Evidence map›Paper›PMID 31221986›Full record

ArticleScientific reports2019

Identification of a Radiosensitivity Molecular Signature Induced by Enzalutamide in Hormone-sensitive and Hormone-resistant Prostate Cancer Cells.

Maryam Ghashghaei, Tamim M Niazi, Adriana Aguilar-Mahecha, Kathleen Oros Klein, Celia M T Greenwood, Mark Basik, Thierry M Muanza

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Drivers of Radioresistance in Prostate Cancer.Journal of clinical medicine · 2022
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
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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

7 authors at 1 institution in 1 country.

Maryam GhashghaeiLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Tamim M NiaziLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Adriana Aguilar-MahechaDepartment of Oncology, Jewish General Hospital, Montreal, QC, Canada.
Kathleen Oros KleinLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
Celia M T GreenwoodSegal Cancer Center, Lady Davis Institute of Research, Jewish General Hospital, McGill University, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-2427-5696
Mark BasikDepartment of Oncology, Jewish General Hospital, Montreal, QC, Canada.
Thierry M MuanzaLady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada. tmuanza@yahoo.com.
Jewish General Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) is the most common cancer amongst men. A novel androgen receptor (AR) antagonist, enzalutamide (ENZA) has recently been demonstrated to enhance the effect of radiation (XRT) by impairing the DNA damage repair process. This study aimed to identify a radiosensitive gene signature induced by ENZA in the PCa cells and to elucidate the biological pathways which influence this radiosensitivity. We treated LNCaP (AR-positive, hormone-sensitive PCa cells) and C4-2 (AR-positive, hormone-resistant PCa cells) cells with ENZA alone and in combination with androgen deprivation therapy (ADT) and XRT. Using one-way ANOVA on the gene expression profiling, we observed significantly differentially expressed (DE) genes in inflammation-and metabolism-related genes in hormone-sensitive and hormone-resistant PCa cell lines respectively. Survival analysis in both the TCGA PRAD and GSE25136 datasets suggested an association between the expression of these genes and time to recurrence. These results indicated that ENZA alone or in combination with ADT enhanced the effect of XRT through immune and inflammation-related pathways in LNCaP cells and metabolic-related pathways in C4-2 cells. Kaplan-Meier analysis and Cox proportional hazard models showed that low expression of all the candidate genes except for PTPRN2 were associated with tumor progression and recurrence in a PCa cohort.

Indexed as

BenzamidesCell Line, TumorGene Expression ProfilingGenes, NeoplasmHumansInflammationMaleMetabolismNitrilesPhenylthiohydantoinProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantRadiation ToleranceBenzamidesenzalutamideNitrilesPhenylthiohydantoin

Identifiers

PMID31221986
PMCPMC6586860
OpenAlexW2951506965

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.