Reciprocal interplays between MicroRNAs and pluripotency transcription factors in dictating stemness features in human cancers

被引:13
作者
Vishnubalaji, Radhakrishnan [1 ]
Shaath, Hibah [1 ]
Al-Alwan, Monther [2 ,3 ]
Abdelalim, Essam M. [4 ,5 ]
Alajez, Nehad M. [1 ,5 ,6 ]
机构
[1] Hamad Bin Khalifa Univ HBKU, Qatar Fdn QF, Qatar Biomed Res Inst QBRI, Translat Canc & Immun Ctr TCIC, POB 34110, Doha, Qatar
[2] King Faisal Specialist Hosp & Res Ctr, Stem Cell & Tissue Reengn Program, Riyadh 11211, Saudi Arabia
[3] Al Faisal Univ, Coll Med, Riyadh 11533, Saudi Arabia
[4] Hamad Bin Khalifa Univ HBKU, Qatar Fdn, Qatar Biomed Res Inst QBRI, Diabet Res Ctr DRC, POB 34110, Doha, Qatar
[5] Hamad Bin Khalifa Univ HBKU, Qatar Fdn QF, Coll Hlth & Life Sci, POB 34110, Doha, Qatar
[6] Hamad Bin Khalifa Univ HBKU, Qatar Fdn, Qatar Biomed Res Inst QBRI, Translat Canc & Immun Ctr TCIC, Doha, Qatar
关键词
Transcription factors; MYC; OCT4; NANOG; SOX2; KLF4; CSCs; MiRNA; MiRNA-TF networks; Cancer; TUMOR-INITIATING CELLS; TARGETING C-MYC; COLORECTAL-CANCER; SELF-RENEWAL; MESENCHYMAL TRANSITION; PANCREATIC-CANCER; MIR-200; FAMILY; PROSPECTIVE IDENTIFICATION; HEPATOCELLULAR-CARCINOMA; MULTIDRUG-RESISTANCE;
D O I
10.1016/j.semcancer.2022.10.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The interplay between microRNAs (miRNAs) and pluripotency transcription factors (TFs) orchestrates the acquisition of cancer stem cell (CSC) features during the course of malignant transformation, rendering them essential cancer cell dependencies and therapeutic vulnerabilities. In this review, we discuss emerging themes in tumor heterogeneity, including the clonal evolution and the CSC models and their implications in resistance to cancer therapies, and then provide thorough coverage on the roles played by key TFs in maintaining normal and malignant stem cell pluripotency and plasticity. In addition, we discuss the reciprocal interactions between miRNAs and MYC, OCT4, NANOG, SOX2, and KLF4 pluripotency TFs and their contributions to tumorigenesis. We provide our view on the potential to interfere with key miRNA-TF networks through the use of RNA-based therapeutics as single agents or in combination with other therapeutic strategies, to abrogate the CSC state and render tumor cells more responsive to standard and targeted therapies.
引用
收藏
页码:1 / 16
页数:16
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