Evidence map›Paper›PMID 40758167›Full record

ArticleBiochemical Society transactions2025

Anticancer drug development against ribosome synthesis and the nucleolus.

Andrew Loiacono, Sui Huang

Erratum issuedAbstract read
In one paragraph

Article in Biochemical Society transactions, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Andrew LoiaconoDepartment of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, U.S.A.ORCID 0009-0008-7146-6752
Sui HuangDepartment of Cell and Developmental Biology, Northwestern University Feinberg School of Medicine, Chicago, U.S.A.ORCID 0000-0002-2400-4319

Funding

Phenotypic marker-guided development of selective antimetastasis therapeutic leadsR01CA269967 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Kevin J. Frankowski, Sui HUANG · 2022 to 2026
$3.2M
NCI NIH HHS R01 CA269967
6 · The paper itself

Abstract

Nucleoli, the most prominent nuclear organelle, form around ribosomal DNA (rDNA) clusters at the p-arms of the five acrocentric chromosomes. Nucleoli are centers of ribosome synthesis, a vital activity in cell proliferation and organism viability. Ribosome biogenesis is a complex process involving the activity of all three RNA polymerases and numerous cellular factors. This energy-consuming process is, therefore, highly regulated, with the transcription of rDNA being the rate-limiting step. Given that uncontrolled cell proliferation is a hallmark of cancer, enhanced ribosome biogenesis plays a crucial role in sustaining tumor growth. In addition, nucleoli are multi-functional organelles, participating in genome organization, cell cycle, stress sensing, macromolecular trafficking, and the sequestration of cellular factors-functions that are also significantly altered in cancerous conditions. This review focuses on summarizing the role of nucleoli in carcinogenesis and anticancer therapeutics that target nucleoli and ribosome synthesis.

Indexed as

cancerdrug developmentnucleolusnucleusribosome biogenesis

Identifiers

PMID40758167
PMCPMC12409996

What OpenQuestion holds

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LicenceCC BY
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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.