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KISS1 in metastatic cancer research and treatment: potential and paradoxes
Thuc Ly1, Sitaram Harihar2, Danny R Welch3,4
1Department of Cancer Biology, Kansas University Medical Center, 3901 Rainbow Blvd. - MS1071, Kansas City, KS, 66160, USA.
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.
Insights
The KISS1 gene, initially known for suppressing metastasis, has broader roles as a neuropeptide in various bodily functions. Further research into its signaling pathways could unlock its potential in cancer therapy and diagnostics.
Area of Science:
- Oncology
- Endocrinology
- Molecular Biology
Background:
- The KISS1 gene was initially identified for its role in suppressing cancer metastasis.
- Its function as a neuropeptide influencing numerous physiological processes is increasingly recognized.
- Clinical trials are exploring KISS1 in reproductive and metabolic conditions, but its oncologic applications remain under investigation.
Purpose of the Study:
- To review and synthesize data from both cancer and non-cancer research on KISS1 signaling.
- To identify shared and distinct signaling pathways relevant to clinical development in oncology.
- To inform the therapeutic and biomarker potential of KISS1 in cancer treatment.
Main Methods:
- Literature review collating data from diverse scientific fields.
- Analysis of signaling pathways involving KISS1 and its receptor.
- Examination of evidence for and against the canonical KISS1 pathway.
Main Results:
- KISS1 exhibits complex signaling with implications beyond metastasis suppression.
- Shared and disparate signaling mechanisms exist between cancer and non-cancer contexts.
- The canonical KISS1 pathway, involving kisspeptin 54 and its receptor, requires further scrutiny.
Conclusions:
- Understanding the multifaceted roles of KISS1 is crucial for realizing its therapeutic potential.
- Further investigation into KISS1 signaling covariates is needed for clinical applications.
- KISS1 holds promise as a target for cancer therapeutics and biomarkers.
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