Expression and function of a novel isoform of Sox5 in malignant B cells.

Leuk Res

Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, United States; Rutgers Cancer Institute of New Jersey, United States. Electronic address:

Published: March 2014

Using a mouse model with the tumor suppressor TRAF3 deleted from B cells, we identified Sox5 as a gene strikingly up-regulated in B lymphomas. Sox5 proteins were not detected in normal or premalignant TRAF3(-/-) B cells even after treatment with B cell stimuli. The Sox5 expressed in TRAF3(-/-) B lymphomas represents a novel isoform of Sox5, and was localized in the nucleus of malignant B cells. Overexpression of Sox5 inhibited cell cycle progression, and up-regulated the protein levels of p27 and β-catenin in human multiple myeloma cells. Together, our findings indicate that Sox5 regulates the proliferation of malignant B cells.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3947564PMC
http://dx.doi.org/10.1016/j.leukres.2013.12.016DOI Listing

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