Understanding the role of TNFR2 signaling in the tumor microenvironment of breast cancer

被引:0
|
作者
Ali Mussa [1 ]
Nor Hayati Ismail [2 ]
Mahasin Hamid [1 ]
Mohammad A. I. Al-Hatamleh [3 ]
Anthony Bragoli [4 ]
Khalid Hajissa [5 ]
Noor Fatmawati Mokhtar [6 ]
Rohimah Mohamud [7 ]
Vuk Uskoković [8 ]
Rosline Hassan [9 ]
机构
[1] Universiti Sains Malaysia,Department of Haematology, School of Medical Sciences
[2] Omdurman Islamic University,Department of Biology, Faculty of Education
[3] Xiangya School of Pharmaceutical Sciences,Department of Pharmaceutics
[4] Central South University,Department of Zoology, Faculty of Sciences and Information Technology
[5] Hunan Province,Division of Hematology and Oncology, Department of Medicine
[6] University of Nyala,Department of Immunology
[7] UPMC Hillman Cancer Center,Department of Zoology, Faculty of Science and Technology
[8] University of Pittsburgh,Institute for Research in Molecular Medicine (iNFORMM)
[9] University of Pittsburgh,Department of Immunology, School of Medical Sciences
[10] Omdurman Islamic University,Division of Natural Sciences
[11] Universiti Sains Malaysia,undefined
[12] Universiti Sains Malaysia,undefined
[13] TardigradeNano LLC,undefined
[14] Fullerton College,undefined
关键词
Immune checkpoint; Immunosuppressive TME; TNF; TNFRSF1B; CD120b;
D O I
10.1186/s13046-024-03218-1
中图分类号
学科分类号
摘要
Breast cancer (BC) is the most frequently diagnosed malignancy among women. It is characterized by a high level of heterogeneity that emerges from the interaction of several cellular and soluble components in the tumor microenvironment (TME), such as cytokines, tumor cells and tumor-associated immune cells. Tumor necrosis factor (TNF) receptor 2 (TNFR2) appears to play a significant role in microenvironmental regulation, tumor progression, immune evasion, drug resistance, and metastasis of many types of cancer, including BC. However, the significance of TNFR2 in BC biology is not fully understood. This review provides an overview of TNFR2 biology, detailing its activation and its interactions with important signaling pathways in the TME (e.g., NF-κB, MAPK, and PI3K/Akt pathways). We discuss potential therapeutic strategies targeting TNFR2, with the aim of enhancing the antitumor immune response to BC. This review provides insights into role of TNFR2 as a major immune checkpoint for the future treatment of patients with BC.
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