Evidence map›Paper›PMID 38400673›Full record

ArticleCancer medicine2024

Low nuclear expression of HIF-hydroxylases PHD2/EGLN1 and PHD3/EGLN3 are associated with poor recurrence-free survival in clear cell renal cell carcinoma.

Lassi Luomala, Kalle Mattila, Paula Vainio, Harry Nisén, Teijo Pellinen, Jouni Lohi, Teemu D Laajala, Petrus Järvinen, Anna-Riina Koskenniemi, Panu Jaakkola and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 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
0.6field-weighted citation impact, top 35% 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, 2 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

11 authors at 2 institutions in 1 country.

Lassi LuomalaDept. of Urology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.ORCID 0000-0003-0053-7302
Kalle MattilaDepartment of Oncology and Radiotherapy, FICAN West Cancer Centre, University of Turku, Turku University Hospital, Turku, Finland.
Paula VainioDept. of Pathology, Turku University Hospital, University of Turku, Turku, Finland.
Harry NisénDept. of Urology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Teijo PellinenInstitute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Jouni LohiDiagnostic Center, HUSLAB Laboratory Services, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Teemu D LaajalaDiagnostic Center, HUSLAB Laboratory Services, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Petrus JärvinenDept. of Urology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
Anna-Riina KoskenniemiDept. of Pathology, Turku University Hospital, University of Turku, Turku, Finland.
Panu JaakkolaDepartment of Oncology and Radiotherapy, FICAN West Cancer Centre, University of Turku, Turku University Hospital, Turku, Finland.
Tuomas MirttiDiagnostic Center, HUSLAB Laboratory Services, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
University of Helsinki · FIUniversity of Turku · FI

Funding

Cancer Foundation Finland (Syöpäsäätiö)Diagnostic Center, Helsinki University HospitalFinnish urological association (Suomen urologiyhdistys)Kidney Foundation (Munuaissäätiö)
6 · The paper itself

Abstract

backgroundHypoxia inducible factors, HIF-1α and HIF-2α, and their main regulators, the prolyl hydroxylase domain proteins (PHDs), mediate cellular response to hypoxia and contribute to tumor progression in clear cell renal cell carcinoma (ccRCC). These biomarkers may improve the value of traditional histopathological features in predicting disease progression after nephrectomy for localized ccRCC and guide patient selection for adjuvant treatments. PATIENTS AND

methodsIn this study, we analyzed the associations of PHD2 and PHD3 with histopathological tumor features and recurrence-free survival (RFS) in a retrospective cohort of 173 patients who had undergone surgery for localized ccRCC at Helsinki University Hospital (HUH), Finland. An external validation cohort of 191 patients was obtained from Turku University Hospital (TUH), Finland. Tissue-microarrays (TMA) were constructed using the primary tumor samples. Clinical parameters and follow-up information from 2006 to 2019 were obtained from electronic medical records. The cytoplasmic and nuclear expression of PHD2, and PHD3 were scored based on immunohistochemical staining and their associations with histopathological features and RFS were evaluated.

resultsNuclear PHD2 and PHD3 expression in cancer cells were associated with lower pT-stage and Fuhrman grade compared with negative nuclei. Patients with positive nuclear expression of PHD2 and PHD3 in cancer cells had favorable RFS compared with patients having negative tumors. The nuclear expression of PHD2 was independently associated with a decreased risk of disease recurrence or death from RCC in multivariable analysis. These results were observed in both cohorts.

conclusionsThe absence of nuclear PHD2 and PHD3 expression in ccRCC was associated with poor RFS and the nuclear expression of PHD2 predicted RFS regardless of other known histopathological prognostic factors. Nuclear PHD2 and PHD3 are potential prognostic biomarkers in patients with localized ccRCC and should be further investigated and validated in prospective studies.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsBiomarkersHumansHypoxiaHypoxia-Inducible Factor 1, alpha SubunitHypoxia-Inducible Factor-Proline DioxygenasesMixed Function OxygenasesNeoplasm Recurrence, LocalProspective StudiesRetrospective StudiesBiomarkersEGLN1 protein, humanEGLN3 protein, humanHypoxia-Inducible Factor 1, alpha SubunitHypoxia-Inducible Factor-Proline DioxygenasesMixed Function Oxygenasesbiomarkerhydroxylase-domain proteins (PHD)hypoxia inducible factors (HIF)recurrence-free survivalrenal cell carcinoma (RCC)

Identifiers

PMID38400673
PMCPMC10891444
OpenAlexW4392131571

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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.