Evidence map›Paper›PMID 31619579›Full record

ArticleAging2019

Long non-coding SBF2-AS1 acting as a competing endogenous RNA to sponge microRNA-142-3p to participate in gemcitabine resistance in pancreatic cancer via upregulating TWF1.

Yong-Qiang Hua, Yao-Dong Zhu, Guo-Qun Xie, Ke Zhang, Jie Sheng, Zhen-Feng Zhu, Zhou-Yu Ning, Hao Chen, Zhen Chen, Zhi-Qiang Meng and 1 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 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

11 authors at 1 institution in 1 country.

Yong-Qiang HuaMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Yao-Dong ZhuChinese Integrative Medicine Oncology Department, First Affiliated Hospital of Medical University of Anhui, Hefei 230000, Anhui Province, PR China.
Guo-Qun XieOncology Department, Yueyang Hospital of Integrative Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 200437, PR China.
Ke ZhangMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Jie ShengMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Zhen-Feng ZhuMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Zhou-Yu NingMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Hao ChenMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Zhen ChenMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Zhi-Qiang MengMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Lu-Ming LiuMinimally Invasive Treatment Center, Fudan University Shanghai Cancer Center, Shanghai 200032, PR China.
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study is implemented to probe into the function of lncRNA SBF2-AS1 as a competing endogenous RNA (ceRNA) to sponge microRNA-142-3p (miR-142-3p) in modulating TWF1 expression in the gemcitabine resistance of pancreatic cancer.

resultsLncRNA SBF2-AS1 was highly expressed in pancreatic cancer tissues and cells. SBF2-AS1 was found to be associated with gemcitabine resistance in pancreatic cancer. Knock-down of SBF2-AS1 inhibited proliferation, epithelial-mesenchymal transition, while promoting apoptosis of gemcitabine resistant pancreatic cancer cells. SBF2-AS1 inhibited the expression of TWF1 by competitively binding with miR-142-3p in pancreatic cancer.

conclusionOur study demonstrates that knock-down of SBF2-AS1 inhibits the expression of TWF1 by competitively binding with miR-142-3p to induce gemcitabine resistance in pancreatic cancer.

methodsExpression of SBF2-AS1 was tested in pancreatic cancer tissues and cells. Construction of AsPC-1/GEM and PANC-1/GEM cells with low expression of SBF2-AS1 was performed to determine the biological behaviors of drug-resistant cells. AsPC-1 and PANC-1 cells expressing SBF2-AS1 and/or miR-142-3p were constructed and treated with different concentrations of gemcitabine to detect the sensitivity of the cells to gemcitabine. The binding relationship between SBF2-AS1 and miR-142-3p and between miR-142-3p and TWF1 were determined.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsCell Line, TumorDeoxycytidineFemaleGemcitabineGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMaleMicrofilament ProteinsMicroRNAsMiddle AgedPancreatic NeoplasmsProtein-Tyrosine KinasesRNA, Long NoncodingAntineoplastic AgentsDeoxycytidineGemcitabinelong non-coding RNA SBF2-AS1, humanMicrofilament ProteinsMicroRNAsMIRN142 microRNA, humanProtein-Tyrosine KinasesRNA, Long NoncodingTWF1 protein, humancompeting endogenous RNAgemcitabine resistancelong non-coding SBF2-AS1microRNA-142-3ppancreatic cancer

Identifiers

PMID31619579
PMCPMC6834408
OpenAlexW2981205949

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.