Insight into the role of p62 in the cisplatin resistant mechanisms of ovarian cancer.
Xiao-Yu YanXian-Zhi QuLong XuSi-Hang YuRui TianXin-Ru ZhongLian-Kun SunJing SuPublished in: Cancer cell international (2020)
Cisplatin is a platinum-based first-line drug for treating ovarian cancer. However, chemotherapy tolerance has limited the efficacy of cisplatin for ovarian cancer patients. Research has demonstrated that cisplatin causes changes in cell survival and death signaling pathways through its interaction with macromolecules and organelles, which indicates that investigation into the DNA off-target effects of cisplatin may provide critical insights into the mechanisms underlying drug resistance. The multifunctional protein p62 works as a signaling hub in the regulation of pro-survival transcriptional factors NF-κB and Nrf2 and connects autophagy and apoptotic signals, which play important roles in maintaining cell homeostasis. In this review, we discuss the role of p62 in cisplatin resistance by exploring p62-associated signaling pathways based on current studies and our work. Insights into these resistance mechanisms may lead to more effective therapeutic strategies for ovarian cancer by targeting p62.
Keyphrases
- signaling pathway
- oxidative stress
- cell death
- pi k akt
- drug delivery
- gene expression
- stem cells
- single cell
- emergency department
- cancer therapy
- squamous cell carcinoma
- cell proliferation
- epithelial mesenchymal transition
- transcription factor
- small molecule
- anti inflammatory
- immune response
- radiation therapy
- endoplasmic reticulum stress
- induced apoptosis
- cell free
- inflammatory response
- locally advanced
- binding protein
- mesenchymal stem cells
- heat shock
- lps induced
- network analysis