Abizadeh Ethan, Berglas Eli, Abizadeh Aaron, Glatman Julia, Lavi Aaron B, Spivak Mark, Sapir Tzuriel, Shifteh David
College of Medicine, SUNY Downstate Health Sciences University, Brooklyn, NY 11203, USA.
Zucker School of Medicine, Hofstra University, Hempstead, NY 11549, USA.
Int J Mol Sci. 2025 Sep 6;26(17):8696. doi: 10.3390/ijms26178696.
The ERK1/2 and PI3K signaling pathways play important roles in cellular proliferation, survival, differentiation, and metabolism. In cancer, these pathways are frequently dysregulated and overactivated, resulting in poor patient prognosis and resistance to treatment. These pathways are activated by receptor tyrosine kinases and send downstream signals to effectors such as RAS, RAF, MEK, AKT, and mTOR. In this review, we highlight the key components of the ERK1/2 and PI3K pathways, the roles they play in tumor progression, and the development of inhibitors and combination therapies designed to enhance therapeutic outcomes and address treatment resistance. Our review demonstrates the need and promise for future research and clinical trials for inhibitors and combination therapies for the ERK1/2 and PI3K pathways in cancer.
ERK1/2和PI3K信号通路在细胞增殖、存活、分化和代谢中发挥重要作用。在癌症中,这些信号通路常常失调并过度激活,导致患者预后不良和治疗耐药。这些信号通路由受体酪氨酸激酶激活,并向下游效应器如RAS、RAF、MEK、AKT和mTOR发送信号。在本综述中,我们重点介绍了ERK1/2和PI3K信号通路的关键组成部分、它们在肿瘤进展中所起的作用,以及旨在提高治疗效果和解决治疗耐药性的抑制剂和联合疗法的开发。我们的综述表明,未来针对癌症中ERK1/2和PI3K信号通路的抑制剂和联合疗法的研究及临床试验具有必要性和前景。