Evidence map›Paper›PMID 26036635›Full record

ArticleOncotarget2015

Tanshinones suppress AURKA through up-regulation of miR-32 expression in non-small cell lung cancer.

Zhong-Liang Ma, Bing-Jie Zhang, D Tao Wang, Xue Li, Jia-Li Wei, Bo-Tao Zhao, Yan Jin, Yan-Li Li, You-Xin Jin

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

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  13. Frontiers in pharmacology · 2022
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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.

Zhong-Liang MaSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Bing-Jie ZhangSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
D Tao WangSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Xue LiSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Jia-Li WeiSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Bo-Tao ZhaoSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Yan JinInstitute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.
Yan-Li LiSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
You-Xin JinSchool of Life Sciences, Shanghai University, Shanghai 200444, China.
Shanghai University · CNShenzhen Institutes of Advanced Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tanshinone is the liposoluble constituent of Salia miltiorrhiza, a root used in traditional herbal medicine which is known to possess certain health benefits. Although it is known that tanshinones, including tanshinone I (T1), tanshinone IIA (T2A), and cryptotanshinone (CT), can inhibit the growth of lung cancer cells in vitro, the mechanism under which they act is still unclear. AURKA, an oncogene, encodes a serine-threonine kinase which regulates mitotic processes in mammalian cells. Here, we reported that tanshinones mediate AURKA suppression partly through up-regulating the expression of miR-32. We found that tanshinones could inhibit cell proliferation, promote apoptosis, and impede cell-cycle progression, thus performing an antineoplastic function in non-small cell lung cancer (NSCLC). Additionally, we demonstrated that tanshinones attained these effects in part by down-regulating AURKA, corroborating previous reports. Our results showed that in NSCLC, similar effects were obtained with knock-down of the AURKA gene by siRNA. We also verified that AURKA was the direct target of miR-32. Collectively, our results demonstrated that tanshinones could inhibit NSCLC by suppressing AURKA via up-regulating the expressions of miR-32 and other related miRNAs.

Indexed as

AbietanesAntineoplastic Agents, PhytogenicApoptosisAurora Kinase ACarcinoma, Non-Small-Cell LungCell CycleCell Line, TumorCell ProliferationHEK293 CellsHumansLung NeoplasmsMicroRNAsUp-RegulationAbietanesAntineoplastic Agents, PhytogenicAURKA protein, humanAurora Kinase AMicroRNAsMIRN23a microRNA, humantanshinoneAURKAmiRNAnon-small cell lung cancertanshinone

Identifiers

PMID26036635
PMCPMC4652991
OpenAlexW1912417670

What OpenQuestion holds

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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.