Evidence map›Paper›PMID 33923231›Full record

ArticleJournal of personalized medicine2021

Combination of Talazoparib and Palbociclib as a Potent Treatment Strategy in Bladder Cancer.

Florian G Klein, Charlène Granier, Yuling Zhao, Qi Pan, Zhichao Tong, Jürgen E Gschwend, Per Sonne Holm, Roman Nawroth

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  10. Landscape of targeted therapies for advanced urothelial carcinoma.Exploration of targeted anti-tumor therapy · 2024
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  14. CDK4/6 inhibitors downregulate the ubiquitin-conjugating enzymes UBE2C/S/T involved in the ubiquitin-proteasome pathway in ER + breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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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

8 authors at 2 institutions in 2 countries.

Florian G KleinDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.ORCID 0000-0003-0802-5838
Charlène GranierDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Yuling ZhaoDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Qi PanDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Zhichao TongDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Jürgen E GschwendDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Per Sonne HolmDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
Roman NawrothDepartment of Urology, Klinikum Rechts der Isar, Technical University of Munich, D-81675 Munich, Germany.
TUM Klinikum · DEInnsbruck Medical University · AT

Funding

Stiftung der Deutschen Wirtschaft PhD scholarship for Florian G. Klein
6 · The paper itself

Abstract

The use of cyclin-dependent kinase 4/6 (CDK4/6) inhibitors represents a potent strategy for cancer therapy. Due to the complex molecular network that regulates cell cycle progression, cancer cells often acquire resistance mechanisms against these inhibitors. Previously, our group identified molecular factors conferring resistance to CDK4/6 inhibition in bladder cancer (BLCA) that also included components within the DNA repair pathway. In this study, we validated whether a combinatory treatment approach of the CDK4/6 inhibitor Palbociclib with Poly-(ADP-Ribose) Polymerase (PARP) inhibitors improves therapy response in BLCA. First, a comparison of PARP inhibitors Talazoparib and Olaparib showed superior efficacy of Talazoparib in vitro and displayed high antitumor activity in xenografts in the chicken chorioallantoic membrane (CAM) model. Moreover, the combination of Talazoparib and the CDK4/6 inhibitor Palbociclib synergistically reduced tumor growth in Retinoblastoma protein (RB)-positive BLCA in vitro and in a CAM model, an effect that relies on Palbociclib-induced cell cycle arrest in G0/G1-phase complemented by a G2 arrest induced by Talazoparib. Interestingly, Talazoparib-induced apoptosis was reduced by Palbociclib. The combination of Palbociclib and Talazoparib effectively enhances BLCA therapy, and RB is a molecular biomarker of response to this treatment regimen.

Indexed as

apoptosisbladder cancerchorioallantoic membrane modelcombination therapyOlaparibPalbociclibRetinoblastoma proteinTalazoparib

Identifiers

PMID33923231
PMCPMC8145096
OpenAlexW3159197080

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.