Evidence map›Paper›PMID 29296880›Full record

ArticleBlood advances2017

CD86 regulates myeloma cell survival.

Catherine M Gavile, Benjamin G Barwick, Scott Newman, Paola Neri, Ajay K Nooka, Sagar Lonial, Kelvin P Lee, Lawrence H Boise

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Why are long-lived plasma cells long-lived?Frontiers in immunology · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Endogenous CD28 drives CAR T cell responses in multiple myeloma.bioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. 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

8 authors at 4 institutions in 2 countries.

Catherine M GavileDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Benjamin G BarwickDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Scott NewmanSt. Jude Children's Research Hospital, Memphis, TN.
Paola NeriDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada; and.
Ajay K NookaDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Sagar LonialDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Kelvin P LeeDepartment of Immunology, Roswell Park Cancer Institute, Buffalo, NY.
Lawrence H BoiseDepartment of Hematology and Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
Emory University · USRoswell Park Comprehensive Cancer Center · USSt. Jude Children's Research Hospital · USUniversity of Calgary · CA

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
CD28-mediated Regulation of Multiple Myeloma Cell Proliferation and SurvivalR01CA121044 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI LEE, KELVIN P. · 2007 to 2023
$4.8M
The Role of CD86 in Multiple MyelomaR01CA192844 · NCI · EMORY UNIVERSITY · PI BOISE, LAWRENCE H. · 2016 to 2020
$1.9M
Proteosome inhibitor sensitivity in multiple myeloma: The role of ER stressR01CA127910 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BOISE, LAWRENCE H. · 2008 to 2012
$1.6M
NCI NIH HHS P30 CA138292NCI NIH HHS R01 CA121044NCI NIH HHS R01 CA127910NCI NIH HHS R01 CA192844
6 · The paper itself

Abstract

Although prognosis for patients with multiple myeloma has improved over the past decade, research toward discovery of new therapeutic avenues is important and could lead to a cure for this plasma cell malignancy. Here we show that blocking the CD28-CD86 pathway via silencing of either CD28 or CD86 leads to myeloma cell death. Inhibiting this pathway leads to downregulation of integrins and IRF4, a known myeloma survival factor. Our data also indicate that CD86, the canonical ligand in this pathway, has prosurvival activity that is dependent on its cytosolic domain. These findings indicate that targeting of this pathway is a promising therapeutic avenue for myeloma, because it leads to modulation of different processes important in cell viability.

Identifiers

PMID29296880
PMCPMC5729629
OpenAlexW2770790219

What OpenQuestion holds

Textmetadata
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.