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S100A8 and S100A9 in Hematologic Malignancies: From Development to Therapy
Farnaz Razmkhah1, Sena Kim1, Sora Lim1
1Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
S100A8 and S100A9 proteins, and calprotectin, significantly impact hematologic malignancies by altering the bone marrow microenvironment. They show potential as diagnostic biomarkers and therapeutic targets throughout cancer progression.
Area of Science:
- Biochemistry
- Immunology
- Oncology
Background:
- S100A8 and S100A9 are multifunctional proteins involved in cellular signaling and immune cell function.
- These proteins are frequently dysregulated in various cancers, including hematologic malignancies, affecting disease progression and treatment response.
Purpose of the Study:
- To review the critical roles of S100A8, S100A9, and calprotectin in the malignant bone marrow microenvironment.
- To explore their potential as biomarkers and therapeutic targets in hematologic malignancies.
Main Methods:
- Literature review focusing on the functions of S100A8, S100A9, and calprotectin.
- Analysis of their involvement in cellular processes relevant to hematologic malignancies.
- Examination of their potential clinical applications.
Main Results:
- S100A8 and S100A9 modulate cell phenotype, influencing viability, differentiation, chemosensitivity, and trafficking.
- Calprotectin, formed by S100A8/S100A9 heterodimers/heterotetramers, actively promotes the malignant bone marrow microenvironment.
- These proteins play dual roles, potentially driving oncogenesis or ameliorating symptoms.
Conclusions:
- S100A8, S100A9, and calprotectin are key players in shaping the bone marrow microenvironment in hematologic malignancies.
- Their involvement across different disease stages highlights their significance from diagnosis to therapy.
- Targeting these proteins offers promising avenues for novel diagnostic and therapeutic strategies in hematologic cancers.
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