New Computational Tools Identify Alternative Splicing Changes in Aggressive Cancers

Researchers at UCLA and CHOP find a strong cancer driver gene is linked to gene changes that regulate the splicing process
Dana Bate
Friday, February 21, 2020
Dr. Owen Witte
Dr. Owen Witte

A multi-institutional group of researchers at UCLA and Children’s Hospital of Philadelphia (CHOP) has linked a strong cancer driver gene to changes in proteins that regulate alternative splicing. The researchers created new computational tools and biological model systems for the study. This collaborative research, led by Owen Witte, M.D., founding director of the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research at UCLA, and Yi Xing, Ph.D., at CHOP, was published today in the Proceedings of the National Academy of Sciences.

“Our study provides insight into the relationship between an important cancer driver gene and alternative splicing changes that could be used to guide the development of splicing-targeted cancer therapy,” said Xing, director of the Center for Computational and Genomic Medicine at CHOP and co-senior author of the study.

The collaborative effort involved researchers at CHOP, UCLA, and the Roswell Park Comprehensive Cancer Center. John Phillips, M.D., Ph.D., a researcher at UCLA, and Yang Pan, M.S., a visiting scholar at CHOP and graduate student at UCLA, were first authors of the study.

Alternative splicing is an essential process that allows for one gene to code for many gene products, based on where the RNA is cut, or spliced, before being translated into proteins. Cancer cells often take advantage of this process to produce proteins that promote growth and survival, allowing them to replicate uncontrollably and metastasize. This happens in many cancers, including prostate cancer, which is associated with shifts in splicing patterns. Yet scientists do not fully understand the process that leads to this change.

To better understand the causes and consequences of alternative splicing changes during cancer progression, the team looked at RNA sequences from nearly 900 prostate tissue samples, ranging from healthy prostate tissue to localized or aggressive metastatic tumor tissue. In order to efficiently analyze such large datasets, the team created a new computational program called rMATS-turbo. Using this program, the researchers identified more than 13,000 alternative splicing events that varied across these 900 prostate samples.

Next, the team developed an analytic tool, dubbed PEGASAS (Pathway Enrichment-Guided Activity Study of Alternative Splicing), to find potential cancer driver genes and pathways that correlated with these alternative splicing changes. They found that Myc, a gene involved in normal cell functions and is amplified in many cancers, was linked to alternative splicing changes in genes that themselves regulate alternative splicing. Using human prostate cells that were engineered to turn on or off Myc activity, researchers further confirmed that these alternative splicing changes were indeed driven by Myc.

"Advances in immunotherapy for solid tumors are critically dependent on finding the right targets,” said Witte, professor of microbiology, immunology and molecular genetics and member of the UCLA Jonsson Comprehensive Cancer Center. “A detailed analysis of prostate cancer transcriptomics that includes exon discovery could provide the right specificity for new therapeutics."

Researchers then applied the same PEGASAS strategy to breast cancer and lung cancer datasets and found the same association between Myc activity and alternative splicing, suggesting Myc activation – and thus disruptions in splicing – occurs in many cancers.

“The successful application of PEGASAS to prostate, breast, and lung cancer datasets suggests that this strategy could be useful in analyzing pathway-driven alternative splicing in many cancer types,” said Xing. “Given the involvement of oncogenic pathways such as the Myc pathway in pediatric cancers, these tools could reveal pathways and targets for treating pediatric cancers as well.”

The study was supported in part by the Immuno-Oncology Translational Network of the National Cancer Institute’s Cancer Moonshot Initiative, other National Cancer Institute funding, along with funding from the Parker Institute for Cancer Immunotherapy, the UCLA Tumor Cell Biology Training Grant, and the Prostate Cancer Research Program under the Office of the Assistant Secretary of Defense for Health Affairs.

Media Contact: 

Dana Bate
Children’s Hospital of Philadelphia
Phone: (267) 426-6055
bated@email.chop.edu
 

Mirabai Vogt-James
UCLA Broad Stem Cell Research Center
Phone: (310) 983-1163
mvogt@mednet.ucla.edu