Evidence map›Paper›PMID 31231778›Full record

ReviewCurrent hematologic malignancy reports2019

Targeting Translation of mRNA as a Therapeutic Strategy in Cancer.

Ipsita Pal, Maryam Safari, Marko Jovanovic, Susan E Bates, Changchun Deng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hematologic malignancy reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 47 citations in OpenAlex.

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  13. Pancreatic Cancer: Nucleic Acid Drug Discovery and Targeted Therapy.Frontiers in cell and developmental biology · 2022
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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

5 authors at 2 institutions in 1 country.

Ipsita PalDepartment of Medicine, Center for Lymphoid Malignancies, Columbia University Irving Medical Center, New York, NY, USA.
Maryam SafariDivison of Hematology and Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Marko JovanovicDepartment of Biological Sciences, Columbia University, New York, NY, USA.
Susan E BatesDivison of Hematology and Oncology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.
Changchun DengDepartment of Medicine, Center for Lymphoid Malignancies, Columbia University Irving Medical Center, New York, NY, USA. cd2448@cumc.columbia.edu.
Columbia University Irving Medical Center · USColumbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewTo highlight recent results in targeting mRNA translation and discuss the results and prospects of translation inhibitors in cancer therapy. RECENT

findingsUntil recently, inhibitors of mRNA translation have been thought to likely lack a therapeutic window. In 2012, the Food and Drug Administration (FDA) approved omacetaxine mepesuccinate (homoharringtonine) for the treatment of adults with chronic myelogenous leukemia (CML) who are resistant to at least two tyrosine kinase inhibitors. Since then, a few drugs, notably tomivosertib (eFT-508), selinexor (KPT-330), and ribavirin, have entered clinical trials. These drugs are known to inhibit mRNA translation. More recently, a number of interesting studies report that discrete subsets of proteins in cancer cells may be selectively targeted at the translation step, through inhibiting signals such as phospho-4E-BP1, eIF4A, and eIF4E. Promising therapies using these strategies have demonstrated potent anti-tumor activity in preclinical cancer models. The growing number of translation inhibitors with diverse mechanisms, coupled with emerging insights into translational regulation of different cancer-promoting genes, suggests a bright new horizon for the field of therapeutic targeting of mRNA translation in cancer.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsBiomarkersGene Expression Regulation, NeoplasticHumansNeoplasmsProtein BiosynthesisRNA, MessengerSignal TransductionAntineoplastic AgentsBiomarkersRNA, Messenger4E-BP1eIF4AeIF4EOmacetaxineSelinexorTranslationTranslation inhibitorUmbralisib

Identifiers

PMID31231778
OpenAlexW2951271467

What OpenQuestion holds

Textmetadata
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.