Evidence map›Paper›PMID 32100006›Full record

ArticleJournal of radiation research2020

The malignancy of liver cancer cells is increased by IL-4/ERK/AKT signaling axis activity triggered by irradiated endothelial cells.

Sung Dae Kim, Ji Sue Baik, Jae-Hye Lee, Seo-Won Mun, Joo Mi Yi, Moon-Taek Park

Open access · goldAbstract read
In one paragraph

Article in Journal of radiation research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Involvement of IL-4, IL-13 and Their Receptors in Pancreatic Cancer.International journal of molecular sciences · 2021
    Review
  9. 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 2 institutions in 1 country.

Sung Dae KimResearch Center, Dongnam Institute of Radiological & Medical Sciences (DIRAMS), Busan, Republic of Korea.
Ji Sue BaikResearch Center, Dongnam Institute of Radiological & Medical Sciences (DIRAMS), Busan, Republic of Korea.
Jae-Hye LeeResearch Center, Dongnam Institute of Radiological & Medical Sciences (DIRAMS), Busan, Republic of Korea.
Seo-Won MunResearch Center, Dongnam Institute of Radiological & Medical Sciences (DIRAMS), Busan, Republic of Korea.
Joo Mi YiDepartment of Microbiology and Immunology, College of Medicine, Inje University, Busan, Republic of Korea.
Moon-Taek ParkResearch Center, Dongnam Institute of Radiological & Medical Sciences (DIRAMS), Busan, Republic of Korea.
Dongnam Institute of Radiological & Medical Sciences · KRInje University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The malignant traits involved in tumor relapse, metastasis and the expansion of cancer stem-like cells are acquired via the epithelial-mesenchymal transition (EMT) process in the tumor microenvironment. In addition, the tumor microenvironment strongly supports the survival and growth of malignant tumor cells and further contributes to the reduced efficacy of anticancer therapy. Ionizing radiation can influence the tumor microenvironment, because it alters the biological functions of endothelial cells composing tumor vascular systems. However, to date, studies on the pivotal role of these endothelial cells in mediating the malignancy of cancer cells in the irradiated tumor microenvironment are rare. We previously evaluated the effects of irradiated endothelial cells on the malignant traits of human liver cancer cells and reported that endothelial cells irradiated with 2 Gy reinforce the malignant properties of these cancer cells. In this study, we investigated the signaling mechanisms underlying these events. We revealed that the increased expression level of IL-4 in endothelial cells irradiated with 2 Gy eventually led to enhanced migration and invasion of cancer cells and further expansion of cancer stem-like cells. In addition, this increased level of IL-4 activated the ERK and AKT signaling pathways to reinforce these events in cancer cells. Taken together, our data indicate that ionizing radiation may indirectly modulate malignancy by affecting endothelial cells in the tumor microenvironment. Importantly, these indirect effects on malignancy are thought to offer valuable clues or targets for overcoming the tumor recurrence after radiotherapy.

Indexed as

Cell Line, TumorCell MovementCulture Media, ConditionedEndothelial CellsEpithelial-Mesenchymal TransitionExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsInterleukin-4Liver NeoplasmsNeoplasm InvasivenessNeoplasm MetastasisNeoplasm Recurrence, LocalProto-Oncogene Proteins c-aktRadiation, IonizingAKT1 protein, humanCulture Media, ConditionedExtracellular Signal-Regulated MAP KinasesIL4 protein, humanInterleukin-4Proto-Oncogene Proteins c-aktRNA, Small Interferingcancer stem-like cellsendothelial cellsepithelial–mesenchymal transitioninvasionionizing radiationmigration

Identifiers

PMID32100006
PMCPMC7299255
OpenAlexW3007568697

What OpenQuestion holds

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LicenceCC BY-NC
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.