Tumoral EHF predicts the efficacy of anti-PD1 therapy in pancreatic ductal adenocarcinoma

Author:

Liu Jing12,Jiang Wenna13,Zhao Kaili1,Wang Hongwei1,Zhou Tianxing1,Bai Weiwei1,Wang Xiuchao1,Zhao Tiansuo1,Huang Chongbiao1,Gao Song1,Qin Tai1,Yu Wenwen1,Yang Bo4,Li Xin1,Fu Danqi1,Tan Wei5,Yang Shengyu6,Ren He1ORCID,Hao Jihui1ORCID

Affiliation:

1. Department of Pancreatic Cancer, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China

2. Department of Breast Oncoplastic Surgery, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, China

3. Department of Clinical Laboratory, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin’s Clinical Research Center for Cancer, China

4. Department of Pathology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, China

5. Biosion, Inc., Jiangsu, China

6. Department of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, PA

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a highly immune-suppressive tumor with a low response rate to single checkpoint blockade therapy. ETS homologous factor (EHF) is a tumor suppressor in PDAC. Here, we report a novel function of EHF in pancreatic cancer immune microenvironment editing and efficacy prediction for anti-PD1 therapy. Our findings support that the deficiency of tumoral EHF induced the accumulation of regulatory T (T reg) cells and myeloid-derived suppressor cells (MDSCs) and a decrease in the number of tumor-infiltrating CD8+ T cells. Mechanistically, EHF deficiency induced the conversion and expansion of T reg cells and MDSCs through inhibiting tumor TGFβ1 and GM-CSF secretion. EHF suppressed the transcription of TGFB1 and CSF2 by directly binding to their promoters. Mice bearing EHF overexpression tumors exhibited significantly better response to anti-PD1 therapy than those with control tumors. Our findings delineate the immunosuppressive mechanism of EHF deficiency in PDAC and highlight that EHF overexpression may improve PDAC checkpoint immunotherapy.

Funder

National Natural Science Foundation of China

National Key Clinical Specialist Construction Programs of China

Key Program of Prevention and Treatment of Chronic Diseases of Tianjin

Key Program of Public Health Bureau Foundation of Tianjin

Science and Technology Development Fund of Tianjin Education Commission for Higher Education

Foundation of Tianjin Medical University

National Cancer Institute

Elsa U. Pardee Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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