Evidence map›Paper›PMID 28161904›Full record

ArticleCancer science2017

Immune-complex level of cofilin-1 in sera is associated with cancer progression and poor prognosis in pancreatic cancer.

Mamoru Satoh, Shigetsugu Takano, Kazuyuki Sogawa, Kenta Noda, Hideyuki Yoshitomi, Masumi Ishibashi, Kaoru Mogushi, Hirotaka Takizawa, Masayuki Otsuka, Hiroaki Shimizu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Cofilin(s) and Mitochondria: Function Beyond Actin Dynamics.International journal of molecular sciences · 2025
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Cofilin: A Promising Protein Implicated in Cancer Metastasis and Apoptosis.Frontiers in cell and developmental biology · 2021
    Review
  19. Review
  20. 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

12 authors at 3 institutions in 1 country.

Mamoru SatohDivision of Clinical Mass Spectrometry, Chiba University Hospital, Chiba, Japan.
Shigetsugu TakanoDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.ORCID http://orcid.org/0000-0002-6495-0422
Kazuyuki SogawaDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kenta NodaR&D Department, Nittobo Medical Co., Ltd., Koriyama, Japan.
Hideyuki YoshitomiDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masumi IshibashiDepartment of Molecular Diagnosis, Graduate School of Medicine, Chiba University, Chiba, Japan.
Kaoru MogushiCenter for Genomic and Regenerative Medicine, Juntendo University, Tokyo, Japan.
Hirotaka TakizawaKashiwado Clinic in Port-Square, Kashiwado Memorial Foundation, Chiba, Japan.
Masayuki OtsukaDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Hiroaki ShimizuDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Masaru MiyazakiDepartment of General Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Fumio NomuraDivision of Clinical Mass Spectrometry, Chiba University Hospital, Chiba, Japan.
Chiba University · JPJuntendo University · JPNitto Boseki (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal malignancies. To improve its outcome, reliable biomarkers are urgently needed. In this study, we aimed to elucidate the key molecules involved in PDAC progression using proteomics approaches. First, we undertook 2-D electrophoresis to identify the proteins overexpressed in PDAC tissues. Following the analysis of agarose gel spots, cofilin-1 was identified and verified as a candidate protein commonly upregulated in PDAC tissues. In immunohistochemistry, cofilin-1 was strongly expressed in the cytoplasm of PDAC cells. Samples were divided into two groups based on the level of cofilin-1 expression. The high expression group showed significantly higher incidence of hematogenous dissemination in relapsed patients than the low expression group (P = 0.0083). In in vitro experiments, knockdown of cofilin-1 significantly decreased chemotaxis in PDAC cell lines. After we confirmed that cofilin-1 was secreted from PDAC cells, we established a detection system for the immune-complex of cofilin-1 in sera. Using this system, we measured the IC levels of cofilin-1 in sera and observed that the IC levels of cofilin-1 in PDAC patients were higher than those in healthy volunteers and patients with pancreatitis (PDAC vs. healthy volunteers, P < 0.0001; PDAC vs. patients with pancreatitis, P < 0.026). Notably, the IC levels of cofilin-1 showed a stepwise increase during PDAC progression (P = 0.0034), and high IC levels of cofilin-1 indicated poor prognosis of patients after surgery (P = 0.039). These results suggest that the IC of cofilin-1 in sera is a potentially attractive serum biomarker for the prognosis of PDAC.

Indexed as

AgedAntigen-Antibody ComplexBiomarkers, TumorBlotting, WesternCarcinoma, Pancreatic DuctalCell Line, TumorCofilin 1Disease ProgressionElectrophoresis, Gel, Two-DimensionalFemaleHumansImmunohistochemistryMaleMiddle AgedPancreatic NeoplasmsPrognosisAntigen-Antibody ComplexBiomarkers, TumorCofilin 1Cofilin-1immune-complexpancreatic cancerprognosisserum biomarker

Identifiers

PMID28161904
PMCPMC5406537
OpenAlexW2583786675

What OpenQuestion holds

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LicenceCC BY-NC
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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.