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Identification of miRNAs Present in Cell- and Plasma-Derived Extracellular Vesicles-Possible Biomarkers of Colorectal Cancer.
Lenart, Marzena; Sieminska, Izabela; Szatanek, Rafal; Mordel, Anna; Szczepanik, Antoni; Rubinkiewicz, Mateusz; Siedlar, Maciej; Baj-Krzyworzeka, Monika.
Afiliación
  • Lenart M; Department of Clinical Immunology, Medical College, Jagiellonian University, 30-663 Krakow, Poland.
  • Sieminska I; Department of Clinical Immunology, Medical College, Jagiellonian University, 30-663 Krakow, Poland.
  • Szatanek R; Institute of Veterinary Sciences, University Center of Veterinary Medicine JU-AU, University of Agriculture in Krakow, 30-059 Krakow, Poland.
  • Mordel A; Department of Clinical Immunology, Medical College, Jagiellonian University, 30-663 Krakow, Poland.
  • Szczepanik A; Department of Clinical Immunology, University Children's Hospital of Cracow, 30-663 Krakow, Poland.
  • Rubinkiewicz M; Third Department of Surgery, Faculty of Medicine, Jagiellonian University Medical College, 31-202 Krakow, Poland.
  • Siedlar M; Second Department of Surgery, Jagiellonian University Medical College, 30-688 Krakow, Poland.
  • Baj-Krzyworzeka M; Department of Clinical Immunology, Medical College, Jagiellonian University, 30-663 Krakow, Poland.
Cancers (Basel) ; 16(13)2024 Jul 05.
Article en En | MEDLINE | ID: mdl-39001526
ABSTRACT
Globally, an increasing prevalence of colorectal cancer (CRC) prompts a need for the development of new methods for early tumor detection. MicroRNAs (also referred to as miRNAs) are short non-coding RNA molecules that play a pivotal role in the regulation of gene expression. MiRNAs are effectively transferred to extracellular vesicle (EVs) membrane sacs commonly released by cells. Our study aimed to examine the expression of miRNAs in four CRC cell lines and EVs derived from them (tumor EVs) in comparison to the normal colon epithelium cell line and its EVs. EVs were isolated by ultracentrifugation from the culture supernatant of SW480, SW620, SW1116, HCT116 and normal CCD841CoN cell lines and characterized according to the MISEV2023 guidelines. MiRNAs were analyzed by small RNA sequencing and validated by quantitative PCR. The performed analysis revealed 22 common miRNAs highly expressed in CRC cell lines and effectively transferred to tumor EVs, including miR-9-5p, miR-182-5p, miR-196b-5p, miR-200b-5p, miR-200c-3p, miR-425-5p and miR-429, which are associated with development, proliferation, invasion and migration of colorectal cancer cells, as well as in vesicle maturation and transport-associated pathways. In parallel, normal cells expressed miRNAs, such as miR-369 and miR-143, which play a role in proinflammatory response and tumor suppression. The analysis of selected miRNAs in plasma-derived EVs and tumor samples from CRC patients showed the similarity of miRNA expression profile between the patients' samples and CRC cell lines. Moreover, miR-182-5p, miR-196-5p, miR-425-5p and miR-429 were detected in several EV samples isolated from patients' plasma. Our results suggest that miR-182-5p, miR-196b-5p and miR-429 are differentially expressed between EVs from CRC patients and healthy donors, which might have clinical implications.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancers (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Polonia
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