Evidence map›Paper›PMID 33125117›Full record

ArticleInternational journal of molecular medicine2020

Hesperidin administration suppresses the proliferation of lung cancer cells by promoting apoptosis via targeting the miR‑132/ZEB2 signalling pathway.

Song Tan, Lingling Dai, Pengcheng Tan, Wei Liu, Yuejun Mu, Jinguo Wang, Xiaoming Huang, Aihua Hou

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 35 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

8 authors at 1 institution in 1 country.

Song TanDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Lingling DaiDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Pengcheng TanDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Wei LiuDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Yuejun MuDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Jinguo WangDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Xiaoming HuangDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Aihua HouDepartment of Oncology, Yantai Hospital of Traditional Chinese Medicine, Yantai, Shandong 264000, P.R. China.
Yantaishan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This aim of the present study was to identify the relationship between hesperidin and microRNA (miR)‑132, and to study the role of hesperidin and miR‑132 in the pathogenesis of non‑small cell lung cancer (NSCLC). Computational analysis and luciferase assays were performed to identify the target of miR‑132. Subsequently, reverse transcription‑quantitative PCR and western blot assays were used to detect the effect of miR‑132 and hesperidin on the expression of haematological and neurological expressed 1 (HN1) and zinc finger E‑box binding homeobox 2 (ZEB2). Finally, MTT assays and flow cytometry analysis were used to investigate the effect of hesperidin on cell proliferation and apoptosis. ZEB2 was identified as a target gene of miR‑132, and transfection with miR‑132 mimic reduced the luciferase activity of the wild‑type ZEB2 3'‑untranslated region (3'‑UTR) but not that of the mutant ZEB2 3'‑UTR. By contrast, neither transfection with miR‑132 mimic nor hesperidin treatment affected HN1 expression. Furthermore, hesperidin evidently inhibited cell proliferation and promoted apoptosis in a dose‑dependent manner. Furthermore, the tumour volume in rats transplanted with NSCLC cells and treated with hesperidin was notably smaller compared with that in rats transplanted with NSCLC cells alone, while treatment with hesperidin significantly reduced the colony formation efficiency of NSCLC cells by increasing miR‑132 expression and decreasing ZEB2 expression. To the best of our knowledge, the present study demonstrated for the first time that the administration of hesperidin decreased the expression of ZEB2 by upregulating the expression of miR‑132, which in turn promoted apoptosis and inhibited the proliferation of NSCLC cells.

Indexed as

ApoptosisSignal TransductionAnimalsBase SequenceCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHesperidinHumansLung NeoplasmsMaleMicroRNAsRats, Sprague-DawleyTumor BurdenTumor Stem Cell AssayHesperidinMicroRNAsMIRN132 microRNA, humanZEB2 protein, humanZinc Finger E-box Binding Homeobox 2

Identifiers

PMID33125117
PMCPMC7595658
OpenAlexW3093119708

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.