Evidence map›Paper›PMID 27634385›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Overexpression of Long Non-Coding RNA TUG1 Promotes Colon Cancer Progression.

Hui-Yuan Zhai, Ming-Hua Sui, Xiao Yu, Zhen Qu, Jin-Chen Hu, Hai-Qing Sun, Hai-Tao Zheng, Kai Zhou, Li-Xin Jiang

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 citations in OpenAlex.

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  9. Role of long noncoding RNA taurine-upregulated gene 1 in cancers.Molecular medicine (Cambridge, Mass.) · 2021
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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

9 authors at 2 institutions in 1 country.

Hui-Yuan ZhaiDepartment of Gastrointestinal Surgery, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Ming-Hua SuiDepartment of Oncology, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Xiao YuDepartment ofEndocrinology, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Zhen QuDepartment of Oncology, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Jin-Chen HuDepartment of Gastrointestinal Surgery, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Hai-Qing SunDepartment of Gastrointestinal Surgery, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Hai-Tao ZhengDepartment of Gastrointestinal Surgery, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Kai ZhouInpatient Area Of Genenral Surgery Department II, The First People`s Hospital Of Taian, Taian, Shandong, China (mainland).
Li-Xin JiangDepartment of Gastrointestinal Surgery, Yantai Yuhuangding Hospital, Yantai, Shandong, China (mainland).
Yuhuangding Hospital · CNTaizhou First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Colon cancer is one of the most prevalent and deadly cancers worldwide. It is still necessary to further define the mechanisms and explore therapeutic targets of colon cancer. Dysregulation of long noncoding RNAs (lncRNAs) has been shown to be correlated with diverse biological processes, including tumorigenesis. This study aimed to characterize the biological mechanism of taurine-upregulated gene 1 (TUG1) in colon cancer. MATERIAL AND METHODS qRT-PCR was used to analyze the expression level of TUG1 and p63 in 75 colon cancer tissues and the matched adjacent non-tumor tissue. In vitro, cultured colon cancer cell lines HCT-116 and LoVo were used as cell models. TUG1 and p63 were silenced via transferring siRNA into HCT-116 or LoVo. The effects of TUG1 were investigated by examining cell proliferation, apoptosis, and migration. RESULTS Among the 75 colon cancer cases, the expression of TUG1 was significantly higher in colon cancer tissues compared with the matched adjacent non-tumor tissue, while p63 expression was lower in the tumor tissue. In HCT-116 and LoVo, the expression of TUG1 was significantly increased by p63 siRNA transfection. Furthermore, down-regulation of TUG1 by siRNA significantly inhibited the cell proliferation and promoted colon cancer cell apoptosis. In addition, inhibition of TUG1 expression significantly blocked the cell migration ability of colon cancer cells. CONCLUSIONS LncRNA TUG1 may serve as a potential oncogene for colon cancer. Overexpressed TUG1 may contribute to promoting cell proliferation and migration in colon cancer cells.

Indexed as

AdultAgedAged, 80 and overApoptosisCell Line, TumorCell MovementCell ProliferationColonic NeoplasmsDisease ProgressionFemaleHumansMaleMembrane ProteinsMiddle AgedRNA, Long NoncodingRNA, Small InterferingCKAP4 protein, humanMembrane ProteinsRNA, Long NoncodingRNA, Small InterferingTaurineTUG1 long noncoding RNA, human

Identifiers

PMID27634385
PMCPMC5027858
OpenAlexW2518772378

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.