Small-molecule drugs of colorectal cancer: Current status and future directions

被引:7
作者
Yang, Yiren [1 ]
Liu, Pengyu [1 ]
Zhou, Mingyang [2 ]
Yin, Linzhou [1 ]
Wang, Miao [1 ]
Liu, Ting [1 ]
Jiang, Xiaowen [1 ]
Gao, Huiyuan [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[2] Univ Penn, Philadelphia, PA 19104 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2024年 / 1870卷 / 01期
关键词
Colorectal cancer; Consensus molecular subtypes; Signaling pathways; Small -molecule drug; Drug combination; TYROSINE KINASE INHIBITOR; NF-KAPPA-B; COLON-CANCER; BIOLOGICAL EVALUATION; NETWORK PHARMACOLOGY; SIGNALING PATHWAYS; MAPK PATHWAY; MITOMYCIN-C; STEM-CELLS; DNA-REPAIR;
D O I
10.1016/j.bbadis.2023.166880
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer (CRC) is the third most commonly diagnosed cancer and the world's fourth most deadly cancer. CRC, as a genetic susceptible disease, faces significant challenges in optimizing prognosis through optimal drug treatment modalities. In recent decades, the development of innovative small-molecule drugs is expected to provide targeted interventions that accurately address the different molecular characteristics of CRC. Although the clinical application of single-target drugs is limited by the heterogeneity and high metastasis of CRC, novel small-molecule drug treatment strategies such as dual/multiple-target drugs, drug repurposing, and combination therapies can help overcome these challenges and provide new insights for improving CRC treatment. In this review, we focus on the current status of a range of small molecule drugs that are being considered for CRC therapy, including single-target drugs, dual/multiple-target drugs, drug repurposing and combination strategies, which will pave the way for targeting CRC vulnerabilities with small-molecule drugs in future personalized treatment.
引用
收藏
页数:26
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