“…However, in GCB DLBCL type, the overexpression of BCL2 is related to the presence of the t (14,18) translocation, whereas in ABC DLBCL, this overexpression is promoted by other mechanisms, such as transcriptional upregulation and gene amplification [31]. Moreover, in patients following R-CHOP treatment [10,11,17], the overexpression of BCL2 appears to pertain negative prognostic impact in GCB DLBCL whereas in ABC DLBCL, rituximab mediates BCL2 downregulation [32]. On this way, the use of BCL2 inhibitors appears to be a promising therapy for DLBCL, namely in GCB subtype [33].…”