Evidence map›Paper›PMID 21355078›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2011

Identification of a soluble form of B7-H1 that retains immunosuppressive activity and is associated with aggressive renal cell carcinoma.

Xavier Frigola, Brant A Inman, Christine M Lohse, Christopher J Krco, John C Cheville, R Houston Thompson, Bradley Leibovich, Michael L Blute, Haidong Dong, Eugene D Kwon

Open access · greenAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 215 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
215citing papers in PubMed, 7 pooled it
5.4field-weighted citation impact, top 3% 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

215 citing papers in PubMed, 7 syntheses or guidelines pooled it, 353 citations in OpenAlex.

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  12. Prognostic value of PD-L1 in patients with metastatic renal cell carcinoma (mRCC) treated with antiangiogenic first line drugs (PROANG-SOGUG study).Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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155 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

10 authors at 4 institutions in 1 country.

Xavier FrigolaDepartment of Immunology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.
Brant A Inman
Christine M Lohse
Christopher J Krco
John C Cheville
R Houston Thompson
Bradley Leibovich
Michael L Blute
Haidong Dong
Eugene D Kwon
Duke University · USDuke Medical Center · USDuke University Hospital · USMayo Clinic · US

Funding

Clinical Impact of B7-H Immune Cell Coregulators in Renal Cell CarcinomaR01CA134345 · NCI · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG, KWON, EUGENE D. · 2009 to 2014
$1.5M
NCI NIH HHS CA134345NCI NIH HHS R01 CA134345
6 · The paper itself

Abstract

purposeRelease of inhibitory coregulatory proteins into the circulation may represent one mechanism by which tumors thwart immune responses. Our objective was to determine whether soluble B7-H1 (sB7-H1) levels in patients with clear cell renal cell carcinoma (ccRCC) are associated with pathologic features and patient outcome. EXPERIMENTAL

designWe developed an ELISA for quantification of sB7-H1 in biological fluids. Biochemical confirmation of the measured analyte as sB7-H1 was done by protein microsequencing using supernates from tumor cell lines. Biological activity of sB7-H1 was assessed in vitro utilizing T-cell apoptosis assays. We tested sB7-H1 levels in the sera from 172 ccRCC patients and correlated sB7-H1 levels with pathologic features and patient outcome.

resultssB7-H1 was detected in the cell supernatants of some B7-H1-positive tumor cell lines. Protein sequencing established that the measured sB7-H1 retained its receptor-binding domain and could deliver proapoptotic signals to T cells. Higher preoperative sB7-H1 levels were associated with larger tumors (P < 0.001), tumors of advanced stage (P = 0.017) and grade (P = 0.044), and tumors with necrosis (P = 0.003). A doubling of sB7-H1 levels was associated with a 41% increased risk of death (P = 0.010).

conclusionOur observations suggest that sB7-H1 may be detected in the sera of ccRCC patients and that sB7-H1 may systemically impair host immunity, thereby fostering cancer progression and subsequent poor clinical outcome.

Indexed as

AdultAgedAged, 80 and overAmino Acid SequenceAntigens, CDApoptosisB7-H1 AntigenCarcinoma, Renal CellCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorCulture Media, ConditionedEnzyme-Linked Immunosorbent AssayFemaleHumansImmunosuppressive AgentsAntigens, CDB7-H1 AntigenCD274 protein, humanCulture Media, ConditionedImmunosuppressive AgentsRecombinant Proteins

Identifiers

PMID21355078
PMCPMC3241002
OpenAlexW2145758395

What OpenQuestion holds

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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.