Evidence map›Paper›PMID 37894751›Full record

ArticleInternational journal of molecular sciences2023

The IGF-Independent Role of IRS-2 in the Secretion of MMP-9 Enhances the Growth of Prostate Carcinoma Cell Line PC3.

Haruka Furuta, Yina Sheng, Ayaka Takahashi, Raku Nagano, Naoyuki Kataoka, Claire Marie Perks, Rachel Barker, Fumihiko Hakuno, Shin-Ichiro Takahashi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

9 authors at 2 institutions in 2 countries.

Haruka FurutaDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.
Yina ShengDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.
Ayaka TakahashiDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.
Raku NaganoDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.ORCID 0009-0005-7016-3539
Naoyuki KataokaDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.ORCID 0000-0002-4498-7420
Claire Marie PerksIGFs & Metabolic Endocrinology Group, Learning & Research Building, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 1TH, UK.ORCID 0000-0003-1562-891X
Rachel BarkerIGFs & Metabolic Endocrinology Group, Learning & Research Building, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 1TH, UK.ORCID 0000-0003-0309-2708
Fumihiko HakunoDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.ORCID 0000-0002-4447-6225
Shin-Ichiro TakahashiDepartment of Animal Sciences and Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo 113-8654, Japan.ORCID 0000-0002-2323-2010
The University of Tokyo · JPUniversity of Bristol · GB

Funding

Bio-oriented Technology Research Advancement Institution Cross-ministerial Moonshot Agriculture, Forestry, and Fisheries Research and Development Program, "Technologies for Smart Bio-industry and Agriculture"Bio-oriented Technology Research Advancement Institution R&D matching funds on the field for Knowledge Integration and InnovationChina Scholarship Council 201906010326Japan Society for the Promotion of Science Core-to-core program A. A. Advanced Research NetworksJapan Society for the Promotion of Science Grant-in-Aid for Scientific Research (S) #25221204 and Scientific Research (A) #18H03972Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research (B) #15H04583, Scientific Research (B) #24380152 and Scientific Research (B) #22H02528NIHR Applied Research Collaboration West, Bristol Biomedical Research Centre
6 · The paper itself

Abstract

Insulin receptor substrate-2 (IRS-2), a substrate of the insulin-like growth factor (IGF)-I receptor, is highly expressed in the prostate cancer cell line, PC3. We recently demonstrated that extracellular signal-regulated kinase (Erk1/2), a kinase downstream of IGF signaling, is activated in PC3 cells under serum starvation, and this activation can be inhibited by IRS-2 knockdown. Here, we observed that adding an IGF-I-neutralizing antibody to the culture medium inhibited the activation of Erk1/2. Suppression of Erk1/2 in IRS-2 knockdown cells was restored by the addition of a PC3 serum-free conditioned medium. In contrast, the IRS-2-silenced PC3 conditioned medium could not restore Erk1/2 activation, suggesting that IRS-2 promotes the secretion of proteins that activate the IGF signaling pathway. Furthermore, gelatin zymography analysis of the conditioned medium showed that matrix metalloproteinase-9 (MMP-9) was secreted extracellularly in an IRS-2 dependent manner when PC3 was cultured under serum starvation conditions. Moreover, MMP-9 knockdown suppressed Erk1/2 activation, DNA synthesis, and migratory activity. The IRS-2 levels were positively correlated with Gleason grade in human prostate cancer tissues. These data suggest that highly expressed IRS-2 activates IGF signaling by enabling the secretion of MMP-9, which is associated with hyperproliferation and malignancy of prostate cancer cell line, PC3.

Indexed as

CarcinomaProstatic NeoplasmsCell LineCulture Media, ConditionedHumansInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsMaleMatrix Metalloproteinase 9PC-3 CellsPhosphoproteinsPhosphorylationProstateCulture Media, ConditionedInsulin-Like Growth Factor IInsulin Receptor Substrate ProteinsIRS2 protein, humanMatrix Metalloproteinase 9MMP9 protein, humanPhosphoproteinsIRS-2MMP-9PC3prostate cancer cellssecretion

Identifiers

PMID37894751
PMCPMC10606031
OpenAlexW4387539924

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.