Evidence map›Paper›PMID 31462499›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Neutrophils promote tumor resistance to radiation therapy.

Amy J Wisdom, Cierra S Hong, Alexander J Lin, Yu Xiang, Daniel E Cooper, Jin Zhang, Eric S Xu, Hsuan-Cheng Kuo, Yvonne M Mowery, David J Carpenter and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 2 pooled it
6.6field-weighted citation impact, top 2% 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

97 citing papers in PubMed, 2 syntheses or guidelines pooled it, 169 citations in OpenAlex.

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37 more citing papers are in PubMed but not listed here.

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

21 authors at 4 institutions in 1 country.

Amy J WisdomDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708.ORCID 0000-0002-6098-5353
Cierra S HongDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708.
Alexander J LinDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63110.
Yu XiangDepartment of Cell Biology, Duke University Medical Center, Durham, NC 27708.
Daniel E CooperDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Jin ZhangDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63110.
Eric S XuDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Hsuan-Cheng KuoDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708.
Yvonne M MoweryDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
David J CarpenterDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Kushal T KadakiaDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708.
Jonathon E HimesDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708.
Lixia LuoDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Yan MaDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Nerissa WilliamsDepartment of Radiation Oncology, Duke University Medical Center, Durham, NC, 27708.
Diana M CardonaDepartment of Pathology, Duke University Medical Center, Durham, NC 27708.
Malay HaldarDepartment of Pathology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.
Yarui DiaoDepartment of Cell Biology, Duke University Medical Center, Durham, NC 27708.
Stephanie MarkovinaDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63110.
Julie K SchwarzDepartment of Radiation Oncology, Washington University School of Medicine, St. Louis, MO 63110.
David G KirschDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27708; david.kirsch@duke.edu.ORCID 0000-0002-2086-205X
Duke Medical Center · USWashington University in St. Louis · USDuke University · USUniversity of Pennsylvania · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Washington University Paul Calabresi K12 Career Development Award for Clinical OncologyK12CA167540 · NCI · WASHINGTON UNIVERSITY · PI John F. Dipersio, Ramaswamy Govindan · 2012 to 2026
$11.7M
Advancing Cancer Therapy through Ground Breaking Research in Radiation BiologyR35CA197616 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI David Guy Kirsch · 2016 to 2026
$10.7M
Optimizing radiation therapy through the manipulation of glutamine metabolismR01CA181745 · NCI · WASHINGTON UNIVERSITY · PI SCHWARZ, JULIE KRISTINA · 2014 to 2025
$3.4M
Mechanisms of radiation-induced tumor cell death and survival in cervical cancerK08CA237822 · NCI · WASHINGTON UNIVERSITY · PI MARKOVINA, STEPHANIE · 2019 to 2023
$1.1M
Dissecting the role of the immune system in the radiation response of Kras-mutant tumorsF30CA221268 · NCI · DUKE UNIVERSITY · PI WISDOM, AMY JORDAN · 2017 to 2020
$154k
NCI NIH HHS F30 CA221268NCI NIH HHS K08 CA237822NCI NIH HHS K12 CA167540NCI NIH HHS R01 CA181745NCI NIH HHS R35 CA197616NIGMS NIH HHS T32 GM007171
6 · The paper itself

Abstract

Nearly two-thirds of cancer patients are treated with radiation therapy (RT), often with the intent to achieve complete and permanent tumor regression (local control). RT is the primary treatment modality used to achieve local control for many malignancies, including locally advanced cervical cancer, head and neck cancer, and lung cancer. The addition of concurrent platinum-based radiosensitizing chemotherapy improves local control and patient survival. Enhanced outcomes with concurrent chemoradiotherapy may result from increased direct killing of tumor cells and effects on nontumor cell populations. Many patients treated with concurrent chemoradiotherapy exhibit a decline in neutrophil count, but the effects of neutrophils on radiation therapy are controversial. To investigate the clinical significance of neutrophils in the response to RT, we examined patient outcomes and circulating neutrophil counts in cervical cancer patients treated with definitive chemoradiation. Although pretreatment neutrophil count did not correlate with outcome, lower absolute neutrophil count after starting concurrent chemoradiotherapy was associated with higher rates of local control, metastasis-free survival, and overall survival. To define the role of neutrophils in tumor response to RT, we used genetic and pharmacological approaches to deplete neutrophils in an autochthonous mouse model of soft tissue sarcoma. Neutrophil depletion prior to image-guided focal irradiation improved tumor response to RT. Our results indicate that neutrophils promote resistance to radiation therapy. The efficacy of chemoradiotherapy may depend on the impact of treatment on peripheral neutrophil count, which has the potential to serve as an inexpensive and widely available biomarker.

Indexed as

ChemoradiotherapyAdolescentAdultAgedAged, 80 and overAnimalsDisease-Free SurvivalDisease Models, AnimalFemaleHumansKaplan-Meier EstimateLeukocyte CountMiceMice, TransgenicMiddle AgedNeutrophilscancer biologygenetically engineered mouse modelneutrophilradiation therapyradiosensitivity

Identifiers

PMID31462499
PMCPMC6744874
OpenAlexW2971180845

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.