Evidence map›Paper›PMID 33603952›Full record

ArticleOxidative medicine and cellular longevity2021

Testis-Specific Thioredoxins TXNDC2, TXNDC3, and TXNDC6 Are Expressed in Both Testicular and Systemic DLBCL and Correlate with Clinical Disease Presentation.

Mikko C Chan, Janette Savela, Riina K Ollikainen, Hanna-Riikka Teppo, Ilkka Miinalainen, Risto Pirinen, Esa J M Kari, Hanne Kuitunen, Taina Turpeenniemi-Hujanen, Outi Kuittinen and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. 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
0.2field-weighted citation impact, top 49% 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. Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins.International journal of molecular sciences · 2026
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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

11 authors at 4 institutions in 1 country.

Mikko C ChanCancer and Translational Medicine Research Unit, University of Oulu, Finland.ORCID https://orcid.org/0000-0002-1244-7905
Janette SavelaCancer and Translational Medicine Research Unit, University of Oulu, Finland.
Riina K OllikainenCancer and Translational Medicine Research Unit, University of Oulu, Finland.
Hanna-Riikka TeppoCancer and Translational Medicine Research Unit, University of Oulu, Finland.ORCID https://orcid.org/0000-0002-9145-5902
Ilkka MiinalainenBiocenter, University of Oulu, Oulu, Finland.
Risto PirinenDepartment of Pathology, North Karelia Central Hospital, Joensuu, Finland.
Esa J M KariDepartment of Oncology and Radiotherapy and Medical Research Center, Oulu University Hospital, Oulu, Finland.
Hanne KuitunenDepartment of Oncology and Radiotherapy and Medical Research Center, Oulu University Hospital, Oulu, Finland.
Taina Turpeenniemi-HujanenCancer and Translational Medicine Research Unit, University of Oulu, Finland.
Outi KuittinenDepartment of Oncology and Radiotherapy and Medical Research Center, Oulu University Hospital, Oulu, Finland.
Milla E L KuusistoCancer and Translational Medicine Research Unit, University of Oulu, Finland.
Oulu University Hospital · FINorth Karelia Central Hospital · FIUniversity of Eastern Finland · FIUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DLBCL is the most common type of non-Hodgkin lymphoma with a substantial group of patients suffering a poor prognosis. Therefore more specific markers are required for better understanding of disease biology and treatment. This study demonstrates that testis-specific antioxidant enzymes TXNDC2, TXNDC3, and TXNDC6 alongside oxidative stress marker 8-OHdG are expressed in both testicular and systemic DLBCL, and their presence or absence has correlations with clinical risk factors such as the number of extranodal effusion, the appearance of B-symptoms, and treatment response. Biopsy samples were collected from 28 systemic and 21 testicular male DLBCL patients. The samples were histostained with TXNDC2, TXNDC3, TXNDC6, and 8-OHdG, then graded by a hematopathologist blinded to clinical data. Immunoelectron microscopy was used as a second method to confirm the reliability of the acquired immunohistochemistry data. The absence of nuclear TXNDC2 expression in testicular DLBCL cells correlated with worse primary treatment response, cytoplasmic TXNDC3 expression in testicular and systemic DLBCL associated with lower frequency of B-symptoms, and TXNDC6 expression in cytoplasm in systemic DLBCL had a clinical significance with higher LD levels suggesting a role in the biological nature of these lymphomas. Overall, TXNDC3 cytoplasmic expression is correlated with a more positive outcome in both testicular and systemic DLBCL, while TXNDC6 cytoplasmic expression is associated with a negative outcome in systemic DLBCL.

Indexed as

8-Hydroxy-2'-DeoxyguanosineCell Line, TumorHumansLymphoma, Large B-Cell, DiffuseMaleMembrane ProteinsMiddle AgedOrgan SpecificityTesticular NeoplasmsTestisThioredoxins8-Hydroxy-2'-DeoxyguanosineMembrane ProteinsNME8 protein, humanNME9 protein, humanThioredoxinsTXNDC2 protein, human

Identifiers

PMID33603952
PMCPMC7870302
OpenAlexW3126842727

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Registered trials

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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.