Evidence map›Paper›PMID 28792527›Full record

ArticlePloS one2017

The long noncoding RNA XIAP-AS1 promotes XIAP transcription by XIAP-AS1 interacting with Sp1 in gastric cancer cells.

Jun Cai, Dong Wang, Zhi-Gang Bai, Jie Yin, Jun Zhang, Zhong-Tao Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Jun CaiDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.
Dong WangDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.
Zhi-Gang BaiDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.
Jie YinDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.
Jun ZhangDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.
Zhong-Tao ZhangDepartment of General Surgery, Beijing Friendship Hospital Affiliated to Capital Medical University, Beijing, China.ORCID http://orcid.org/0000-0001-6406-4829
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play roles in the tumorigenesis, proliferation and metastasis of tumor cells. Previous studies indicate that the transcription factor Sp1 is responsible for transcription of the XIAP gene, but it is unknown whether lncRNAs are involved in XIAP transcription. Herein, we identified a novel lncRNA, denoted as XIAP-AS1, transcribed from the first intron of the complementary strand of the XIAP gene. Using RNA FISH, cell fractionation and qRT-PCR, XIAP-AS1 was determined to be located primarily in the nucleus. After various XIAP-AS1 deletion mutants were expressed, RIP assays showed that only the full-length XIAP-AS1 RNA interacted with Sp1 and thereby participated in XIAP transcription. ChIP assays showed that XIAP-AS1 knockdown decreased the binding of Sp1 to the promoter region of XIAP. XIAP-AS1 knockdown promoted tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL)-induced apoptosis in gastric tumor cells, as cleaved caspase-3 and caspase-9 was detected. Moreover, in an in vivo mouse xenograft model, tumor cell proliferation was inhibited by XIAP-AS1 knockdown in response to TRAIL administration. In conclusion, our results indicate that XIAP-AS1 is involved in XIAP transcription by interacting with Sp1. Additionally, XIAP-AS1 is a potential target for TRAIL-induced apoptosis in gastric cancer cells.

Indexed as

AnimalsApoptosisCarcinogenesisCell Line, TumorCell NucleusCell ProliferationCytoplasmFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMice, Inbred BALB CMice, NudeNeoplasm TransplantationPromoter Regions, GeneticRNA, Long Noncodinglong noncoding RNA XIAP-AS1, humanRNA, Long NoncodingSp1 Transcription FactorTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanXIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID28792527
PMCPMC5549724
OpenAlexW2743760745

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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.