LTA4H improves the tumor microenvironment and prevents HCC progression via targeting the HNRNPA1/LTBP1/TGF-β axis

Leukotriene A4 hydrolase (LTA4H), an inflammatory mediator, has garnered attention for its role in the development of chronic lung diseases and various cancers. Our study highlights the protective role of LTA4H in hepatocellular carcinoma (HCC) occurrence and progression. LTA4H is downregulated in clinical and mouse HCC tumors. LTA4H deficiency exacerbates hepatocyte damage by restraining JNK activation and promotes CD206<sup>+</sup> macrophage polarization through the upregulation of LTBP1 expression and downstream transforming growth factor β (TGF-β) secretion and activation. Mechanistically, LTA4H induces heterogeneous nuclear ribonucleoprotein A1 (HNRNPA1) phosphorylation, enhancing their interaction and leading to the functional inhibition of HNRNPA1 in regulating Ltbp1 mRNA maturation and processing in the nucleus. LTA4H-deficient patients exhibit poor prognosis and immunotherapy resistance. Combination therapy targeting TGF-β and PD-1 significantly improves the immunotherapy resistance of LTA4H-knockout Hepa1-6 tumors. Our findings reveal the previously unreported role of LTA4H in regulating the tumor microenvironment and provide insights into potential diagnostic and therapeutic strategies for patients with LTA4H-deficient HCC.

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Publication Details

Journal
Cell Reports Medicine
Published
2025-03-01
DOI
https://doi.org/10.1016/j.xcrm.2025.102000
Citations
8
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
7.49
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article

LTA4H improves the tumor microenvironment and prevents HCC progression via targeting the HNRNPA1/LTBP1/TGF-β axis

Shuai Yang, Zihan Zhao, Jing Wu, Ji Hu et al.
8 citations
Cell Reports Medicine
Cancer-related molecular mechanisms research
7.49
article

LTA4H improves the tumor microenvironment and prevents HCC progression via targeting the HNRNPA1/LTBP1/TGF-β axis

Shuai Yang, Zihan Zhao, Jing Wu, Ji Hu, Mixue Bai, Bo Zheng, Dongdong Xue, Xinyao Qiu, Lei Chen, Mengye Wu, Yangqianwen Zhang, Jianmin Wu, Tao Zhou, Jinxia Bao, Siyun Shen, Shuowu Liu, Yin Wang, Yani Zhang, Yixian Wang, Yingcheng Yang, Shan Wang, Meiyu Bao
article en
8 citations

Abstract

Leukotriene A4 hydrolase (LTA4H), an inflammatory mediator, has garnered attention for its role in the development of chronic lung diseases and various cancers. Our study highlights the protective role of LTA4H in hepatocellular carcinoma (HCC) occurrence and progression. LTA4H is downregulated in clinical and mouse HCC tumors. LTA4H deficiency exacerbates hepatocyte damage by restraining JNK activation and promotes CD206<sup>+</sup> macrophage polarization through the upregulation of LTBP1 expression and downstream transforming growth factor β (TGF-β) secretion and activation. Mechanistically, LTA4H induces heterogeneous nuclear ribonucleoprotein A1 (HNRNPA1) phosphorylation, enhancing their interaction and leading to the functional inhibition of HNRNPA1 in regulating Ltbp1 mRNA maturation and processing in the nucleus. LTA4H-deficient patients exhibit poor prognosis and immunotherapy resistance. Combination therapy targeting TGF-β and PD-1 significantly improves the immunotherapy resistance of LTA4H-knockout Hepa1-6 tumors. Our findings reveal the previously unreported role of LTA4H in regulating the tumor microenvironment and provide insights into potential diagnostic and therapeutic strategies for patients with LTA4H-deficient HCC.

Cell Reports MedicineVol. 6(3)
Ministry of Education of the People's Republic of China (CN), Second Military Medical University (CN), Shanghai Jiao Tong University (CN), Fudan University (CN), Renji Hospital (CN), Fudan University Shanghai Cancer Center (CN), Shanghai Cancer Institute (CN), Model Animal Research Center (CN), Eastern Hepatobiliary Surgery Hospital (CN), State Key Laboratory of Oncogene and Related Genes (CN), Nanjing University (CN)
Zero hunger
Openalex Percentile: Top 3%
Cancer-related molecular mechanisms research
7.49
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