Targeting Wnt Signaling in Endometrial Cancer.
Iram FatimaSusmita BarmanRajani RaiKristina W W ThielVishal ChandraPublished in: Cancers (2021)
This review presents new findings on Wnt signaling in endometrial carcinoma and implications for possible future treatments. The Wnt proteins are essential mediators in cell signaling during vertebrate embryo development. Recent biochemical and genetic studies have provided significant insight into Wnt signaling, in particular in cell cycle regulation, inflammation, and cancer. The role of Wnt signaling is well established in gastrointestinal and breast cancers, but its function in gynecologic cancers, especially in endometrial cancers, has not been well elucidated. Development of a subset of endometrial carcinomas has been attributed to activation of the APC/β-catenin signaling pathway (due to β-catenin mutations) and downregulation of Wnt antagonists by epigenetic silencing. The Wnt pathway also appears to be linked to estrogen and progesterone, and new findings implicate it in mTOR and Hedgehog signaling. Therapeutic interference of Wnt signaling remains a significant challenge. Herein, we discuss the Wnt-activating mechanisms in endometrial cancer and review the current advances and challenges in drug discovery.
Keyphrases
- endometrial cancer
- cell proliferation
- cell cycle
- drug discovery
- stem cells
- oxidative stress
- signaling pathway
- gene expression
- dna methylation
- squamous cell carcinoma
- estrogen receptor
- pregnant women
- single cell
- childhood cancer
- papillary thyroid
- epithelial mesenchymal transition
- current status
- cancer therapy
- copy number
- squamous cell
- bone marrow