Emerging roles for HMGA2 in colorectal cancer.
Emerging roles for HMGA2 in colorectal cancer.
复制标题
HMGA2 在结直肠癌中的新作用
DOI:
10.1016/j.tranon.2020.100894
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发表时间:
2021-01
影响因子:
5
通讯作者:
Wu J
中科院分区:
文献类型:
--
作者:
Wang X;Wang J;Wu J
HMGA2 (High Mobility Group AT-hook 2) has been reported to promote colorectal cancer (CRC) development by regulating the transcription of target genes. It participates in nearly all aspects of cellular processes, including cell transformation, proliferation, apoptosis, senescence, metastasis, epithelial-to-mesenchymal transition (EMT), DNA repair and stem cell self-renewal. In the past decades, a group of downstream targets and binding partners have been identified in a wide range of cancers. Our findings of HMGA2 as a key factor in the MDM2/p53, IL11/STAT3 and Wnt/β-catenin signaling pathways prompt us to summarize current advances in the functional and molecular basis of HMGA2 in CRC. In this review, we address the roles of HMGA2 in the oncogenic networks of CRC based on recent advances. We review its aberrant expression, explore underlying mechanisms, discuss its pro-tumorigenic effects, and highlight promising small-molecule inhibitors based on targeting HMGA2 here. However, the understanding of HMGA2 in CRC progression is still elusive, thus we also discuss the future perspectives in this review. Collectively, this review provides novel insights into the oncogenic properties of HMGA2, which has potential implications in the diagnosis and treatment of CRC. HMGA2 promotes colorectal cancer (CRC) development by regulating the transcriptions of target genes. Circulating cell-free HMGA2 mRNA has been identified as a potential screening marker in CRC. HMGA2 appears to be a key factor in the networks of MDM2/p53, IL11/STAT3 and Wnt/β-catenin signaling pathways in CRC. Many agents and siRNAs serve as potential therapeutic approaches by targeting HMGA2 for the treatment of CRC. Deciphering HMGA2-mediated machinery helps to conceive effective therapy strategies and develop novel inhibitors in CRC.
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DOI:
10.1038/nrc.2017.99
发表时间:
2018-01
期刊:
Nature reviews. Cancer
影响因子:
--
作者:
Anastasiadou E;Jacob LS;Slack FJ
通讯作者:
Slack FJ
影响因子:
11.2
作者:
Frankenberger C;Rabe D;Bainer R;Sankarasharma D;Chada K;Krausz T;Gilad Y;Becker L;Rosner MR
通讯作者:
Rosner MR
影响因子:
12.4
作者:
Chang HY;Ye SP;Pan SL;Kuo TT;Liu BC;Chen YL;Huang TC
通讯作者:
Huang TC
影响因子:
4.6
作者:
Chang KP;Lin SJ;Liu SC;Yi JS;Chien KY;Chi LM;Kao HK;Liang Y;Lin YT;Chang YS;Yu JS
通讯作者:
Yu JS
影响因子:
11.2
作者:
Gao D;Vahdat LT;Wong S;Chang JC;Mittal V
通讯作者:
Mittal V