Evidence map›Paper›PMID 36743211›Full record

ArticleFrontiers in molecular biosciences2023

A Boolean-based machine learning framework identifies predictive biomarkers of HSP90-targeted therapy response in prostate cancer.

Sung-Young Shin, Margaret M Centenera, Joshua T Hodgson, Elizabeth V Nguyen, Lisa M Butler, Roger J Daly, Lan K Nguyen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Advances in Prostate Cancer Biomarkers and Probes.Cyborg and bionic systems (Washington, D.C.) · 2024
    Review
  6. Review
  7. Review
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

7 authors at 3 institutions in 1 country.

Sung-Young ShinDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
Margaret M CenteneraSouth Australian Immunogenomics Cancer Institute and Freemasons Foundation Centre for Men's Health, University of Adelaide, Adelaide, SA, Australia.
Joshua T HodgsonSouth Australian Immunogenomics Cancer Institute and Freemasons Foundation Centre for Men's Health, University of Adelaide, Adelaide, SA, Australia.
Elizabeth V NguyenDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
Lisa M ButlerSouth Australian Immunogenomics Cancer Institute and Freemasons Foundation Centre for Men's Health, University of Adelaide, Adelaide, SA, Australia.
Roger J DalyDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
Lan K NguyenDepartment of Biochemistry and Molecular Biology, Monash University, Clayton, VIC, Australia.
Monash University · AUSouth Australian Health and Medical Research Institute · AUUniversity of Adelaide · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precision medicine has emerged as an important paradigm in oncology, driven by the significant heterogeneity of individual patients' tumour. A key prerequisite for effective implementation of precision oncology is the development of companion biomarkers that can predict response to anti-cancer therapies and guide patient selection for clinical trials and/or treatment. However, reliable predictive biomarkers are currently lacking for many anti-cancer therapies, hampering their clinical application. Here, we developed a novel machine learning-based framework to derive predictive multi-gene biomarker panels and associated expression signatures that accurately predict cancer drug sensitivity. We demonstrated the power of the approach by applying it to identify response biomarker panels for an Hsp90-based therapy in prostate cancer, using proteomic data profiled from prostate cancer patient-derived explants. Our approach employs a rational feature section strategy to maximise model performance, and innovatively utilizes Boolean algebra methods to derive specific expression signatures of the marker proteins. Given suitable data for model training, the approach is also applicable to other cancer drug agents in different tumour settings.

Indexed as

17-AAGBoolean function minimizationfeature selectionHsp90 inhibitormachine learningprecision oncologypredictive biomarkerprostate cancer

Identifiers

PMID36743211
PMCPMC9892654
OpenAlexW4317387681

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.