Evidence map›Paper›PMID 35986207›Full record

ArticleScientific reports2022

Cross-platform validation of a mouse blood gene signature for quantitative reconstruction of radiation dose.

Shanaz A Ghandhi, Igor Shuryak, Brian Ponnaiya, Xuefeng Wu, Guy Garty, Shad R Morton, Salan P Kaur, Sally A Amundson

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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 23% 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, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Sex differences in radiation research.International journal of radiation biology · 2024
    Article
  8. Article
  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

8 authors at 1 institution in 1 country.

Shanaz A GhandhiCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA. sg2423@cumc.columbia.edu.
Igor ShuryakCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Brian PonnaiyaCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Xuefeng WuCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Guy GartyCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Shad R MortonCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Salan P KaurCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Sally A AmundsonCenter for Radiological Research, Columbia University Irving Medical Center, 630, W 168th Street, VC11-237, New York, NY, 10032, USA.
Columbia University Irving Medical Center · US

Funding

Sample Engineering CoreU19AI067773 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AMUNDSON, SALLY A. · 2005 to 2024
$105.4M
NIAID NIH HHS U19A1067773NIAID NIH HHS U19 AI067773
6 · The paper itself

Abstract

In the search for biological markers after a large-scale exposure of the human population to radiation, gene expression is a sensitive endpoint easily translatable to in-field high throughput applications. Primarily, the ex-vivo irradiated healthy human blood model has been used to generate available gene expression datasets. This model has limitations i.e., lack of signaling from other irradiated tissues and deterioration of blood cells cultures over time. In vivo models are needed; therefore, we present our novel approach to define a gene signature in mouse blood cells that quantitatively correlates with radiation dose (at 1 Gy/min). Starting with available microarray datasets, we selected 30 radiation-responsive genes and performed cross-validation/training-testing data splits to downselect 16 radiation-responsive genes. We then tested these genes in an independent cohort of irradiated adult C57BL/6 mice (50:50 both sexes) and measured mRNA by quantitative RT-PCR in whole blood at 24 h. Dose reconstruction using net signal (difference between geometric means of top 3 positively correlated and top 4 negatively correlated genes with dose), was highly improved over the microarrays, with a root mean square error of ± 1.1 Gy in male and female mice combined. There were no significant sex-specific differences in mRNA or cell counts after irradiation.

Indexed as

Blood CellsAdultAnimalsDose-Response Relationship, RadiationFemaleHumansMaleMiceMice, Inbred C57BLRNA, MessengerRNA, Messenger

Identifiers

PMID35986207
PMCPMC9391341
OpenAlexW4292315410

What Socratic 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 Socratic graph.