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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2015 pubmed

[Suppression of Kiss-1 gene inhibits HCT116 human colorectal carcinoma cell migration in vitro via nuclear factor-κB signaling pathway].

Chen. Shaoqin S; Su. Xiaobao X; Gao. Ji J; Han. Hongjing H; Chen. Zhihua Z; Lin. Suyong S

Key Findings

  • Kiss-1 over‑expression raised I‑κB levels, which blocks NF‑κB signaling
  • MMP‑9, a protein that helps cancer cells invade, dropped when Kiss-1 was increased
  • Cell growth, invasion, and migration were all significantly reduced in the lab model

Practical Outcomes

  • The study shows kisspeptin can slow cancer cell behavior in a petri dish, but it offers no direct guidance for human use, dosing, or safety. Biohackers should view this as early‑stage evidence of a possible anti‑cancer pathway, not a ready‑to‑apply supplement or protocol.

Summary

Scientists put extra copies of the kisspeptin gene (Kiss-1) into colon cancer cells in a dish and found the cells grew and spread less, likely because the gene turned down a pathway (NF‑κB) that helps tumors move.

Abstract

To investigate the effect of Kiss-1 gene suppression on the metastatic capacity of HCT116 human colorectal carcinoma cells in vitro and the involvement of nuclear factor-κB (NF-κB) signaling pathway. A recombinant lentiviral vector of Kiss-1 gene pGC-LV-Kiss-1-EGFP or the empty vector was transfected in HCT116 cells. Cell Counting Kit-8 (CCK8) and Transwell chamber assay were used to detect the changes in cell proliferation, invasion and migration ability after the transfection. Western blotting was used to detect the expression of I-κB, the inhibitive protein of NF-κB signal pathway, and the expression of the downstream effector MMP-9 before and after transfection. In cells over-expressing Kiss-1, I-κB expression increased and MMP-9 expression decreased significantly compared to those in the blank control and vector-transfected cells (P<0.05). Kiss-1 gene over-expression resulted in significant inhibition of HCT116 cell proliferation, invasion, and migration as compared to the control cells (P<0.05). Lentivirus-mediated Kiss-1 gene over-expression can inhibit the proliferation, invasion, and migration of HCT116 cells via the NF-B signaling pathway.

Study Information

Provider

pubmed

Year

2015