Evidence map›Paper›PMID 30862004›Full record

ArticleInternational journal of molecular sciences2019

Ginsenoside Rk1 Induces Apoptosis in Neuroblastoma Cells Through Loss of Mitochondrial Membrane Potential and Activation of Caspases.

Jung-Mi Oh, Jeongwoo Lee, Wan-Taek Im, Sungkun Chun

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Therapeutic Applications of Ginseng Natural Compounds for Health Management.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Emerging therapeutic targets for neuroblastoma.Expert opinion on therapeutic targets · 2020
    Review
  9. Review
  10. Article
  11. 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

4 authors at 3 institutions in 1 country.

Jung-Mi OhDepartment of Physiology, Chonbuk National University Medical School, Jeonju 54907, Korea. biojmi@jbnu.ac.kr.
Jeongwoo LeeDepartment of Anesthesiology and Pain Medicine, Chonbuk National University Hospital, Jeonju 54907, Korea. jw88lee@gmail.com.ORCID 0000-0002-2186-3134
Wan-Taek ImDepartment of Biotechnology, Hankyoung National University, Anseong 17579, Korea. wandra@hknu.ac.kr.
Sungkun ChunDepartment of Physiology, Chonbuk National University Medical School, Jeonju 54907, Korea. sungkun.chun@jbnu.ac.kr.ORCID 0000-0001-9837-2299
Jeonbuk National University Hospital · KRHankyong National University · KRJeonbuk National University · KR

Funding

Korea Health Industry Development Institute HI17C1510National Research Foundation of Korea NRF-2017R1A5A2015061National Research Foundation of Korea NRF-2017R1D1A1B03035125
6 · The paper itself

Abstract

Neuroblastoma (NB) is the most common childhood cancer, with a very poor prognosis. More than 60% of children with NB die within five years; therefore, a more effective therapy for NB is required. Although ginsenoside has been shown to significantly inhibit the growth of various cancers, the effect of ginsenoside Rk1 on neuroblastoma has not been known yet. Hence, we examined the anticancer effects of highly pure Rk1 on neuroblastoma cell lines. The apoptotic effects of Rk1 on neuroblastoma cells were examined using cell viability assay, flow cytometry and cell staining assay, and the change in gene expression levels were analysed using RT-PCR, western blots, and immunohistochemistry. The metastatic effect of Rk1 was monitored by wound healing assay, invasion and migration with Matrigels. Rk1 inhibited neuroblastoma cell viability dose-dependently. Rk1-induced apoptosis was investigated through nuclear condensation and mitochondrial membrane potential loss, and it showed that Rk1 can induce cell cycle arrest at the G0/G1 phase but also inhibit the metastatic ability of neuroblastoma cells. Moreover, Rk1 (30 mg/kg) injections markedly inhibited xenograft tumor growth. These findings demonstrate that Rk1 might be valuable in the development of anti-cancer agents for neuroblastoma treatment.

Indexed as

AnimalsApoptosisApoptosis Regulatory ProteinsCaspasesCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationCell SurvivalDisease Models, AnimalDose-Response Relationship, DrugEpithelial-Mesenchymal TransitionGinsenosidesHumansMaleMembrane Potential, MitochondrialApoptosis Regulatory ProteinsCaspasesginsenoside Rk1Ginsenosidesapoptosisginsenoside Rk1metastasisneuroblastomaproliferation

Identifiers

PMID30862004
PMCPMC6429382
OpenAlexW2922215784

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.