Evidence map›Paper›PMID 39310778›Full record

ArticleiScience2024

Structural analysis of genomic and proteomic signatures reveal dynamic expression of intrinsically disordered regions in breast cancer.

Nicole Zatorski, Yifei Sun, Abdulkadir Elmas, Christian Dallago, Timothy Karl, David Stein, Burkhard Rost, Kuan-Lin Huang, Martin Walsh, Avner Schlessinger

Abstract read
In one paragraph

Article in iScience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Nicole ZatorskiDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Yifei SunDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Abdulkadir ElmasDepartment of Genetic and Genomic Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Christian DallagoNVIDIA DE GmbH, Einsteinstraße 172, 81677 München, Germany.
Timothy KarlFaculty of Informatics, Bioinformatics & Computational Biology, Technical University Munich (TUM), 85748 Garching, Germany.
David SteinDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Burkhard RostFaculty of Informatics, Bioinformatics & Computational Biology, Technical University Munich (TUM), 85748 Garching, Germany.
Kuan-Lin HuangDepartment of Genetic and Genomic Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Martin WalshDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.
Avner SchlessingerDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, One Gustave Levey Pl, New York, NY 10029, USA.

Funding

Prenatal medication exposure in autism, birth complications and developmental disabilitiesR01HD107528 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MAGDALENA JANECKA, ABRAHAM REICHENBERG · 2022 to 2026
$3.4M
Multi-modal data integration to identify kinase substratesU01CA271318 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PANDEY, GAURAV, SCHLESSINGER, AVNER · 2022 to 2023
$1.0M
Compound Cardiovascular Activity Prediction Using Structural and Genomic FeaturesF30HL160179 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZATORSKI, NICOLE · 2021 to 2024
$182k
NCI NIH HHS U01 CA271318NHLBI NIH HHS F30 HL160179NICHD NIH HHS R01 HD107528
6 · The paper itself

Abstract

Structural features of proteins capture underlying information about protein evolution and function, which enhances the analysis of proteomic and transcriptomic data. Here, we develop Structural Analysis of Gene and protein Expression Signatures (SAGES), a method that describes expression data using features calculated from sequence-based prediction methods and 3D structural models. We used SAGES, along with machine learning, to characterize tissues from healthy individuals and those with breast cancer. We analyzed gene expression data from 23 breast cancer patients and genetic mutation data from the Catalog of Somatic Mutations In Cancer database as well as 17 breast tumor protein expression profiles. We identified prominent expression of intrinsically disordered regions in breast cancer proteins as well as relationships between drug perturbation signatures and breast cancer disease signatures. Our results suggest that SAGES is generally applicable to describe diverse biological phenomena including disease states and drug effects.

Indexed as

BioinformaticsBiological sciencesComputer science

Identifiers

PMID39310778
PMCPMC11416222

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Registered trials

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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.