Cheng Linna, Huang Shenzhen, Chen Lijuan, Dong Xiaoyan, Zhang Lei, Wu Chengye, Ye Kaihong, Shao Fengmin, Zhu Zunmin, Thorne Rick F
Institute of Hematology, Henan Key Laboratory of Stem Cell Differentiation and Modification, Henan Provincial People\'s Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan, 450003, China.
Henan Eye Institute, Henan Eye Hospital and Henan Key Laboratory of Ophthalmology and Visual Science, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Henan University People's Hospital, Zhengzhou, Henan, 450003, China.
Curr Med Chem. 2022;29(13):2261-2273. doi: 10.2174/0929867328666210709110721.
Doublecortin-like kinase 1 (DCLK1) has emerged over the last decade as a unique stem cell marker within gastrointestinal tissues. Evidence from mouse models shows that high Dclk1 expression denotes a population of cells that promote tissue regeneration and serve as potential cancer stem cells. Moreover, since certain DCLK1 isoforms are overexpressed in many cancers and not normal cells, targeting the expression or kinase activity of DCLK1 has the potential to inhibit cancer cell growth. Here, we review the evidence for DCLK1 as a prospective cancer target including its isoform-specific expression and mutational status in human cancers. We further discuss the challenges and current progress in the development of small molecule inhibitors of DCLK1.
在过去十年中,双皮质素样激酶1(DCLK1)已成为胃肠道组织中一种独特的干细胞标志物。来自小鼠模型的证据表明,Dclk1高表达表示一群促进组织再生并充当潜在癌症干细胞的细胞。此外,由于某些DCLK1异构体在许多癌症中而非正常细胞中过表达,靶向DCLK1的表达或激酶活性有可能抑制癌细胞生长。在此,我们综述了DCLK1作为潜在癌症靶点的证据,包括其在人类癌症中的异构体特异性表达和突变状态。我们还进一步讨论了DCLK1小分子抑制剂开发中的挑战和当前进展。