Evidence map›Paper›PMID 28182302›Full record

ArticleCancer science2017

Podoplanin promotes progression of malignant pleural mesothelioma by regulating motility and focus formation.

Shinji Takeuchi, Koji Fukuda, Tadaaki Yamada, Sachiko Arai, Satoshi Takagi, Genichiro Ishii, Atsushi Ochiai, Shotaro Iwakiri, Kazumi Itoi, Hisanori Uehara and 3 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Genomics and Functional Genomics of Malignant Pleural Mesothelioma.International journal of molecular sciences · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
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  15. 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

13 authors at 6 institutions in 1 country.

Shinji TakeuchiDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Koji FukudaDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Tadaaki YamadaDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Sachiko AraiDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Satoshi TakagiCancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.
Genichiro IshiiDivision of Pathology, Research Center for Innovative Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Atsushi OchiaiDivision of Pathology, Research Center for Innovative Oncology, National Cancer Center Hospital East, Kashiwa, Japan.
Shotaro IwakiriDepartment of Respiratory Surgery, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
Kazumi ItoiDepartment of Respiratory Surgery, Hyogo Prefectural Amagasaki General Medical Center, Amagasaki, Japan.
Hisanori UeharaDepartment of Pathology and Laboratory Medicine, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Hiroshi NishiharaDepartment of Translational Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Naoya FujitaCancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.
Seiji YanoDivision of Medical Oncology, Cancer Research Institute, Kanazawa University, Kanazawa, Japan.
Kanazawa University · JPHyogo Prefectural Amagasaki General Medical Center · JPJapanese Foundation For Cancer Research · JPNational Cancer Center Hospital East · JPHokkaido University · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant pleural mesothelioma (MPM) is characterized by dissemination and aggressive growth in the thoracic cavity. Podoplanin (PDPN) is an established diagnostic marker for MPM, but the function of PDPN in MPM is not fully understood. The purpose of this study was to determine the pathogenetic function of PDPN in MPM. Forty-seven of 52 tumors (90%) from Japanese patients with MPM and 3/6 (50%) MPM cell lines tested positive for PDPN. Knocking down PDPN in PDPN-high expressing MPM cells resulted in decreased cell motility. In contrast, overexpression of PDPN in PDPN-low expressing MPM cells enhanced cell motility. PDPN stimulated motility was mediated by activation of the RhoA/ROCK pathway. Moreover, knocking down PDPN with short hairpin (sh) RNA in PDPN-high expressing MPM cells resulted in decreased development of a thoracic tumor in mice with severe combined immune deficiency (SCID). In sharp contrast, transfection of PDPN in PDPN-low expressing MPM cells resulted in an increase in the number of Ki-67-positive proliferating tumor cells and it promoted progression of a thoracic tumor in SCID mice. Interestingly, PDPN promoted focus formation in vitro, and a low level of E-cadherin expression and YAP1 activation was observed in PDPN-high MPM tumors. These findings indicate that PDPN is a diagnostic marker as well as a pathogenetic regulator that promotes MPM progression by increasing cell motility and inducing focus formation. Therefore, PDPN might be a pathogenetic determinant of MPM dissemination and aggressive growth and may thus be an ideal therapeutic target.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsBlotting, WesternCadherinsCell Line, TumorCell MovementDisease ProgressionHumansImmunohistochemistryKi-67 AntigenMembrane GlycoproteinsMesotheliomaMice, SCIDPhosphoproteinsPleural NeoplasmsPodoplaninAdaptor Proteins, Signal TransducingCadherinsKi-67 AntigenMembrane GlycoproteinsPDPN protein, humanPhosphoproteinsPodoplaninrho-Associated Kinasesrho GTP-Binding ProteinsTranscription FactorsYAP1 protein, humanYAP-Signaling Proteinsfocus formationmesotheliomamotilitypodoplaninYAP1

Identifiers

PMID28182302
PMCPMC5406599
OpenAlexW2586987301

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.