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학술저널
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이예은 (강원대학교) 이지연 (Yonsei University College of Medicine) 이용선 (국립암센터국제암대학원대학교) Jiyoung Joan Jang (National Cancer Center) Hyeonju Woo (Ewha Womans University) 최해인 (한양대학교) Young Gyu Chai (Hanyang University) 김태경 (POSTECH) 김태수 (이화여자대학교) 김락균 (연세대학교) Sun Shim Choi (Kangwon National University)
저널정보
한국분자세포생물학회 Molecules and Cells Molecules and Cells 제44권 제9호
발행연도
2021.9
수록면
658 - 669 (12page)
DOI
10.14348/molcells.2021.0173

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Enhancers have been conventionally perceived as cis-acting elements that provide binding sites for trans-acting factors. However, recent studies have shown that enhancers are transcribed and that these transcripts, called enhancer RNAs (eRNAs), have a regulatory function. Here, we identified putative eRNAs by profiling and determining the overlap between noncoding RNA expression loci and eRNA-associated histone marks such as H3K27ac and H3K4me1 in hepatocellular carcinoma (HCC) cell lines. Of the 132 HCC-derived noncoding RNAs, 74 overlapped with the eRNA loci defined by the FANTOM consortium, and 65 were located in the proximal regions of genes differentially expressed between normal and tumor tissues in TCGA dataset. Interestingly, knockdown of two selected putative eRNAs, THUMPD3-AS1 and LINC01572, led to downregulation of their target mRNAs and to a reduction in the proliferation and migration of HCC cells. Additionally, the expression of these two noncoding RNAs and target mRNAs was elevated in tumor samples in the TCGA dataset, and high expression was associated with poor survival of patients. Collectively, our study suggests that noncoding RNAs such as THUMPD3-AS1 and LINC01572 (i.e., putative eRNAs) can promote the transcription of genes involved in cell proliferation and differentiation and that the dysregulation of these noncoding RNAs can cause cancers such as HCC.

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