Med Hypotheses. 2012 Sep;79(3):421-2. doi: 10.1016/j.mehy.2012.05.026. Epub 2012 Jun 1.
MicroRNAs (miRNAs) are a kind of RNA, produced copies of endogenous hairpin-shaped, are 21-25 nucleotide length, small, and single chain. Recent studies have revealed that hundreds of miRNAs are found in the human genome and are responsible for diverse cellular processes including the control of developmental timing, cell proliferation, apoptosis and tumorigenesis. miRNAs can activate the initiation of apoptosis, cessation of the cell cycle and aging in case of DNA damage by stimulating the tumor suppressor target gene p53 directly and indirectly. DNA damage is composed by multiple stress factors including ionizing radiation, reactive oxygen species, UV exposure and drugs like doxorubicin and camptothecin. Radiation is used widely in health, academic area, and industry for producing electricity. As a result of using radiation widely in different fields, environmental radiation exposure is increasing as well. Whereas high dose radiation exposure causes DNA damage and gives rise to ionization to molecules of living cells by accelerating malignant tumor formation. Fields receiving high dose radiation are evaluated in terms of adverse effects, therapeutic efficacy and secondary malignancies in radiotherapy applications. Dose distributions are re-created when it is required. On the other hand, fields received low dose and the doses that the patient is exposure in simulation and/or portal imaging are often overlooked. The changes in miRNA levels arising in low dose radiation field and its effect to neoplastic process in cell will be pathfinder in terms of secondary cancers or second primary cancers. It is shown that there are differences between the level changes of miRNA in low dose fields which are overlooked in daily practical applications because of not resulting with acute or chronic side effect and the level changes of miRNA in high dose fields. With the help of verifying so-called differences in low dose fields which are seen in advanced radiation techniques, radiation oncologists must be careful when using these techniques in childhood cancers and the patient group which have long overall survival period. Additionally, demonstrating the pathway which is influenced by miRNA changes can provide us the opportunity to focus on the exact cancer type which has to be followed. So that we can detect the secondary cancers earlier and can treat them with long expected survival period.
微小 RNA(miRNA)是一种 RNA,产生内源性发夹形的副本,长 21-25 个核苷酸,小且单链。最近的研究表明,人类基因组中存在数百种 miRNA,它们负责多种细胞过程,包括控制发育时间、细胞增殖、细胞凋亡和肿瘤发生。miRNA 可以通过直接和间接刺激肿瘤抑制靶基因 p53,激活 DNA 损伤诱导的细胞凋亡、细胞周期停滞和衰老。DNA 损伤由多种应激因素组成,包括电离辐射、活性氧、紫外线暴露以及多柔比星和喜树碱等药物。辐射广泛用于发电的健康、学术和工业领域。由于不同领域广泛使用辐射,环境辐射暴露也在增加。虽然高剂量辐射暴露会导致 DNA 损伤,并通过加速恶性肿瘤形成导致活细胞分子电离。在放射治疗应用中,会评估高剂量辐射场的不良反应、治疗效果和继发性恶性肿瘤。需要时会重新创建剂量分布。另一方面,低剂量辐射场和模拟和/或门户成像中患者接受的剂量往往被忽视。低剂量辐射场中 miRNA 水平的变化及其对细胞肿瘤发生过程的影响将成为继发性癌症或第二原发癌症的探索者。研究表明,由于没有导致急性或慢性副作用,低剂量场中 miRNA 水平的变化与日常应用中忽略的高剂量场中 miRNA 水平的变化之间存在差异。随着验证所谓的低剂量场差异的帮助,放射肿瘤学家在儿童癌症和具有长期总体生存时间的患者群体中使用这些技术时必须小心。此外,证明受 miRNA 变化影响的途径可以为我们提供关注必须随访的确切癌症类型的机会。这样,我们可以更早地发现继发性癌症,并通过长期预期的生存时间对其进行治疗。