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Engineering Artificial Factors to Specifically Manipulate Alternative Splicing in Human Cells
Published on: April 26, 2017
Therapeutic Targeting of Alternative RNA Splicing in Gastrointestinal Malignancies and Other Cancers
Ilyas Sahin1, Andrew George2,3, Attila A Seyhan4,5,6,7
1Division of Hematology Oncology, Department of Medicine, University of Florida Health Cancer Center, Gainesville, FL 32610, USA.
Abstract:
Recent comprehensive genomic studies including single-cell RNA sequencing and characterization have revealed multiple processes by which protein-coding and noncoding RNA processing are dysregulated in many cancers. More specifically, the abnormal regulation of mRNA and precursor mRNA (pre-mRNA) processing, which includes the removal of introns by splicing, is frequently altered in tumors, producing multiple different isoforms and diversifying protein expression. These alterations in RNA processing result in numerous cancer-specific mRNAs and pathogenically spliced events that generate altered levels of normal proteins or proteins with new functions, leading to the activation of oncogenes or the inactivation of tumor suppressor genes. Abnormally spliced pre-mRNAs are also associated with resistance to cancer treatment, and certain cancers are highly sensitive to the pharmacological inhibition of splicing. The discovery of these alterations in RNA processing has not only provided new insights into cancer pathogenesis but identified novel therapeutic vulnerabilities and therapeutic opportunities in targeting these aberrations in various ways (e.g., small molecules, splice-switching oligonucleotides (SSOs), and protein therapies) to modulate alternative RNA splicing or other RNA processing and modification mechanisms. Some of these strategies are currently progressing toward clinical development or are already in clinical trials. Additionally, tumor-specific neoantigens produced from these pathogenically spliced events and other abnormal RNA processes provide a potentially extensive source of tumor-specific therapeutic antigens (TAs) for targeted cancer immunotherapy. Moreover, a better understanding of the molecular mechanisms associated with aberrant RNA processes and the biological impact they play might provide insights into cancer initiation, progression, and metastasis. Our goal is to highlight key alternative RNA splicing and processing mechanisms and their roles in cancer pathophysiology as well as emerging therapeutic alternative splicing targets in cancer, particularly in gastrointestinal (GI) malignancies.
Insights
Cancer cells frequently alter RNA processing, leading to abnormal protein production and therapeutic resistance. Targeting these splicing defects offers new cancer treatment strategies and immunotherapy opportunities, especially in gastrointestinal cancers.
Area of Science:
- Oncology
- Molecular Biology
- Genomics
Background:
- Comprehensive genomic studies reveal widespread dysregulation of RNA processing in cancers.
- Abnormal messenger RNA (mRNA) and precursor mRNA (pre-mRNA) processing, including splicing, is common in tumors.
- Altered RNA processing generates cancer-specific transcripts, diversifies protein expression, and impacts oncogene/tumor suppressor gene activity.
Purpose of the Study:
- To review key alternative RNA splicing and processing mechanisms in cancer pathophysiology.
- To highlight emerging therapeutic targets for modulating RNA splicing in cancer.
- To focus on gastrointestinal (GI) malignancies as a specific area of interest.
Main Methods:
- Analysis of recent comprehensive genomic studies, including single-cell RNA sequencing.
- Review of literature on RNA processing alterations in cancer.
- Identification of therapeutic strategies targeting RNA splicing.
Main Results:
- Aberrant splicing produces altered proteins, contributing to oncogenesis and tumor suppressor inactivation.
- Abnormally spliced pre-mRNAs are linked to cancer treatment resistance.
- Targeting RNA processing aberrations presents novel therapeutic vulnerabilities and opportunities.
Conclusions:
- Dysregulated RNA processing is a hallmark of cancer, impacting pathogenesis and treatment response.
- Therapeutic strategies targeting RNA splicing, such as small molecules and splice-switching oligonucleotides (SSOs), are advancing to clinical trials.
- Tumor-specific splice variants can serve as neoantigens for targeted cancer immunotherapy.
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