Evidence map›Paper›PMID 30511015›Full record

ArticleNPJ breast cancer2018

Cyclin E1 and Rb modulation as common events at time of resistance to palbociclib in hormone receptor-positive breast cancer.

Cristina Guarducci, Martina Bonechi, Matteo Benelli, Chiara Biagioni, Giulia Boccalini, Dario Romagnoli, Roberto Verardo, Rachel Schiff, C Kent Osborne, Carmine De Angelis and 3 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 2 pooled it
7.7field-weighted citation impact, top 2% 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

94 citing papers in PubMed, 2 syntheses or guidelines pooled it, 131 citations in OpenAlex.

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  6. Next-generation CDK inhibitors in HR+/HER2- breast cancer.The Journal of clinical investigation · 2026
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34 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

13 authors at 3 institutions in 2 countries.

Cristina Guarducci *1"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Martina Bonechi *1"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Matteo Benelli2Bioinformatics Unit, Hospital of Prato, Prato, Italy.
Chiara Biagioni2Bioinformatics Unit, Hospital of Prato, Prato, Italy.
Giulia Boccalini1"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Dario Romagnoli2Bioinformatics Unit, Hospital of Prato, Prato, Italy.
Roberto VerardoLaboratorio Nazionale CIB (LNCIB), Area Science Park, Functional Genomics & Bioinformatics Units, Trieste, Italy.
Rachel Schiff5Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX USA.
C Kent Osborne5Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX USA.
Carmine De Angelis5Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX USA.
Angelo Di Leo3"Sandro Pitigliani" Medical Oncology Department, Hospital of Prato, Prato, Italy.
Luca Malorni *1"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Ilenia Migliaccio *1"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Hospital of Prato · ITChildren's Cancer Center · USAREA Science Park · IT

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DAVID R ROWLEY · 2007 to 2026
$73.9M
TUMOR SUPPRESSOR GENES IN BREAST CANCER DEVELOPMENTP50CA058183 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI OSBORNE, C KENT · 1992 to 2012
$30.9M
Translational Research in Breast Cancer (SPORE)P50CA186784 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Xiang Zhang · 2014 to 2026
$24.5M
NCI NIH HHS P30 CA125123NCI NIH HHS P50 CA058183NCI NIH HHS P50 CA186784
6 · The paper itself

Abstract

CDK4/6 inhibitors represent a new treatment standard for hormone receptor-positive (HR+), HER2-negative advanced breast cancer (BC) patients. Although efficacious, resistance to these agents is universal. Here, we profiled a large panel of HR+ BC cell lines with conditioned resistance to the CDK4/6 inhibitor palbociclib, and analyzed cell cycle-related markers by gene expression profiles (GEP) and western blot (WB). GEP showed high molecular heterogeneity among the models, with E2F targets being significantly enriched both during treatment and at the time of resistance. By both WB and GEP, a common molecular feature at the time of palbociclib resistance was the concomitant overexpression of cyclin E1 and down-regulation of Rb.

Identifiers

PMID30511015
PMCPMC6261939
OpenAlexW2901425242

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.