STUDY OF VARIABILITY IN THE ACTIVITY OF RIBOSOMAL CISTRONES IN COLORECTAL CANCER

Nino Chigvinadze, I. Pantsulaia, T. Jokhadze
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Abstract

According to the World Health Organization, colon cancer is one of the most common cancers. By 2020, approximately 1,900,000 cases of CRC were detected worldwide (a total of 10%). In 2020, American Cancer Society 104,610 new cases of CRC were identified and 53,200 patients died. Similar to other tumors colon cancer (CRC) is a genetically inherited multifactorial disease. It is established that genetic, immunologic, as well as environmental factors, all play significant role in CRC development and metastasis. As mentioned, carcinogenesis is associated with the whole number of genetic phenomena ongoing in certain groups of the genes; it is of staged nature and includes interactions of gene suppressors and oncogenes. Many genes responsible for CRC development were identified, family forms were described as well. In particular, high risk of CRC development in case of family history of adenomatous polyposis was demonstrated. As mentioned, neoplastic variability of the tumors is associated with changed morphogenesis of the nucleus, in turn, playing certain role in regulation of the suppressor genes p53, APC and pro-carcinogenesis KRAS.
结直肠癌中核糖体顺酮活性变异性的研究
根据世界卫生组织的数据,结肠癌是最常见的癌症之一。到2020年,全球约有190万例结直肠癌被发现(总数为10%)。2020年,美国癌症协会发现了104,610例新的结直肠癌病例,53,200例患者死亡。与其他肿瘤类似,结肠癌(CRC)是一种遗传性多因素疾病。研究发现,遗传、免疫和环境因素在结直肠癌的发生和转移中都起着重要的作用。如前所述,致癌作用与某些基因群中正在发生的一系列遗传现象有关;它是阶段性的,包括基因抑制因子和癌基因的相互作用。许多与结直肠癌发展有关的基因被确定,家族形式也被描述。特别是,有腺瘤性息肉病家族史的人患结直肠癌的风险较高。如前所述,肿瘤的肿瘤变异性与细胞核形态发生的改变有关,进而对抑制基因p53、APC和促癌基因KRAS起一定的调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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