Evidence map›Paper›PMID 20395438›Full record

ArticleThe American journal of pathology2010

The insulin-like growth factor receptor I promotes motility and invasion of bladder cancer cells through Akt- and mitogen-activated protein kinase-dependent activation of paxillin.

David Metalli, Francesca Lovat, Farida Tripodi, Marco Genua, Shi-Qiong Xu, Michela Spinelli, Lilia Alberghina, Marco Vanoni, Raffaele Baffa, Leonard G Gomella and 2 more

Abstract read
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

52 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
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  8. Review
  9. Article
  10. Role of tyrosine kinases in bladder cancer progression: an overview.Cell communication and signaling : CCS · 2020
    Review
  11. Article
  12. Docosahexaenoic Acid Reverted the All-Journal of clinical medicine · 2020
    Article
  13. Article
  14. PHIP drives glioblastoma motility and invasion by regulating the focal adhesion complex.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  15. Article
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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.

David MetalliDepartment of Urology, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Francesca Lovat
Farida Tripodi
Marco Genua
Shi-Qiong Xu
Michela Spinelli
Lilia Alberghina
Marco Vanoni
Raffaele Baffa
Leonard G Gomella
Renato V Iozzo
Andrea Morrione

Funding

NEOPLASTIC MODULATION OF PROTEOGLYCAN METABOLISMR01CA039481 · NCI · UNIVERSITY OF PENNSYLVANIA · PI IOZZO, RENATO V. · 1985 to 2020
$7.1M
The Biology of Perlecan in Cancer and AngiogenesisR01CA047282 · NCI · THOMAS JEFFERSON UNIVERSITY · PI IOZZO, RENATO V. · 1990 to 2019
$5.7M
Proepithelin Signaling in Urothelial CellsR01DK068419 · NIDDK · THOMAS JEFFERSON UNIVERSITY · PI MORRIONE, ANDREA · 2005 to 2009
$1.2M
NCI NIH HHS R01 CA039481NCI NIH HHS R01 CA047282NCI NIH HHS R01 CA39481NIDDK NIH HHS R01 DK068419
6 · The paper itself

Abstract

The insulin-like growth factor receptor I (IGF-IR) plays an essential role in transformation by promoting cell growth and protecting cancer cells from apoptosis. Aberrant IGF-IR signaling is implicated in several types of tumors, including carcinomas of the lung, breast, prostate, pancreas, liver, and colon. However, the contribution of the IGF-IR to the development of the transformed phenotype in urothelial cells has not been clearly established. In this study we demonstrated that the IGF-IR is overexpressed in invasive bladder cancer tissues compared with nonmalignant controls. We have investigated the role of the IGF-IR in bladder cancer by using urothelial carcinoma-derived 5637 and T24 cells. Although activation of the IGF-IR did not appreciably affect their growth, it did promote migration and stimulate in vitro wound closure and invasion. These effects required the activation of the Akt and Mitogen-activated protein kinase (MAPK) pathways as well as IGF-I-induced Akt- and MAPK-dependent phosphorylation of paxillin, which relocated at dynamic focal adhesions and was necessary for promoting motility in bladder cancer cells. Our results provide the first evidence for a role of the IGF-IR in motility and invasion of bladder cancer cells and support the hypothesis that the IGF-IR may play a critical role in the establishment of the invasive phenotype in urothelial neoplasia. Thus, the IGF-IR may also serve as a novel biomarker for bladder cancer.

Indexed as

Cell Line, TumorCell MovementCell Transformation, NeoplasticFocal Adhesion Protein-Tyrosine KinasesHumansMitogen-Activated Protein KinasesNeoplasm InvasivenessPaxillinProto-Oncogene Proteins c-aktReceptor, IGF Type 1RNA, Small InterferingSignal TransductionUrinary Bladder NeoplasmsFocal Adhesion Protein-Tyrosine KinasesMitogen-Activated Protein KinasesPaxillinProto-Oncogene Proteins c-aktReceptor, IGF Type 1RNA, Small Interfering

Identifiers

PMID20395438
PMCPMC2877859

What OpenQuestion holds

Textmetadata
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.