The Hippo pathway as a drug target in gastric cancer

The Hippo tumor suppressor pathway is critical for balancing cellular differentiation and proliferation in response to cell-cell contact, mechanical signals and diffusible signals such as lysophosphatidic acid. Hippo pathway signaling is frequently dysregulated in gastric cancer (GC), as well as man...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer letters 2018-04, Vol.420, p.14-25
Hauptverfasser: Qiao, Yiting, Li, Tongyu, Zheng, Shusen, Wang, Hangxiang
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The Hippo tumor suppressor pathway is critical for balancing cellular differentiation and proliferation in response to cell-cell contact, mechanical signals and diffusible signals such as lysophosphatidic acid. Hippo pathway signaling is frequently dysregulated in gastric cancer (GC), as well as many other kinds of solid tumors, contributing to multiple aspects of malignant progression including unchecked cell division and metastasis. Considering the importance of this Hippo pathway in cancer, its pharmacological disruption may be of huge benefit in the fight against this disease. In this review, we summarize the components of the Hippo pathway, its crosstalk with other major oncogenic signaling pathways, common mechanisms of its dysregulation, as well as potential therapeutic approaches of targeting this pathway for cancer treatment, specifically in a GC context. •This review highlighted the clinical significance of Hippo pathway in gastric cancer from the aspects of functions and mechanisms of dysregulation.•This review summarized the interplay between Hippo pathway and H. pylori infection, one of the strongest risk factors for gastric cancer.•This review conducted a comprehensive discussion regarding advances for targeting Hippo pathway for the treatment of cancer, including gastric cancer.
ISSN:0304-3835
1872-7980
DOI:10.1016/j.canlet.2018.01.062