Evidence map›Paper›PMID 39300957›Full record

ArticleCancer medicine2024

Aging-related biomarkers in testicular cancer survivors after different oncologic treatments.

A Carballo-Muñoz, G Lima, L Llorente, Y A Remolina-Bonilla, S Jaime-Casas, A Otamendi-Lopez, R A Ortiz-Guerra, Hugo E Velazquez, Y Atisha-Fregoso, M T Bourlon

Abstract 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

A Carballo-MuñozDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.ORCID https://orcid.org/0000-0002-2380-5886
G LimaDepartment of Inmunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
L LlorenteDepartment of Inmunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
Y A Remolina-BonillaDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.ORCID https://orcid.org/0000-0003-2388-5844
S Jaime-CasasDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
A Otamendi-LopezDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
R A Ortiz-GuerraDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
Hugo E VelazquezRadiology Department, National Institute of Cardiology, Mexico City, Tlalpan, Mexico.
Y Atisha-FregosoInstitute of Molecular Medicine, Feinstein Institutes for Medical Research, New York, New York, USA.
M T BourlonDepartment of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.ORCID https://orcid.org/0000-0002-3116-912X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTesticular cancer survivors (TCS) exposed to chemotherapy have an increased expression of CDKN2A/p16

methodsCase-control study of TCS, disease-free ≥3 months and stratified by primary treatment modality into orchiectomy only, chemotherapy, or bone marrow transplant (BMT). Each group was compared with age-matched healthy controls (HC). We measured the relative proportions of lymphocyte subpopulations using flow cytometry, levels of C-reactive protein, and relative expression of CDKN2A/p16

resultsWe included 65 patients; 19 were treated with orchiectomy only, 35 received different doses of chemotherapy, and 11 underwent BMT. The chemotherapy and BMT groups had decreased naïve CD4 cells compared to HC. The chemotherapy group showed increased central and effector memory CD4 cells, as well as effector and terminally differentiated CD8 cells, compared to HC. Chemotherapy (chemotherapy 1.84 vs. HC 0.92; p < 0.01) and BMT (BMT 6.96 vs. HC 1.25; p < 0.005) groups had higher expression of CDKN2A/p16

conclusionsAmong TCS, only patients exposed to cytotoxic agents developed an immunosenescent phenotype. This finding supports the attribution of this alteration to the cytotoxic treatment.

Indexed as

Cancer SurvivorsCyclin-Dependent Kinase Inhibitor p16OrchiectomyTesticular NeoplasmsAdultAgingBone Marrow TransplantationCase-Control StudiesHumansImmunosenescenceMaleMiddle AgedYoung AdultCDKN2A protein, humanCyclin-Dependent Kinase Inhibitor p16biomarkerscancer care continuumchemotherapygerm cell tumorsurvival

Identifiers

PMID39300957
PMCPMC11413499

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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.