Evidence map›Paper›PMID 31746388›Full record

ArticleMolecular medicine reports2020

Hydroxypropyl‑β‑cyclodextrin attenuates the epithelial‑to‑mesenchymal transition via endoplasmic reticulum stress in MDA‑MB‑231 breast cancer cells.

Yifan Wu, Yiyang Zhao, Xuanhong He, Zhiqiang He, Tian Wang, Linxi Wan, Lai Chen, Nianlong Yan

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  7. Role of theFrontiers in cell and developmental biology · 2022
    Review
  8. Article
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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 2 institutions in 1 country.

Yifan Wu *Department of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Yiyang Zhao *Department of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Xuanhong HeDepartment of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Zhiqiang HeDepartment of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Tian WangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Linxi WanDepartment of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Lai ChenLaboratory Animal Research Center for Science and Technology, Jiangxi University of Traditional Chinese Medicine, Nanchang, Jiangxi 330004, P.R. China.
Nianlong YanDepartment of Biochemistry and Molecular Biology, School of Basic Medical Science, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Nanchang University · CNJiangxi University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial‑to‑mesenchymal transition (EMT) has been reported to serve vital roles in regulating the progress of cancer metastasis. In addition, lipid rafts enriched in sphingolipids and cholesterol serve important roles in physiological and biochemical processes as a signaling platform. The present study explored the effects of hydroxypropyl‑β‑cyclodextrin (HP‑β‑CD), a cholesterol‑depleting agent of lipid rafts, on the transforming growth factor (TGF)‑β/Smad signaling pathway and endoplasmic reticulum (ER) stress in mediating EMT in MDA‑MB‑231 breast cancer cells. HP‑β‑CD treatment inhibited TGF‑β1‑induced EMT, based on increased expression of E‑cadherin and decreased expression of vimentin. HP‑β‑CD reduced the expression of the TGF receptor TβRI and blocked the phosphorylation of Smad2. In addition, HP‑β‑CD increased the expression of ER stress‑related proteins (binding immunoglobulin protein and activating transcription factor 6), but TGF‑β1 could reverse these changes. Sodium 4‑phenylbutyrate, an inhibitor of ER stress, suppressed these effects of HP‑β‑CD on EMT and TGF‑β/Smad signaling pathway inhibition in breast cancer cells. Thus, HP‑β‑CD can block the TGF‑β/Smad signaling pathway via diminishing the expression of TβRI which helps to activate ER stress and attenuate EMT in MDA‑MB‑231 cells, highlighting a potential target of lipid rafts for breast cancer treatment.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinBreast NeoplasmsCadherinsCell Line, TumorCell MovementCell ProliferationEndoplasmic Reticulum StressEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansPhenylbutyratesPhosphorylationReceptor, Transforming Growth Factor-beta Type ISmad2 ProteinTransforming Growth Factor beta12-Hydroxypropyl-beta-cyclodextrin4-phenylbutyric acidCadherinsPhenylbutyratesReceptor, Transforming Growth Factor-beta Type ISmad2 ProteinSMAD2 protein, humanTGFB1 protein, humanTransforming Growth Factor beta1Vimentinendoplasmic reticulum stressepithelial-mesenchymal transitionhydroxypropyl-β-cyclodextrinipid raftsMda-MB-231 cells

Identifiers

PMID31746388
PMCPMC6896369
OpenAlexW2984524873

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.