Evidence map›Paper›PMID 41719623›Full record

ReviewThe Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases

Molecular factors associated with lung cancer in people living with HIV.

Ivonne Denisse Bautista-Rojas, Jesus Figueroa-Navarrete, Diana Laura Reyes-Hernandez, Evelyn Rivera-Toledo

Abstract readReview
In one paragraph

Review in The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Ivonne Denisse Bautista-RojasUniversidad Nacional Autónoma de México (UNAM), Facultad de Medicina, Departamento de Microbiología y Parasitología, Mexico City, Mexico.
Jesus Figueroa-NavarreteUniversidad Nacional Autónoma de México (UNAM), Facultad de Medicina, Departamento de Microbiología y Parasitología, Mexico City, Mexico.
Diana Laura Reyes-HernandezUniversidad Nacional Autónoma de México (UNAM), Facultad de Medicina, Departamento de Microbiología y Parasitología, Mexico City, Mexico.
Evelyn Rivera-ToledoUniversidad Nacional Autónoma de México (UNAM), Facultad de Medicina, Departamento de Microbiología y Parasitología, Mexico City, Mexico. Electronic address: evelyn.rivera@unam.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the most common Non-AIDS-Defining Cancer (NADC) and a leading cause of cancer-related death in People Living With HIV (PLWH). Despite antiretroviral therapy, PLWH are at higher risk of developing cancer compared to the general population. This increased susceptibility reflects a combination of immunosuppression, chronic inflammation, smoking, and direct oncogenic effects of HIV proteins. Tat, gp120, and Nef modulate cell cycle control, apoptosis, epithelial-mesenchymal transition, angiogenesis, and immune evasion. Persistent HIV reservoirs in lung tissue (mainly effector memory CD4⁺ T-cells and alveolar macrophages) sustain local immune dysregulation. Extracellular vesicles carrying viral proteins or nucleic acids activate oncogenic pathways, while HIV integration disrupts tumor suppressor genes such as PTEN and induces epigenetic silencing of regulators like P16

Indexed as

HIV InfectionsLung NeoplasmsHumansRisk FactorsHIVLung cancerNon-AIDS-defining cancersOncogenic HIV proteins

Identifiers

PMID41719623
PMCPMC12933453

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.