Yavorski John M, Blanck George
a Department of Molecular Medicine , Morsani College of Medicine, University of South Florida , Tampa , FL , USA.
b Immunology Program, H. Lee Moffitt Cancer Center and Research Institute , Tampa , FL , USA.
Cell Cycle. 2016 Aug 17;15(16):2157-2163. doi: 10.1080/15384101.2016.1195532. Epub 2016 Jun 29.
Oncogene mutations are primarily thought to facilitate uncontrolled cell growth. However, overexpression of oncoproteins likely leads to apoptosis in a feed forward mechanism, whereby a certain level of oncoprotein leads to the activation of pro-proliferation effector genes and higher levels lead to activation of pro-apoptotic effector genes. TCGA STAD barcodes having no oncoprotein coding region mutations represented reduced expression of the apoptosis-effector genes compared with barcodes with multiple oncoprotein coding region mutations. Furthermore, STAD barcodes in a "no-subsequent tumor" group, representing 224 samples, and in a "positive outcome" group, had more oncoprotein coding regions mutated, on average, than barcodes of the new tumor and negative outcome groups, respectively. BRAF, CTNNB1, KRAS and MTOR coding region mutations (as a group) had the strongest association with the no-subsequent tumor group. Tumor suppressor coding region mutations were also correlated with no-subsequent tumor. These results are consistent with an oncoprotein-mediated, feed-forward mechanism of apoptosis in patients. Importantly, the no-subsequent tumor group also had more overall mutations. This result leads to considerations of unhealthy cells or cells with more neo-antigens for immune rejection. However, a probabilistic aspect of mutagenesis is also consistent with more oncoprotein and tumor suppressor protein mutations, in cases of more overall mutations, and thus a higher likelihood of activation of feed forward apoptosis pathways.
癌基因突变主要被认为会促进细胞的失控生长。然而,癌蛋白的过表达可能会以前馈机制导致细胞凋亡,即一定水平的癌蛋白会导致促增殖效应基因的激活,而更高水平则会导致促凋亡效应基因的激活。与具有多个癌蛋白编码区突变的条形码相比,没有癌蛋白编码区突变的TCGA STAD条形码显示凋亡效应基因的表达降低。此外,代表224个样本的“无后续肿瘤”组和“阳性结果”组中的STAD条形码,平均而言,分别比新肿瘤组和阴性结果组的条形码有更多的癌蛋白编码区发生突变。BRAF、CTNNB1、KRAS和MTOR编码区突变(作为一个整体)与无后续肿瘤组的关联最强。肿瘤抑制因子编码区突变也与无后续肿瘤相关。这些结果与患者中癌蛋白介导的前馈凋亡机制一致。重要的是,无后续肿瘤组也有更多的总体突变。这一结果引发了对不健康细胞或具有更多新抗原以供免疫排斥的细胞的思考。然而,在总体突变较多的情况下,诱变的概率方面也与更多的癌蛋白和肿瘤抑制蛋白突变一致,因此前馈凋亡途径激活的可能性更高。