Evidence map›Paper›PMID 29381682›Full record

ArticleBritish journal of cancer2018

Treatment with docetaxel in combination with Aneustat leads to potent inhibition of metastasis in a patient-derived xenograft model of advanced prostate cancer.

Sifeng Qu, Xinpei Ci, Hui Xue, Xin Dong, Jun Hao, Dong Lin, Pier-Luc Clermont, Rebecca Wu, Colin C Collins, Peter W Gout and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
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

11 authors at 3 institutions in 1 country.

Sifeng QuDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Xinpei CiDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Hui XueDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Xin DongDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Jun HaoDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Dong LinDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Pier-Luc ClermontFaculty of Medicine, Université Laval, Québec, QC G1V 0A6, Canada.
Rebecca WuDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Colin C CollinsVancouver Prostate Centre, Vancouver, BC V6H 3Z6, Canada.
Peter W GoutDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
Yuzhuo WangDepartment of Experimental Therapeutics, BC Cancer Agency, Vancouver, BC V5Z 1L3 Canada.
BC Cancer Agency · CAUniversity of British Columbia · CAUniversité Laval · CA

Funding

CIHR
6 · The paper itself

Abstract

backgroundDocetaxel used for first-line treatment of advanced prostate cancer (PCa) is only marginally effective. We previously showed, using the LTL-313H subrenal capsule patient-derived metastatic PCa xenograft model, that docetaxel combined with Aneustat (OMN54), a multivalent plant-derived therapeutic, led to marked synergistic tumour growth inhibition. Here, we investigated the effect of docetaxel+Aneustat on metastasis.

methodsC4-2 cells were incubated with docetaxel, Aneustat and docetaxel+Aneustat to assess effects on cell migration. The LTL-313H model, similarly treated, was analysed for effects on lung micro-metastasis and kidney invasion. The LTL-313H gene expression profile was compared with profiles of PCa patients (obtained from Oncomine) and subjected to IPA to determine involvement of cancer driver genes.

resultsDocetaxel+Aneustat markedly inhibited C4-2 cell migration and LTL-313H lung micro-metastasis/kidney invasion. Oncomine analysis indicated that treatment with docetaxel+Aneustat was associated with improved patient outcome. The drug combination markedly downregulated expression of cancer driver genes such as FOXM1 (and FOXM1-target genes). FOXM1 overexpression reduced the anti-metastatic activity of docetaxel+Aneustat.

conclusionsDocetaxel+Aneustat can inhibit PCa tissue invasion and metastasis. This activity appears to be based on reduced expression of cancer driver genes such as FOXM1. Use of docetaxel+Aneustat may provide a new, more effective regimen for therapy of metastatic PCa.

Indexed as

AnimalsAntineoplastic Combined Chemotherapy ProtocolsCell MovementCell ProliferationDocetaxelDrugs, Chinese HerbalDrug SynergismForkhead Box Protein M1HumansLung NeoplasmsMaleMiceNeoplasm InvasivenessNeoplasm MetastasisProstatic NeoplasmsTranscriptomeDocetaxelDrugs, Chinese HerbalForkhead Box Protein M1FOXM1 protein, human

Identifiers

PMID29381682
PMCPMC5877435
OpenAlexW2787764040

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.