Evidence map›Paper›PMID 27058426›Full record

ReviewOncotarget2016

Molecules that target nucleophosmin for cancer treatment: an update.

Adele Di Matteo, Mimma Franceschini, Sara Chiarella, Serena Rocchio, Carlo Travaglini-Allocatelli, Luca Federici

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% of its field
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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

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  18. KPNA2 promotes renal cell carcinoma proliferation and metastasis via NPM.Journal of cellular and molecular medicine · 2021
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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

6 authors at 3 institutions in 1 country.

Adele Di MatteoIstituto di Biologia e Patologia Molecolari, Consiglio Nazionale delle Ricerche, Rome, Italy.
Mimma FranceschiniDipartimento di Scienze Mediche, Orali e Biotecnologiche, Università di Chieti "G. d'Annunzio", Chieti, Italy.
Sara ChiarellaDipartimento di Scienze Mediche, Orali e Biotecnologiche, Università di Chieti "G. d'Annunzio", Chieti, Italy.
Serena RocchioDipartimento di Scienze Biochimiche "A. Rossi Fanelli", Università di Roma "Sapienza", Rome, Italy.
Carlo Travaglini-AllocatelliDipartimento di Scienze Biochimiche "A. Rossi Fanelli", Università di Roma "Sapienza", Rome, Italy.
Luca FedericiDipartimento di Scienze Mediche, Orali e Biotecnologiche, Università di Chieti "G. d'Annunzio", Chieti, Italy.
University of Chieti-Pescara · ITSapienza University of Rome · ITInstitute of Molecular Biology and Pathology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleophosmin is a highly and ubiquitously expressed protein, mainly localized in nucleoli but able to shuttle between nucleus and cytoplasm. Nucleophosmin plays crucial roles in ribosome maturation and export, centrosome duplication, cell cycle progression, histone assembly and response to a variety of stress stimuli. Much interest in this protein has arisen in the past ten years, since the discovery of heterozygous mutations in the terminal exon of the NPM1 gene, which are the most frequent genetic alteration in acute myeloid leukemia. Nucleophosmin is also frequently overexpressed in solid tumours and, in many cases, its overexpression correlates with mitotic index and metastatization. Therefore it is considered as a promising target for the treatment of both haematologic and solid malignancies. NPM1 targeting molecules may suppress different functions of the protein, interfere with its subcellular localization, with its oligomerization properties or drive its degradation. In the recent years, several such molecules have been described and here we review what is currently known about them, their interaction with nucleophosmin and the mechanistic basis of their toxicity. Collectively, these molecules exemplify a number of different strategies that can be adopted to target nucleophosmin and we summarize them at the end of the review.

Indexed as

Amino Acid SequenceAntineoplastic AgentsHematologic NeoplasmsHumansIndolesMolecular StructureMolecular Targeted TherapyNeoplasmsNuclear ProteinsNucleophosminSequence Homology, Amino AcidAntineoplastic AgentsIndolesNPM1 protein, humanNSC 348884Nuclear ProteinsNucleophosminacute myeloid leukemiaB23nucleophosminsolid tumourstargeted therapy

Identifiers

PMID27058426
PMCPMC5190137
OpenAlexW2330101120

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.