Tumor Immune Microenvironment in Lymphoma: Focus on Epigenetics.
Daniel José García-DomínguezLourdes Hontecillas-PrietoNatalia Palazón-CarriónCarlos Jiménez-CorteganaVíctor Sánchez-MargaletLuis de la Cruz MerinoPublished in: Cancers (2022)
Lymphoma is a neoplasm arising from B or T lymphocytes or natural killer cells characterized by clonal lymphoproliferation. This tumor comprises a diverse and heterogeneous group of malignancies with distinct clinical, histopathological, and molecular characteristics. Despite advances in lymphoma treatment, clinical outcomes of patients with relapsed or refractory disease remain poor. Thus, a deeper understanding of molecular pathogenesis and tumor progression of lymphoma is required. Epigenetic alterations contribute to cancer initiation, progression, and drug resistance. In fact, over the past decade, dysregulation of epigenetic mechanisms has been identified in lymphomas, and the knowledge of the epigenetic aberrations has led to the emergence of the promising epigenetic therapy field in lymphoma tumors. However, epigenetic aberrations in lymphoma not only have been found in tumor cells, but also in cells from the tumor microenvironment, such as immune cells. Whereas the epigenetic dysregulation in lymphoma cells is being intensively investigated, there are limited studies regarding the epigenetic mechanisms that affect the functions of immune cells from the tumor microenvironment in lymphoma. Therefore, this review tries to provide a general overview of epigenetic alterations that affect both lymphoma cells and infiltrating immune cells within the tumor, as well as the epigenetic cross-talk between them.
Keyphrases
- diffuse large b cell lymphoma
- dna methylation
- gene expression
- induced apoptosis
- healthcare
- acute myeloid leukemia
- stem cells
- acute lymphoblastic leukemia
- squamous cell carcinoma
- signaling pathway
- genome wide
- mesenchymal stem cells
- long non coding rna
- papillary thyroid
- cell proliferation
- hodgkin lymphoma
- squamous cell