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B cells and their mediators as targets for therapy in solid tumors

Research output: Contribution to journalReview articlepeer-review

Abstract

B cells have recently been appreciated as paracrine mediators of solid tumor development. Their ability to influence various hallmarks of cancer development, aside from antigen presentation, can be attributed to the diversity of soluble mediators they express, including cytokines and immunoglobulins, that can act directly and indirectly on the diversity of leukocyte subsets that infiltrate developing tumors, evolving neoplastic cells, as well as select T cell populations in secondary lymphoid organs and within tumor stroma. Herein, we review the literature supporting these interactions and discuss novel approaches to ameliorate protumoral B cell effects for anti-cancer therapy.

Original languageEnglish (US)
Pages (from-to)1644-1649
Number of pages6
JournalExperimental Cell Research
Volume319
Issue number11
DOIs
StatePublished - Jul 1 2013

Funding

The authors thank members of the Coussens laboratory for critical discussions on content. AJG is supported by T32I078903-04 . LMC acknowledges support from the NIH/NCI, a DOD BCRP Era of Hope Scholar Expansion Award, Susan B Komen Foundation, and the Breast Cancer Research Foundation.

FundersFunder number
Susan B. Komen Foundation
Author National Institutes of Health National Institutes of Health National Institutes of Health National Institutes of Health The Bev Hartig Huntington's Disease Foundation National Institutes of Health
U.S. Department of Defense
National Institute of Health-National Cancer InstituteR01CA130980
Breast Cancer Research Foundation

    Keywords

    • B cells
    • Cancer
    • Inflammation
    • Leukocytes
    • Myeloid cells

    ASJC Scopus subject areas

    • Cell Biology

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