Evidence map›Paper›PMID 40126183›Full record

ArticleOncoimmunology2025

Cellular and secretome profiling uncover immunological biomarkers in the prognosis of renal cell carcinoma patients.

Le Tong, Veronika Kremer, Shi Yong Neo, Christina Seitz, Nicholas P Tobin, Barbara Seliger, Ulrika Harmenberg, Eugenia Colón, Ann-Helén Scherman Plogell, Lisa L Liu and 1 more

Abstract read
In one paragraph

Article in Oncoimmunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

11 authors.

Le TongDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Veronika KremerDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Shi Yong NeoDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Christina SeitzInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Nicholas P TobinDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Barbara SeligerInstitute for Medical Immunology, Martin-Luther University Halle-Wittenberg, Halle, Germany.
Ulrika HarmenbergDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Eugenia ColónDepartment of Women's and Children's Health, Karolinska Institutet and S:t Göran's Hospital-Unilabs, Stockholm, Sweden.
Ann-Helén Scherman PlogellDepartment of Surgery and Oncology, S:t Göran's Hospital, Stockholm, Sweden.
Lisa L LiuDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Andreas LundqvistDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-9709-2970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal cell carcinoma (RCC) is recognized as an immunogenic tumor, yet tumor-infiltrating lymphocytes often exhibit diminished effector function. However, the mechanisms underlying reduced T and NK cell activity in RCC remain unclear. Here, we examined the immune contexture in RCC patients undergoing nephrectomy to identify immune-related biomarkers associated with disease progression. Immune cell phenotypes and secretion profiles were assessed using flow cytometry and Luminex multiplex analysis. Supervised multivariate analysis revealed several changes of which frequencies of T and NK cells expressing CCR5, CXCR3, and PD-1 were elevated within tumors compared with peripheral blood. In addition, higher levels of regulatory T cells, PD-1+, and CXCR3+ T and NK cells were observed in patients with relapse following nephrectomy. With regards to soluble factors, tumor-derived CXCL8 was associated with higher Fuhrman grade and increased frequency of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs). These biomarkers demonstrate potential relevance in the progression of RCC and merit further investigation in prospective studies.

Indexed as

Biomarkers, TumorCarcinoma, Renal CellKidney NeoplasmsAgedFemaleHumansKiller Cells, NaturalLymphocytes, Tumor-InfiltratingMaleMiddle AgedMyeloid-Derived Suppressor CellsNephrectomyPrognosisBiomarkers, TumorBiomarkersCXCL8NK cellsPD-1prognosisrenal cell carcinomaT cells

Identifiers

PMID40126183
PMCPMC11934188

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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.