AI Article Synopsis

  • A study on 18 patients with splenic marginal zone lymphoma (SMZL) compared the effectiveness of novel mitogenic agents (ODN + IL-2) to traditional inducers (TPA and LPS) in promoting cell proliferation and karyotyping.
  • Results revealed that ODN + IL-2 led to significantly better proliferation rates (94.4%) and quality of chromosome banding (77.7%) compared to TPA and LPS (55% and 44.4%, respectively).
  • The ODN + IL-2 method not only defined karyotypes in all patients but also detected more clonal aberrations, indicating its potential for future studies on the prognostic significance of genetic changes in SMZL.

Article Abstract

To compare the efficiency of novel mitogenic agents and traditional mitosis inductors, 18 patients with splenic marginal zone lymphoma (SMZL) were studied. Three cultures using oligodeoxynucleotide (ODN) plus interleukin-2 (IL-2), or TPA, or LPS were setup in each patient. Seventeen/18 cases with ODN + IL2 had moderate/good proliferation (94, 4%) as compared with 10/18 cases with TPA and LPS (55%) (P = .015); 14/18 (77, 7%) cases with ODN + IL2 had sufficient good quality of banding as compared with 8/18 cases (44, 4%) with TPA and LPS. The karyotype could be defined from ODN + IL2-stimulated cultures in all 18 patients, 14 of whom (77, 7%) had a cytogenetic aberration, whereas clonal aberrations could be documented in 9 and in 3 cases by stimulation with LPS and TPA, respectively. Recurrent chromosome aberrations in our series were represented by aberrations of chromosome 14q in 5 patients, by trisomy 12 and 7q deletion in 4 cases each, and by abnormalities involving 11q and 13q in two cases each. These findings show that stimulation with ODN + IL2 offers more mitotic figures of better quality and results in an increased rate of clonal aberrations in SMZL, making this method ideal for prospective studies aiming at the definition of the prognostic impact of cytogenetic aberrations in this disorder.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100609PMC
http://dx.doi.org/10.1155/2011/691493DOI Listing

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