Evidence map›Paper›PMID 24481448›Full record

ArticleCell death & disease2014

miR-1207-5p and miR-1266 suppress gastric cancer growth and invasion by targeting telomerase reverse transcriptase.

L Chen, M-H Lü, D Zhang, N-B Hao, Y-H Fan, Y-Y Wu, S-M Wang, R Xie, D-C Fang, H Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 2 pooled it
10.1field-weighted citation impact, top 1% 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

80 citing papers in PubMed, 2 syntheses or guidelines pooled it, 135 citations in OpenAlex.

  1. Pooled it
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  8. Role of Non-Coding RNAs in Colorectal Cancer: Focus on Long Non-Coding RNAs.International journal of molecular sciences · 2022
    Review
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20 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.

L ChenDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
M-H LüDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
D ZhangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
N-B HaoDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
Y-H FanDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
Y-Y WuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
S-M WangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
R XieDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
D-C FangInstitute of Gastroenterology, Southwest Hospital, Third Military Medical University, Chongqing 400037, China.
H ZhangDepartment of Gastroenterology, The Second Affiliated Hospital, Chongqing Medical University, Chongqing 400037, China.
C-J HuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
S-M YangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China.
Army Medical University · CNXinqiao Hospital · CNDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

hTERT is the catalytic subunit of the telomerase complex. Elevated expression of hTERT is associated with the expansion and metastasis of gastric tumor. In this study, we aimed to identify novel tumor suppressor miRNAs that restrain hTERT expression. We began our screen for hTERT-targeting miRNAs with a miRNA microarray. miRNA candidates were further filtered by bioinformatic analysis, general expression pattern in different cell lines, gain-of-function effects on hTERT protein and the potential of these effects to suppress hTERT 3' untranslated region (3'UTR) luciferase activity. The clinical relevance of two miRNAs (miR-1207-5p and miR-1266) was evaluated by real-time RT-PCR. The effects of these miRNAs on cell growth, cell cycle and invasion of gastric cancer cells were measured with CCK-8, flow cytometry and transwell assays. Finally, the ability of these miRNAs to suppress the transplanted tumors was also investigated. Fourteen miRNAs were identified using a combination of bioinformatics and miRNA microarray analysis. Of these fourteen miRNAs, nine were expressed at significantly lower levels in hTERT-positive cell lines compared with hTERT-negative cell lines and five could downregulate hTERT protein expression. Only miR-1207-5p and miR-1266 interacted with the 3' UTR of hTERT and the expression levels of these two miRNAs were significantly decreased in gastric cancer tissues. These two miRNAs also inhibited gastric tumor growth in vitro and in vivo. Altogether, miR-1207-5p and miR-1266 were determined to be hTERT suppressors in gastric cancer, and the delivery of these two miRNAs represents a novel therapeutic strategy for gastric cancer treatment.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsCell ProliferationDown-RegulationHumansMicroRNAsNeoplasm InvasivenessStomach NeoplasmsTelomerase3' Untranslated RegionsMicroRNAsMIRN1207 microRNA, humanMIRN1266 microRNA, humanTelomeraseTERT protein, human

Identifiers

PMID24481448
PMCPMC4040688
OpenAlexW1964425329

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.