pubmed-article:17267661 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C0004561 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C0205282 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C1425349 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C1420809 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C1521840 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C0769707 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C1517333 | lld:lifeskim |
pubmed-article:17267661 | lifeskim:mentions | umls-concept:C0626649 | lld:lifeskim |
pubmed-article:17267661 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:17267661 | pubmed:dateCreated | 2007-2-19 | lld:pubmed |
pubmed-article:17267661 | pubmed:abstractText | B lymphocyte stimulator (BLyS) is crucial for B-cell survival, and the biological effects of BLyS are mediated by three cell surface receptors designated B cell-activating factor receptor (BAFF-R), transmembrane activator and calcium modulator and cyclophilin ligand interactor (TACI), and B-cell maturation antibody (BCMA). Increased expression of BLyS and its receptors has been identified in numerous B-cell malignancies. We generated a fusion toxin designated rGel/BLyS for receptor-mediated delivery of the recombinant gelonin (rGel) toxin to neoplastic B cells, and we characterized its activity against various B-cell tumor lines. Three mantle cell lymphoma (MCL) cell lines (JeKo-1, Mino, and SP53) and two diffuse large B-cell lymphoma (DLBCL) cell lines (SUDHL-6 and OCI-Ly3) expressing all three distinct BLyS receptors were found to be the most sensitive to the fusion toxin (IC(50) = 2-5 pmol/L and 0.001-5 nmol/L for MCL and DLBCL, respectively). The rGel/BLyS fusion toxin showed specific binding to cells expressing BLyS receptors and rapid internalization of the rGel component into target cells. The cytotoxic effects of rGel/BLyS were inhibited by pretreatment with free BLyS or with soluble BAFF-R, TACI, and BCMA decoy receptors. This suggests that the cytotoxic effects of the fusion toxin are mediated through BLyS receptors. The rGel/BLyS fusion toxin inhibited MCL cell growth through induction of apoptosis associated with caspase-3 activation and poly (ADP-ribose) polymerase cleavage. Our results suggest that BLyS has the potential to serve as an excellent targeting ligand for the specific delivery of cytotoxic molecules to neoplastic B cells expressing the BLyS receptors, and that the rGel/BLyS fusion toxin may be an excellent candidate for the treatment of B-cell malignancies especially MCL and DLBCL. | lld:pubmed |
pubmed-article:17267661 | pubmed:language | eng | lld:pubmed |
pubmed-article:17267661 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17267661 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17267661 | pubmed:month | Feb | lld:pubmed |
pubmed-article:17267661 | pubmed:issn | 1535-7163 | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:AguiarRicardo... | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:RosenblumMich... | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:MarksJohn WJW | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:HittelmanWalt... | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:CheungLawrenc... | lld:pubmed |
pubmed-article:17267661 | pubmed:author | pubmed-author:LyuMi-AeMA | lld:pubmed |
pubmed-article:17267661 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17267661 | pubmed:volume | 6 | lld:pubmed |
pubmed-article:17267661 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17267661 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17267661 | pubmed:pagination | 460-70 | lld:pubmed |
pubmed-article:17267661 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:17267661 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17267661 | pubmed:articleTitle | The rGel/BLyS fusion toxin specifically targets malignant B cells expressing the BLyS receptors BAFF-R, TACI, and BCMA. | lld:pubmed |
pubmed-article:17267661 | pubmed:affiliation | Immunopharmacology and Targeted Therapy Section, Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, Unit 0044, 1515 Holcombe Boulevard, Houston, TX 77030, USA. | lld:pubmed |
pubmed-article:17267661 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17267661 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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