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Role of Hippo pathway dysregulation from gastrointestinal premalignant lesions to cancer. | LitMetric

AI Article Synopsis

  • - The Hippo pathway, first found in fruit flies, is crucial for regulating tissue health and organ growth, with YAP and TAZ being key players in controlling cell behavior.
  • - Dysregulation of Hippo signaling is common in gastrointestinal cancers, and abnormal activation of YAP/TAZ is linked to chronic inflammation that may lead to cancer development.
  • - More research is needed to understand how disruptions in Hippo signaling contribute to cancer initiation, which could help in creating new early treatment options targeting this pathway.

Article Abstract

Background: First identified in Drosophila melanogaster, the Hippo pathway is considered a major regulatory cascade controlling tissue homeostasis and organ development. Hippo signaling components include kinases whose activity regulates YAP and TAZ final effectors. In response to upstream stimuli, YAP and TAZ control transcriptional programs involved in cell proliferation, cytoskeletal reorganization and stemness.

Main Text: While fine tuning of Hippo cascade components is essential for maintaining the balance between proliferative and non-proliferative signals, pathway signaling is frequently dysregulated in gastrointestinal cancers. Also, YAP/TAZ aberrant activation has been described in conditions characterized by chronic inflammation that precede cancer development, suggesting a role of Hippo effectors in triggering carcinogenesis. In this review, we summarize the architecture of the Hippo pathway and discuss the involvement of signaling cascade unbalances in premalignant lesions of the gastrointestinal tract, providing a focus on the underlying molecular mechanisms.

Conclusions: The biology of premalignant Hippo signaling dysregulation needs further investigation in order to elucidate the evolutionary trajectories triggering cancer inititation and develop effective early therapeutic strategies targeting the Hippo/YAP pathway.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10903154PMC
http://dx.doi.org/10.1186/s12967-024-05027-8DOI Listing

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