Evidence map›Paper›PMID 22396490›Full record

ArticleCancer research2012

Impact of intertumoral heterogeneity on predicting chemotherapy response of BRCA1-deficient mammary tumors.

Sven Rottenberg, Marieke A Vollebergh, Bas de Hoon, Jorma de Ronde, Philip C Schouten, Ariena Kersbergen, Serge A L Zander, Marina Pajic, Janneke E Jaspers, Martijn Jonkers and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Docetaxel response in BRCA1,p53-deficient mammary tumor cells is affected by Huntingtin and BAP1.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. The Lasker-Koshland Special Achievement Award in Medical Science awarded to Piet Borst.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Article
  7. Heterogeneity derived fromCancer medicine · 2022
    Article
  8. Pleiotropic Roles of ABC Transporters in Breast Cancer.International journal of molecular sciences · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. PretreatmentThe oncologist · 2018
    Article
  14. Review
  15. New tools for old drugs: Functional genetic screens to optimize current chemotherapy.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2018
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  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

21 authors at 6 institutions in 2 countries.

Sven RottenbergDivision of Molecular Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands. s.rottenberg@nki.nl
Marieke A Vollebergh
Bas de Hoon
Jorma de Ronde
Philip C Schouten
Ariena Kersbergen
Serge A L Zander
Marina Pajic
Janneke E Jaspers
Martijn Jonkers
Martin Lodén
Wendy Sol
Eline van der Burg
Jelle Wesseling
Jean-Pierre Gillet
Michael M Gottesman
Joost Gribnau
Lodewyk Wessels
Sabine C Linn
Jos Jonkers
Piet Borst
Center for Cancer Research · USErasmus MC · NLNational Cancer Institute · USErasmus MC Cancer Institute · NLErasmus University Rotterdam · NLMRC Holland (Netherlands) · NL

Funding

Mechanisms of non-classical multidrug resistance in cancerZIABC010830 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GOTTESMAN, MICHAEL · 2009 to 2025
$19.6M
Intramural NIH HHS ZIA BC010830
6 · The paper itself

Abstract

The lack of markers to predict chemotherapy responses in patients poses a major handicap in cancer treatment. We searched for gene expression patterns that correlate with docetaxel or cisplatin response in a mouse model for breast cancer associated with BRCA1 deficiency. Array-based expression profiling did not identify a single marker gene predicting docetaxel response, despite an increase in Abcb1 (P-glycoprotein) expression that was sufficient to explain resistance in several poor responders. Intertumoral heterogeneity explained the inability to identify a predictive gene expression signature for docetaxel. To address this problem, we used a novel algorithm designed to detect differential gene expression in a subgroup of the poor responders that could identify tumors with increased Abcb1 transcript levels. In contrast, standard analytical tools, such as significance analysis of microarrays, detected a marker only if it correlated with response in a substantial fraction of tumors. For example, low expression of the Xist gene correlated with cisplatin hypersensitivity in most tumors, and it also predicted long recurrence-free survival of HER2-negative, stage III breast cancer patients treated with intensive platinum-based chemotherapy. Our findings may prove useful for selecting patients with high-risk breast cancer who could benefit from platinum-based therapy.

Indexed as

AnimalsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1BRCA1 ProteinBreast NeoplasmsCisplatinDocetaxelFemaleGene Expression ProfilingMammary Neoplasms, ExperimentalMiceMice, TransgenicRandomized Controlled Trials as TopicTaxoidsAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 1BRCA1 ProteinBRCA1 protein, humanCisplatinDocetaxelTaxoids

Identifiers

PMID22396490
PMCPMC3518318
OpenAlexW2151864343

What OpenQuestion holds

Textmetadata
LicenceTDM
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.