» Articles » PMID: 27132279

Role of the Tumor Microenvironment in Mature B-cell Lymphoid Malignancies

Abstract

The tumor microenvironment is the cellular and molecular environment in which the tumor exists and with which it continuously interacts. In B-cell lymphomas, this microenvironment is intriguing in that it plays critical roles in the regulation of tumor cell survival and proliferation, fostering immune escape as well as the development of treatment resistance. The purpose of this review is to summarize the proceedings of the Second Annual Summit on the Immune Microenvironment in Hematologic Malignancies that took place on September 11-12, 2014 in Dublin, Ireland. We provide a timely overview of the composition and biological relevance of the cellular and molecular microenvironment interface and discuss the role of interactions between the microenvironment and neoplastic cells in a variety of B-cell lymphomas. In addition, we focus on various novel therapeutic strategies that target the tumor microenvironment, including agents that modulate B-cell receptor pathways and immune-checkpoints, chimeric antigen receptor T cells and immunomodulatory agents.

Citing Articles

In Vitro 3D Models of Haematological Malignancies: Current Trends and the Road Ahead?.

Mattioda C, Voena C, Ciardelli G, Mattu C Cells. 2025; 14(1.

PMID: 39791739 PMC: 11720277. DOI: 10.3390/cells14010038.


Multi-Omics Profiling Unveils the Complexity and Dynamics of Immune Infiltrates in Intrahepatic Cholangiocarcinoma.

Li X, Wang Y, Guan R, Sheng N, Zhang S Biology (Basel). 2024; 13(10).

PMID: 39452125 PMC: 11504529. DOI: 10.3390/biology13100816.


EZB-type diffuse large B-cell lymphoma cell lines have superior migration capabilities compared to MCD-type.

Sherif M, Schafer H, Scharf S, van Oostendorp V, Sadeghi Shoreh Deli A, Loth A Br J Haematol. 2024; 205(6):2327-2337.

PMID: 39355919 PMC: 11637725. DOI: 10.1111/bjh.19778.


Tumor microenvironment as a complex milieu driving cancer progression: a mini review.

Li Z, Li J, Bai X, Huang X, Wang Q Clin Transl Oncol. 2024; .

PMID: 39342061 DOI: 10.1007/s12094-024-03697-w.


Harnessing natural killer cells for refractory/relapsed non-Hodgkin lymphoma: biological roles, clinical trials, and future prospective.

Bakhtiyaridovvombaygi M, Yazdanparast S, Kheyrandish S, Safdari S, Amiri Samani F, Sohani M Biomark Res. 2024; 12(1):66.

PMID: 39020411 PMC: 11253502. DOI: 10.1186/s40364-024-00610-z.


References
1.
Burger J, Keating M, Wierda W, Hartmann E, Hoellenriegel J, Rosin N . Safety and activity of ibrutinib plus rituximab for patients with high-risk chronic lymphocytic leukaemia: a single-arm, phase 2 study. Lancet Oncol. 2014; 15(10):1090-9. PMC: 4174348. DOI: 10.1016/S1470-2045(14)70335-3. View

2.
Ahmadzadeh M, Johnson L, Heemskerk B, Wunderlich J, Dudley M, White D . Tumor antigen-specific CD8 T cells infiltrating the tumor express high levels of PD-1 and are functionally impaired. Blood. 2009; 114(8):1537-44. PMC: 2927090. DOI: 10.1182/blood-2008-12-195792. View

3.
Dotti G, Savoldo B, Pule M, Straathof K, Biagi E, Yvon E . Human cytotoxic T lymphocytes with reduced sensitivity to Fas-induced apoptosis. Blood. 2005; 105(12):4677-84. PMC: 1895003. DOI: 10.1182/blood-2004-08-3337. View

4.
Wu L, Adams M, Carter T, Chen R, Muller G, Stirling D . lenalidomide enhances natural killer cell and monocyte-mediated antibody-dependent cellular cytotoxicity of rituximab-treated CD20+ tumor cells. Clin Cancer Res. 2008; 14(14):4650-7. DOI: 10.1158/1078-0432.CCR-07-4405. View

5.
Pegram H, Lee J, Hayman E, Imperato G, Tedder T, Sadelain M . Tumor-targeted T cells modified to secrete IL-12 eradicate systemic tumors without need for prior conditioning. Blood. 2012; 119(18):4133-41. PMC: 3359735. DOI: 10.1182/blood-2011-12-400044. View