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ADAMTS-8 and kallikrein-related peptidases 10 and 5 proteases also have a tumor suppression role
Eva G Palacios Serrato1, Karen H Medina-Abreu1, Enrique Oropeza-Martínez1
1Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, Mexico City 03100, Mexico.
Abstract:
Proteases are essential for homeostasis, and their primary function is proteolytic in extracellular and intracellular compartments. The deregulation of expression, abundance, and activity of proteases has been related to several pathologies, including cancer. This deregulation contributes to their pro-tumorigenic activity since they participate in the degradation of extracellular matrix components and adhesion molecules, and the activation of growth factors. However, some proteases, such as ADAM metallopeptidase with thrombospondin type 1 motif 8 and kallikrein-related peptidases 5 and 10, have emerged as tumor suppressors due to their antitumoral actions in specific cancer contexts. In this article, we discuss the antitumoral effects of ADAM metallopeptidase with thrombospondin type 1 motif 8, kallikrein-related peptidases 5 and 10 that have been described to date, suggesting their potential use as novel biomarkers and therapeutic targets in cancer.
Insights
Certain proteases, like ADAM metallopeptidase with thrombospondin type 1 motif 8 and kallikrein-related peptidases 5 and 10, act as tumor suppressors. Their antitumoral effects suggest potential as cancer biomarkers and therapeutic targets.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Proteases are crucial for cellular homeostasis, regulating extracellular and intracellular processes.
- Deregulation of protease activity is linked to various pathologies, notably cancer, where they can promote tumor growth.
- Some proteases, including ADAM metallopeptidase with thrombospondin type 1 motif 8 (ADAMTS8) and kallikrein-related peptidases (KLKs) 5 and 10, exhibit tumor-suppressive roles.
Purpose of the Study:
- To review the known antitumoral effects of ADAMTS8, KLK5, and KLK10.
- To explore the potential of these proteases as cancer biomarkers.
- To discuss their therapeutic potential in oncology.
Main Methods:
- Literature review of studies investigating ADAMTS8, KLK5, and KLK10 in cancer.
- Analysis of reported antitumoral mechanisms and contexts.
- Synthesis of findings regarding biomarker and therapeutic applications.
Main Results:
- ADAMTS8, KLK5, and KLK10 demonstrate tumor-suppressive activities in specific cancer types.
- These proteases influence extracellular matrix degradation, cell adhesion, and growth factor signaling.
- Evidence suggests their potential utility in cancer diagnostics and treatment strategies.
Conclusions:
- ADAMTS8, KLK5, and KLK10 represent a class of proteases with significant antitumoral functions.
- Their roles highlight the complex involvement of proteases in cancer, with both pro- and anti-tumorigenic potential.
- These findings support further investigation into ADAMTS8, KLK5, and KLK10 as novel cancer biomarkers and therapeutic targets.
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