Ras and Wnt Interaction Contribute in Prostate Cancer Bone Metastasis.
Chia-Hsiang ChangNtlotlang MokgautsiYen-Nien LiuPublished in: Molecules (Basel, Switzerland) (2020)
Prostate cancer (PCa) is one of the most prevalent and malignant cancer types in men, which causes more than three-hundred thousand cancer death each year. At late stage of PCa progression, bone marrow is the most often metastatic site that constitutes almost 70% of metastatic cases of the PCa population. However, the characteristic for the osteo-philic property of PCa is still puzzling. Recent studies reported that the Wnt and Ras signaling pathways are pivotal in bone metastasis and that take parts in different cytological changes, but their crosstalk is not well studied. In this review, we focused on interactions between the Wnt and Ras signaling pathways during each stage of bone metastasis and present the fate of those interactions. This review contributes insights that can guide other researchers by unveiling more details with regard to bone metastasis and might also help in finding potential therapeutic regimens for preventing PCa bone metastasis.
Keyphrases
- prostate cancer
- bone mineral density
- bone marrow
- stem cells
- signaling pathway
- soft tissue
- bone loss
- cell proliferation
- bone regeneration
- squamous cell carcinoma
- small cell lung cancer
- papillary thyroid
- radical prostatectomy
- postmenopausal women
- pi k akt
- epithelial mesenchymal transition
- squamous cell
- wild type
- induced apoptosis
- ultrasound guided