Evidence map›Paper›PMID 37470810›Full record

ArticleCancer research2023

Radiotherapy-Induced Neurocognitive Impairment Is Driven by Heightened Apoptotic Priming in Early Life and Prevented by Blocking BAX.

Rumani Singh, Stacey Yu, Marwa Osman, Zintis Inde, Cameron Fraser, Abigail H Cleveland, Nicole Almanzar, Chuan Bian Lim, Gaurav N Joshi, Johan Spetz and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
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  8. bioRxiv : the preprint server for biology · 2023
    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

20 authors at 5 institutions in 2 countries.

Rumani SinghJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-4324-3753
Stacey YuJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0001-5540-4027
Marwa OsmanJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0001-6219-9025
Zintis IndeJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0001-5564-1698
Cameron FraserJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-8180-5913
Abigail H ClevelandDepartment of Neurology, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0002-3502-5940
Nicole AlmanzarMolecular and Integrative Physiological Sciences Program, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0001-9829-0402
Chuan Bian LimJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-0848-6426
Gaurav N JoshiJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-6789-6783
Johan SpetzJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-5216-9786
Xingping QinJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0003-3263-0843
Sneh M TopraniJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-2388-5425
Zachary NagelJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0003-2104-2093
Matthew C HockingDepartment of Psychiatry, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-1368-0856
Robert A CormackDepartment of Medicine, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-5553-9984
Torunn I YockDepartment of Medicine, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-6408-8011
Jeffrey W MillerDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0001-7718-1581
Zhi-Min YuanJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0003-4812-251X
Timothy GershonDepartment of Neurology, University of North Carolina, Chapel Hill, North Carolina.ORCID 0000-0001-7034-6400
Kristopher A SarosiekJohn B. Little Center for Radiation Sciences, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.ORCID 0000-0002-4618-5085
Harvard University · USUniversity of North Carolina at Chapel Hill · USBrigham and Women's Hospital · USChildren's Hospital of Philadelphia · USDepartment of Physiological Sciences · RU

Funding

Translational Research Support CoreP30ES000002 · NIEHS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI Marc G Weisskopf · 1985 to 2026
$44.6M
Training Program in Molecular and Integrative Physiological SciencesT32HL007118 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI LU, QUAN · 1985 to 2025
$14.3M
CANCER CELL BIOLOGY TRAINING PROGRAMT32CA071341 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHANNING J. DER, Yuliya Pylayeva-Gupta · 1996 to 2026
$5.0M
Developmental regulation of apoptosis as a modifiable driver of radiotherapy-induced neurocognitive impairment in pediatric patientsR37CA248565 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Kristopher Andrew Sarosiek · 2020 to 2026
$2.6M
Bcl-xL-regulated apoptosis in cerebellar development and medulloblastoma treatmentR01NS102627 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GERSHON, TIMOTHY · 2018 to 2022
$1.8M
Identifying targetable apoptotic vulnerabilities for the treatment of AL amyloidosisR01DK125263 · NIDDK · HARVARD SCHOOL OF PUBLIC HEALTH · PI SAROSIEK, KRISTOPHER ANDREW · 2020 to 2023
$1.4M
Regulation of Apoptotic Priming and Competence in Healthy and Cancerous CellsR00CA188679 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI SAROSIEK, KRISTOPHER ANDREW · 2017 to 2019
$747k
Regulation of apoptotic priming and competence in healthy and cancerous cellsK99CA188679 · NCI · DANA-FARBER CANCER INST · PI SAROSIEK, KRISTOPHER ANDREW · 2014 to 2015
$178k
Optimizing the therapeutic index for pediatric medulloblastomas by targeting apoptosisF31CA246811 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI YU, STACEY JESSICA · 2020 to 2022
$101k
Apoptotic Regulation and Neuroinflammation in Alzheimer's DiseaseF32AG077861 · NIA · HARVARD SCHOOL OF PUBLIC HEALTH · PI INDE, ZINTIS · 2022 to 2022
$68k
NCI NIH HHS F31 CA246811NCI NIH HHS K99 CA188679NCI NIH HHS R00 CA188679NCI NIH HHS R37 CA248565NCI NIH HHS T32 CA071341NHLBI NIH HHS T32 HL007118NIA NIH HHS F32 AG077861NIDDK NIH HHS R01 DK125263NIEHS NIH HHS P30 ES000002NINDS NIH HHS R01 NS102627
6 · The paper itself

Abstract

Although external beam radiotherapy (xRT) is commonly used to treat central nervous system (CNS) tumors in patients of all ages, young children treated with xRT frequently experience life-altering and dose-limiting neurocognitive impairment (NI) while adults do not. The lack of understanding of mechanisms responsible for these differences has impeded the development of neuroprotective treatments. Using a newly developed mouse model of xRT-induced NI, we found that neurocognitive function is impaired by ionizing radiation in a dose- and age-dependent manner, with the youngest animals being most affected. Histologic analysis revealed xRT-driven neuronal degeneration and cell death in neurogenic brain regions in young animals but not adults. BH3 profiling showed that neural stem and progenitor cells, neurons, and astrocytes in young mice are highly primed for apoptosis, rendering them hypersensitive to genotoxic damage. Analysis of single-cell RNA sequencing data revealed that neural cell vulnerability stems from heightened expression of proapoptotic genes including BAX, which is associated with developmental and mitogenic signaling by MYC. xRT induced apoptosis in primed neural cells by triggering a p53- and PUMA-initiated, proapoptotic feedback loop requiring cleavage of BID and culminating in BAX oligomerization and caspase activation. Notably, loss of BAX protected against apoptosis induced by proapoptotic signaling in vitro and prevented xRT-induced apoptosis in neural cells in vivo as well as neurocognitive sequelae. On the basis of these findings, preventing xRT-induced apoptosis specifically in immature neural cells by blocking BAX, BIM, or BID via direct or upstream mechanisms is expected to ameliorate NI in pediatric patients with CNS tumor. SIGNIFICANCE: Age- and differentiation-dependent apoptotic priming plays a pivotal role in driving radiotherapy-induced neurocognitive impairment and can be targeted for neuroprotection in pediatric patients.

Indexed as

ApoptosisApoptosis Regulatory ProteinsAnimalsbcl-2-Associated X ProteinCell DeathChildChild, PreschoolHumansMiceSignal TransductionTumor Suppressor Protein p53Apoptosis Regulatory ProteinsBax protein, mousebcl-2-Associated X ProteinTumor Suppressor Protein p53

Identifiers

PMID37470810
PMCPMC10570680
OpenAlexW4384818879

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Registered trials

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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.