Guest guest Posted January 17, 2011 Report Share Posted January 17, 2011 A paper by Herishanu et al and a commentary by Friedberg are worth reading in the latest issue of the journal Blood, DOI 10.1182/blood-2010-05-284984 Herishanu and colleagues elegantly demonstrated that the lymph nodes are key sites in pathogenesis of CLL, where increased signalling through the B-cell receptor (BCR) contributes to proliferation and tumour progression. Treatments like Cal 101, PCI-32765, AVL-292 etc. target elements of the BCR pathway. Fostamatinib disodium has been found to inhibit Syk, which is also involved. Friedberg states: " We now understand the importance of BCR signalling in maintaining the CLL nodal malignant microenvironment, which sheds light on these clinical observations. Given the importance of BCR signalling in maintaining the CLL nodal malignant microenvironment, we have even more reason to pursue this pathway as a rational therapeutic target for this disease. " Article: http://cllcanada.ca Blood: http://bloodjournal.hematologylibrary.org/cgi/content/abstract/117/2/563 http://bloodjournal.hematologylibrary.org/cgi/content/full/117/2/377 Quote Link to comment Share on other sites More sharing options...
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