Evidence map›Paper›PMID 28991157›Full record

ArticleInternational journal of molecular sciences2017

Geranylgeranylacetone Ameliorates Intestinal Radiation Toxicity by Preventing Endothelial Cell Dysfunction.

Na-Kyung Han, Ye Ji Jeong, Bo-Jeong Pyun, Yoon-Jin Lee, Sung-Ho Kim, Hae-June Lee

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. 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
1.5field-weighted citation impact, top 17% 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, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Geranylgeranyl Transferase Inhibitors Mitigate Intestinal Radiation Toxicity.International journal of radiation oncology, biology, physics · 2026
    Article
  4. Review
  5. Article
  6. Biomimetics (Basel, Switzerland) · 2022
    Article
  7. Mechanisms of radiation-induced endothelium damage: Emerging models and technologies.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2021
    Review
  8. Review
  9. Article
  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

6 authors at 3 institutions in 1 country.

Na-Kyung HanDivision of Basic Radiation Bioscience, Korea Institute of Radiological and Medical Sciences, Seoul 01812 Korea. gmxvz@hanmail.net.
Ye Ji JeongDivision of Basic Radiation Bioscience, Korea Institute of Radiological and Medical Sciences, Seoul 01812 Korea. brightwisdm0914@gmail.com.
Bo-Jeong PyunKorean Medicine Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon 34054, Korea. bjpyun@kiom.re.kr.
Yoon-Jin LeeDivision of Basic Radiation Bioscience, Korea Institute of Radiological and Medical Sciences, Seoul 01812 Korea. yjlee8@kirams.re.kr.
Sung-Ho KimCollege of Veterinary Medicine, Chonnam National University, Gwangju 61186, Korea. shokim@chonnam.ac.kr.
Hae-June LeeDivision of Basic Radiation Bioscience, Korea Institute of Radiological and Medical Sciences, Seoul 01812 Korea. hjlee@kirams.re.kr.ORCID 0000-0002-7743-0151
Korea Institute of Radiological and Medical Sciences · KRChonnam National University · KRKorea Institute of Oriental Medicine · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Radiation-induced intestinal toxicity is common among cancer patients after radiotherapy. Endothelial cell dysfunction is believed to be a critical contributor to radiation tissue injury in the intestine. Geranylgeranylacetone (GGA) has been used to treat peptic ulcers and gastritis. However, the protective capacity of GGA against radiation-induced intestinal injury has not been addressed. Therefore, we investigated whether GGA affects intestinal damage in mice and vascular endothelial cell damage in vitro. GGA treatment significantly ameliorated intestinal injury, as evident by intestinal crypt survival, villi length and the subsequently prolonged survival time of irradiated mice. In addition, intestinal microvessels were also significantly preserved in GGA-treated mice. To clarify the effect of GGA on endothelial cell survival, we examined endothelial function by evaluating cell proliferation, tube formation, wound healing, invasion and migration in the presence or absence of GGA after irradiation. Our findings showed that GGA plays a role in maintaining vascular cell function; however, it does not protect against radiation-induced vascular cell death. GGA promoted endothelial function during radiation injury by preventing the loss of VEGF/VEGFR1/eNOS signaling and by down-regulating TNFα expression in endothelial cells. This finding indicates the potential impact of GGA as a therapeutic agent in mitigating radiation-induced intestinal damage.

Indexed as

AnimalsBlotting, WesternCell MovementCell ProliferationDiterpenesEndothelial CellsFemaleHumansHuman Umbilical Vein Endothelial CellsIntestinal MucosaIntestinesMiceMice, Inbred C57BLWound HealingDiterpenesgeranylgeranylacetoneangiogenesisendothelial dysfunctiongeranylgeranylacetone (GGA)radiation enteropathy

Identifiers

PMID28991157
PMCPMC5666785
OpenAlexW2761432760

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.