Castel Pau, Toska Eneda, Engelman Jeffrey A, Scaltriti Maurizio
Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA.
Department of Oncology, Sidney Kimmel Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Nat Cancer. 2021 Jun;2(6):587-597. doi: 10.1038/s43018-021-00218-4. Epub 2021 Jun 17.
Phosphoinositide-3- kinase (PI3K) signaling regulates cellular proliferation, survival and metabolism, and its aberrant activation is one of the most frequent oncogenic events across human cancers. In the last few decades, research focused on the development of PI3K inhibitors, from preclinical tool compounds to the highly specific medicines approved to treat patients with cancer. Herein we discuss current paradigms for PI3K inhibitors in cancer therapy, focusing on clinical data and mechanisms of action. We also discuss current limitations in the use of PI3K inhibitors including toxicities and mechanisms of resistance, with specific emphasis on approaches aimed to improve their efficacy.
磷酸肌醇-3-激酶(PI3K)信号传导调节细胞增殖、存活和代谢,其异常激活是人类癌症中最常见的致癌事件之一。在过去几十年中,研究重点是PI3K抑制剂的开发,从临床前工具化合物到已获批用于治疗癌症患者的高度特异性药物。在此,我们讨论PI3K抑制剂在癌症治疗中的当前范式,重点关注临床数据和作用机制。我们还讨论了PI3K抑制剂使用中的当前局限性,包括毒性和耐药机制,并特别强调旨在提高其疗效的方法。