Evidence map›Paper›PMID 32273767›Full record

ArticleCancer management and research2020

Acetyl-11-keto-β-boswellic Acid Inhibits Precancerous Breast Lesion MCF-10AT Cells via Regulation of LINC00707/miR-206 that Reduces Estrogen Receptor-α.

Xuefeng Jiang, Yusheng Liu, Guijuan Zhang, Shujun Lin, Naijun Yuan, Jieyan Wu, Xianxin Yan, Yi Ma, Min Ma

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
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.

Xuefeng Jiang *College of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.ORCID 0000-0002-1526-9470
Yusheng Liu *College of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.
Guijuan Zhang *The First Affiliated Hospital of Jinan University, Guangzhou, People's Republic of China.
Shujun LinCollege of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.
Naijun YuanCollege of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.ORCID 0000-0002-0096-9570
Jieyan WuCollege of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.ORCID 0000-0002-9650-9228
Xianxin YanCollege of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.
Yi MaInstitute of Biomedicine and Department of Cellular Biology, Jinan University, Guangzhou, People's Republic of China.
Min MaCollege of Traditional Chinese Medicine of Jinan University, Guangzhou, People's Republic of China.
Jinan University · CNFirst Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAcetyl-11-keto-β-boswellic acid (AKBA) has therapeutic effects on a range of diseases, including tumours. lncRNAs, as competing endogenous RNAs (ceRNAs), can interact with miRNAs to regulate the expression of target genes, which can affect the development of tumors. Here, we examined the effects of AKBA on breast precancerous lesions MCF-10AT cells.

methodsThe expression profiles of breast cancer (BC) tissue were collated from The Cancer Genome Atlas (TCGA), and the lncRNA-miRNA-mRNA ceRNA network was constructed. AKBA targets were predicted by network pharmacology. The expression of long intergenic nonprotein-coding RNA 707 (LINC00707), miR-206 and ER-α was determined by qRT-PCR. Cell viability, apoptosis and cycle were assessed by CCK-8 and flow cytometry. Protein levels were measured by Western blotting.

resultsA total of 3205 differentially expressed mRNAs, 104 miRNAs, and 605 lncRNAs were identified. The ceRNA network consisting of 9 lncRNAs, 15 miRNAs and 82 mRNAs was constructed. We found that LINC00707 was up-regulated and miR-206 was down-regulated in MCF-10AT cells. Transfected si-LINC00707 could inhibit cell proliferation, induce cell apoptosis and cycle arrest of MCF-10AT cells. In addition, network pharmacology predicted that AKBA may regulate the ESR1 in the treatment of BC. Our research demonstrated that AKBA could induce cell apoptosis and G1-phase arrest and inhibit ER-α expression via LINC00707/miR-206 in MCF-10AT cells.

conclusionAKBA inhibited MCF-10AT cells via regulation of LINC00707/miR-206 that reduces ER-α.

Indexed as

acetyl-11-keto-β-boswellic acidbreast precancerous lesionceRNAESR1LINC00707miR-206

Identifiers

PMID32273767
PMCPMC7108719
OpenAlexW3013108834

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.