Evidence map›Paper›PMID 24658029›Full record

ArticlePloS one2014

Gene expression profiling associated with angiotensin II type 2 receptor-induced apoptosis in human prostate cancer cells.

Nana Pei, Feilong Jie, Jie Luo, Renqiang Wan, Yanling Zhang, Xinglu Chen, Zhibing Liang, Hongyan Du, Andrew Li, Baihong Chen and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. The Angiotensin ATPharmacological reviews · 2022
    Review
  3. Article
  4. Article
  5. Angiotensin II type 2 receptor promotes apoptosis and inhibits angiogenesis in bladder cancer.Journal of experimental & clinical cancer research : CR · 2017
    Article
  6. Article
  7. Article
  8. Review
  9. 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

15 authors at 3 institutions in 2 countries.

Nana PeiSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Feilong JieSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Jie LuoSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Renqiang WanDepartment of Otolaryngology-Head and Neck Surgery, Guangdong No. 2 Provincial People's Hospital, Guangzhou, Guangdong, China.
Yanling ZhangSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Xinglu ChenSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Zhibing LiangSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Hongyan DuSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Andrew LiDepartment of Neuroscience, University of Florida, Gainesville, Florida, United States of America.
Baihong ChenSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Yi ZhangDepartment of Pharmacology, University of Florida, Gainesville, Florida, United States of America.
Colin SumnersDepartment of Physiology and Functional Genomics, University of Florida, Gainesville, Florida, United States of America.
Jinlong LiSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Weiwang GuInstitute of Comparative Medicine and Center of Laboratory Animals, Southern Medical University, Guangzhou, Guangdong, China.
Hongwei LiSchool of Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Southern Medical University · CNUniversity of Florida · USGuangdong Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increased expression of angiotensin II type 2 receptor (AT2R) induces apoptosis in numerous tumor cell lines, with either Angiotensin II-dependent or Angiotensin II-independent regulation, but its molecular mechanism remains poorly understood. Here, we used PCR Array analysis to determine the gene and microRNA expression profiles in human prostate cancer cell lines transduced with AT2R recombinant adenovirus. Our results demonstrated that AT2R over expression leads to up-regulation of 6 apoptosis-related genes (TRAIL-R2, BAG3, BNIPI, HRK, Gadd45a, TP53BP2), 2 cytokine genes (IL6 and IL8) and 1 microRNA, and down-regulation of 1 apoptosis-related gene TNFSF10 and 2 cytokine genes (BMP6, BMP7) in transduced DU145 cells. HRK was identified as an up-regulated gene in AT2R-transduced PC-3 cells by real-time RT-PCR. Next, we utilized siRNAs to silence the up-regulated genes to further determine their roles on AT2R overexpression mediated apoptosis. The results showed downregulation of Gadd45a reduced the apoptotic effect by ∼30% in DU145 cells, downregulation of HRK reduced AT2R-mediated apoptosis by more than 50% in PC-3 cells, while downregulation of TRAIL-R2 enhanced AT2R-mediated apoptosis more than 4 times in DU145 cells. We also found that the effects on AT2R-mediated apoptosis caused by downregulation of Gadd45a, TRAIL-R2 and HRK were independent in activation of p38 MAPK, p44/42 MAPK and p53. Taken together, our results demonstrated that TRAIL-R2, Gadd45a and HRK may be novel target genes for further study of the mechanism of AT2R-mediated apoptosis in prostate cancer cells.

Indexed as

ApoptosisCell Line, TumorDown-RegulationGene Expression ProfilingHumansMaleMicroarray AnalysisMicroRNAsProstatic NeoplasmsReceptor, Angiotensin, Type 2Transduction, GeneticUp-RegulationMicroRNAsReceptor, Angiotensin, Type 2

Identifiers

PMID24658029
PMCPMC3962398
OpenAlexW2095063113

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Registered trials

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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.