Evidence map›Paper›PMID 38699227›Full record

ArticleiScience2024

Network-based approach elucidates critical genes in BRCA subtypes and chemotherapy response in triple negative breast cancer.

Piyush Agrawal, Navami Jain, Vishaka Gopalan, Annan Timon, Arashdeep Singh, Padma S Rajagopal, Sridhar Hannenhalli

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Characterizing the pan-cancer role of exosomal miRNAs in metastasis across cancers.Computational and structural biotechnology journal · 2025
    Article
  6. Article
  7. Characterizing the role of exosomal miRNAs in metastasis.bioRxiv : the preprint server for biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Piyush AgrawalCancer Data Science Lab, National Cancer Institute, NIH, Bethesda, MD, USA.
Navami JainStanford University, Stanford, CA, USA.
Vishaka GopalanCancer Data Science Lab, National Cancer Institute, NIH, Bethesda, MD, USA.
Annan TimonUniversity of Pennsylvania, Philadelphia, PA, USA.
Arashdeep SinghCancer Data Science Lab, National Cancer Institute, NIH, Bethesda, MD, USA.
Padma S RajagopalCancer Data Science Lab, National Cancer Institute, NIH, Bethesda, MD, USA.
Sridhar HannenhalliCancer Data Science Lab, National Cancer Institute, NIH, Bethesda, MD, USA.

Funding

Gene interactions in cancerZIABC011984 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HANNENHALLI, SRIDHAR · 2020 to 2025
$1.4M
Transcriptional heterogeneity and regulatory mechanisms in tumor microenvironmentZIABC012176 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HANNENHALLI, SRIDHAR · 2024 to 2025
$1.3M
Leveraging RNA and synthetic lethality to predict response to treatment in breast cancer (including BRCA-mutated)ZIABC012057 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RAJAGOPAL, PADMA · 2021 to 2025
$759k
Long-Read DNA Sequencing and RNA Sequencing in LFS-Like FamiliesZIABC012144 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RAJAGOPAL, PADMA · 2023 to 2025
$449k
6 · The paper itself

Abstract

Breast cancers (BRCA) exhibit substantial transcriptional heterogeneity, posing a significant clinical challenge. The global transcriptional changes in a disease context, however, are likely mediated by few key genes which reflect disease etiology better than the differentially expressed genes (DEGs). We apply our network-based tool PathExt to 1,059 BRCA tumors across 4 subtypes to identify key mediator genes in each subtype. Compared to conventional differential expression analysis, PathExt-identified genes exhibit greater concordance across tumors, revealing shared and subtype-specific biological processes; better recapitulate BRCA-associated genes in multiple benchmarks, and are more essential in BRCA subtype-specific cell lines. Single-cell transcriptomic analysis reveals a subtype-specific distribution of PathExt-identified genes in multiple cell types from the tumor microenvironment. Application of PathExt to a TNBC chemotherapy response dataset identified subtype-specific key genes and biological processes associated with resistance. We described putative drugs that target key genes potentially mediating drug resistance.

Indexed as

cancercancer systems biologygene network

Identifiers

PMID38699227
PMCPMC11063905

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.