Related Experiment Video
Updated: May 20, 2026

Wild-type Blocking PCR Combined with Direct Sequencing as a Highly Sensitive Method for Detection of Low-Frequency Somatic Mutations
Published on: March 29, 2017
Molecular pathogenesis of Waldenstrom's macroglobulinemia
Esteban Braggio1, Casey Philipsborn, Anne Novak
1Department of Hematology-Oncology, Mayo Clinic in Arizona, 13400 East Shea Boulevard, Collaborative Research Building, Room 1-105, Scottsdale, AZ 85259-5494, USA.
Abstract:
Waldenström's macroglobulinemia is an indolent, lymphoproliferative disease, characterized by a heterogeneous lymphoplasmacytic bone marrow infiltrate and high immunoglobulin M production. While technological advances over the past several decades have dramatically improved the possibilities of studying the molecular basis of Waldenström's macroglobulinemia, the pathogenesis of the disease remains fragmented. Undoubtedly, research has been successful in uncovering underlying aberrations and deregulated mechanisms in this disease, providing useful information for identifying biomarkers for disease diagnosis, risk stratification and therapeutic intervention, but there is still a long way to go before the pathogenesis of Waldenström's macroglobulinemia is fully revealed. In addition, the low number of in vitro or in vivo models significantly challenges extensive analysis. In this manuscript, we review the molecular basis of this disease.
Related Concept Videos
Myasthenia Gravis ll: Pathophysiology
Cytotoxic Edema: Pathophysiology
Cytomegalovirus Disease
