2017-01-18T00:00:00.000Z

DOI

10.1159/000452108

Citations

5

References

30