Evidence map›Paper›PMID 30015828›Full record

ArticleInternational journal of molecular medicine2018

Alantolactone induces apoptosis and suppresses migration in MCF‑7 human breast cancer cells via the p38 MAPK, NF‑κB and Nrf2 signaling pathways.

Jianli Liu, Meijia Liu, Shuai Wang, Yin He, Yapeng Huo, Zhijun Yang, Xiangyu Cao

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2018. 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
2.2field-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

25 citing papers in PubMed, 39 citations in OpenAlex.

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  20. Terpenoids as Potential Geroprotectors.Antioxidants (Basel, Switzerland) · 2020
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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

7 authors at 1 institution in 1 country.

Jianli LiuDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Meijia LiuDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Shuai WangDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Yin HeDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Yapeng HuoDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Zhijun YangDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Xiangyu CaoDepartment of Biological Sciences, School of Life Science, Liaoning University, Shenyang, Liaoning 110036, P.R. China.
Liaoning University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human breast cancer is a malignant type of cancer with high prevalence. In the present study, the anticancer effects of alantolactone, a sesquiterpene lactone, on the human breast cancer cell line MCF‑7 were investigated in vitro. The MCF‑7 cell morphology changed from diamond to round subsequent to treatment with alantolactone, and the cell viability reduced significantly compared with that of the control cells. Alantolactone induced apoptosis of MCF‑7 cells by regulating the protein expression levels of B‑cell lymphoma 2 (Bcl‑2), Bcl‑2‑associated X protein, p53, caspase‑3 and caspase‑12, which are associated with the apoptotic pathway, and suppressed colony formation and migration by regulating the protein expression of matrix metalloproteinase (MMP)‑2, MMP‑7 and MMP‑9. Cell signaling pathway analysis confirmed that alantolactone increased the phosphorylation of p38, and decreased the nuclear expression levels of p65 and nuclear factor erythroid 2‑related factor 2 (Nrf2), suggesting that the apoptosis‑promoting and migration‑suppressing effect of alantolactone may partially depend on regulating the p38 MAPK, NF‑κB and Nrf2 pathways. These results also suggested that alantolactone may become a potential therapeutic strategy for treating breast cancer.

Indexed as

ApoptosisBreast NeoplasmsCell MovementFemaleHumansLactonesMAP Kinase Signaling SystemMCF-7 CellsNeoplasm ProteinsNF-E2-Related Factor 2NF-kappa Bp38 Mitogen-Activated Protein KinasesSesquiterpenes, EudesmanealantolactoneLactonesNeoplasm ProteinsNFE2L2 protein, humanNF-E2-Related Factor 2NF-kappa Bp38 Mitogen-Activated Protein KinasesSesquiterpenes, Eudesmane

Identifiers

PMID30015828
PMCPMC6108867
OpenAlexW2810392784

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.