Characterization of Estrogen Receptors in Pancreatic Adenocarcinoma with Tertiary Lymphoid Structures

Author:

Zou Xuan1234,Liu Yu1234,Lin Xuan1234,Wang Ruijie1234,Dai Zhengjie1234,Chen Yusheng1234,Ma Mingjian1234,Tasiheng Yesiboli1234,Yan Yu1234,Wang Xu12345ORCID,Yu Xianjun1234,Cheng He1234,Liu Chen1234

Affiliation:

1. Department of Pancreatic Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China

2. Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China

3. Shanghai Pancreatic Cancer Institute, Shanghai 200032, China

4. Pancreatic Cancer Institute, Fudan University, Shanghai 200032, China

5. Cancer Institute, Shanghai Key Laboratory of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China

Abstract

The role of estrogen signaling in antitumor immunology remains unknown for non-traditional sex-biased cancer types such as pancreatic adenocarcinoma (PAAD). Tertiary lymphoid structures (TLS) are active zones composed of multiple types of immune cells, whose presence indicates anti-tumor immune responses. In this study, we employed a 12-chemokine signature to characterize potential gene categories associated with TLS development and identified seventeen major gene categories including estrogen receptors (ERs). Immunohistochemistry staining revealed the expression patterns of three ERs (ERα, ERβ, and GPER) in 174 PAAD samples, and their correlation with clinicopathological characteristics, immune cell infiltration levels, and intratumoral TLS presence was analyzed. The results indicated that ERα (+) and ERβ (+) were correlated with high tumor grade, and ERβ (+) and GPER (+) were correlated with lower TNM stage, and both ERα (+) and GPER (+) displayed a beneficial effect on prognosis in this cohort. Interestingly, positive staining of all three ERs was significantly correlated with the presence of intratumoral TLSs and infiltration of more active immune cells into the microenvironment. Moreover, the chemotaxis of CD8+T-cells to PAAD cells was significantly increased in vitro with upregulated expression of ERα or ERβ on PAAD cells. To conclude, our study showed a novel correlation between ER expression and TLS development, suggesting that ERs may play a protective role by enhancing anti-tumor immune responses in PAAD.

Funder

National Natural Science Foundation of China

Scientific Innovation Project of Shanghai Education Committee

Shanghai Municipal Science and Technology Major Project

Clinical and Scientific Innovation Project of Shanghai Hospital Development Center

Clinical Research Plan of Shanghai Hospital Development Center

National Key Research and Development Program of China

Xuhui District Artificial Intelligence Medical Hospital Cooperation Project

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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