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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Mustafin, R.N.</author>
    </authors>
   </contributors>
   <titles>
    <title>INTERRELATION OF CIRCULAR RNAs WITH RETROELEMENTS AND microRNAs IN COLORECTAL CANCER DEVELOPMENT</title>
   </titles>
   <keywords>
    <keyword>circRNA</keyword>
    <keyword>colorectal cancer</keyword>
    <keyword>long noncoding RNA</keyword>
    <keyword>microRNA</keyword>
    <keyword>retroelements</keyword>
    <keyword>viral mimicry</keyword>
    <keyword>Scopus</keyword>
    <keyword>Белый список</keyword>
   </keywords>
   <dates>
    <year>2025</year>
    <pub-dates>
     <date>2026-05-02</date>
    </pub-dates>
   </dates>
   <doi>10.24412/2500-2295-2025-2-89-113</doi>
   <journal>OPERA MEDICA ET PHYSIOLOGICA</journal>
   <abstract>Abstract. Colorectal cancer (CRC) is characterized by a high mutational load and resistance to chemotherapy. Therefore, new approaches in the treatment of CRC include viral mimicry aimed at activating the expression of&#13;
retroelements to stimulate the immune response against cancer. However, the role of activated retroelements in CRC&#13;
carcinogenesis must be considered. Retroelements are implicated in CRC-specific chromothripsis and one of the&#13;
highest percentages of retroelement insertions in CRC of any cancer type has been identified. In addition,&#13;
retroelements are evolutionarily and functionally related to long noncoding RNAs, microRNAs, and circular RNAs.&#13;
Therefore, a differentiated approach is needed in targeted therapy of CRC using circular RNAs as tools (as the most&#13;
stable non-coding RNAs) to control the activity of retroelements. This article describes the analysis of scientific&#13;
literature on the relationship in the mechanisms of CRC development of retroelements with circular RNAs,&#13;
microRNAs and long non-coding RNAs. Data on the func-tioning of specific circular RNAs as tumor suppressors and&#13;
oncogenes with their influence on microRNA and the ex-pression of protein-coding genes are systematized. The&#13;
nature of changes in the expression of transposon-derived microRNAs interacting with circRNAs and long noncoding&#13;
RNAs in CRC is presented. The obtained data may form the basis for more correct epigenetic therapy of CRC with&#13;
activation of only those retroelements that are not involved in CRC carcinogenesis.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/5220</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/5413</url>
    </pdf-urls>
   </urls>
  </record>
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