Home > Publications database > Assessment of a Serum Microrna Risk Score for Colorectal Cancer among Participants of Screening Colonoscopy at Various Stages of Colorectal Carcinogenesis. > print |
001 | 181117 | ||
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100 | 1 | _ | |a Raut, Janhavi |0 P:(DE-He78)43ea0369702f56d45fa4a32df9f49aca |b 0 |e First author |u dkfz |
245 | _ | _ | |a Assessment of a Serum Microrna Risk Score for Colorectal Cancer among Participants of Screening Colonoscopy at Various Stages of Colorectal Carcinogenesis. |
260 | _ | _ | |a Basel |c 2022 |b MDPI |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1660554892_9214 |2 PUB:(DE-HGF) |
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520 | _ | _ | |a We recently derived and validated a serum-based microRNA risk score (miR-score) which predicted colorectal cancer (CRC) occurrence with very high accuracy within 14 years of follow-up in a large population-based cohort. Here, we aimed to assess and compare the distribution of the miR-score among participants of screening colonoscopy at various stages of colorectal carcinogenesis. MicroRNAs (miRNAs) were profiled by quantitative-real-time-polymerase-chain-reaction in the serum samples of screening colonoscopy participants with CRC (n = 52), advanced colorectal adenoma (AA, n = 100), non-advanced colorectal adenoma (NAA, n = 88), and participants free of colorectal neoplasms (n = 173). The mean values of the miR-score were compared between groups by the Mann-Whitney U test. The associations of the miR-score with risk for colorectal neoplasms were evaluated using logistic regression analyses. MicroRNA risk scores were significantly higher among participants with AA than among those with NAA (p = 0.027) and those with CRC (p = 0.014), whereas no statistically significant difference was seen between those with NAA and those with no colorectal neoplasms (p = 0.127). When comparing adjacent groups, miR-scores were inversely associated with CRC versus AA and positively associated with AA versus NAA [odds ratio (OR), 0.37 (95% confidence interval (CI), 0.16-0.86) and OR, 2.22 (95% CI, 1.06-4.64) for the top versus bottom tertiles, respectively]. Our results are consistent with the hypothesis that a high miR-score may be indicative of an increased CRC risk by an increased tendency of progression from non-advanced to advanced colorectal neoplasms, along with a change of the miR-patterns after CRC manifestation. |
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650 | _ | 7 | |a blood-based |2 Other |
650 | _ | 7 | |a colorectal cancer |2 Other |
650 | _ | 7 | |a miRNA |2 Other |
650 | _ | 7 | |a risk stratification |2 Other |
650 | _ | 7 | |a risk-adapted screening |2 Other |
700 | 1 | _ | |a Bhardwaj, Megha |0 P:(DE-He78)ac7aed57f26354e8a484b5d257f7bada |b 1 |u dkfz |
700 | 1 | _ | |a Niedermaier, Tobias |0 P:(DE-He78)20dc4ad11ff465acf5b99f1e679e10b7 |b 2 |u dkfz |
700 | 1 | _ | |a Miah, Kaya |0 P:(DE-He78)b97fc5666ea8f9db9ef499de6b2397cf |b 3 |u dkfz |
700 | 1 | _ | |a Schrotz-King, Petra |0 P:(DE-He78)01ef71f71b01a3ec3b698653fd43fe86 |b 4 |u dkfz |
700 | 1 | _ | |a Brenner, Hermann |0 P:(DE-He78)90d5535ff896e70eed81f4a4f6f22ae2 |b 5 |e Last author |u dkfz |
773 | _ | _ | |a 10.3390/cells11152462 |g Vol. 11, no. 15, p. 2462 - |0 PERI:(DE-600)2661518-6 |n 15 |p 2462 |t Cells |v 11 |y 2022 |x 2073-4409 |
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