Department of Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, 9700 RB Groningen, The Netherlands.
Neogenix Laboratoire SDB BHD, Petaling Jaya 47301, Malaysia.
Genes (Basel). 2022 Jan 25;13(2):227. doi: 10.3390/genes13020227.
We previously described involvement of the MYC/miR-150/MYB/ZDHHC11 network in the growth of Burkitt lymphoma (BL) cells. Here we studied the relevance of this network in the two other B-cell lymphomas: Hodgkin lymphoma (HL) and diffuse large B-cell lymphoma (DLBCL). Expression levels of the network components were assessed at the RNA and protein level. The effect of modulating levels of the network components on cell growth was determined through GFP competition assay. AGO2-RNA immunoprecipitation was performed to validate targeting by miR-150. Expression levels of MYC, MYB and ZDHHC11 were increased, while miR-150 levels were decreased similar to the pattern observed in BL. The knockdown of MYC, MYB and ZDHHC11 decreased the growth of HL and DLBCL cells. In contrast, overexpression of miR-150 did not induce clear phenotypes in HL, and limited the effects in DLBCL. This could not be explained by the differences in overexpression levels. Furthermore, we showed that in HL, ZDHHC11 and MYB are efficiently targeted by miR-150. To conclude, MYC, MYB and ZDHHC11 are critical for the growth of HL and DLBCL cells consistent with the role observed in BL cells, while low endogenous miR-150 levels appeared to be less critical for the growth of HL and DLBCL cells despite the effective targeting of ZDHHC11 and MYB.
我们之前描述了 MYC/miR-150/MYB/ZDHHC11 网络在伯基特淋巴瘤 (BL) 细胞生长中的作用。在这里,我们研究了该网络在另外两种 B 细胞淋巴瘤:霍奇金淋巴瘤 (HL) 和弥漫性大 B 细胞淋巴瘤 (DLBCL) 中的相关性。在 RNA 和蛋白质水平评估网络组件的表达水平。通过 GFP 竞争测定确定调节网络组件水平对细胞生长的影响。进行 AGO2-RNA 免疫沉淀以验证 miR-150 的靶向作用。MYC、MYB 和 ZDHHC11 的表达水平增加,而 miR-150 水平降低,与 BL 中观察到的模式相似。MYC、MYB 和 ZDHHC11 的敲低降低了 HL 和 DLBCL 细胞的生长。相比之下,miR-150 的过表达在 HL 中并未诱导明显表型,并且在 DLBCL 中的影响有限。这不能用过表达水平的差异来解释。此外,我们表明在 HL 中,ZDHHC11 和 MYB 被 miR-150 有效靶向。总之,MYC、MYB 和 ZDHHC11 对 HL 和 DLBCL 细胞的生长至关重要,与在 BL 细胞中观察到的作用一致,而尽管 ZDHHC11 和 MYB 被有效靶向,但内源性 miR-150 水平较低似乎对 HL 和 DLBCL 细胞的生长不太关键。