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April 5, 2026Cancer Research0 citations

Abstract 1522: FMNL1 overexpression enhances tumor-specific TIL and CAR-T cell accumulation and therapeutic efficacy in solid tumors

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JCJeffrey W. ChungJOJessica Olivas-CorralAWAshley Wood

Key Points

  • The study aims to determine if overexpressing FMNL1 can enhance T cell accumulation and efficacy against solid tumors.
  • Engineered tumor-specific TILs and CAR-T cells to overexpress FMNL1.
  • Assessed T cell activation and cytotoxicity in vitro.
  • Evaluated T cell infiltration and therapeutic efficacy in murine models of melanoma and lung carcinoma.
  • FMNL1-overexpressing T cells showed normal activation and increased cytotoxicity.
  • In vivo studies revealed significant increases in TIL and CAR-T cell accumulation at tumor sites with FMNL1 overexpression.
  • Adoptive transfer of FMNL1-overexpressing CAR-T cells extended survival in melanoma-bearing mice compared to controls.

Abstract

Abstract Purpose: Adoptive T cell therapies such as tumor-infiltrating lymphocytes (TIL) and chimeric antigen receptor (CAR)-T cells show limited efficacy against solid tumors. This is due in part to physical barriers in solid tumors, including abnormal vasculature and dense extracellular matrix, which limit T cell infiltration and persistence within restrictive tumor microenvironments. We investigated whether overexpression of Formin-like-1 (FMNL1), a cytoskeletal regulator of T cell migration, could overcome these physical barriers and improve T cell accumulation and therapeutic activity in solid tumors. Methods: We engineered tumor-specific TILs and CAR-T cells to overexpress FMNL1 using a bioengineering platform. We first assessed control and FMNL1-overexpressing T cell activation, cytotoxicity, and restimulation in vitro. Then using murine tumor models, we evaluated tumor infiltration and therapeutic efficacy of adoptively transferred control and FMNL1-overexpressing TILs and CAR-T cells in melanoma and lung carcinoma models. Results: FMNL1-overexpressing T cells maintained normal activation and tumor cell killing compared to control T cells. In vivo, FMNL1 overexpression significantly increased TIL and CAR-T cell accumulation at melanoma and lung carcinoma solid tumor sites compared to controls. Importantly, adoptive transfer of FMNL1-overexpressing CAR-T cells prolonged survival in melanoma tumor-bearing mice relative to control CAR-T cells, in both immunodeficient and immunocompetent recipient mice. Conclusions: This is the first demonstration that enhancing cytoskeletal dynamics via FMNL1 overexpression increases T cell accumulation in solid tumors and improves therapeutic efficacy. These findings highlight a novel, tumor antigen and CAR construct independent strategy to overcome physical barriers in the tumor microenvironment and suggest translational potential for improving CAR-T cell therapy in patients with solid tumors. Citation Format: Jeffrey W. Chung, Jessica Olivas-Corral, Ashley M. Wood, Ashton L. Sigler, Edward Ning, Michelle E. Allen, Kayla Fairweather, Jordan Jacobelli, . FMNL1 overexpression enhances tumor-specific TIL and CAR-T cell accumulation and therapeutic efficacy in solid tumors 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 1522.

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Cite This Study

Chung et al. (2026) studied this question.

synapsesocial.com/papers/69d1fd73a79560c99a0a37e8https://doi.org/10.1158/1538-7445.am2026-1522
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