Evidence map›Paper›PMID 35847718›Full record

ArticleEJHaem2020

Marginal zone lymphoma expression of histidine-rich glycoprotein correlates with improved survival.

Tor Persson Skare, Elin Sjöberg, Mattias Berglund, Ross O Smith, Francis P Roche, Cecilia Lindskog, Birgitta Sander, Ingrid Glimelius, Alex R Gholiha, Gunilla Enblad and 2 more

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2020. 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
0.1field-weighted citation impact, top 51% 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. Article
  2. Article
  3. 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

12 authors at 2 institutions in 1 country.

Tor Persson SkareDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Elin SjöbergDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Mattias BerglundDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Ross O SmithDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Francis P RocheDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Cecilia LindskogDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Birgitta SanderDept of Laboratory Medicine Division of Pathology Karolinska Institutet and Karolinska University Hospital Stockholm Sweden.
Ingrid GlimeliusDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Alex R GholihaDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.ORCID https://orcid.org/0000-0002-3393-1106
Gunilla EnbladDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.
Rose-Marie AminiDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.ORCID https://orcid.org/0000-0003-0901-5252
Lena Claesson-WelshDepartment of Immunology Genetics and Pathology Science for Life and Beijer Laboratories and Unit of Experimental and Clinical Oncology Uppsala University Uppsala Sweden.ORCID https://orcid.org/0000-0003-4275-2000
Uppsala University · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The abundant hepatocyte-expressed plasma protein histidine-rich glycoprotein (HRG) enhances antitumor immunity by polarizing inflammatory and immune cells in several mouse models, however, the clinical relevance of HRG in human cancer is poorly explored. The expression and role of HRG in human B-cell lymphomas was investigated in order to find new tools for prognosis and treatment. Findings: Immunohistochemical (IHC) analysis and RNA hybridization of tissue microarrays showed that (i) HRG was expressed by tumor cells in marginal zone lymphoma (MZL), in 36% of 59 cases. Expression was also detected in follicular lymphoma (22%), mantle cell lymphoma (19%), and indiffuse large B-cell lymphoma (DLBCL;5%) while primary CNS lymphoma (PCNSL) lacked expression of HRG. (ii) MZL patients positive for HRG showed a superior overall survival outcome (HR = 0.086, 95% CI = 0.014-0.518, Conclusion: HRG expression by MZL tumor cells correlates with an altered transcription profile and improved overall survival.

Indexed as

alpha defensin 1gene expressionhistidine rich glycoproteinmarginal zone lymphomasurvival

Identifiers

PMID35847718
PMCPMC9175683
OpenAlexW3047950584

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.