Evidence map›Paper›PMID 23114578›Full record

ReviewDiscovery medicine2012

T cell coinhibition and immunotherapy in human breast cancer.

Murali Janakiram, Yael M Abadi, Joseph A Sparano, Xingxing Zang

Abstract readReview
In one paragraph

Review in Discovery medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Wide Expression and Significance of Alternative Immune Checkpoint Molecules, B7x and HHLA2, in PD-L1-Negative Human Lung Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  10. Article
  11. The association betweenBioscience reports · 2017
    Article
  12. Article
  13. Article
  14. HHLA2, a New Immune Checkpoint Member of the B7 Family, Is Widely Expressed in Human Lung Cancer and Associated with EGFR Mutational Status.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  15. Article
  16. Article
  17. Expression, Clinical Significance, and Receptor Identification of the Newest B7 Family Member HHLA2 Protein.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Murali JanakiramDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Yael M Abadi
Joseph A Sparano
Xingxing Zang
Albert Einstein College of Medicine · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
New T Cell Coinhibitory Pathway and Type 1 DiabetesDP2DK083076 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ZANG, XINGXING · 2008 to 2010
$2.6M
NCI NIH HHS P30 CA013330NCI NIH HHS P30CA013330NIDDK NIH HHS DP2 DK083076NIDDK NIH HHS DP2DK083076NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32GM007491
6 · The paper itself

Abstract

Costimulation and coinhibition generated by the B7 family and their receptor CD28 family have key roles in regulating T lymphocyte activation and tolerance. These pathways are very attractive therapeutic targets for human cancers including breast cancer. Gene polymorphisms of B7x (B7-H4/B7S1), PD-1 (CD279), and CTLA-4 (CD152) are associated with increased risk of developing breast cancer although the underlying mechanisms are unclear. In human breast cancer microenvironment, up-regulation of coinhibitory B7/CD28 members B7x, B7-H3 (CD276), and PD-L1 (B7-H1/CD274) on tumor cells as well as PD-1 and PD-L1 on tumor-infiltrating immune cells are emerging as immune evasion pathways. Chemotherapy can affect the expression of these molecules, and therefore may dampen the immune response against breast cancer. Immunotherapy targeting T cell coinhibition as monotherapy or combined with standard therapies are in early stages of clinical development, but hold great promise for treatment of human breast cancer.

Indexed as

Breast NeoplasmsDNA AdductsFemaleHumansImmunotherapyT-LymphocytesDNA Adducts

Identifiers

PMID23114578
PMCPMC4107447
OpenAlexW150346066

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.