Our study was designed to compare cellular kinetic parameters of classical Hodgkin's disease (HD) with those of anaplastic large cell lymphomas (ALCL-C, common type; and ALCL-HL, Hodgkin's like), with a particular focus on the G 2 /M transition. These disorders share some phenotypic properties, e.g.
Expression of p34cdc2 and cyclins A and B compared to other proliferative features of non-Hodgkin's lymphomas: A multivariate cluster analysis
โ Scribed by Lorenzo Leoncini; Antonio Cossu; Tiziana Megha; Cristiana Bellan; Stefano Lazzi; Pietro Luzi; Piero Tosi; Paolo Barbini; Gabriele Cevenini; Stefano Pileri; Antonio Giordano; Rainer Kraft; Jean A. Laissue; Hans Cottier
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 172 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
โฆ Synopsis
In view of recent knowledge on proteins regulating the cell cycle, we re-evaluated proliferative features of 98 diffusely growing non-Hodgkin's lymphomas. The combined use of 5 proliferation-associated variables (mitotic indices and percentages of Ki-67 ุ , p34 cdc2ุ , cyclin A ุ and cyclin B ุ cells) and their entry into a multivariate cluster analysis separated, without overlaps, the entire cohort into 3 groups (clusters) with (1) low, (2) intermediate and (3) high proliferative activity. Conversely, bivariate plots exposed considerable cluster overlaps. Multivariate stepwise discriminant analysis of all cases revealed a decreasing order of discriminant power for % Ki-67 ุ cells G % p34 cdc2ุ cells G mitotic index G % cyclin A ุ cells G % cyclin B ุ cells. The combined use of 2 variables only, mitotic index and % p34 cdc2ุ cells, allowed a clear-cut separation of clusters 2 and 3. In bivariate plots, correlations were best between % Ki-67 ุ cells and % cyclin A ุ cells and between mitotic indices and % cyclin B ุ cells. Except for chronic lymphocytic leukemias, immunocytomas and marginal zone lymphomas (all in cluster 1), individual lymphoma entities were distributed among at least 2 clusters. There was, however, a marked preponderance of mantle cell lymphomas and diffuse follicular center lymphomas in cluster 1 and of diffuse large B-cell lymphomas and peripheral T-cell lymphomas in cluster 2. Anaplastic large-cell lymphomas predominated in cluster 3 and responded best to therapy. Int.
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