Evidence map›Paper›PMID 37923249›Full record

ArticleThe American journal of pathology2024

Specific Polo-Like Kinase 1 Expression in Nodular Lymphocyte-Predominant Hodgkin Lymphoma Suggests an Intact Immune Surveillance Program.

Jonathan Weiss, Kathryn Gibbons, Vida Ehyaee, Vanessa Perez-Silos, Alejandro Zevallos, Mark Maienschein-Cline, Eileen Brister, Maria Sverdlov, Eshana Shah, Jayalakshmi Balakrishna and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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

23 authors at 8 institutions in 1 country.

Jonathan WeissDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Kathryn GibbonsDepartment of Pathology, Henry Ford Hospital, Detroit, Michigan.
Vida EhyaeeDepartment of Pathology, Rush University, Chicago, Illinois.
Vanessa Perez-SilosDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois.
Alejandro ZevallosDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois.
Mark Maienschein-ClineResearch Informatics Core, University of Illinois at Chicago, Chicago, Illinois.
Eileen BristerResearch Tissue Imaging Core and Research Histology Core, University of Illinois at Chicago, Chicago, Illinois.
Maria SverdlovResearch Tissue Imaging Core and Research Histology Core, University of Illinois at Chicago, Chicago, Illinois.
Eshana ShahDepartment of Internal Medicine, University of Illinois at Chicago, Chicago, Illinois.
Jayalakshmi BalakrishnaDepartment of Pathology, Ohio State University, Columbus, Ohio.
Emily SymesDepartment of Pathology, University of Chicago, Chicago, Illinois.
John K FrederiksenDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois.
Peter H GannDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois.
Robert PostDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois.
Nicolas Lopez-HisijosDepartment of Pathology, Rush University, Chicago, Illinois.
John ReneauDepartment of Internal Medicine, Ohio State University, Columbus, Ohio.
Girish VenkataramanDepartment of Pathology, University of Chicago, Chicago, Illinois.
Nathanael BaileyDepartment of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
Noah A BrownDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Mina L XuDepartment of Pathology, Yale University, New Haven, Connecticut.
Ryan A WilcoxDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Kedar InamdarDepartment of Pathology, Henry Ford Hospital, Detroit, Michigan. Electronic address: kinamda1@hfhs.org.
Carlos Murga-ZamalloaDepartment of Pathology, University of Illinois at Chicago, Chicago, Illinois. Electronic address: catto@uic.edu.
University of Illinois Chicago · USUniversity of Michigan · USHenry Ford Hospital · USRush University · USThe Ohio State University · USUniversity of Chicago · USUniversity of Pittsburgh Medical Center · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) is a rare and relatively indolent B-cell lymphoma. Characteristically, the [lymphocyte-predominant (LP)] tumor cells are embedded in a microenvironment enriched in lymphocytes. More aggressive variants of mature B-cell and peripheral T-cell lymphomas exhibit nuclear expression of the polo-like kinase 1 (PLK1) protein, stabilizing MYC (alias c-myc) and associated with worse clinical outcomes. This study demonstrated expression of PLK1 in the LP cells in 100% of NLPHL cases (n = 76). In contrast, <5% of classic Hodgkin lymphoma cases (n = 70) showed PLK1 expression within the tumor cells. Loss-of-function approaches demonstrated that the expression of PLK1 promoted cell proliferation and increased MYC stability in NLPHL cell lines. Correlation with clinical parameters revealed that the increased expression of PLK1 was associated with advanced-stage disease in patients with NLPHL. A multiplex immunofluorescence panel coupled with artificial intelligence algorithms was used to correlate the composition of the tumor microenvironment with the proliferative stage of LP cells. The results showed that LP cells with PLK1 (high) expression were associated with increased numbers of cytotoxic and T-regulatory T cells. Overall, the findings demonstrate that PLK1 signaling increases NLPHL proliferation and constitutes a potential vulnerability that can be targeted with PLK1 inhibitors. An active immune surveillance program in NLPHL may be a critical mechanism limiting PLK1-dependent tumor growth.

Indexed as

Hodgkin DiseaseLymphoma, B-CellArtificial IntelligenceHumansLymphocytesPolo-Like Kinase 1Tumor MicroenvironmentPLK1 protein, humanPolo-Like Kinase 1

Identifiers

PMID37923249
PMCPMC10768536
OpenAlexW4388283553

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.