Evidence mapPaperPMID 30936679Full record

ArticleCancer informatics2019

High-Throughput Mutation Data Now Complement Transcriptomic Profiling: Advances in Molecular Pathway Activation Analysis Approach in Cancer Biology.

Anton Buzdin, Maxim Sorokin, Elena Poddubskaya, Nicolas Borisov

Open access · goldAbstract readComment
In one paragraph

Article in Cancer informatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-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

10 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Anton BuzdinInstitute for Personalized Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
Maxim SorokinInstitute for Personalized Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
Elena PoddubskayaInstitute for Personalized Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.
Nicolas BorisovInstitute for Personalized Medicine, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.ORCID https://orcid.org/0000-0002-1671-5524
Sechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We recently reviewed the current progress in the use of high-throughput molecular "omics" data for the quantitative analysis of molecular pathway activation. These quantitative metrics may be used in many ways, and we focused on their application as tumor biomarkers. Here, we provide an update of the most recent conceptual findings related to pathway analysis in tumor biology, which were not included in the previous review. The major novelties include a method enabling calculation of pathway-scale tumor mutation burden termed "Pathway Instability" and its application for scoring of anticancer target drugs. A new technique termed Shambhala emerged that enables accurate common harmonization of any number of gene expression profiles obtained using any number of experimental platforms. This may be helpful for merging various gene expression data sets and for comparing their pathway activation characteristics. Another recent bioinformatics method, termed FLOating-Window Projective Separator (FloWPS), has the potential to significantly enhance the value of pathway activation profiles as biomarkers of cancer response to treatments. It reduces the minimum required number of training samples needed to construct a machine-learning-based classifier. Finally, several documented clinical cases have been recently published, in which gene-expression-based pathway analysis was successfully used for personalized off-label prescription of target drugs to metastatic cancer patients.

Indexed as

bioinformaticscancermachine learningmutation profilingsignaling pathways

Identifiers

PMID30936679
PMCPMC6434430
OpenAlexW2932621682

What Socratic holds

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LicenceCC BY-NC
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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 Socratic graph.