Related Experiment Video
Updated: Apr 2, 2026

Genome-Wide CRISPR Screen for Unveiling Radiosensitive and Radioresistant Genes
Published on: May 23, 2025
In vivo CRISPR screens identify CBX4 as an epigenetic regulator for cancer immunotherapy
Zhibo Ma1,2, Wenlong Jia3, Xi Zhou1,2
1Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Abstract:
Epigenetic dysregulation is associated with immune evasion and immune checkpoint blockade (ICB) resistance. Here, using in vivo CRISPR/Cas9 screens targeting epigenetics-related factors in mouse tumor models treated with ICB, we identified chromobox 4 (CBX4) as a key negative regulator of the immune tumor microenvironment (TME). Single-cell RNA-seq and spatial transcriptomics analyses of patients receiving neoadjuvant anti-programmed cell death protein 1 (anti-PD-1) therapy revealed high CBX4 expression in both tumor cells and immunosuppressive tumor-associated macrophage subpopulations, with preferential accumulation in nonresponders. Deficiency of CBX4 in macrophages or tumor cells induced robust antitumor immunity and increased infiltration and the cytotoxic activity of CD8+ T cells and NK cells, thereby heightening the sensitivity of ICB treatment. Mechanistically, CBX4 targeted H3K9me3- and H3K27me3-marked endogenous retroelements such as RLTR4-Mm-int. Loss of CBX4 derepressed retrotransposons, activating cytosolic RNA-sensing pathways and triggering the type I IFN response, ultimately leading to a robustly inflamed TME. Moreover, we uncovered a negative correlation between CBX4 expression, immune responses, and retrotransposon levels, and were able to determine the prognosis of patients with hepatocellular carcinoma (HCC) undergoing ICB therapy. Our study establishes CBX4 as an epigenetic immune checkpoint through the epigenetic silencing of retrotransposons, remodeling the immune TME and thus providing a promising therapeutic target to enhance tumor immunogenicity and overcome immunotherapy resistance.
Insights
Chromobox 4 (CBX4) silences retrotransposons, hindering anti-tumor immunity and causing resistance to immune checkpoint blockade (ICB) therapy. Targeting CBX4 can enhance immune responses and overcome resistance in cancer treatment.
Area of Science:
- Immunology
- Epigenetics
- Oncology
Background:
- Epigenetic alterations contribute to immune evasion and resistance to immune checkpoint blockade (ICB).
- Understanding the epigenetic regulators of the tumor immune microenvironment is crucial for improving cancer immunotherapy.
Purpose of the Study:
- To identify epigenetic factors regulating the tumor immune microenvironment and ICB response.
- To investigate the role of Chromobox 4 (CBX4) in immune evasion and ICB resistance.
Main Methods:
- In vivo CRISPR-Cas9 screens in mouse tumor models treated with ICB.
- Single-cell RNA sequencing and spatial transcriptomics in patients receiving neoadjuvant anti-PD-1 therapy.
- Analysis of epigenetic modifications (H3K9me3, H3K27me3) and retrotransposon activity.
Main Results:
- CBX4 was identified as a key negative regulator of the anti-tumor immune response.
- High CBX4 expression in tumor cells and macrophages correlated with ICB resistance and poor prognosis in hepatocellular carcinoma (HCC) patients.
- CBX4 deficiency enhanced CD8+ T cell and NK cell infiltration and activity, increasing ICB sensitivity.
- CBX4 epigenetically silences endogenous retroelements, and its loss activates type I interferon responses.
Conclusions:
- CBX4 acts as an epigenetic immune checkpoint by silencing retrotransposons and suppressing anti-tumor immunity.
- Targeting CBX4 presents a promising therapeutic strategy to enhance immunogenicity and overcome ICB resistance.
Related Concept Videos
Epigenetic Regulation
X-chromosome...
Epigenetic Regulation
Genetic Screens
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
CRISPR
CRISPR

