Evidence map›Paper›PMID 35085599›Full record

ArticleHuman pathology2022

Global assessment of IRF8 as a novel cancer biomarker.

Daniel C McQuaid, Gauri Panse, Wei-Lien Wang, Geraldine S Pinkus, Samuel G Katz, Mina L Xu

Open access · greenAbstract read
In one paragraph

Article in Human pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Daniel C McQuaidDepartment of Pathology, Yale New-Haven Hospital, Yale School of Medicine, New Haven, CT, 06510, USA.
Gauri PanseDepartment of Pathology, Yale New-Haven Hospital, Yale School of Medicine, New Haven, CT, 06510, USA.
Wei-Lien WangDepartment of Pathology and Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Geraldine S PinkusDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.
Samuel G KatzDepartment of Pathology, Yale New-Haven Hospital, Yale School of Medicine, New Haven, CT, 06510, USA. Electronic address: samuel.katz@yale.edu.
Mina L XuDepartment of Pathology, Yale New-Haven Hospital, Yale School of Medicine, New Haven, CT, 06510, USA. Electronic address: mina.xu@yale.edu.
Yale New Haven Hospital · USBrigham and Women's Hospital · USThe University of Texas MD Anderson Cancer Center · US

Funding

Medical Scientist Training ProgramT32GM136651 · NIGMS · YALE UNIVERSITY · PI BARBARA I KAZMIERCZAK · 2020 to 2026
$16.5M
NIGMS NIH HHS T32 GM136651
6 · The paper itself

Abstract

Interferon regulatory factor 8 (IRF8) is a member of the IRF family that is specific to the hematopoietic cell and is involved in regulating the development of human monocytic and dendritic-lineage cells, as well as B-cells. Because its utility as a sensitive and specific monoblast marker in the context of acute monocytic leukemias has been recently demonstrated, we hypothesized that it may also be useful as a novel immunohistochemical marker in myeloid sarcomas and blastic plasmacytoid dendritic cell neoplasms (BPDCNs) with respect to their differential diagnoses. In this retrospective study, we analyzed the IHC expression pattern of IRF8 in 385 patient samples across 30 types of cancers, referenced to their mRNA expression data available through The Cancer Genome Atlas. In addition, we assessed IRF8 in 35 myeloid sarcomas and 15 BPDCNs. Twenty-four of 35 cases of myeloid sarcomas (68.5%) showed positivity for IRF8, with six cases (17.1%) demonstrating IRF8 expression in the absence of CD34 and MPO. All 15 of 15 BPDCNs (100%) showed strong uniform expression of IRF8 and were occasionally more definitive than CD123. IRF8 was negative in all desmoplastic small round cell tumors, Ewing sarcomas, synovial sarcomas, and undifferentiated pleomorphic sarcomas, as well as all epithelial malignancies tested except for 2 triple negative breast cancers that showed subset weak staining. In conclusion, IRF8 is a novel marker helpful in identifying extranodal hematopoietic tumors that can otherwise be difficult to diagnose given the broad differential diagnoses and frequent loss of more common lineage-defining markers.

Indexed as

Biomarkers, TumorInterferon Regulatory FactorsNeoplasmsSarcomaHumansInterferon Regulatory Factor-8Retrospective StudiesBiomarkers, TumorInterferon Regulatory Factor-8Interferon Regulatory FactorsBlastic plasmacytoid dendritic neoplasmsCancer tissue microarraysIRF8Myeloid sarcoma

Identifiers

PMID35085599
PMCPMC10621657
OpenAlexW4206936559

What OpenQuestion holds

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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.