Evidence map›Paper›PMID 35325326›Full record

ArticleJournal of molecular histology2022

Echinacoside inhibits the proliferation, migration, invasion and angiogenesis of ovarian cancer cells through PI3K/AKT pathway.

Juan Liu, Ni Tang, Ni Liu, Panpan Lei, Fang Wang

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular histology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Echinacea: Bioactive Compounds and Agronomy.Plants (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Article
  12. Molecules (Basel, Switzerland) · 2023
    Review
  13. A Novel Strategy for Screening Active Components inJournal of analytical methods in chemistry · 2023
    Article
  14. 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

5 authors at 1 institution in 1 country.

Juan LiuDepartment of Gynecology, Weinan Maternal and Child Health Hospital, No. 114, Dongfeng Street, Weinan, 714000, Shaanxi, China.
Ni TangDepartment of Gynecology, Weinan Maternal and Child Health Hospital, No. 114, Dongfeng Street, Weinan, 714000, Shaanxi, China.
Ni LiuDepartment of Gynecology, Weinan Maternal and Child Health Hospital, No. 114, Dongfeng Street, Weinan, 714000, Shaanxi, China.
Panpan LeiDepartment of Gynecology, Weinan Maternal and Child Health Hospital, No. 114, Dongfeng Street, Weinan, 714000, Shaanxi, China.
Fang WangDepartment of Gynecology, Weinan Maternal and Child Health Hospital, No. 114, Dongfeng Street, Weinan, 714000, Shaanxi, China. wangfanggyn@126.com.
Weinan Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Echinacoside is a group of natural compounds extracted from medicinal plants Cistanche and Echinacea, which has neuroprotective, antiaging, immunomodulatory and anticancer effects, but its specific role and mechanism in tumor remains partially unclear. To our knowledge, it was the first time to reported the effect of Echinacoside in ovarian cancer. Colony formation, TUNEL staining, Transwell and tube formation assays were conducted to analyze the proliferation, apoptosis, invasion and tube formation abilities of serous ovarian carcinoma cells (SKOV3 and OVCAR-3), respectively. The expressions of apoptosis-, invasion- and PI3K/AKT pathway-related proteins were measured by western blotting. In addition, PI3K agonist (740Y-P) was used to assess the regulatory effect of Echinacoside on PI3K/AKT signaling in ovarian cancer. Finally, the anti-tumor effect of Echinacoside on SKOV3-xenografted mice was evaluated by xenograft tumor mouse model. Our results demonstrated Echinacoside concentration-dependently reduced the proliferation, migration and angiogenesis of ovarian cancer cells, whereas promoted apoptosis. Moreover, western blotting revealed that Echinacoside suppressed the growth of ovarian cancer cells by downregulating the phosphorylation levels of PI3K, AKT and mTOR, which could be partially reversed by 740Y-P. Further, in vivo results showed that Echinacoside could effectively alleviate the tumor growth of xenograft mice, accompanied by the decrease of PI3K/AKT signaling. In general, our results demonstrate that Echinacoside could reduce the ovarian cancer progression through inhibition of PI3K/AKT pathway, suggesting that Echinacoside may be a new treatment option for ovarian cancer.

Indexed as

Ovarian NeoplasmsPhosphatidylinositol 3-KinasesAnimalsApoptosisCell Line, TumorCell MovementCell ProliferationFemaleGlycosidesHumansMiceNeovascularization, PathologicProto-Oncogene Proteins c-aktechinacosideGlycosidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAngiogenesisEchinacosideOvarian cancerPI3K/AKT pathway

Identifiers

PMID35325326
OpenAlexW4220724604

What OpenQuestion holds

Textmetadata
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.