Genome-wide gain-of-function screening characterized lncRNA regulators for tumor immune response.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36475797.
- Also identified by DOI 10.1126/sciadv.add0005 and PMC identifier 9728976.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The majority of lncRNAs' roles in tumor immunology remain elusive. This project performed a CRISPR activation screening of 9744 lncRNAs in melanoma cells cocultured with human CD8<sup>+</sup> T cells. We identified 16 lncRNAs potentially regulating tumor immune response. Further integrative analysis using tumor immunogenomics data revealed that <i>IL10RB-DT</i> and <i>LINC01198</i> are significantly correlated with tumor immune response and survival in melanoma and breast cancer. Specifically, <i>IL10RB-DT</i> suppresses CD8<sup>+</sup> T cells activation via inhibiting IFN-γ-JAK-STAT1 signaling and antigen presentation in melanoma and breast cancer cells. On the other hand, <i>LINC01198</i>'s up-regulation sensitizes the killing of tumor cells by CD8<sup>+</sup> T cells. Mechanistically, <i>LINC01198</i> interacts and activates NF-κB component p65 to trigger the type I and type II interferon responses in melanoma and breast cancer cells. Our study systematically characterized novel lncRNAs involved in tumor immune response.
Medical subject headings
- RNA, Long Noncoding
- Melanoma
- Breast Neoplasms