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Publication : Genetic imbalances in preleukemic thymuses.

First Author  Verlaet M Year  2001
Journal  Biochem Biophys Res Commun Volume  283
Issue  1 Pages  12-8
PubMed ID  11322760 Mgi Jnum  J:71014
Mgi Id  MGI:2148954 Doi  10.1006/bbrc.2001.4731
Citation  Verlaet M, et al. (2001) Genetic imbalances in preleukemic thymuses. Biochem Biophys Res Commun 283(1):12-8
abstractText  To understand the molecular mechanisms involved in preleukemia, the suppression subtractive hybridization method was used in a murine radiation-induced thymic lymphoma model. Seventeen mRNAs overexpressed in preleukemic thymuses were identified: mouse laminin binding protein (p40/37LBP), E25 protein, Rattus norvegicus clone BB.1.4.1, profilin, poly(A) binding protein (PABP), mouse high mobility group protein 1, topoisomerase I, clusterin, proteasome RC1 subunit, rat prostatein C3 and C1 subunits; two ESTs and four unknown genes. The overexpression of PABP, clusterin, profilin, and the p40/37LBP mRNAs was confirmed in preleukemic thymuses and can be related to some cellular events observed during the preleukemic period, i.e., alterations of cell cycle and apoptosis properties. The p40/37LBP and 67-kDa laminin receptor proteins were upregulated during the preleukemic period. The data suggest that additional studies on p40/37LBP and 67-kDa laminin receptor regulation are required to evaluate their potential role in the lymphoma prevention by TNF-alpha and IFN-gamma. Copyright 2001 Academic Press.
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