High-Temperature Requirement A1 (Htra1) - A Novel Regulator of Canonical Wnt Signaling.

Sci Rep

Department of Clinical Microbiology and Immunology, Sackler School of Medicine, Tel Aviv University, Tel Aviv, 69978, Israel.

Published: December 2017

AI Article Synopsis

  • The canonical Wnt signaling pathway is linked to various diseases, particularly colorectal cancer (CRC), and is primarily driven by the protein β-catenin, which activates Wnt target genes.
  • High-Temperature Requirement A1 (HTRA1) is identified as a new component of the Wnt pathway that inhibits Wnt/β-catenin signaling and influences the expression of Wnt target genes.
  • HTRA1 interacts with β-catenin and decreases cell proliferation, suggesting it plays a role as a suppressor of the canonical Wnt signaling pathway.

Article Abstract

Different cancer types as well as many other diseases are caused by aberrant activation of the canonical Wnt signal transduction pathway, and it is especially implicated in the development and progression of colorectal cancer (CRC). The main effector protein of the canonical Wnt signaling cascade is β-catenin, which binds to the T- cell factor/lymphoid enhancer factor (TCF/LEF) and triggers the activation of Wnt target genes. Here, we identify the serine protease High-Temperature Requirement A1 (HTRA1) as a novel component of the canonical Wnt pathway. We show that the HTRA1 protein inhibits the Wnt/β-catenin signaling, in both paracrine and autocrine manners, and affects the expression of several Wnt target genes. Moreover, HTRA1 forms a complex with β-catenin and reduces the proliferation rates of cells. Taken together, our findings indicate that HTRA1 functions as a novel suppressor of the canonical Wnt signaling pathway.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740065PMC
http://dx.doi.org/10.1038/s41598-017-18203-2DOI Listing

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