Key actors in cancer therapy: epigenetic modifiers.
Remzi Okan AkarSelin SelviEngin UlukayaNazlıhan AztopalPublished in: Turkish journal of biology = Turk biyoloji dergisi (2019)
Epigenetic reprogramming plays a crucial role in the tumorigenicity and maintenance of tumor-specific gene expression that especially occurs through DNA methylation and/or histone modifications. It has well-defined mechanisms. It is known that alterations in the DNA methylation pattern and/or the loss of specific histone acetylation/methylation markers are related to several hallmarks of cancer, such as drug resistance, stemness, epithelial-mesenchymal transition, and metastasis. It has also recently been highlighted that epigenetic alterations are critical for the regulation of the stemlike properties of cancer cells (tumor-initiating cells; cancer stem cells). Cancer stem cells are thought to be responsible for the recurrence of cancer which makes the patient return to the clinic with metastatic tumor tissue. Hence, the dysregulation of epigenetic machinery represents potential new therapeutic targets. Therefore, compounds with epigenetic activities have become crucial for developing new therapy regimens (e.g., antimetastatic agents) in the fight against cancer. Here, we review the epigenetic modifiers that have already been used in the clinic and/or in clinical trials, related preclinical studies in cancer therapy, and the smart combination strategies that target cancer stem cells along with the other cancer cells. The emerging role of epitranscriptome (RNA epigenetic) in cancer therapy has also been included in this review as a new avenue and potential target for the better management of cancer-beneficial epigenetic machinery.
Keyphrases
- dna methylation
- gene expression
- cancer stem cells
- cancer therapy
- genome wide
- papillary thyroid
- epithelial mesenchymal transition
- clinical trial
- squamous cell
- drug delivery
- small cell lung cancer
- copy number
- stem cells
- squamous cell carcinoma
- childhood cancer
- induced apoptosis
- lymph node metastasis
- mesenchymal stem cells
- cell proliferation
- young adults
- cell death
- climate change
- risk assessment
- study protocol
- cell cycle arrest
- nucleic acid