Itaconate transporter SLC13A3 impairs tumor immunity via endowing ferroptosis resistance

Immune checkpoint blockade (ICB) triggers tumor ferroptosis. However, most patients are unresponsive to ICB. Tumors might evade ferroptosis in the tumor microenvironment (TME). Here, we discover SLC13A3 is an itaconate transporter in tumor cells and endows tumor ferroptosis resistance, diminishing tumor immunity and ICB efficacy. Mechanistically, tumor cells uptake itaconate via SLC13A3 from tumor-associated macrophages (TAMs), thereby activating the NRF2-SLC7A11 pathway and escaping from immune-mediated ferroptosis. Structural modeling and molecular docking analysis identify a functional inhibitor for SLC13A3 (SLC13A3i). Deletion of ACOD1 (an essential enzyme for itaconate synthesis) in macrophages, genetic ablation of SLC13A3 in tumors, or treatment with SLC13A3i sensitize tumors to ferroptosis, curb tumor progression, and bolster ICB effectiveness. Thus, we identify the interplay between tumors and TAMs via the SLC13A3-itaconate-NRF2-SLC7A11 axis as a previously unknown immune ferroptosis resistant mechanism in the TME and SLC13A3 as a promising immunometabolic target for treating SLC13A3<sup>+</sup> cancer.

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Publication Details

Journal
Cancer Cell
Published
2024-11-07
DOI
https://doi.org/10.1016/j.ccell.2024.10.010
Citations
66
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
27.65

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article

Itaconate transporter SLC13A3 impairs tumor immunity via endowing ferroptosis resistance

Jwala Priyadarsini Sivaccumar, Ilona Kryczek, Lana X. Garmire, Sara Grove et al.
66 citations
Cancer Cell
Ferroptosis and cancer prognosis
27.65
article

Itaconate transporter SLC13A3 impairs tumor immunity via endowing ferroptosis resistance

Jwala Priyadarsini Sivaccumar, Ilona Kryczek, Lana X. Garmire, Sara Grove, Jiali Yu, Zhiqiang An, Ashwin Ramesh, Linda Vatan, Shuang Wei, Yatrik M. Shah, Peng Liao, Thomas M. Vigil, Kole Tison, Richard M. Mortensen, Paul D. Kirchhoff, Shaomeng Wang, Michael Pitter, Hannah Yang, Weiping Zou, Ningyan Zhang, Jiajia Zhou, Chan Kim, Heng Lin, Yuheng Du, Weichao Wang
article en
66 citations

Abstract

Immune checkpoint blockade (ICB) triggers tumor ferroptosis. However, most patients are unresponsive to ICB. Tumors might evade ferroptosis in the tumor microenvironment (TME). Here, we discover SLC13A3 is an itaconate transporter in tumor cells and endows tumor ferroptosis resistance, diminishing tumor immunity and ICB efficacy. Mechanistically, tumor cells uptake itaconate via SLC13A3 from tumor-associated macrophages (TAMs), thereby activating the NRF2-SLC7A11 pathway and escaping from immune-mediated ferroptosis. Structural modeling and molecular docking analysis identify a functional inhibitor for SLC13A3 (SLC13A3i). Deletion of ACOD1 (an essential enzyme for itaconate synthesis) in macrophages, genetic ablation of SLC13A3 in tumors, or treatment with SLC13A3i sensitize tumors to ferroptosis, curb tumor progression, and bolster ICB effectiveness. Thus, we identify the interplay between tumors and TAMs via the SLC13A3-itaconate-NRF2-SLC7A11 axis as a previously unknown immune ferroptosis resistant mechanism in the TME and SLC13A3 as a promising immunometabolic target for treating SLC13A3<sup>+</sup> cancer.

Cancer CellVol. 42(12)
University of Michigan (US), Michigan Medicine (US), Michigan Center for Translational Pathology (US), CHA University Bundang Medical Center (KR), Brown Foundation (US), The University of Texas Health Science Center at Houston (US)
Welch Foundation, National Institutes of Health, Rogel Cancer Center, University of Michigan, National Cancer Institute
Openalex Percentile: Top 0%
Ferroptosis and cancer prognosis
27.65
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