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A narrative review of the roles of muscle segment homeobox transcription factor family in cancer.

作者信息

Liu Chao, Huang Mengxi, Han Chao, Li Huiyu, Wang Jing, Huang Yadi, Chen Yanyan, Zhu Jialong, Fu Gongbo, Yu Hanqing, Lei Zengjie, Chu Xiaoyuan

机构信息

Department of Medical Oncology, Jinling Hospital, Nanjing Medical University, Nanjing, China.

Department of Medical Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing University, Nanjing, China.

出版信息

Ann Transl Med. 2021 May;9(9):810. doi: 10.21037/atm-21-220.


DOI:10.21037/atm-21-220
PMID:34268423
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8246185/
Abstract

Deregulation of many homeobox genes has been observed in various cancers and has caused functional implications in the tumor progression. In this review, we will focus on the roles of the human muscle segment homeobox (MSX) transcription factor family in the process of tumorigenesis. The MSX transcription factors, through complex downstream regulation mechanisms, are promoters or inhibitors of diverse cancers by participating in cell proliferation, cell invasion, cell metastasis, cell apoptosis, cell differentiation, drug resistance of tumors, maintenance of tumor stemness, and tumor angiogenesis. Moreover, their upstream regulatory mechanisms in cancers may include: gene mutation and chromosome aberration; DNA methylation and chromatin modification; regulation by non-coding RNAs; regulation by other transcription factors and post-translational modification. These mechanisms may provide a better understanding of why MSX transcription factors are abnormally expressed in tumors. Notably, intermolecular interactions and post-translational modification can regulate the transcriptional activity of MSX transcription factors. It is also crucial to know what affects the transcriptional activity of MSX transcription factors in tumors for possible interventions in them in the future. This systematic summary of the regulatory patterns of the MSX transcription factor family may help to further understand the mechanisms involved in transcriptional regulation and also provide new therapeutic approaches for tumor progression.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/8246185/2ad6313eef16/atm-09-09-810-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/8246185/316ec1d4ced4/atm-09-09-810-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/8246185/2ad6313eef16/atm-09-09-810-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/8246185/316ec1d4ced4/atm-09-09-810-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/8246185/2ad6313eef16/atm-09-09-810-f2.jpg

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本文引用的文献

[1]
Identification and Validation of MSX1 as a Key Candidate for Progestin Resistance in Endometrial Cancer.

Onco Targets Ther. 2020-11-13

[2]
Homeoprotein Msx1-PIASy Interaction Inhibits Angiogenesis.

Cells. 2020-8-7

[3]
MSX1-A Potential Marker for Uterus-Preserving Therapy of Endometrial Carcinomas.

Int J Mol Sci. 2020-6-25

[4]
Overexpression of kinesin superfamily members as prognostic biomarkers of breast cancer.

Cancer Cell Int. 2020-4-15

[5]
The Role of CHK1 Varies with the Status of Oestrogen-receptor and Progesterone-receptor in the Targeted Therapy for Breast Cancer.

Int J Biol Sci. 2020

[6]
QMEANDisCo-distance constraints applied on model quality estimation.

Bioinformatics. 2020-4-15

[7]
The FBXW2-MSX2-SOX2 axis regulates stem cell property and drug resistance of cancer cells.

Proc Natl Acad Sci U S A. 2019-9-23

[8]
MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.

BMC Med Genomics. 2019-7-1

[9]
Analysis of circulating blood and tissue biopsy PDX1 and MSX2 gene expression in patients with pancreatic cancer: A case-control experimental study.

Medicine (Baltimore). 2019-6

[10]
microRNA-203 promotes proliferation, differentiation, and migration of osteoblasts by upregulation of Msh homeobox 2.

J Cell Physiol. 2019-3-10

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