Evidence map›Paper›PMID 31470581›Full record

ArticleNutrients2019

Korean Red Ginseng Extract Increases Apoptosis by Activation of the Noxa Pathway in Colorectal Cancer.

Yoon A Jeong, Bo Ram Kim, Dae Young Kim, Soyeon Jeong, Yoo Jin Na, Jung Lim Kim, Hye Kyeong Yun, Bu Gyeom Kim, Seong Hye Park, Min Jee Jo and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Anti-Colorectal Cancer Activity ofInternational journal of molecular sciences · 2025
    Review
  2. Article
  3. Article
  4. 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

14 authors at 2 institutions in 1 country.

Yoon A JeongGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Bo Ram KimDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Dae Young KimGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Soyeon JeongDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Yoo Jin NaGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Jung Lim KimDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Hye Kyeong YunGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Bu Gyeom KimGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Seong Hye ParkDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Min Jee JoGraduate School of Medicine, Korea University College of Medicine, Seoul 02841, Korea.
Sun Il LeeDepartment of Surgery, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Byung-Cheol HanKorea Ginseng Research Institute, Korea Ginseng Corporation, Daejeon 34337, Korea.
Dae-Hee LeeDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea.
Sang Cheul OhDepartment of Oncology, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Korea. sachoh@korea.ac.kr.
Korea University · KRKorea University Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough the anticancer activity of Korean Red Ginseng (KRG) has been known in various cancers, the mechanism of KRG-induced apoptosis is unknown in colorectal cancer (CRC). In our study, we examined whether KRG induces apoptosis in CRC cells.

methodsIn the cell viability assay, the concentration of the appropriate KRG extracts was fixed at 2.5 mg/mL in numerous CRC cells. This fixed concentration was in other experiments, and it was confirmed that the KRG extracts induce apoptosis in CRC cells.

resultsWe found that KRG induced Noxa activation and apoptosis and increased endoplasmic reticulum stress via reactive oxygen species production. This indicated that KRG efficiently enhanced cell death in CRC cells.

conclusionOur results show that KRG can be used as a possible anticancer drug for patients with CRC.

Indexed as

Antineoplastic Agents, PhytogenicApoptosisColorectal NeoplasmsEndoplasmic Reticulum StressGene Expression Regulation, NeoplasticHCT116 CellsHT29 CellsHumansPanaxPlant ExtractsProto-Oncogene Proteins c-bcl-2Reactive Oxygen SpeciesSignal TransductionAntineoplastic Agents, PhytogenicPlant ExtractsPMAIP1 protein, humanProto-Oncogene Proteins c-bcl-2Reactive Oxygen Speciesendoplasmic reticulum stresskorean red ginsengNoxareactive oxygen species

Identifiers

PMID31470581
PMCPMC6770724
OpenAlexW2970942381

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.