Evidence map›Paper›PMID 25835975›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Ginsenoside Rh2 inhibits metastasis of glioblastoma multiforme through Akt-regulated MMP13.

Ning Guan, Xiaochuan Huo, Zhenxing Zhang, Shoudan Zhang, Junsheng Luo, Wenshi Guo

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
  7. Review
  8. Anticancer Activities of Ginsenosides, the Main Active Components of Ginseng.Evidence-based complementary and alternative medicine : eCAM · 2021
    Review
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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

6 authors at 2 institutions in 1 country.

Ning GuanDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China.
Xiaochuan HuoDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China.
Zhenxing ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China.
Shoudan ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China.
Junsheng LuoDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China.
Wenshi GuoDepartment of Neurosurgery, The First Affiliated Hospital of Liaoning Medical University, 2 Renmin Road, Jinzhou, 121001, China. wenshi_guo@163.com.
Jinzhou Medical University · CNFirst Affiliated Hospital of Liaoning Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is the most malignant type of primary brain tumor. Although the growth of the tumor cells in a relatively closed space may partially account for its malignancy, highly invasive nature of glioblastoma cells has been suggested to be the main reason for the failure of current therapeutic approaches. Ginsenoside Rh2 (GRh2) has recently been shown to significantly suppress the growth and survival of GBM through inhibiting epidermal growth factor receptor signaling, whereas its effects on the invasion and metastasis have not been examined. Here, we showed that GRh2 dose-dependently decreased GBM cell invasiveness in both scratch wound healing assay and Transwell cell migration assay. Moreover, the inhibitory effects of GRh2 on cell migration seemed to be conducted through decreased expression of matrix metalloproteinase (MMP)-13. Furthermore, using specific inhibitors, we found that GRh2 inhibited MMP13 through PI3k/Akt signaling pathway. Finally, high MMP13 levels were detected in GBM specimen from the patients. Together, these data suggest that GRh2 may suppress GBM migration through inhibiting Akt-mediated MMP13 activation. Thus, our data highlight a previous unappreciated role for GRh2 in suppressing GBM cell metastasis.

Indexed as

AdultCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGinsenosidesGlioblastomaHumansMaleMatrix Metalloproteinase 13Middle AgedNeoplasm InvasivenessNeoplasm MetastasisOncogene Protein v-aktPhosphatidylinositol 3-Kinasesginsenoside Rh2GinsenosidesMatrix Metalloproteinase 13MMP13 protein, humanOncogene Protein v-aktPhosphatidylinositol 3-KinasesAktGinsenoside Rh2 (GRh2)Glioblastoma multiforme (GBM)Matrix metalloproteinase (MMP)-13PI3k

Identifiers

PMID25835975
OpenAlexW1972486807

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.