医学
吉非替尼
酪氨酸激酶抑制剂
酪氨酸激酶
癌症
靶向治疗
表皮生长因子受体
癌症研究
抗药性
埃罗替尼
表皮生长因子受体抑制剂
肺癌
药理学
恶性肿瘤
肿瘤科
内科学
受体
生物
微生物学
作者
Qingqing Pan,Yao Lu,Xie Li,Di Wu,Rong Liu,Wenxia Gao,Kui Luo,Bin He,Yuji Pu
标识
DOI:10.1021/acs.molpharmaceut.2c00792
摘要
Epidermal growth factor receptor (EGFR) plays a key role in signal transduction pathways associated with cell proliferation, growth, and survival. Its overexpression and aberrant activation in malignancy correlate with poor prognosis and short survival. Targeting inhibition of EGFR by small-molecular tyrosine kinase inhibitors (TKIs) is emerging as an important treatment model besides of chemotherapy, greatly reshaping the landscape of cancer therapy. However, they are still challenged by the off-targeted toxicity, relatively limited cancer types, and drug resistance after long-term therapy. In this review, we summarize the recent progress of oral, pulmonary, and injectable drug delivery systems for enhanced and targeting TKI delivery to tumors and reduced side effects. Importantly, EGFR-TKI-based combination therapies not only greatly broaden the applicable cancer types of EGFR-TKI but also significantly improve the anticancer effect. The mechanisms of TKI resistance are summarized, and current strategies to overcome TKI resistance as well as the application of TKI in reversing chemotherapy resistance are discussed. Finally, we provide a perspective on the future research of EGFR-TKI-based cancer therapy.
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