Transcriptional factors targeting in cancer stem cells for tumor modulation

被引:32
作者
Chaudhary, Archana [1 ]
Raza, Syed Shadab [2 ]
Haque, Rizwanul [1 ]
机构
[1] Cent Univ South Bihar, Sch Earth Biol & Environm Sci, Dept Biotechnol, Gaya, Bihar, India
[2] Era Univ, Eras Lucknow Med Coll & Hosp, Lab Stem Cell & Restorat Neurol, Lucknow, India
关键词
Cancer Stem Cells (CSC); Transcription factors (TFs); Octamer-binding transcription factor 4 (OCT-4); Sex determining region Y-box 2 (SOX-2); GENE-EXPRESSION SIGNATURE; LYMPH-NODE METASTASIS; CARBON ION-BEAM; BREAST-CANCER; POOR-PROGNOSIS; DRUG-RESISTANCE; SELF-RENEWAL; NESTIN EXPRESSION; C-MYC; NANOG;
D O I
10.1016/j.semcancer.2022.12.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer Stem Cells (CSCs) are now considered the primary "seeds" for the onset, development, metastasis, and recurrence of tumors. Despite therapeutic breakthroughs, cancer remains the leading cause of death worldwide. This is because the tumor microenvironment contains a key population of cells known as CSCs, which promote tumor aggression. CSCs are self-renewing cells that aid tumor recurrence by promoting tumor growth and persisting in patients after many traditional cancer treatments. According to reports, numerous transcription factors (TF) play a key role in maintaining CSC pluripotency and its self-renewal property. The understanding of the functions, structures, and interactional dynamics of these transcription factors with DNA has modified the hypothesis, paving the way for novel transcription factor-targeted therapies. These TFs, which are crucial and are required by cancer cells, play a vital function in the etiology of human cancer. Such CSC TFs will help with gene expression profiling, which provides crucial data for predicting the prognosis of patients. To overcome anticancer medication resistance and completely eradicate cancer, a potent therapy combining TFs-based CSC targets with traditional chemotherapy may be developed. In order to develop therapies that could eliminate CSCs, we here concentrated on the effect of TFs and other components of signalling pathways on cancer stemness.
引用
收藏
页码:123 / 137
页数:15
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