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.

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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