4.6 Review

Transcription Factors in Cancer Development and Therapy

Journal

CANCERS
Volume 12, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/cancers12082296

Keywords

cancer; transcription factors; oncogenes; therapeutic-resistance

Categories

Funding

  1. National Institutes of Health National Cancer Institute [CA178063, CA219764, CA176846, CA216410]
  2. Veterans Affairs Merit Award [BX003296, BX002703]
  3. Veterans Affairs Career Scientist Award [BX004855]
  4. University of Illinois Cancer Center Pilot Grant Award

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Cancer is a multi-step process and requires constitutive expression/activation of transcription factors (TFs) for growth and survival. Many of the TFs reported so far are critical for carcinogenesis. These include pro-inflammatory TFs, hypoxia-inducible factors (HIFs), cell proliferation and epithelial-mesenchymal transition (EMT)-controlling TFs, pluripotency TFs upregulated in cancer stem-like cells, and the nuclear receptors (NRs). Some of those, including HIFs, Myc, ETS-1, and beta-catenin, are multifunctional and may regulate multiple other TFs involved in various pro-oncogenic events, including proliferation, survival, metabolism, invasion, and metastasis. High expression of some TFs is also correlated with poor prognosis and chemoresistance, constituting a significant challenge in cancer treatment. Considering the pivotal role of TFs in cancer, there is an urgent need to develop strategies targeting them. Targeting TFs, in combination with other chemotherapeutics, could emerge as a better strategy to target cancer. So far, targeting NRs have shown promising results in improving survival. In this review, we provide a comprehensive overview of the TFs that play a central role in cancer progression, which could be potential therapeutic candidates for developing specific inhibitors. Here, we also discuss the efforts made to target some of those TFs, including NRs.

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