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MiR-30a and miR-200c differentiate cholangiocarcinomas from gastrointestinal cancer liver metastasesopen access

Authors
Park, Jun WonJeong, Jong MinCho, Kye SooCho, Soo YoungCheon, Jae HeeChoi, Dong HoPark, Sang JaeKim, Hark Kyun
Issue Date
Apr-2021
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS ONE, v.16, no.4, pp.1 - 14
Indexed
SCIE
SCOPUS
Journal Title
PLOS ONE
Volume
16
Number
4
Start Page
1
End Page
14
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/1248
DOI
10.1371/journal.pone.0250083
ISSN
1932-6203
Abstract
Prior studies have demonstrated the utility of microRNA assays for predicting some cancer tissue origins, but these assays need to be further optimized for predicting the tissue origins of adenocarcinomas of the liver. We performed microRNA profiling on 195 frozen primary tumor samples using 14 types of tumors that were either adenocarcinomas or differentiated from adenocarcinomas. The 1-nearest neighbor method predicted tissue-of-origin in 33 samples of a test set, with an accuracy of 93.9% at feature selection p values ranging from 10(-4) to 10(-10). According to binary decision tree analyses, the overexpression of miR-30a and the underexpression of miR-200 family members (miR-200c and miR-141) differentiated intrahepatic cholangiocarcinomas from extrahepatic adenocarcinomas. When binary decision tree analyses were performed using the test set, the prediction accuracy was 84.8%. The overexpression of miR-30a and the reduced expressions of miR-200c, miR-141, and miR-425 could distinguish intrahepatic cholangiocarcinomas from liver metastases from the gastrointestinal tract.
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