Evidence map›Paper›PMID 30894541›Full record

ArticleNature communications2019

Multiple ABCB1 transcriptional fusions in drug resistant high-grade serous ovarian and breast cancer.

Elizabeth L Christie, Swetansu Pattnaik, Jessica Beach, Anthony Copeland, Nineveh Rashoo, Sian Fereday, Joy Hendley, Kathryn Alsop, Samuel L Brady, Greg Lamb and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed
9.5field-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

111 citing papers in PubMed, 190 citations in OpenAlex.

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  20. Therapeutic Potential of Metal-Based and PARP Inhibitor Chemotherapy forInternational journal of molecular sciences · 2025
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51 more citing papers are in PubMed but not listed here.

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

15 authors at 6 institutions in 2 countries.

Elizabeth L ChristiePeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Swetansu PattnaikKinghorn Cancer Centre, Garvan Institute for Medical Research, Darlinghurst, 2010, NSW, Australia.
Jessica BeachPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Anthony CopelandPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Nineveh RashooPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Sian FeredayPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Joy HendleyPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Kathryn AlsopPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Samuel L BradyThe University of Utah, Salt Lake City, UT, 84112, USA.ORCID http://orcid.org/0000-0001-5518-7800
Greg LambThe University of Utah, Salt Lake City, UT, 84112, USA.
Ahwan PandeyPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Anna deFazioCentre for Cancer Research, The Westmead Institute for Medical Research, Westmead, 2145, NSW, Australia.
Heather ThornePeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Andrea BildThe University of Utah, Salt Lake City, UT, 84112, USA.ORCID http://orcid.org/0000-0002-4727-5533
David D L BowtellPeter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia. d.bowtell@petermac.org.
Peter MacCallum Cancer Centre · AUGarvan Institute of Medical Research · AUUniversity of Utah · USCity Of Hope National Medical Center · USThe University of Melbourne · AUThe University of Sydney · AU

Funding

Project 2: Targeting Cooperative Phenotypes Common in Spatial HeterogeneityU54CA209978 · NCI · UNIVERSITY OF UTAH · PI BILD, ANDREA HOPE · 2017 to 2021
$10.5M
NCI NIH HHS U54 CA209978
6 · The paper itself

Abstract

ABCB1 encodes Multidrug Resistance protein (MDR1), an ATP-binding cassette member involved in the cellular efflux of chemotherapeutic drugs. Here we report that ovarian and breast samples from chemotherapy treated patients are positive for multiple transcriptional fusions involving ABCB1, placing it under the control of a strong promoter while leaving its open reading frame intact. We identified 15 different transcriptional fusion partners involving ABCB1, as well as patients with multiple distinct fusion events. The partner gene selected depended on its structure, promoter strength, and chromosomal proximity to ABCB1. Fusion positivity was strongly associated with the number of lines of MDR1-substrate chemotherapy given. MDR1 inhibition in a fusion positive ovarian cancer cell line increased sensitivity to paclitaxel more than 50-fold. Convergent evolution of ABCB1 fusion is therefore frequent in chemotherapy resistant recurrent ovarian cancer. As most currently approved PARP inhibitors (PARPi) are MDR1 substrates, prior chemotherapy may precondition resistance to PARPi.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedAged, 80 and overAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BBreast NeoplasmsCohort StudiesCystadenocarcinoma, SerousDrug Resistance, NeoplasmFemaleHumansMiddle AgedNeoplasm GradingOncogene Proteins, FusionOvarian NeoplasmsABCB1 protein, humanAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily BOncogene Proteins, FusionPaclitaxelPoly(ADP-ribose) Polymerases

Identifiers

PMID30894541
PMCPMC6426934
OpenAlexW2924441988

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.