Evidence map›Paper›PMID 28117679›Full record

ReviewInternational journal of molecular sciences2017

The Potential of Targeting Ribosome Biogenesis in High-Grade Serous Ovarian Cancer.

Shunfei Yan, Daniel Frank, Jinbae Son, Katherine M Hannan, Ross D Hannan, Keefe T Chan, Richard B Pearson, Elaine Sanij

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

  1. Telomerase-Associated Genes as Prognostic Markers in High-Grade Serous Ovarian Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2026
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  8. The Interplay Between theInternational journal of molecular sciences · 2024
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  17. Reduced rDNA transcription diminishes skeletal muscle ribosomal capacity and protein synthesis in cancer cachexia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 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

8 authors at 3 institutions in 1 country.

Shunfei YanResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. Shunfei.yan@petermac.org.
Daniel FrankResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. dfrank@student.unimelb.edu.au.
Jinbae SonResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. jinbae.son@petermac.org.
Katherine M HannanDepartment of Biochemistry and Molecular Biology, University of Melbourne, Parkville, VIC 3010, Australia. kate.hannan@anu.edu.au.
Ross D HannanResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. ross.hannan@anu.edu.au.
Keefe T ChanResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. keefe.chan@petermac.org.
Richard B PearsonResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. rick.pearson@petermac.org.
Elaine SanijResearch Division, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia. elaine.sanij@petermac.org.
Peter MacCallum Cancer Centre · AUUniversity of Melbourne · AUAustralian National University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overall survival for patients with ovarian cancer (OC) has shown little improvement for decades meaning new therapeutic options are critical. OC comprises multiple histological subtypes, of which the most common and aggressive subtype is high-grade serous ovarian cancer (HGSOC). HGSOC is characterized by genomic structural variations with relatively few recurrent somatic mutations or dominantly acting oncogenes that can be targeted for the development of novel therapies. However, deregulation of pathways controlling homologous recombination (HR) and ribosome biogenesis has been observed in a high proportion of HGSOC, raising the possibility that targeting these basic cellular processes may provide improved patient outcomes. The poly (ADP-ribose) polymerase (PARP) inhibitor olaparib has been approved to treat women with defects in HR due to germline

Indexed as

BenzothiazolesCystadenocarcinoma, SerousFemaleHumansModels, GeneticMolecular Targeted TherapyNaphthyridinesOvarian NeoplasmsPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsRNA, RibosomalBenzothiazolesCX 5461NaphthyridinesolaparibPhthalazinesPiperazinesPoly(ADP-ribose) Polymerase InhibitorsRNA, RibosomalCX-5461high-grade serous carcinomahomologous recombinationPol Iribosome biogenesis

Identifiers

PMID28117679
PMCPMC5297839
OpenAlexW2578423810

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.