Abstract 4257: F5446 epigenetically reprograms T cells to boost CEA CAR T cell immunotherapy efficacy in human colorectal cancer metastasis

Abstract Chimeric Antigen Receptor (CAR) T cell therapy emerges as a promising cell-based immunotherapy for human cancer; however, it has shown little efficacy in solid tumors. Recent studies have shown that SUV39H1 decreases CAR T cell persistence and knocking out SUV39H1 increased CAR T efficacy in tumor-bearing mice. Analysis of human colon cancer liver metastases scRNA-seq datasets revealed that histone methyltransferases of H3K9me3 are upregulated in colon tumor and expressed in subsets of T cells in liver metastases of human colon cancer patients. To overcome human colon cancer resistance to CAR T cell immunotherapy, we have developed a SUV39H1-specific small molecule inhibitor F5446. Previously, we found that H3K9me3 promotes differentiation of Tex cells and targeting H3K9me3 is an effective approach to increase IFNγhi Tex-int cells to reinvigorate CTL functionality to suppress colon cancer liver metastasis. Based on this data, we hypothesize that F5446 is effective in increasing persistence of CAR T cells to suppress metastatic human colon cancer growth in NSG mice. A phase I clinical trial for α-CEA CAR T cell immunotherapy found it is well tolerated in patients with colorectal cancer with modest efficacy. Based on this, we generated second and third generation α-CEA CAR T plasmids for lentivirus transduction of primary T cells. We utilize an experimental liver metastasis model to induce liver metastasis of human colorectal cancer in a humanized mouse model. Mice are then treated with one dose of α-CEA CAR T cells and treated every three days with F5446 until endpoint. Extracted tumors are digested and the CAR T cell phenotypes (memory, effector, naïve, or exhausted) are determined via flow cytometry. We anticipate that F5446 will increase the persistence of CAR T cells in the liver metastases compared to CAR T therapy alone. F5446 is a promising conjunctive treatment with CAR T cell therapy to increase efficacy in solid tumor colon cancer. Citation Format: Kendra Fick, Patrick Czabala, Zainab Tiamiyu, Dafeng Yang, Kebin Liu, . F5446 epigenetically reprograms T cells to boost CEA CAR T cell immunotherapy efficacy in human colorectal cancer metastasis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4257.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-4257
Primary Topic
CAR-T cell therapy research
Type
article
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article

Abstract 4257: F5446 epigenetically reprograms T cells to boost CEA CAR T cell immunotherapy efficacy in human colorectal cancer metastasis

Zainab Tiamiyu, Patrick Czabala, K. R. Fick, Kebin Liu et al.
Cancer Research
CAR-T cell therapy research
article

Abstract 4257: F5446 epigenetically reprograms T cells to boost CEA CAR T cell immunotherapy efficacy in human colorectal cancer metastasis

Zainab Tiamiyu, Patrick Czabala, K. R. Fick, Kebin Liu, Dafeng Yang
article en

Abstract

Abstract Chimeric Antigen Receptor (CAR) T cell therapy emerges as a promising cell-based immunotherapy for human cancer; however, it has shown little efficacy in solid tumors. Recent studies have shown that SUV39H1 decreases CAR T cell persistence and knocking out SUV39H1 increased CAR T efficacy in tumor-bearing mice. Analysis of human colon cancer liver metastases scRNA-seq datasets revealed that histone methyltransferases of H3K9me3 are upregulated in colon tumor and expressed in subsets of T cells in liver metastases of human colon cancer patients. To overcome human colon cancer resistance to CAR T cell immunotherapy, we have developed a SUV39H1-specific small molecule inhibitor F5446. Previously, we found that H3K9me3 promotes differentiation of Tex cells and targeting H3K9me3 is an effective approach to increase IFNγhi Tex-int cells to reinvigorate CTL functionality to suppress colon cancer liver metastasis. Based on this data, we hypothesize that F5446 is effective in increasing persistence of CAR T cells to suppress metastatic human colon cancer growth in NSG mice. A phase I clinical trial for α-CEA CAR T cell immunotherapy found it is well tolerated in patients with colorectal cancer with modest efficacy. Based on this, we generated second and third generation α-CEA CAR T plasmids for lentivirus transduction of primary T cells. We utilize an experimental liver metastasis model to induce liver metastasis of human colorectal cancer in a humanized mouse model. Mice are then treated with one dose of α-CEA CAR T cells and treated every three days with F5446 until endpoint. Extracted tumors are digested and the CAR T cell phenotypes (memory, effector, naïve, or exhausted) are determined via flow cytometry. We anticipate that F5446 will increase the persistence of CAR T cells in the liver metastases compared to CAR T therapy alone. F5446 is a promising conjunctive treatment with CAR T cell therapy to increase efficacy in solid tumor colon cancer. Citation Format: Kendra Fick, Patrick Czabala, Zainab Tiamiyu, Dafeng Yang, Kebin Liu, . F5446 epigenetically reprograms T cells to boost CEA CAR T cell immunotherapy efficacy in human colorectal cancer metastasis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4257.

Cancer ResearchVol. 86(7_Supplement)
Augusta University Health (US)
Good health and well-being
Openalex Percentile: Top 10%
CAR-T cell therapy research
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