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. Author manuscript; available in PMC: 2024 Mar 2.
Published in final edited form as: Cancer Chemother Pharmacol. 2023 Mar 2;91(3):281–290. doi: 10.1007/s00280-023-04511-0

Fig. 1.

Fig. 1

Flow cytometric analysis of pre- and post-treatment samples. PBMCs were isolated at baseline (Pre-) and 24 h after (Post*-) treatment. PBMC from each sample were analyzed for levels of Bim, p-cdc2 Y15, p-cdc2 T14, p-Chk1, gH2AX, and p-HH3. Analysis of biomarkers were performed on the CD45dim SSlow CD3-CD20-population. The mean fluorescence intensity (MFI) ratio of signal to its isocontrol for pretreatment samples from each patient was set as 100%. Results of analysis showed as bar charts displaying the relative levels of the assayed proteins in samples after averaging triplicate determinations, including standard deviation bars. Asterisks indicate significant post-treatment changes with * = significance with p values between 0.04 and 0.01; ** = significance with p values between 0.009 and 0.002; and *** = significance with p values between 0.0003 and 0.00007