Figure 2
Figure 2. Quantitative RT-PCR validation of 8 differentially expressed genes in CD4+CD7− Sezary cells from SS patients. The expression of several genes identified in the microarray comparing AHI-1–suppressed Hut 78/sh4 cells with Hut 78 control cells were evaluated by quantitative RT-PCR in both CD4+CD7− primary leukemic cells from 6 SS patients and 5 CD4+ normal controls. (A) Validation of up-regulated genes in primary SS samples compared with normal controls: AHI-1 and PALM2-AKAP2. (B) Validation of down-regulated genes in primary SS samples compared with normal controls: HCK, BIN1, NKG7, REPS2, SPIB, and BRDG1. Values shown are the mean ± SEM. The P values presented are the result of 2-sample t tests comparing the SS patient expression data with that of normal controls.

Quantitative RT-PCR validation of 8 differentially expressed genes in CD4+CD7 Sezary cells from SS patients. The expression of several genes identified in the microarray comparing AHI-1–suppressed Hut 78/sh4 cells with Hut 78 control cells were evaluated by quantitative RT-PCR in both CD4+CD7 primary leukemic cells from 6 SS patients and 5 CD4+ normal controls. (A) Validation of up-regulated genes in primary SS samples compared with normal controls: AHI-1 and PALM2-AKAP2. (B) Validation of down-regulated genes in primary SS samples compared with normal controls: HCK, BIN1, NKG7, REPS2, SPIB, and BRDG1. Values shown are the mean ± SEM. The P values presented are the result of 2-sample t tests comparing the SS patient expression data with that of normal controls.

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