Simão Éder Maiquel, Sinigaglia Marialva, Bugs Cristhian Augusto, Castro Mauro Antonio Alves, Librelotto Giovani Rubert, Alves Ronnie, Mombach José Carlos Merino
Departamento de Física, Universidade Federal de Santa Maria, Brazil.
Mol Biosyst. 2012 Nov;8(11):3003-9. doi: 10.1039/c2mb25242b.
A recent model proposing that a barrier is raised against tumor evolution in pre-cancer tissues is investigated. For that we quantify expression alterations in genome maintenance pathways: DNA damage response, death pathways and cell cycle and also differentially expressed genes in transcriptomes of pre-cancerous and cancerous lesions deposited in the GEO database. We find that the main alterations in pre-cancer samples comprising the barrier are: (1) DNA double strand-breaks signaling and repair pathways induction, (2) upregulation of cyclin-dependent kinases, (3) p53 dependent (and independent) repair and apoptosis pathways induction and (4) replicative senescence induction early in tissue transformation. In the cancer samples we find that the induced pathways in pre-cancer are systematically inhibited and the only remaining induced pathway is p53, whereas the retinoblastoma pathway arises induced in most samples. The results give support to the model, furthermore they reveal the involvement of additional mechanisms in pre-cancer, including the early induction of replicative senescence and of p53 independent apoptosis.
我们对最近提出的一种模型进行了研究,该模型认为癌前组织中会对肿瘤进化形成一种屏障。为此,我们量化了基因组维持途径中的表达变化:DNA损伤反应、死亡途径和细胞周期,以及存储在GEO数据库中的癌前病变和癌性病变转录组中的差异表达基因。我们发现,构成该屏障的癌前样本中的主要变化包括:(1)DNA双链断裂信号传导和修复途径的诱导;(2)细胞周期蛋白依赖性激酶的上调;(3)p53依赖性(和非依赖性)修复及凋亡途径的诱导;(4)在组织转化早期诱导复制性衰老。在癌症样本中,我们发现癌前诱导的途径被系统性抑制,唯一剩下的诱导途径是p53,而视网膜母细胞瘤途径在大多数样本中被诱导产生。这些结果支持了该模型,此外,它们还揭示了癌前阶段涉及的其他机制,包括复制性衰老和p53非依赖性凋亡的早期诱导。