| Literature DB >> 31128213 |
Zhe Cao1, Qianjin Liao1, Min Su1, Kai Huang2, Junfei Jin2, Deliang Cao3.
Abstract
Phosphatidylinositol 3-kinase (PI3K)/AKT pathway regulates cell growth, proliferation, survival, mobility and invasion. Mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) pathway is also an important mitogenic signaling pathway involved in various cellular progresses. AKT, also named protein kinase B (PKB), is a primary mediator of the PI3K signaling pathway; and ERK at the end of MAPK signaling is the unique substrate and downstream effector of mitogen-activated protein/extracellular signal-regulated kinase (MEK). The AKT and ERK signaling are both aberrantly activated in a wide range of human cancers and have long been targeted for cancer therapy, but the clinical benefits of these targeted therapies have been limited due to complex cross-talk. Novel strategies, such as AKT/ERK dual inhibitors, may be needed.Entities:
Keywords: MAPK/ERK pathway; ONC201; PI3K/AKT pathway; Protein kinase inhibitors; Targeted cancer therapy
Mesh:
Substances:
Year: 2019 PMID: 31128213 DOI: 10.1016/j.canlet.2019.05.025
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679