Evidence map›Paper›PMID 30451820›Full record

ArticleCell death & disease2018

Long non-coding RNA H19 confers 5-Fu resistance in colorectal cancer by promoting SIRT1-mediated autophagy.

Meng Wang, Dong Han, Ziming Yuan, Hanqing Hu, Zhixun Zhao, Runkun Yang, Yinghu Jin, Chaoxia Zou, Yinggang Chen, Guiyu Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
6.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

117 citing papers in PubMed, 186 citations in OpenAlex.

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  14. The role of SIRT1 in the development of gastrointestinal tumors.Frontiers in cell and developmental biology · 2025
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57 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Meng WangDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Dong HanDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, 150081, China.
Ziming YuanDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Hanqing HuDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Zhixun ZhaoDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Runkun YangDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Yinghu JinDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Chaoxia ZouDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, 150081, China.
Yinggang ChenDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Guiyu WangDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China.
Xu GaoDepartment of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, 150081, China. gaoxu_671227@163.com.
Xishan WangDepartment of Colorectal Surgery, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150081, China. wxshan1208@126.com.
Second Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy failure is the major cause of recurrence and poor prognosis in colorectal cancer (CRC) patients. The role of the differentially expressed lncRNAs in 5-Fluorouracil chemoresistance has not fully explained. Here, we observed lncRNA H19 was associated with the 5-Fu resistance in CRC. Quantitative analysis indicated that H19 was significantly increased in recurrent CRC patient samples. Kaplan-Meier survival analysis indicated that high H19 expression in CRC tissues was significantly associated with poor recurrent free survival. Our functional studies demonstrated that H19 promoted colorectal cells 5-Fu resistance. Mechanistically, H19 triggered autophagy via SIRT1 to induce cancer chemoresistance. Furthermore, bioinformatics analysis showed that miR-194-5p could directly bind to H19, suggesting H19 might work as a ceRNA to sponge miR-194-5p, which was confirmed by Dual-luciferase reporter assay and Immunoprecipitation assay. Extensively, our study also showed that SIRT1 is the novel direct target of miR-194-5p in CRC cells. Taken together, our study suggests that H19 mediates 5-Fu resistance in CRC via SIRT1 mediated autophagy. Our finding provides a novel mechanistic role of H19 in CRC chemoresistance, suggesting that H19 may function as a marker for prediction of chemotherapeutic response to 5-Fu.

Indexed as

AgedAutophagyCell Line, TumorCell ProliferationColorectal NeoplasmsDrug Resistance, NeoplasmFemaleFluorouracilGene Expression Regulation, NeoplasticHumansMaleMicroRNAsMiddle AgedRNA, Long NoncodingSirtuin 1FluorouracilH19 long non-coding RNAMicroRNAsMIRN194 microRNA, humanRNA, Long NoncodingSIRT1 protein, humanSirtuin 1

Identifiers

PMID30451820
PMCPMC6242979
OpenAlexW2901854772

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.