Evidence map›Paper›PMID 29781054›Full record

ArticleDigestive diseases and sciences2018

Isoalantolactone Inhibits Esophageal Squamous Cell Carcinoma Growth Through Downregulation of MicroRNA-21 and Derepression of PDCD4.

Shi-Wang Wen, Yue-Feng Zhang, Yong Li, Yan-Zhao Xu, Zhen-Hua Li, Huilai Lü, Yong-Gang Zhu, Zhen-Xu Liu, Zi-Qiang Tian

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Article in Digestive diseases and sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 10 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

9 authors at 2 institutions in 1 country.

Shi-Wang WenDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Yue-Feng ZhangDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Yong LiDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Yan-Zhao XuDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Zhen-Hua LiDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Huilai LüDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Yong-Gang ZhuDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Zhen-Xu LiuDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China.
Zi-Qiang TianDepartment of Thoracic Surgery, Fourth Hospital, Hebei Medical University, Shijiazhuang, 050011, China. tizq12@vip.163.com.
Hebei Medical University · CNFourth Hospital of Hebei Medical University · CN

Funding

the Key Projects of Medical Research 20110488
6 · The paper itself

Abstract

backgroundThis study was designed to explore the anticancer potential of isoalantolactone, a sesquiterpene lactone, on esophageal squamous cell carcinoma (ESCC) cells and associated molecular mechanisms.

methodsESCC cell lines were treated with isoalantolactone or vehicle and tested for viability, proliferation, cell cycle distribution, and apoptosis. Xenograft tumor studies in nude mice were done to examine the in vivo anticancer effect of isoalantolactone.

resultsIsoalantolactone treatment reduced ESCC cell viability and proliferation in vitro, which was coupled with induction of G0/G1 cell cycle arrest and apoptosis. In vivo studies confirmed the growth-suppressive effect of isoalantolactone on ESCC cells. Mechanistically, isoalantolactone reversed microRNA-21-mediated repression of programmed cell death 4 (PDCD4). Overexpression of microRNA-21 and knockdown of PDCD4 blocked the growth suppression and apoptosis induction by isoalantolactone in ESCC cells.

conclusionsIsoalantolactone shows growth-suppressive activity against ESCC cells, which is ascribed to upregulation of PDCD4 via downregulation of microRNA-21.

Indexed as

AnimalsAntineoplastic AgentsApoptosisApoptosis Regulatory ProteinsCarcinoma, Squamous CellCell Cycle CheckpointsCell Line, TumorCell ProliferationDose-Response Relationship, DrugDown-RegulationEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaGene Expression Regulation, NeoplasticHumansMaleMice, Inbred BALB CAntineoplastic AgentsApoptosis Regulatory ProteinsisoalantolactoneMicroRNAsMIRN21 microRNA, humanPDCD4 protein, humanRNA-Binding ProteinsSesquiterpenesApoptosisEsophageal squamous cell carcinomaIsoalantolactoneMicroRNA-21PDCD4

Identifiers

PMID29781054
OpenAlexW2804535370

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.