KISS1 in metastatic cancer research and treatment: potential and paradoxes
- PMID: 32152912
- PMCID: PMC7483209
- DOI: 10.1007/s10555-020-09868-9
KISS1 in metastatic cancer research and treatment: potential and paradoxes
Abstract
The significance of KISS1 goes beyond its original discovery as a metastasis suppressor. Its function as a neuropeptide involved in diverse physiologic processes is more well studied. Enthusiasm regarding KISS1 has cumulated in clinical trials in multiple fields related to reproduction and metabolism. But its cancer therapeutic space is unsettled. This review focuses on collating data from cancer and non-cancer fields in order to understand shared and disparate signaling that might inform clinical development in the cancer therapeutic and biomarker space. Research has focused on amino acid residues 68-121 (kisspeptin 54), binding to the KISS1 receptor and cellular responses. Evidence and counterevidence regarding this canonical pathway require closer look at the covariates so that the incredible potential of KISS1 can be realized.
Keywords: Dormancy; G protein-coupled receptor; KISS1; KISS1R; Metastasis; Metastasis suppressor.
Conflict of interest statement
References
-
- Lee J-H, Doumen DJ, & Welch DR (1996). Cloning of a novel gene, KiSS-1, which is responsible for metastasis suppression in chromosome 6/human melanoma hybrid cells. PNAS, 37, 531.
-
- Ohtaki T, Shintani Y, Honda S, Matsumoto H, Hori A, Kanehashi K, et al. (2001). Metastasis suppressor gene KiSS1 encodes peptide ligand of a G-protein-coupled receptor. Nature, 411(6837), 613–617. - PubMed
-
- Kotani M, Detheux M, Vandenbogaerde A, Communi D, Vanderwinden JM, Le Poul E, et al. (2001). The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54. J Biol Chem, 276(37), 34631–34636. - PubMed
-
- Muir AI, Chamberlain L, Elshourbagy NA, Michalovich D, Moore DJ, Calamari A, et al. (2001). AXOR12, a novel human G protein-coupled receptor, activated by the peptide KiSS-1. J Biol Chem, 276(31), 28969–28975. - PubMed
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