ReviewMolecular biology reports2026
Acidic nuclear phosphoprotein 32A (ANP32A): structure, function, and its role in disease pathogenesis.
Review in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Acidic nuclear phosphoprotein 32A (ANP32A) is not only a core component of the inhibitor of histone acetyltransferases (INHAT) complex but also a crucial pleiotropic protein regulating cellular homeostasis and disease progression. Its extensive involvement in transcriptional regulation, apoptotic cascades, and signal transduction underpins its pivotal role across virology, neurobiology, and oncology. This review systematically elucidates the structure-function relationship of ANP32A, delineating its role as an essential host factor for viral replication and its complex involvement in neurodegenerative processes. Particular emphasis is placed on its context-dependent duality within oncology, where it exerts a pronounced "double-edged sword" effect by acting as either a tumor suppressor or an oncogene depending on the cellular milieu. Ultimately, this article aims to provide a theoretical foundation for the development of precision-targeted clinical interventions directed at ANP32A.
Indexed as
Identifiers
42474758What OpenQuestion holds
Registered trials
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.