Rationale for the design of combination therapies that are active in T-cell lymphomas?

Published: June 10, 2009
Abstract Views: 154
PDF: 150
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Authors

The lymphomas are the most diverse group of diseases within any single class of malignancy. More than thirty different clinico-pathologic diseases have been identified and classified. Such a variety of diseases of the lymphoid system likely are the result of the unique etiology of each individual tumor type. On the basis of function, T-cells and B-cells have distinctly different functions, and undoubtedly activate genes to drive the different specialized pathways to achieve these purposes. Factors that clearly have a role in lymphomagenesis include illegitimate gene recombination, infection by oncogenic viruses, impaired host immunity, and persistent proliferation driven by inflammation.

Dimensions

Altmetric

PlumX Metrics

Downloads

Citations

Supporting Agencies

How to Cite

Plunkett, W. (2009). Rationale for the design of combination therapies that are active in T-cell lymphomas?. Hematology Meeting Reports (formerly Haematologica Reports), 2(13). https://doi.org/10.4081/hmr.v2i13.498