4.6 Article

Transcriptional factors targeting in cancer stem cells for tumor modulation

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SEMINARS IN CANCER BIOLOGY
卷 88, 期 -, 页码 123-137

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ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2022.12.010

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Cancer Stem Cells (CSC); Transcription factors (TFs); Octamer-binding transcription factor 4 (OCT-4); Sex determining region Y-box 2 (SOX-2)

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Cancer Stem Cells (CSCs) are crucial in the onset, development, metastasis, and recurrence of tumors. Understanding the functions of transcription factors (TFs) and their interaction with DNA has paved the way for novel therapies targeting CSCs. These TFs play a vital role in the etiology of human cancer and can provide important data for predicting patient prognosis. Combining TFs-based CSC targets with traditional chemotherapy may lead to a potent therapy for overcoming cancer resistance.
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.

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