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Exploring SLAMF5/CD84 in Cancer: Advancing the Frontiers of Tumor Immunology

Safia Obaidur RabDepartment of Clinical Laboratory Sciences, College of Applied Medical Science King Khalid University Abha Saudi ArabiaAhmed Hussein ZwamelDepartment of Medical Analysis, Medical Laboratory Technique College The Islamic University Najaf IraqAshok Kumar BishoyiMarwadi University Research Center, Department of Microbiology, Faculty of Science Marwadi University Rajkot Gujarat IndiaSuhas BallalDepartment of Chemistry and Biochemistry, School of Sciences JAIN (Deemed to be University) Bangalore Karnataka IndiaAbhayveer SinghCentre for Research Impact & Outcome, Chitkara University Institute of Engineering and Technology Chitkara University Rajpura Punjab IndiaAnita DeviDepartment of Chemistry, Chandigarh Engineering College Chandigarh Group of Colleges‐Jhanjeri Mohali Punjab IndiaGirish Chandra SharmaDepartment of Applied Sciences–Chemistry, NIMS Institute of Engineering & Technology NIMS University Rajasthan Jaipur IndiaPushpa Negi BhakuniDepartment of Allied Science Graphic Era Hill University Bhimtal Uttarakhand IndiaJasur RizaevDepartment of Public Health and Healthcare Management, Rector Samarkand State Medical University 18, Amir Temur Street Samarkand Uzbekistan
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Аннотация

The Signaling Lymphocytic Activation Molecule (SLAM) family receptors play essential roles in regulating immune cell activation, differentiation, and communication. SLAMF5, also known as CD84, has drawn increasing attention in cancer immunology due to its involvement in both tumor progression and immune modulation. This review explores the expression patterns, signaling mechanisms, and functional roles of SLAMF5/CD84 within the tumor microenvironment. SLAMF5/CD84 is expressed on multiple immune cell types and contributes to immune evasion by enhancing regulatory B cell function, promoting myeloid-derived suppressor cell expansion, and upregulating immune checkpoint molecules such as PD-L1. Its expression has been implicated in various hematologic malignancies and solid tumors, including chronic lymphocytic leukemia, multiple myeloma, and triple-negative breast cancer. Emerging therapeutic approaches targeting SLAMF5/CD84-such as monoclonal antibodies and CAR T-cell therapies-offer promising strategies to counteract immunosuppression and improve treatment outcomes. By highlighting recent findings and therapeutic developments, this review underscores the significance of SLAMF5/CD84 as both a prognostic biomarker and a novel target in cancer immunotherapy. Understanding SLAMF5/CD84's multifaceted roles in the tumor immune landscape could support the development of more effective and personalized cancer treatment strategies.

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