An Update on the Potential Roles of E2F Family Members in Colorectal Cancer.
ZhaoHui XuHui QuYanYing RenZeZhong GongHyok Ju RiXin ChenPublished in: Cancer management and research (2021)
Colorectal cancer (CRC) is a major health burden worldwide, and thus, optimised diagnosis and treatments are imperative. E2F transcription factors (E2Fs) are a family of transcription factors consisting of eight genes, contributing to the oncogenesis and development of CRC. Importantly, E2Fs control not only the cell cycle but also apoptosis, senescence, DNA damage response, and drug resistance by interacting with multiple signaling pathways. However, the specific functions and intricate machinery of these eight E2Fs in human CRC remain unclear in many respects. Evidence on E2Fs and CRC has been scattered on the related regulatory genes, microRNAs (miRNAs), and competing endogenous RNAs (ceRNAs). Accordingly, some drugs targeting E2Fs have been transferred from preclinical to clinical application. Herein, we have systemically reviewed the current literature on the roles of various E2Fs in CRC with the purpose of providing possible clinical implications for patient diagnosis and prognosis and future treatment strategy design, thereby furthering the understanding of the E2Fs.
Keyphrases
- cell cycle
- transcription factor
- dna damage response
- endothelial cells
- genome wide
- public health
- genome wide identification
- cell proliferation
- oxidative stress
- healthcare
- mental health
- gene expression
- dna methylation
- case report
- endoplasmic reticulum stress
- cancer therapy
- epithelial mesenchymal transition
- mesenchymal stem cells
- risk factors
- cell therapy
- protein kinase
- genome wide analysis
- induced pluripotent stem cells
- cell cycle arrest