Evidence map›Paper›PMID 27683557›Full record

ArticleCancer discovery2016

TGFβ1-Mediated SMAD3 Enhances PD-1 Expression on Antigen-Specific T Cells in Cancer.

Benjamin V Park, Zachary T Freeman, Ali Ghasemzadeh, Michael A Chattergoon, Alleluiah Rutebemberwa, Jordana Steigner, Matthew E Winter, Thanh V Huynh, Suzanne M Sebald, Se-Jin Lee and 3 more

Abstract read
In one paragraph

Article in Cancer discovery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 191 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
191citing papers in PubMed, 1 pooled it
7.7field-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

191 citing papers in PubMed, 1 synthesis or guideline pooled it, 276 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Targeting Tumor-Associated Macrophages and Cancer-Associated Fibroblasts to Overcome Therapeutic Resistance in Hepatocellular Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  11. Article
  12. Strategies to target PD-1/PD-L1 in the tumor microenvironment.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  13. Article
  14. Article
  15. Do Metastatic Cells Arise from PD-L1International journal of molecular sciences · 2026
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

131 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

13 authors at 1 institution in 1 country.

Benjamin V ParkDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Zachary T FreemanDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ali GhasemzadehImmunology and Hematopoiesis Division, Department of Oncology, Bloomberg-Kimmel Institute, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Michael A ChattergoonDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Alleluiah RutebemberwaDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jordana SteignerDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Matthew E WinterDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Thanh V HuynhDepartment of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Suzanne M SebaldDepartment of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Se-Jin LeeDepartment of Molecular Biology and Genetics, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Fan PanImmunology and Hematopoiesis Division, Department of Oncology, Bloomberg-Kimmel Institute, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Drew M PardollImmunology and Hematopoiesis Division, Department of Oncology, Bloomberg-Kimmel Institute, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Andrea L CoxDivision of Infectious Diseases, The Johns Hopkins University School of Medicine, Baltimore, Maryland. acox@jhmi.edu.
Johns Hopkins University · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
Scientific CoreU19AI088791 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2010 to 2020
$8.2M
Training Veterinarians for Careers in Biomedical ResearchT32OD011089 · OD · JOHNS HOPKINS UNIVERSITY · PI JOSEPH L MANKOWSKI · 2012 to 2026
$6.7M
Characterization of Myostatin and GDF-11R01AR060636 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEE, SE-JIN · 2010 to 2020
$3.7M
The Role of EOS in Regulatory T-cell Biology.R01AI089830 · NIAID · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M. · 2010 to 2014
$2.0M
Metabolic regulation of T cell fate and tumor immunityR01AI099300 · NIAID · JOHNS HOPKINS UNIVERSITY · PI PAN, FAN · 2013 to 2017
$2.0M
NCI NIH HHS P30 CA006973NIAID NIH HHS R01 AI089830NIAID NIH HHS R01 AI099300NIAID NIH HHS U19 AI088791NIAMS NIH HHS R01 AR060636NIGMS NIH HHS T32 GM007309NIH HHS T32 OD011089
6 · The paper itself

Abstract

Programmed death-1 (PD-1) is a coinhibitory receptor that downregulates the activity of tumor-infiltrating lymphocytes (TIL) in cancer and of virus-specific T cells in chronic infection. The molecular mechanisms driving high PD-1 expression on TILs have not been fully investigated. We demonstrate that TGFβ1 enhances antigen-induced PD-1 expression through SMAD3-dependent, SMAD2-independent transcriptional activation in T cells in vitro and in TILs in vivo The PD-1 SIGNIFICANCE: Engagement of the coinhibitory receptor PD-1 or its ligand, PD-L1, dramatically inhibits the antitumor function of TILs within the TME. Our findings represent a novel immunosuppressive function of TGFβ and demonstrate that TGFβ1 allows tumors to evade host immune responses in part through enhanced SMAD3-mediated PD-1 expression on TILs. Cancer Discov; 6(12); 1366-81. ©2016 AACRThis article is highlighted in the In This Issue feature, p. 1293.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell Line, TumorCytokinesDrug Resistance, NeoplasmHumansJurkat CellsLymphocytes, Tumor-InfiltratingMiceNeoplasmsProgrammed Cell Death 1 ReceptorSignal TransductionSmad3 ProteinTransforming Growth Factor beta1Tumor MicroenvironmentCytokinesPDCD1 protein, humanProgrammed Cell Death 1 ReceptorSmad3 ProteinSMAD3 protein, humanTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID27683557
PMCPMC5295786
OpenAlexW2527634451

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.