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    ИсслСдованиС уровня экспрСссии Π³Π΅Π½ΠΎΠ²-ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ΠΎΠ² ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ‚ΠΈΠ²Π½ΠΎΠΉ активности Π² слизистой ΠΎΠ±ΠΎΠ»ΠΎΡ‡ΠΊΠ΅ толстой кишки ΠΏΡ€ΠΈ Ρ€Π°Π·Π»ΠΈΡ‡Π½ΠΎΠΉ ΠΏΠ°Ρ‚ΠΎΠ»ΠΎΠ³ΠΈΠΈ

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    Background. The search for molecular markers of colon diseases allowing highly specific and sensitive identification and differentiation of pathological processes is a clinically important problem. Expression levels of genes responsible for proliferation can reflect the changes in the affected tissues. The study objective is to perform comparative analysis of molecular and genetic markers of proliferative activity in benign and malignant neoplasms of the colon. Materials and methods. Analysis of the changes in proliferation markers (CCND1, с-MYC, Ki-67, HER2neu, TERT) in adenocarcinoma of the colon (n = 259), resection margin (about 15–20 cm from the tumor lesion) (n = 251), unchanged colon mucosa from healthy donors (n = 247), polyps (n = 28), unchanged colon mucosa intestinal polyposis (10–15 cm from the polyp) (n = 75) was performed using RT-PCR. Results and conclusion. It was shown that morphologically unchanged tissue of intestinal mucosa in malignant tumors has significant differences from normal tissue of healthy donors. Significant differences in the level of expression of genes responsible for the processes of proliferation, с-MYC, CCND1, TERT were found in benign hyperproliferative diseases (polyps). Moreover, these changes were specific to the type of pathological process, which allows us to consider these genes as the most promising candidates in the development of a differential method for diagnosing colon diseases.Π’Π²Π΅Π΄Π΅Π½ΠΈΠ΅. Поиск молСкулярных ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ΠΎΠ² диагностики Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠΉ толстой кишки, способных с высокой Ρ‡ΡƒΠ²ΡΡ‚Π²ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΡΡ‚ΡŒΡŽ ΠΈ ΡΠΏΠ΅Ρ†ΠΈΡ„ΠΈΡ‡Π½ΠΎΡΡ‚ΡŒΡŽ Π²Ρ‹ΡΠ²Π»ΡΡ‚ΡŒ ΠΈ Π΄ΠΈΡ„Ρ„Π΅Ρ€Π΅Π½Ρ†ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ патологичСский процСсс, являСтся Π°ΠΊΡ‚ΡƒΠ°Π»ΡŒΠ½ΠΎΠΉ клиничСски Π²Π°ΠΆΠ½ΠΎΠΉ Π·Π°Π΄Π°Ρ‡Π΅ΠΉ. Π£Ρ€ΠΎΠ²Π΅Π½ΡŒ экспрСссии Π³Π΅Π½ΠΎΠ², отвСтствСнных Π·Π° процСссы ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ†ΠΈΠΈ, ΠΌΠΎΠΆΠ΅Ρ‚ ΠΎΡ‚Ρ€Π°ΠΆΠ°Ρ‚ΡŒ ΠΊΠ°Ρ€Ρ‚ΠΈΠ½Ρƒ ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠΉ Π² тканях ΠΏΠΎΡ€Π°ΠΆΠ΅Π½Π½ΠΎΠ³ΠΎ ΠΎΡ€Π³Π°Π½Π°. ЦСль исслСдования – ΡΡ€Π°Π²Π½ΠΈΡ‚Π΅Π»ΡŒΠ½Ρ‹ΠΉ Π°Π½Π°Π»ΠΈΠ· молСкулярно-гСнСтичСских ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ΠΎΠ² ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ‚ΠΈΠ²Π½ΠΎΠΉ активности ΠΏΡ€ΠΈ доброкачСствСнных ΠΈ злокачСствСнных новообразованиях толстой кишки. ΠœΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π»Ρ‹ ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹. ΠœΠ΅Ρ‚ΠΎΠ΄ΠΎΠΌ ΠΏΠΎΠ»ΠΈΠΌΠ΅Ρ€Π°Π·Π½ΠΎΠΉ Ρ†Π΅ΠΏΠ½ΠΎΠΉ Ρ€Π΅Π°ΠΊΡ†ΠΈΠΈ Π² Ρ€Π΅Π°Π»ΡŒΠ½ΠΎΠΌ Π²Ρ€Π΅ΠΌΠ΅Π½ΠΈ ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½ Π°Π½Π°Π»ΠΈΠ· ΠΈΠ·ΠΌΠ΅Π½Π΅Π½ΠΈΠΉ экспрСссии ΠΌΠ°Ρ€ΠΊΠ΅Ρ€ΠΎΠ² ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ†ΠΈΠΈ (CCND1, с-MYC, Ki-67, HER2neu, TERT) Π² ΡΠ»Π΅Π΄ΡƒΡŽΡ‰ΠΈΡ… тканях: Π°Π΄Π΅Π½ΠΎΠΊΠ°Ρ€Ρ†ΠΈΠ½ΠΎΠΌΡ‹ толстой кишки (n = 259), края Ρ€Π΅Π·Π΅ΠΊΡ†ΠΈΠΈ (ΠΎΠΊΠΎΠ»ΠΎ 15–20 см ΠΎΡ‚ ΠΎΠΏΡƒΡ…ΠΎΠ»Π΅Π²ΠΎΠ³ΠΎ ΡƒΠ·Π»Π°) (n = 251), Π½Π΅ΠΈΠ·ΠΌΠ΅Π½Π΅Π½Π½ΠΎΠΉ слизистой ΠΎΠ±ΠΎΠ»ΠΎΡ‡ΠΊΠΈ толстой кишки Π·Π΄ΠΎΡ€ΠΎΠ²Ρ‹Ρ… Π΄ΠΎΠ½ΠΎΡ€ΠΎΠ² (n = 247), ΠΏΠΎΠ»ΠΈΠΏΠΎΠ² (n = 28), Π½Π΅ΠΈΠ·ΠΌΠ΅Π½Π΅Π½Π½ΠΎΠΉ слизистой ΠΎΠ±ΠΎΠ»ΠΎΡ‡ΠΊΠΈ толстой кишки ΠΏΡ€ΠΈ ΠΏΠΎΠ»ΠΈΠΏΠ°Ρ… (10–15 см ΠΎΡ‚ ΠΏΠΎΠ»ΠΈΠΏΠ°) (n = 75). Π Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹ ΠΈ Π·Π°ΠΊΠ»ΡŽΡ‡Π΅Π½ΠΈΠ΅. УстановлСно, Ρ‡Ρ‚ΠΎ Π² тканях ΠΏΠΎΠ»ΠΈΠΏΠΎΠ² толстой кишки Π½Π°Π±Π»ΡŽΠ΄Π°ΡŽΡ‚ΡΡ достовСрныС различия Π² ΡƒΡ€ΠΎΠ²Π½Π΅ экспрСссии Π³Π΅Π½ΠΎΠ², отвСтствСнных Π·Π° процСссы ΠΏΡ€ΠΎΠ»ΠΈΡ„Π΅Ρ€Π°Ρ†ΠΈΠΈ (с-MYC, CCND1, TERT). ВыявлСнныС различия спСцифичны для Ρ‚ΠΈΠΏΠ° патологичСского процСсса, Ρ‡Ρ‚ΠΎ позволяСт Ρ€Π°ΡΡΠΌΠ°Ρ‚Ρ€ΠΈΠ²Π°Ρ‚ΡŒ Π΄Π°Π½Π½Ρ‹Π΅ Π³Π΅Π½Ρ‹ Π² качСствС Π½Π°ΠΈΠ±ΠΎΠ»Π΅Π΅ пСрспСктивных ΠΊΠ°Π½Π΄ΠΈΠ΄Π°Ρ‚ΠΎΠ² ΠΏΡ€ΠΈ Ρ€Π°Π·Ρ€Π°Π±ΠΎΡ‚ΠΊΠ΅ Π΄ΠΈΡ„Ρ„Π΅Ρ€Π΅Π½Ρ†ΠΈΠ°Π»ΡŒΠ½ΠΎΠ³ΠΎ ΠΌΠ΅Ρ‚ΠΎΠ΄Π° диагностики Π·Π°Π±ΠΎΠ»Π΅Π²Π°Π½ΠΈΠΉ толстой кишки

    Investigation of the expression level of genes-markers of proliferative activity in the mucosa at normal and various pathologies of the colon

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    Background. The search for molecular markers of colon diseases allowing highly specific and sensitive identification and differentiation of pathological processes is a clinically important problem. Expression levels of genes responsible for proliferation can reflect the changes in the affected tissues. The study objective is to perform comparative analysis of molecular and genetic markers of proliferative activity in benign and malignant neoplasms of the colon. Materials and methods. Analysis of the changes in proliferation markers (CCND1, с-MYC, Ki-67, HER2neu, TERT) in adenocarcinoma of the colon (n = 259), resection margin (about 15–20 cm from the tumor lesion) (n = 251), unchanged colon mucosa from healthy donors (n = 247), polyps (n = 28), unchanged colon mucosa intestinal polyposis (10–15 cm from the polyp) (n = 75) was performed using RT-PCR. Results and conclusion. It was shown that morphologically unchanged tissue of intestinal mucosa in malignant tumors has significant differences from normal tissue of healthy donors. Significant differences in the level of expression of genes responsible for the processes of proliferation, с-MYC, CCND1, TERT were found in benign hyperproliferative diseases (polyps). Moreover, these changes were specific to the type of pathological process, which allows us to consider these genes as the most promising candidates in the development of a differential method for diagnosing colon diseases
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