Evidence map›Paper›PMID 40415137›Full record

Observational studyPituitary2025

Genes of the "regulation of lymphocyte activation" pathway may influence immune cells infiltration in growth hormone secreting pituitary tumors.

Sabrina Chiloiro, Flavia Costanza, Giovanni Luca Scaglione, Filippo Russo, Carmela Nardelli, Antonella Giampietro, Pier Paolo Mattogno, Liverana Lauretti, Guido Rindi, Laura De Marinis and 5 more

Abstract readObservational Study
In one paragraph

Observational study in Pituitary, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Clinical characteristics associated with somaticFrontiers in endocrinology · 2026
    Pooled it
  2. 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

15 authors.

Sabrina Chiloiro *Department of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy. sabrina.chiloiro@unicatt.it.ORCID http://orcid.org/0000-0001-9241-2392
Flavia Costanza *Department of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Giovanni Luca Scaglione *Bioinformatic Unit, Istituto Dermopatico dell'Immacolata (IDI), Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00167, Rome, Italy.
Filippo RussoDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131, Naples, Italy.
Carmela NardelliDepartment of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131, Naples, Italy.
Antonella GiampietroDepartment of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Pier Paolo MattognoDepartment of Neurosurgery, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00168, Rome, Italy.
Liverana LaurettiDepartment of Neurosurgery, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00168, Rome, Italy.
Guido RindiDepartment of Woman and Child Health Sciences and Public Health, Anatomic Pathology Unit, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00168, Rome, Italy.
Laura De MarinisDepartment of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Marco GessiDepartment of Woman and Child Health Sciences and Public Health, Anatomic Pathology Unit, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00168, Rome, Italy.
Antonio BianchiDepartment of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy.
Francesco DogliettoDepartment of Neurosurgery, Fondazione Policlinico Universitario A. Gemelli, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), 00168, Rome, Italy.
Ettore Domenico Capoluongo *Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, 80131, Naples, Italy.
Alfredo Pontecorvi *Department of Medical and Surgical Translational Sciences, Catholic University of the Sacred Heart, 00168, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe tumor microenvironment (TME) may provide a useful framework for understanding the heterogeneous behavior of growth hormone (GH) secreting pituitary adenomas. Although the interest in TME in somatotropinomas has increased exponentially over the last few decades, there is limited elucidation of its mechanisms, particularly in relation to genes expression involved in its regulation.

methodsA retrospective, observational, single-center study was conducted on 85 subjects: 46 patients diagnosed with acromegaly and 39 controls. After DNA extraction, clinical exome sequencing was performed and genomic alterations were detected, classified, and filtered using a dedicated bioinformatics pipeline.

results5759 unique genetic variants were found in patients with acromegaly. 33 patients (72%) showed the presence of at least one pathogenic variant in at least one of the following genes: FANCD2, SPTA1, TYRO3, and ZNF335. The enrichment pathway analysis of mutated genes was performed and showed that these genes were included in the same genetic pathway called "regulation of lymphocyte activation" (GO:0051249). Inflammatory infiltrate was analyzed in histological samples in 26 patients. A significantly higher number of CD68 + macrophages (P-value = 0.008), a lower number of CD8 + T lymphocytes (P-value = 0.037) and a higher CD68 + macrophages/ CD8 + T-lymphocytes ratio (P-value = 0.004) were observed in patients with pathogenic variants of genes of "regulation of lymphocyte activation" pathway.

conclusionThis study provides new insights into the genetic basis of the TME in somatotropinomas and suggests that genetics may influence immune cells infiltration in acromegaly.

Indexed as

AdenomaGrowth Hormone-Secreting Pituitary AdenomaLymphocyte ActivationPituitary NeoplasmsAcromegalyAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesTumor MicroenvironmentAcromegalyClinical exome sequencingGeneticsImmune cells infiltrationPituitary adenomasTumor microenvironment

Identifiers

PMID40415137
PMCPMC12104112

What OpenQuestion holds

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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.