ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
NUDT21 Drives T-Cell Acute Lymphoblastic Leukemia Through Dual Regulation of Alternative Polyadenylation and Transcriptional Activation.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
19 authors.
Funding
Abstract
T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy with limited therapeutic options. Here, we identify the alternative polyadenylation (APA) regulator NUDT21 as a key factor in T-ALL maintenance through integrated multi-omics analyses and functional studies. NUDT21 is aberrantly upregulated in T-ALL patients, and its elevated expression is associated with poor clinical outcomes. Mechanistically, NUDT21 exerts dual oncogenic functions. As a core component of the CFIm complex, NUDT21 promotes distal poly(A) site usage of oncogenic transcripts, most prominently UBE2D3, generating long 3'UTR isoforms with enhanced mRNA stability and increased protein expression. Functionally, UBE2D3 acts as a critical downstream effector that sustains leukemia cell proliferation and survival through MYC-dependent signaling. Beyond its canonical role in APA regulation, NUDT21 also localizes to transcriptionally active promoters and interacts with lineage-specific transcription factors, including MYB, RUNX1, and GATA3, to facilitate MYC transcription. Importantly, pharmacological targeting of NUDT21 with ouabain octahydrate induces robust apoptosis in T-ALL cells by promoting NUDT21 protein degradation and concomitant suppression of UBE2D3 and MYC. Collectively, our findings establish NUDT21 as a multimodal oncogenic regulator and a promising therapeutic target in T-ALL.
Indexed as
Identifiers
What 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.