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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2015 pubmed 19 citations

Honokiol suppresses metastasis of renal cell carcinoma by targeting KISS1/KISS1R signaling.

Cheng. Shujie S; Castillo. Victor V; Eliaz. Isaac I; Sliva. Daniel D

Key Findings

  • Honokiol reduced invasion and colony formation of highly metastatic RCC cells in a dose‑dependent manner.
  • Treatment with honokiol markedly increased the expression of the metastasis‑suppressor gene KISS1 and its receptor KISS1R at both mRNA and protein levels.
  • Silencing KISS1 reversed the anti‑invasive effects of honokiol, confirming that KISS1/KISS1R activation mediates the benefit.

Practical Outcomes

  • Honokiol shows promise as a natural agent that may help prevent kidney cancer spread by activating KISS1/KISS1R, but the research is limited to cell cultures. No human dosing, safety, or efficacy data are available yet, so biohackers should treat this as early‑stage evidence and not a ready‑to‑use protocol.

Summary

A study found that honokiol, a compound from magnolia bark, can block the spread of kidney cancer cells in the lab by turning on the KISS1/KISS1R pathway, which normally suppresses metastasis. When the researchers blocked KISS1, the anti‑cancer effect of honokiol went away, showing the pathway is key.

Abstract

Renal cell carcinoma (RCC) is a common urological cancer worldwide and is known to have a high risk of metastasis, which is considered responsible for more than 90% of cancer associated deaths. Honokiol is a small-molecule biphenol isolated from Magnolia spp. bark and has been shown to be a potential anticancer agent involved in multiple facets of signal transduction. In this study, we demonstrated that honokiol inhibited the invasion and colony formation of highly metastatic RCC cell line 786-0 in a dose-dependent manner. DNA-microarray data showed the significant upregulation of metastasis-suppressor gene KISS1 and its receptor, KISS1R. The upregulation was confirmed by qRT-PCR analysis. Overexpression of KISS1 and KISS1R was detected by western blotting at the translation level as well. Of note, the decreased invasive and colonized capacities were reversed by KISS1 knockdown. Taken together, the results first indicate that activation of KISS1/KISS1R signaling by honokiol suppresses multistep process of metastasis, including invasion and colony formation, in RCC cells 786-0. Honokiol may be considered as a natural agent against RCC metastasis.

Study Information

Provider

pubmed

Year

2015

Date

2015-04-02T00:00:00.000Z

DOI

10.3892/ijo.2015.2950

Citations

19

References

53