Sinkovics Joseph G
St. Joseph's Hospital Cancer Institute, 3001 W. Dr. Martin Luther King Jr. Boulevard, Tampa, FL 33607-6307, USA.
Int J Oncol. 2009 Sep;35(3):441-65. doi: 10.3892/ijo_00000357.
Evolving young genomes of archaea, prokaryota and unicellular eukaryota were wide open for the acceptance of alien genomic sequences, which they often preserved and vertically transferred to their descendants throughout three billion years of evolution. Established complex large genomes, although seeded with ancestral retroelements, have come to regulate strictly their integrity. However, intruding retroelements, especially the descendents of Ty3/Gypsy, the chromoviruses, continue to find their ways into even the most established genomes. The simian and hominoid-Homo genomes preserved and accommodated a large number of endogenous retroviral genomic segments. These retroelements may mature into exogenous retroviruses, or into functional new genes. Phages and viruses have been instrumental in incorporating and transferring host cell genes. These events profoundly influenced and altered the course of evolution. Horizontal (lateral) gene transfers (HGT) overwhelmed the genomes of the ancient protocells and the evolving unicellular microorganisms, actually leading to their Cambrian explosion. While the rigidly organized genomes of multicellular organisms increasingly resist H/LGT, de-differentiated cells assuming the metabolism of their onto- or phylogenetic ancestors, open up widely to the practice of H/LGT by direct transfer, or to transfers mediated by viruses, or by cell fusions. This activity is intensified in malignantly transformed cells, thus rendering these subjects receptive to therapy with oncolytic viruses and with viral vectors of tumor-suppressive or immunogenic genetic materials. Naturally formed hybrids of dendritic and tumor cells are often tolerogenic, whereas laboratory products of these unisons may be immunogenic in the hosts of origin. As human breast cancer stem cells are induced by a treacherous class of CD8+ T cells to undergo epithelial to mesenchymal (ETM) transition and to yield to malignant transformation by the omnipresent proto-ocogenes (for example, the ras oncogenes), they become defenseless toward oncolytic viruses. Cell fusions and horizontal exchanges of genes are fundamental attributes and inherent characteristics of the living matter.
古生菌、原核生物和单细胞真核生物不断进化的年轻基因组对外来基因组序列的接受度很高,在长达30亿年的进化过程中,它们常常保留这些序列并垂直传递给后代。已确立的复杂大基因组,尽管最初含有祖先逆转录元件,但后来开始严格调控自身的完整性。然而,入侵的逆转录元件,尤其是Ty3/Gypsy的后代——嗜铬病毒,仍不断进入即使是最稳定的基因组。猿类和类人猿-人类基因组保留并容纳了大量内源性逆转录病毒基因组片段。这些逆转录元件可能成熟为外源性逆转录病毒,或成为功能性新基因。噬菌体和病毒在整合和转移宿主细胞基因方面发挥了重要作用。这些事件深刻影响并改变了进化进程。水平(横向)基因转移(HGT)在古代原始细胞和不断进化的单细胞微生物基因组中占主导地位,实际上导致了它们的寒武纪大爆发。虽然多细胞生物严格组织的基因组越来越抵制水平/横向基因转移(H/LGT),但去分化细胞承担其个体发育或系统发育祖先的代谢功能,通过直接转移、病毒介导的转移或细胞融合,广泛接受H/LGT。这种活动在恶性转化细胞中加剧,从而使这些细胞易于接受溶瘤病毒以及携带肿瘤抑制或免疫原性遗传物质的病毒载体的治疗。自然形成的树突状细胞和肿瘤细胞杂交体通常具有耐受性,而这些融合体的实验室产物在其原始宿主中可能具有免疫原性。由于人类乳腺癌干细胞被一类危险的CD8+ T细胞诱导发生上皮-间质(ETM)转变,并被无处不在的原癌基因(例如ras癌基因)导致恶性转化,它们对溶瘤病毒变得毫无防御能力。细胞融合和基因水平交换是生命物质的基本属性和固有特征。