Evidence map›Paper›PMID 31645597›Full record

ArticleScientific reports2019

Modeling cancer drug response through drug-specific informative genes.

Luca Parca, Gerardo Pepe, Marco Pietrosanto, Giulio Galvan, Leonardo Galli, Antonio Palmeri, Marco Sciandrone, Fabrizio Ferrè, Gabriele Ausiello, Manuela Helmer-Citterich

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
21.4field-weighted citation impact, top 1% 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

36 citing papers in PubMed, 142 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Luca ParcaDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.ORCID http://orcid.org/0000-0002-0924-8518
Gerardo PepeDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Marco PietrosantoDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Giulio GalvanDepartment of Information Engineering, University of Florence, Florence, Italy.ORCID http://orcid.org/0000-0002-0384-0334
Leonardo GalliDepartment of Information Engineering, University of Florence, Florence, Italy.ORCID http://orcid.org/0000-0002-8045-7101
Antonio PalmeriDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Marco SciandroneDepartment of Information Engineering, University of Florence, Florence, Italy.
Fabrizio FerrèDepartment of Pharmacy and Biotechnology, University of Bologna Alma Mater, Bologna, Italy.
Gabriele AusielloDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy.
Manuela Helmer-CitterichDepartment of Biology, University of Rome "Tor Vergata", Rome, Italy. manuela.helmer.citterich@uniroma2.it.ORCID http://orcid.org/0000-0001-9530-7504
University of Rome Tor Vergata · ITUniversity of Florence · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in pharmacogenomics have generated a wealth of data of different types whose analysis have helped in the identification of signatures of different cellular sensitivity/resistance responses to hundreds of chemical compounds. Among the different data types, gene expression has proven to be the more successful for the inference of drug response in cancer cell lines. Although effective, the whole transcriptome can introduce noise in the predictive models, since specific mechanisms are required for different drugs and these realistically involve only part of the proteins encoded in the genome. We analyzed the pharmacogenomics data of 961 cell lines tested with 265 anti-cancer drugs and developed different machine learning approaches for dissecting the genome systematically and predict drug responses using both drug-unspecific and drug-specific genes. These methodologies reach better response predictions for the vast majority of the screened drugs using tens to few hundreds genes specific to each drug instead of the whole genome, thus allowing a better understanding and interpretation of drug-specific response mechanisms which are not necessarily restricted to the drug known targets.

Indexed as

Antineoplastic AgentsCell Line, TumorDose-Response Relationship, DrugGene Expression Regulation, NeoplasticGenome, HumanHumansMachine LearningModels, BiologicalNeoplasmsPharmacogeneticsTranscriptomeAntineoplastic Agents

Identifiers

PMID31645597
PMCPMC6811538
OpenAlexW2981742563

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.