Roles of Wnt Target Genes in the Journey of Cancer Stem Cells

被引:64
|
作者
Kim, Jee-Heun [1 ]
Park, So-Yeon [1 ,2 ]
Jun, Youngsoo [1 ,2 ,3 ]
Kim, Ji-Young [4 ]
Nam, Jeong-Seok [1 ,2 ,3 ]
机构
[1] Gwangju Inst Sci & Technol, Sch Life Sci, Gwangju 61005, South Korea
[2] Gwangju Inst Sci & Technol, Cell Logist Res Ctr, Gwangju 61005, South Korea
[3] Gwangju Inst Sci & Technol, Silver Hlth Bio Res Ctr, Gwangju 61005, South Korea
[4] Gwangju Inst Sci & Technol, Lab Anim Resource Ctr, Gwnagju 61005, South Korea
基金
新加坡国家研究基金会;
关键词
cancer stem cell; Wnt signaling; initiation; persistence; invasion; migration; metastasis; EPITHELIAL-MESENCHYMAL-TRANSITION; CIRCULATING TUMOR-CELLS; WNT/BETA-CATENIN PATHWAY; HUMAN COLORECTAL CANCERS; BETA-CATENIN; BREAST-CANCER; COLON-CANCER; C-MYC; UP-REGULATION; MATRIX METALLOPROTEINASES;
D O I
10.3390/ijms18081604
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
The importance of Wnt/-catenin signaling in cancer stem cells (CSCs) has been acknowledged; however, the mechanism through which it regulates the biological function of CSCs and promotes cancer progression remains elusive. Hence, to understand the intricate mechanism by which Wnt controls stemness, the specific downstream target genes of Wnt were established by analyzing the genetic signatures of multiple types of metastatic cancers based on gene set enrichment. By focusing on the molecular function of Wnt target genes, the biological roles of Wnt were interpreted in terms of CSC dynamics from initiation to metastasis. Wnt signaling participates in cancer initiation by generating CSCs from normal stem cells or non-CSCs and augmenting persistent growth at the primary region, which is resistant to anti-cancer therapy. Moreover, it assists CSCs in invading nearby tissues and in entering the blood stream, during which the negative feedback of the Wnt signaling pathway maintains CSCs in a dormant state that is suitable for survival. When CSCs arrive at distant organs, another burst of Wnt signaling induces CSCs to succeed in re-initiation and colonization. This comprehensive understanding of Wnt target genes provides a plausible explanation for how Wnt allows CSCs variation during cancer progression.
引用
收藏
页数:21
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