Evidence map›Paper›PMID 28930981›Full record

ArticleJournal of visualized experiments : JoVE2017

Generation of Prostate Cancer Cell Models of Resistance to the Anti-mitotic Agent Docetaxel.

Lisa Mohr, Marc Carceles-Cordon, Jungreem Woo, Carlos Cordon-Cardo, Josep Domingo-Domenech, Veronica Rodriguez-Bravo

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. 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
0.6field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Lisa MohrDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai.
Marc Carceles-CordonDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai.
Jungreem WooDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai.
Carlos Cordon-CardoDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai.
Josep Domingo-DomenechDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai.
Veronica Rodriguez-BravoDepartment of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai; Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai; veronica.rodriguez-bravo@mssm.edu.
Icahn School of Medicine at Mount Sinai · US

Funding

Role of GATA2 signaling network in Lethal Prostate CancerR01CA207311 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DOMINGO-DOMENECH, JOSEP MARIA · 2016 to 2020
$2.2M
Genome Stability Regulation by the Nuclear Pore-Chromosome Axis and Defects in Tumor CellsK22CA207458 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RODRIGUEZ-BRAVO, VERONICA · 2016 to 2018
$551k
NCI NIH HHS K22 CA207458NCI NIH HHS R01 CA207311
6 · The paper itself

Abstract

Microtubule targeting agents (MTAs) are a mainstay in the treatment of a wide range of tumors. However, acquired resistance to chemotherapeutic drugs is a common mechanism of disease progression and a prognostic-determinant feature of malignant tumors. In prostate cancer (PC), resistance to MTAs such as the taxane Docetaxel dictates treatment failure as well as progression towards lethal stages of disease that are defined by a poor prognosis and high mortality rates. Though studied for decades, the array of mechanisms contributing to acquired resistance are not completely understood, and thus pose a significant limitation to the development of new therapeutic strategies that could benefit patients in these advanced stages of disease. In this protocol, we describe the generation of Docetaxel-resistant prostate cancer cell lines that mimic lethal features of late-stage prostate cancer, and therefore can be used to study the mechanisms by which acquired chemoresistance arises. Despite potential limitations intrinsic to a cell based model, such as the loss of resistance properties over time, the Docetaxel-resistant cell lines produced by this method have been successfully used in recent studies and offer the opportunity to advance our molecular understanding of acquired chemoresistance in lethal prostate cancer.

Indexed as

Antineoplastic AgentsDocetaxelDrug Resistance, NeoplasmHumansMaleProstatic NeoplasmsTaxoidsAntineoplastic AgentsDocetaxelTaxoids

Identifiers

PMID28930981
PMCPMC5607877
OpenAlexW2752060542

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.