Evidence map›Paper›PMID 27084634›Full record

ArticleInternational journal of radiation oncology, biology, physics2016

Tumor Cells Surviving Exposure to Proton or Photon Radiation Share a Common Immunogenic Modulation Signature, Rendering Them More Sensitive to T Cell-Mediated Killing.

Sofia R Gameiro, Anthony S Malamas, Michael B Bernstein, Kwong Y Tsang, April Vassantachart, Narayan Sahoo, Ramesh Tailor, Rajesh Pidikiti, Chandan P Guha, Stephen M Hahn and 2 more

Open access · greenAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
17.3field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 144 citations in OpenAlex.

  1. Multilevel Mechanisms of Cancer Drug Resistance.International journal of molecular sciences · 2024
    Pooled it
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  4. A Pilot Study of Stereotactic Body Radiation Therapy Combined with Cytoreductive Nephrectomy for Metastatic Renal Cell Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
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  17. Genotype-Directed Synthetic Cytotoxicity of ATR Inhibition with Radiotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
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  20. A perspective on tumor radiation resistance following high-LET radiation treatment.Journal of cancer research and clinical oncology · 2024
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 1 country.

Sofia R GameiroLaboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Anthony S MalamasLaboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Michael B BernsteinDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Kwong Y TsangLaboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
April VassantachartDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Narayan SahooDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Ramesh TailorDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Rajesh PidikitiDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Chandan P GuhaDepartment of Radiation Oncology, Montefiore Medical Center, Bronx, New York.
Stephen M HahnDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
Sunil KrishnanDivision of Radiation Oncology, M. D. Anderson Cancer Center, Houston, Texas.
James W HodgeLaboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: jh241d@nih.gov.
The University of Texas MD Anderson Cancer Center · USCenter for Cancer Research · USMontefiore Medical Center · USNational Cancer Institute · USNational Institutes of Health · US

Funding

Vaccine and Drug Combination Therapy for Human CancersZIABC010661 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HODGE, JAMES · 2009 to 2025
$11.2M
Vaccine and radiation for the therapy of human cancersZIABC010975 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HODGE, JAMES · 2009 to 2025
$11.0M
Vaccine and Drug Combination Therapy for Human CancersZ01BC010661 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HODGE, JAMES W · 2005 to 2008
$1.8M
Vaccine and radiation for the therapy of human cancersZ01BC010975 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HODGE, JAMES · 2008 to 2008
$412k
Intramural NIH HHS Z01 BC010661Intramural NIH HHS Z01 BC010975Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

purposeTo provide the foundation for combining immunotherapy to induce tumor antigen-specific T cells with proton radiation therapy to exploit the activity of those T cells. METHODS AND MATERIALS: Using cell lines of tumors frequently treated with proton radiation, such as prostate, breast, lung, and chordoma, we examined the effect of proton radiation on the viability and induction of immunogenic modulation in tumor cells by flow cytometric and immunofluorescent analysis of surface phenotype and the functional immune consequences.

resultsThese studies show for the first time that (1) proton and photon radiation induced comparable up-regulation of surface molecules involved in immune recognition (histocompatibility leukocyte antigen, intercellular adhesion molecule 1, and the tumor-associated antigens carcinoembryonic antigen and mucin 1); (2) proton radiation mediated calreticulin cell-surface expression, increasing sensitivity to cytotoxic T-lymphocyte killing of tumor cells; and (3) cancer stem cells, which are resistant to the direct cytolytic activity of proton radiation, nonetheless up-regulated calreticulin after radiation in a manner similar to non-cancer stem cells.

conclusionsThese findings offer a rationale for the use of proton radiation in combination with immunotherapy, including for patients who have failed radiation therapy alone or have limited treatment options.

Indexed as

Breast NeoplasmsCalreticulinCarcinoembryonic AntigenCell Line, TumorCell MembraneChordomaCombined Modality TherapyFemaleHLA AntigensHumansImmunomodulationImmunotherapyIntercellular Adhesion Molecule-1Lung NeoplasmsMaleMucin-1CalreticulinCarcinoembryonic AntigenHLA AntigensIntercellular Adhesion Molecule-1Mucin-1

Identifiers

PMID27084634
PMCPMC4834148
OpenAlexW2263844620

What OpenQuestion holds

Textmetadata
LicenceTDM
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.