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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2012 pubmed 24 citations

Kisspeptin-54 levels are increased in patients with colorectal cancer.

Canbay. Emel E; Ergen. Arzu A; Bugra. Dursun D; Yamaner. Sumer S; Eraltan. Ilhan Yaylim IY; Buyukuncu. Yilmaz Y; Bulut. Turker T

Key Findings

  • Plasma kisspeptin-54 levels are significantly higher in colorectal cancer patients than in healthy controls
  • A cutoff of 46 ng/ml distinguishes patients with reasonable sensitivity (63%) and specificity (81.4%)
  • Higher kisspeptin-54 levels correlate with lymph node involvement and predict metastasis

Practical Outcomes

  • For most biohackers, this research doesn’t offer a direct action plan or supplement to improve health. It mainly suggests kisspeptin-54 could become a future blood test for early cancer detection, but there’s no current way to modify its levels for longevity or performance benefits.

Summary

The study found that people with colorectal cancer have higher levels of a protein called kisspeptin-54 in their blood compared to healthy people, and that higher levels are linked to cancer spreading to lymph nodes. However, this is just a diagnostic marker, not something you can take or change with lifestyle or supplements.

Abstract

Recent studies have demonstrated that Kisspeptin, the product of the metastasis suppressor gene KiSS-1, could have a role in tumor progression and invasion. In this pilot study, we investigated the association of plasma Kisspeptin-54 level with colorectal cancer (CRC). Plasma Kisspeptin-54 levels were quantified using enzyme-immunoassay (EIA) kits from blood samples of 81 patients with CRC at their initial staging and 59 age-matched healthy controls. Plasma Kisspeptin-54 levels were significantly higher in CRC patients (86.2 ± 20.5) than in controls (49 ± 12.7; p < 0.005). The cutoff value for Kisspeptin-54 detection was determined as 46 ng/ml, and area under curve (AUC) value was 0.766 with sensitivity 63 %, specificity 81.4 %, positive predictive value 82.2 %, negative predictive value 61.5 %, positive likelihood ratio 3.38, and negative likelihood ratio 0.46. Increased plasma Kisspeptin-54 levels were significantly correlated with nodal involvement of CRC (Spearman, rs = 0.345, p = 0.002). Kisspeptin-54 was also found to be an independent predictive marker for lymph node metastases of CRC (p = 0; Exp(B): 2.053; 95 % CI, 1.255-2.851). Our results reveal that plasma Kisspeptin-54 measurement could be a useful diagnostic and prognostic parameter for CRC. Further prospective evaluation is needed to validate these findings and to establish the clinical usefulness of Kisspeptin-54 for CRC diagnostics.

Study Information

Provider

pubmed

Year

2012

Date

2012-05-03T00:00:00.000Z

DOI

10.1007/s00268-012-1636-7

Citations

24

References

20