Evidence map›Paper›PMID 28486014›Full record

ArticleCell cycle (Georgetown, Tex.)2017

Tissue TGF-β expression following conventional radiotherapy and pulsed low-dose-rate radiation.

Joshua E Meyer, Niklas K Finnberg, Lili Chen, Dusica Cvetkovic, Bin Wang, Lanlan Zhou, Yanqun Dong, Mark A Hallman, Chang-Ming C Ma, Wafik S El-Deiry

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 15% 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, 32 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Emerging evidence for adapting radiotherapy to immunotherapy.Nature reviews. Clinical oncology · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Cryptotanshinone Ameliorates Radiation-Induced Lung Injury in Rats.Evidence-based complementary and alternative medicine : eCAM · 2019
    Article
  14. Rhythmic radiotherapy beats down TGF-β.Cell cycle (Georgetown, Tex.) · 2017
    Article
  15. Understanding the pluses of pulses.Cell cycle (Georgetown, Tex.) · 2017
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Joshua E Meyera Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Niklas K Finnbergb Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Department of Medical Oncology and Molecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania.
Lili Chena Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Dusica Cvetkovica Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Bin Wanga Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Lanlan Zhoub Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Department of Medical Oncology and Molecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania.ORCID http://orcid.org/0000-0001-9471-9099
Yanqun Donga Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Mark A Hallmana Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Chang-Ming C Maa Radiation Oncology Department , Fox Chase Cancer Center , Philadelphia , PA , USA.
Wafik S El-Deiryb Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Department of Medical Oncology and Molecular Therapeutics Program , Fox Chase Cancer Center , Philadelphia , Pennsylvania.
Fox Chase Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The release of inflammatory cytokines has been implicated in the toxicity of conventional radiotherapy (CRT). Transforming growth factor β (TGF-β) has been suggested to be a risk marker for pulmonary toxicity following radiotherapy. Pulsed low-dose rate radiotherapy (PLDR) is a technique that involves spreading out a conventional radiotherapy dose into short pulses of dose with breaks in between to reduce toxicities. We hypothesized that the more tolerable toxicity profile of PLDR compared with CRT may be related to differential expression of inflammatory cytokines such as TGF-β in normal tissues. To address this, we analyzed tissues from mice that had been subjected to lethal doses of CRT and PLDR by histology and immunohistochemistry (IHC). Equivalent physical doses of CRT triggered more cellular atrophy in the bone marrow, intestine, and pancreas when compared with PLDR as indicated by hematoxylin and eosin staining. IHC data indicates that TGF-β expression is increased in the bone marrow, intestine, and lungs of mice subjected to CRT as compared with tissues from mice subjected to PLDR. Our in vivo data suggest that differential expression of inflammatory cytokines such as TGF-β may play a role in the more favorable normal tissue late response following treatment with PLDR.

Indexed as

AnimalsBone MarrowDose-Response Relationship, RadiationIntestine, SmallLungMaleMice, Inbred BALB COrgan SpecificityRadiation Injuries, ExperimentalRadiotherapyTransforming Growth Factor betaTransforming Growth Factor betabone marrowPLDRpulsed low-dose rate radiationradiotherapysmall intestineTGF-βtoxicity

Identifiers

PMID28486014
PMCPMC5499842
OpenAlexW2613154837

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.