摘要
The phosphoinositide 3-kinase (PI3K) pathway, one of the most commonly activated signaling pathways in human cancers, plays a crucial role in the regulation of cell proliferation, differentiation, and survival. This pathway is usually activated by receptor tyrosine kinases (RTKs), whose constitutive and aberrant activation is via gain-of-function mutations, chromosomal rearrangement, gene amplification and autocrine. Blockage of PI3K pathway by targeted therapy on RTKs with tyrosine kinases inhibitors (TKIs) and monoclonal antibodies (mAbs) has achieved great progress in past decades; however, there still remain big challenges during their clinical application. In this review, we provide an overview about the most frequently encountered alterations in RTKs and focus on current therapeutic agents developed to counteract their aberrant functions, accompanied with discussions of two major challenges to the RTKs-targeted therapy in cancer – resistance and toxicity.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 3-22 |
| 页数 | 20 |
| 期刊 | Seminars in Cancer Biology |
| 卷 | 59 |
| DOI | |
| 出版状态 | 已出版 - 12月 2019 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 3 良好健康与福祉
学术指纹
探究 'Receptor tyrosine kinases in PI3K signaling: The therapeutic targets in cancer' 的科研主题。它们共同构成独一无二的指纹。引用此
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