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Related Concept Videos

The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
Lymphoid Cells and Tissues01:18

Lymphoid Cells and Tissues

Lymphoid cells and tissues are integral to the immune system, which is crucial in maintaining our body's defense against harmful pathogens. They form the building blocks of lymphoid organs, which include the spleen, thymus, and lymph nodes.
Lymphoid cells consist of various types of immune system cells. These include B and T lymphocytes, which are responsible for producing antibodies and killing infected cells, respectively. Dendritic cells act as messengers between the innate and adaptive...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...

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The tumour microenvironment in B cell lymphomas.

David W Scott1, Randy D Gascoyne2

  • 1Centre for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver V5Z 1L3, Canada.

Nature Reviews. Cancer
|July 11, 2014
PubMed
Summary

B cell lymphomas rely on interactions with surrounding non-cancerous cells. Understanding the tumour microenvironment offers new therapeutic strategies for these cancers.

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Area of Science:

  • Oncology
  • Immunology
  • Cell Biology

Background:

  • B cell lymphomas originate from immune cells requiring complex interactions for normal development.
  • Tumour cells, despite genetic mutations, remain dependent on their surrounding microenvironment.
  • The tumour microenvironment comprises non-malignant immune and stromal cells crucial for cancer progression.

Purpose of the Study:

  • To highlight the critical role of the tumour microenvironment in B cell lymphoma pathogenesis.
  • To explore how understanding these cellular interactions can reveal new therapeutic targets.
  • To emphasize the importance of studying the tumor microenvironment for future cancer treatments.

Main Methods:

  • This study is a review of existing literature on B cell lymphomas and their microenvironments.
  • It synthesizes findings on the interactions between malignant B cells and stromal/immune cells.
  • Focuses on the conceptual framework rather than specific experimental data.

Main Results:

  • B cell lymphomas are fundamentally dependent on their microenvironment for survival and growth.
  • Interactions with immune and stromal cells influence lymphoma development and progression.
  • Genetic aberrations within cancer cells do not negate their reliance on external cellular support.

Conclusions:

  • A comprehensive understanding of the tumour microenvironment is essential for deciphering B cell lymphoma pathogenesis.
  • Targeting the interactions within the microenvironment presents promising therapeutic avenues.
  • Future cancer therapies should consider the broader cellular ecosystem, not just the cancer cells themselves.