Evidence map›Paper›PMID 30975102›Full record

ArticleBMC cancer2019

Reduced FRG1 expression promotes prostate cancer progression and affects prostate cancer cell migration and invasion.

Ankit Tiwari, Bratati Mukherjee, Md Khurshidul Hassan, Niharika Pattanaik, Archita Mohanty Jaiswal, Manjusha Dixit

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

6 authors at 1 institution in 1 country.

Ankit TiwariSchool of Biological Sciences, National Institute of Science Education and Research Bhubaneswar, HBNI, PO: Bhimpur-Padanpur, Via: Jatni, Odisha, 752050, India.
Bratati MukherjeeSchool of Biological Sciences, National Institute of Science Education and Research Bhubaneswar, HBNI, PO: Bhimpur-Padanpur, Via: Jatni, Odisha, 752050, India.
Md Khurshidul HassanSchool of Biological Sciences, National Institute of Science Education and Research Bhubaneswar, HBNI, PO: Bhimpur-Padanpur, Via: Jatni, Odisha, 752050, India.
Niharika PattanaikSRL Diagnostics Ltd, Plot 2084, Hall Plot 339/4820, Goutam Nagar Unit no. 28, Bhubaneswar, Odisha, 751014, India.
Archita Mohanty JaiswalSRL Diagnostics Ltd, Plot 2084, Hall Plot 339/4820, Goutam Nagar Unit no. 28, Bhubaneswar, Odisha, 751014, India.
Manjusha DixitSchool of Biological Sciences, National Institute of Science Education and Research Bhubaneswar, HBNI, PO: Bhimpur-Padanpur, Via: Jatni, Odisha, 752050, India. manjusha@niser.ac.in.
National Institute of Science Education and Research · IN

Funding

Department of Biotechnology , Ministry of Science and Technology BT/PR-14705/BRB/10/898/2010
6 · The paper itself

Abstract

backgroundProstate cancer is the most common form of cancer in males and accounts for high cancer related deaths. Therapeutic advancement in prostate cancer has not been able to reduce the mortality burden of prostate cancer, which warrants further research. FRG1 which affects angiogenesis and cell migration in Xenopus, can be a potential player in tumorigenesis. In this study, we investigated the role of FRG1 in prostate cancer progression.

methodsImmunohistochemistry was performed to determine FRG1 expression in patient samples. FRG1 expression perturbation was done to investigate the effect of FRG1 on cell proliferation, migration and invasion, in DU145, PC3 and LNCaP cells. To understand the mechanism, we checked expression of various cytokines and MMPs by q-RT PCR, signaling molecules by western blot, in FRG1 perturbation sets. Results were validated by use of pharmacological inhibitor and activator and, western blot.

resultsIn prostate cancer tissue, FRG1 levels were significantly reduced, compared to the uninvolved counterpart. FRG1 expression showed variable effect on PC3 and DU145 cell proliferation. FRG1 levels consistently affected cell migration and invasion, in both DU145 and PC3 cells. Ectopic expression of FRG1 led to significant reduction in cell migration and invasion in both DU145 and PC3 cells, reverse trends were observed with FRG1 knockdown. In androgen receptor positive cell line LNCaP, FRG1 doesn't affect any of the cell properties. FRG1 knockdown led to significantly enhanced expression of GM-CSF, MMP1, PDGFA and CXCL1, in PC3 cells and, in DU145, it led to higher expression of GM-CSF, MMP1 and PLGF. Interestingly, FRG1 knockdown in both the cell lines led to activation of p38 MAPK. Pharmacological activation of p38 MAPK led to increase in the expression of GM-CSF and PLGF in DU145 whereas in PC3 it led to enhanced expression of GM-CSF, MMP1 and CXCL1. On the other hand, inhibition of p38 MAPK led to reduction in the expression of above mentioned cytokines.

conclusionFRG1 expression is reduced in prostate adenocarcinoma tissue. FRG1 expression affects migration and invasion in AR negative prostate cancer cells through known MMPs and cytokines, which may be mediated primarily via p38 MAPK activation.

Indexed as

Cell MovementAdenocarcinomaAgedBiopsy, Large-Core NeedleCarcinogenesisCell Line, TumorCell ProliferationCohort StudiesDisease ProgressionGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansMaleMAP Kinase Signaling SystemMicrofilament ProteinsMiddle AgedAR protein, humanFRG1 protein, humanMicrofilament ProteinsNuclear ProteinsReceptors, AndrogenRNA-Binding ProteinsRNA, Small InterferingCell invasionCell migrationCXCL1FRG1GM-CSFImmunohistochemistryMMP1p38 MAPKPLGFProstate cancer

Identifiers

PMID30975102
PMCPMC6458714
OpenAlexW2945553115

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.