Evidence map›Paper›PMID 23455497›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Host b7x promotes pulmonary metastasis of breast cancer.

Yael M Abadi, Hyungjun Jeon, Kim C Ohaegbulam, Lisa Scandiuzzi, Kaya Ghosh, Kimberly A Hofmeyer, Jun Sik Lee, Anjana Ray, Claudia Gravekamp, Xingxing Zang

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Methodology forBio-protocol · 2020
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. B7-H4 Modulates Regulatory CD4Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  19. Review
  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

10 authors at 1 institution in 1 country.

Yael M AbadiDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Hyungjun Jeon
Kim C Ohaegbulam
Lisa Scandiuzzi
Kaya Ghosh
Kimberly A Hofmeyer
Jun Sik Lee
Anjana Ray
Claudia Gravekamp
Xingxing Zang
Albert Einstein College of Medicine · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
TRAINING IN HORMONE-MEMBRANE INTERACTIONST32DK007513 · NIDDK · YESHIVA UNIVERSITY · PI ZUKIN, R. SUZANNE · 1986 to 2011
$3.7M
New T Cell Coinhibitory Pathway and Type 1 DiabetesDP2DK083076 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ZANG, XINGXING · 2008 to 2010
$2.6M
HEPATOLOGY RESEARCHT32DK007218 · NIDDK · YESHIVA UNIVERSITY · PI CZAJA, MARK J · 1986 to 2011
$2.1M
NCI NIH HHS P30 CA013330NCI NIH HHS P30CA013330NCI NIH HHS PC094137NIDDK NIH HHS DP2 DK083076NIDDK NIH HHS DP2DK083076NIDDK NIH HHS T32 DK007218NIDDK NIH HHS T32DK007218NIDDK NIH HHS T32 DK007513NIDDK NIH HHS T32DK007513NIGMS NIH HHS GM007288NIGMS NIH HHS T32 GM007288NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32GM007491
6 · The paper itself

Abstract

B7x (B7-H4 or B7S1) is an inhibitory member of the B7 family of T cell costimulation. It is expressed in low levels in healthy peripheral tissues, such as the lung epithelium, but is overexpressed in a variety of human cancers with negative clinical associations, including metastasis. However, the function of B7x in the context of cancer, whether expressed on cancer cells or on surrounding "host" tissues, has not been elucidated in vivo. We used the 4T1 metastatic breast cancer model and B7x knockout (B7x (-/-)) mice to investigate the effect of host tissue-expressed B7x on cancer. We found that 4T1 cells were B7x negative in vitro and in vivo, and B7x(-/-) mice had significantly fewer lung 4T1 tumor nodules than did wild-type mice. Furthermore, B7x(-/-) mice showed significantly enhanced survival and a memory response to tumor rechallenge. Mechanistic studies revealed that the presence of B7x correlated with reduced general and tumor-specific T cell cytokine responses, as well as with an increased infiltration of immunosuppressive cells, including tumor-associated neutrophils, macrophages, and regulatory T cells, into tumor-bearing lungs. Importantly, tumor-associated neutrophils strongly bound B7x protein and inhibited the proliferation of both CD4 and CD8 T cells. These results suggest that host B7x may enable metastasizing cancer cells to escape local antitumor immune responses through interactions with the innate and adaptive immune systems. Thus, targeting the B7x pathway holds much promise for improving the efficacy of immunotherapy for metastatic cancer.

Indexed as

AnimalsAntigens, LyBreast NeoplasmsCD11b AntigenCell Line, TumorCytokinesDisease Models, AnimalFemaleImmunologic MemoryLung NeoplasmsLymphocyte ActivationMiceMice, KnockoutNeutrophilsPhenotypeT-LymphocytesAntigens, LyCD11b AntigenCytokinesLy6G antigen, mouseV-Set Domain-Containing T-Cell Activation Inhibitor 1Vtcn1 protein, mouse

Identifiers

PMID23455497
PMCPMC3608819
OpenAlexW1745893103

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.