Evidence map›Paper›PMID 28462831›Full record

ArticleBioorganic & medicinal chemistry letters2017

Brefeldin A enhances docetaxel-induced growth inhibition and apoptosis in prostate cancer cells in monolayer and 3D cultures.

Huarong Huang, Ting Liu, Junxi Guo, Lin Yu, Xiaofeng Wu, Yan He, Dongli Li, Junlei Liu, Kun Zhang, Xi Zheng and 1 more

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. FPOA induces the apoptosis of HepG2 cells.Experimental and therapeutic medicine · 2018
    Article
  7. Review
  8. 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 2 countries.

Huarong HuangAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China. Electronic address: hrhuang@gdut.edu.cn.
Ting LiuAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Junxi GuoAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Lin YuAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Xiaofeng WuAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Yan HeAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Dongli LiDepartment of Chemical Engineering and Environment, Wuyi University, Jiangmen 510060, China.
Junlei LiuAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Kun ZhangAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China.
Xi ZhengAllan H. Conney Laboratory for Anticancer Research, Guangdong University of Technology, Guangzhou 510006, China; Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States. Electronic address: xizheng@pharmacy.rutgers.edu.
Susan GoodinRutgers Cancer Institute of New Jersey, New Brunswick, NJ 08903, United States.
Guangdong University of Technology · CNRutgers, The State University of New Jersey · USWuyi University · CN

Funding

TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Tracie Saunders · 1997 to 2026
$94.5M
Prevention of prostate cancer by Lipitor, Celebrex and voluntary exerciseR03CA133902 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI ZHENG, XI · 2008 to 2009
$155k
NCI NIH HHS P30 CA072720NCI NIH HHS R03 CA133902
6 · The paper itself

Abstract

Docetaxel is a commonly used chemotherapeutic drug for patients with late stage prostate cancer. However, serious side effect and drug resistance limit its clinical success. Brefeldin A is a 16-membered macrolide antibiotic from mangrove-derived Fungus Aspergillus sp. (9Hu), which exhibited potent cytotoxicity against human cancer cells. In the present study, we determined the effect of brefeldin A on docetaxel-induced growth inhibition and apoptosis in human prostate cancer PC-3 cells. Brefeldin A in combination with docetaxel inhibited the growth of PC-3 cells in monolayer and in three dimensional cultures. The combination also potently stimulated apoptosis in PC-3 cells as determined by propidium iodide staining and morphological assessment. Mechanistic studies showed that growth inhibition and apoptosis in PC-3 cells treated with brefeldin A and docetaxel were associated with decrease in the level of Bcl-2. The present study indicates that combined brefeldin A with docetaxel may represent a novel approach for improving the efficacy of docetaxel, and Bcl-2 may serve as a target for brefeldin A to enhance the effects of docetaxel chemotherapy.

Indexed as

ApoptosisBrefeldin ACell Line, TumorCell ProliferationDocetaxelHumansMaleProstatic NeoplasmsTaxoidsBrefeldin ADocetaxelTaxoids3D cultureBcl-2Brefeldin ADocetaxelProstate cancer

Identifiers

PMID28462831
PMCPMC5523854
OpenAlexW2606758932

What OpenQuestion holds

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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.