Evidence map›Paper›PMID 32998700›Full record

ArticleBMC bioinformatics2020

Leveraging TCGA gene expression data to build predictive models for cancer drug response.

Evan A Clayton, Toyya A Pujol, John F McDonald, Peng Qiu

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Harmonized nonhuman cancer database.bioRxiv : the preprint server for biology · 2025
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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

4 authors at 2 institutions in 1 country.

Evan A ClaytonIntegrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Toyya A PujolSchool of Industrial and Systems Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
John F McDonaldIntegrated Cancer Research Center, School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
Peng QiuDepartment of Biomedical Engineering, Georgia Institute of Technology and Emory University, 950 Atlantic Dr NW, 30332-0230, Atlanta, GA, 404-385-1656, USA. peng.qiu@bme.gatech.edu.
Georgia Institute of Technology · USEmory University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMachine learning has been utilized to predict cancer drug response from multi-omics data generated from sensitivities of cancer cell lines to different therapeutic compounds. Here, we build machine learning models using gene expression data from patients' primary tumor tissues to predict whether a patient will respond positively or negatively to two chemotherapeutics: 5-Fluorouracil and Gemcitabine.

resultsWe focused on 5-Fluorouracil and Gemcitabine because based on our exclusion criteria, they provide the largest numbers of patients within TCGA. Normalized gene expression data were clustered and used as the input features for the study. We used matching clinical trial data to ascertain the response of these patients via multiple classification methods. Multiple clustering and classification methods were compared for prediction accuracy of drug response. Clara and random forest were found to be the best clustering and classification methods, respectively. The results show our models predict with up to 86% accuracy; despite the study's limitation of sample size. We also found the genes most informative for predicting drug response were enriched in well-known cancer signaling pathways and highlighted their potential significance in chemotherapy prognosis.

conclusionsPrimary tumor gene expression is a good predictor of cancer drug response. Investment in larger datasets containing both patient gene expression and drug response is needed to support future work of machine learning models. Ultimately, such predictive models may aid oncologists with making critical treatment decisions.

Indexed as

Machine LearningAntineoplastic AgentsArea Under CurveCluster AnalysisDatabases, GeneticDeoxycytidineFluorouracilGemcitabineGene Expression Regulation, NeoplasticHumansNeoplasmsROC CurveAntineoplastic AgentsDeoxycytidineFluorouracilGemcitabineDrug responseMachine learningPersonalized oncologyPredictive models

Identifiers

PMID32998700
PMCPMC7526215
OpenAlexW3090947871

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.