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In Vitro Ubiquitination and Deubiquitination Assays of Nucleosomal Histones
Published on: July 25, 2019
Purine-rich element binding protein alpha: a DNA/RNA binding protein with multiple roles in cancers
Shiyi Yu1,2, Chengyang Jiang1,2, Yawen Yang1,2
1Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou, Jiangsu, China.
Abstract:
Proteins that bind to DNA/RNA are typically evolutionarily conserved with multiple regulatory functions in transcription initiation, mRNA translation, stability of RNAs, and RNA splicing. Therefore, dysregulation of DNA/RNA binding proteins such as purine-rich element binding protein alpha (PURα) disrupts signaling transduction and often leads to human diseases including cancer. PURα was initially recognized as a tumor suppressor in acute myeloid leukemia (AML) and prostate cancer (PC). Most recently, several studies have revealed that PURα is dysregulated in multiple cancers, such as breast cancer (BC) and esophageal squamous cell carcinoma (ESCC). The oncogenic or tumor-suppressive functions of PURα are realized via regulating RNA/protein interaction, mRNA translation, formation of stress granules (SGs), and transcriptional regulation of several oncogenes and tumor suppressors. Although DNA/RNA binding proteins are hardly targeted, novel strategies have been applied to identify compounds targeting PURα and have demonstrated promising anti-tumor efficacy in the preclinical study. The present review summarizes the most recently discovered critical roles of PURα in various cancer types, providing an overview of the biomarker and therapeutic target potential of PURα for patients with cancer.
Insights
Purine-rich element binding protein alpha (PURα) plays a dual role in cancer, acting as a tumor suppressor or oncogene. Targeting PURα shows promise for novel cancer therapies.
Area of Science:
- Molecular Biology
- Cancer Research
- Biochemistry
Background:
- DNA/RNA binding proteins are crucial for gene regulation and are often conserved.
- Dysregulation of these proteins, like purine-rich element binding protein alpha (PURα), contributes to human diseases, particularly cancer.
- PURα has been identified as both a tumor suppressor in acute myeloid leukemia and prostate cancer, and dysregulated in breast and esophageal cancers.
Purpose of the Study:
- To review the multifaceted roles of PURα in various cancer types.
- To explore the potential of PURα as a biomarker and therapeutic target in oncology.
- To summarize recent findings on PURα's involvement in cancer progression and treatment.
Main Methods:
- Literature review of recent studies on PURα in cancer.
- Analysis of PURα's regulatory functions in transcription, translation, RNA stability, and splicing.
- Examination of PURα's role in stress granule formation and RNA/protein interactions.
Main Results:
- PURα exhibits context-dependent oncogenic or tumor-suppressive functions across different cancers.
- PURα influences cancer through regulating mRNA translation, stress granule dynamics, and oncogene/tumor suppressor transcription.
- Novel strategies targeting PURα have shown preclinical anti-tumor efficacy.
Conclusions:
- PURα is a critical regulator in multiple cancer types with significant implications for disease progression.
- PURα represents a promising biomarker and therapeutic target for cancer treatment.
- Further research into PURα-targeting agents could lead to effective anti-cancer therapies.
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