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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2018 pubmed

The role of kisspeptin on aromatase expression in breast cancer.

Yilmaz. M B MB; Oksuz. H H; Ilgaz. N S NS; Ocal. I I; Tazehkand. M Norizadeh MN

Key Findings

  • Kisspeptin raised aromatase (CYP19A1) mRNA levels in MCF7 breast cancer cells.
  • The increase was prevented by a kisspeptin receptor (GPR54) inhibitor, indicating receptor‑mediated action.
  • In SKBR3 breast cancer cells, kisspeptin did not increase aromatase despite raising GPR54 expression.

Practical Outcomes

  • For biohackers considering kisspeptin for hormone or performance tweaks, this study warns that kisspeptin might elevate estrogen production via aromatase in some cell types, potentially worsening estrogen‑sensitive conditions like certain breast cancers. Until human data are available, using kisspeptin for hormonal modulation should be approached with caution, especially for women with a history or risk of breast cancer.

Summary

In lab studies of breast cancer cells, the hormone kisspeptin caused an increase in the gene that makes the estrogen‑producing enzyme aromatase, but only in one type of cancer cell (MCF7). This effect was blocked when the kisspeptin receptor was inhibited, and it did not happen in another breast cancer cell line (SKBR3). The findings suggest kisspeptin could boost estrogen production in certain cancer cells, which might make tumors more aggressive.

Abstract

Kisspeptin is a reproductive peptide hormone that has anti-metastatic roles in several cancer types including colon, lung, and brain cancer. However, in breast cancer, increasing of kisspeptin expression induces aggressiveness of tumors, which in turn exacerbates breast cancer prognosis. Breast cancer cell lines MCF7 and SKBR3 were cultured in MEM (phenol red free) containing 10 % fetal bovine. Treatments were performed, at 70 % confluency, after 24-hour serum deprivation in serum free medium for 6, 24 and 48 hours. Aromatase (CYP19A1) and kisspeptin receptor (GPR54) mRNA expression were determined by real time Taqman Assay. Kisspeptin induced aromatase (CYP19A1) and kisspeptin receptor (GPR54) mRNA expression, while this induction was abolished by kisspeptin receptor inhibitor in MCF7 cells. In SKBR3 cells, however, even though there was an increase in GPR54 mRNA expression with kisspeptin, the induction of CYP19A1 was not observed. The inducing effect of kisspeptin on aromatase expression is possibly mediated via kisspeptin receptor and estrogen receptor dependent mechanisms (Fig. 5, Ref. 27).

Study Information

Provider

pubmed

Year

2018

DOI

10.4149/bll_2018_141