Evidence map›Paper›PMID 21251614›Full record

ArticleCancer cell2011

Endogenous T cell responses to antigens expressed in lung adenocarcinomas delay malignant tumor progression.

Michel DuPage, Ann F Cheung, Claire Mazumdar, Monte M Winslow, Roderick Bronson, Leah M Schmidt, Denise Crowley, Jianzhu Chen, Tyler Jacks

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02710396 (Identifying Genetic Predictors of Durable Clinical Benefit to Pembrolizumab in Advanced Non-small Cell Lung Cancer), which is not on this map. Cited by 168 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
168citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 93% 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.

NCT02710396 phase2terminatednot on this mapstarted 2016, after this paper: background citation

Identifying Genetic Predictors of Durable Clinical Benefit to Pembrolizumab in Advanced Non-small Cell Lung Cancer (NSCLC) Alone and in Combination With Chemotherapy.

TypeinterventionalSponsorColumbia UniversityRan2016 to 2021Enrolled19ConditionsCarcinoma, Non-Small-Cell LungArmsPembrolizumab, Carboplatin, Nab-paclitaxel, Pemetrexed
3 · Its place in the literature

Who cites it

168 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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  20. Precision models in hepatocellular carcinoma.Nature reviews. Gastroenterology & hepatology · 2025
    Review

108 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

9 authors at 3 institutions in 1 country.

Michel DuPageKoch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Ann F Cheung
Claire Mazumdar
Monte M Winslow
Roderick Bronson
Leah M Schmidt
Denise Crowley
Jianzhu Chen
Tyler Jacks
Massachusetts Institute of Technology · USHoward Hughes Medical Institute · USNew England Disabled Sports · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
Tumor-Stroma Interacions in the Tumor MicroenvironmentU54CA126515 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HYNES, RICHARD O · 2006 to 2010
$6.5M
Howard Hughes Medical InstituteNCI NIH HHS 1 U54 CA126515-01NCI NIH HHS P30 CA014051NCI NIH HHS P30-CA14051NCI NIH HHS U54 CA126515
6 · The paper itself

Abstract

Neoantigens derived from somatic mutations in tumors may provide a critical link between the adaptive immune system and cancer. Here, we describe a system to introduce exogenous antigens into genetically engineered mouse lung cancers to mimic tumor neoantigens. We show that endogenous T cells respond to and infiltrate tumors, significantly delaying malignant progression. Despite continued antigen expression, T cell infiltration does not persist and tumors ultimately escape immune attack. Transplantation of cell lines derived from these lung tumors or prophylactic vaccination against the autochthonous tumors, however, results in rapid tumor eradication or selection of tumors that lose antigen expression. These results provide insight into the dynamic nature of the immune response to naturally arising tumors.

Indexed as

AdenocarcinomaAdenocarcinoma of LungAdoptive TransferAnimalsAntigen PresentationAntigens, NeoplasmAntigens, SurfaceApoptosisApoptosis Regulatory ProteinsB-LymphocytesCancer VaccinesCD3 ComplexCD8-Positive T-LymphocytesCell CountCell ProliferationCytokinesAntigens, NeoplasmAntigens, SurfaceApoptosis Regulatory ProteinsCancer VaccinesCD3 ComplexCytokinesHistocompatibility Antigens Class IInterleukin-7 Receptor alpha SubunitOligopeptidesOVA 323-339OVA-8OvalbuminPdcd1 protein, mousePeptide FragmentsProgrammed Cell Death 1 Receptorsuperagonist SIYR

Identifiers

PMID21251614
PMCPMC3069809
OpenAlexW1552804793

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.