Evidence map›Paper›PMID 25465204›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2015

Metastatic bladder cancer cells distinctively sense and respond to physical cues of collagen fibril-mimetic nanotopography.

James N Iuliano, Paul D Kutscha, N J Biderman, Sita Subbaram, Timothy R Groves, Scott A Tenenbaum, Nadine Hempel

Abstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
  4. LncRNA MAFG-AS1 is involved in human cancer progression.European journal of medical research · 2023
    Review
  5. 3D Tumor Models in Urology.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Article
  8. 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

7 authors.

James N IulianoNanobioscience Constellation, College of Nanoscale Science, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA University at Albany, State University of New York, Albany, NY 12203, USA.
Paul D KutschaNanobioscience Constellation, College of Nanoscale Science, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA University at Albany, State University of New York, Albany, NY 12203, USA.
N J BidermanNanoengineering Constellation, College of Nanoscale Engineering, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA University at Albany, State University of New York, Albany, NY 12203, USA.
Sita SubbaramCenter for Cell Biology and Cancer Research, Albany Medical College, Albany, NY 12209, USA.
Timothy R GrovesNanoengineering Constellation, College of Nanoscale Engineering, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA.
Scott A TenenbaumNanobioscience Constellation, College of Nanoscale Science, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA.
Nadine HempelNanobioscience Constellation, College of Nanoscale Science, SUNY Polytechnic Institute, State University of New York, Albany, NY 12203, USA nhempel@sunycnse.com.

Funding

Mitochondrial Redox Control of MetastasisR00CA143229 · NCI · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI HEMPEL, NADINE · 2012 to 2014
$709k
NCI NIH HHS R00 CA143229NCI NIH HHS R00CA143229
6 · The paper itself

Abstract

Tumor metastasis is characterized by enhanced invasiveness and migration of tumor cells through the extracellular matrix (ECM), resulting in extravasation into the blood and lymph and colonization at secondary sites. The ECM provides a physical scaffold consisting of components such as collagen fibrils, which have distinct dimensions at the nanoscale. In addition to the interaction of peptide moieties with tumor cell integrin clusters, the ECM provides a physical guide for tumor cell migration. Using nanolithography we set out to mimic the physical dimensions of collagen fibrils using lined nanotopographical silicon surfaces and to explore whether metastatic tumor cells are uniquely able to respond to these physical dimensions. Etched silicon surfaces containing nanoscale lined patterns with varying trench and ridge sizes (65-500 nm) were evaluated for their ability to distinguish between a non-metastatic (253 J) and a highly metastatic (253 J-BV) derivative bladder cancer cell line. Enhanced alignment was distinctively observed for the metastatic cell lines on feature sizes that mimic the dimensions of collagen fibrils (65-100 nm lines, 1:1-1:1.5 pitch). Further, these sub-100 nm lines acted as guides for migration of metastatic cancer cells. Interestingly, even at this subcellular scale, metastatic cell migration was abrogated when cells were forced to move perpendicular to these lines. Compared to flat surfaces, 65 nm lines enhanced the formation of actin stress fibers and filopodia of metastatic cells. This was accompanied by increased formation of focal contacts, visualized by immunofluorescent staining of phospho-focal adhesion kinase along the protruding lamellipodia. Simple lined nanotopography appears to be an informative platform for studying the physical cues of the ECM in a pseudo-3D format and likely mimics physical aspects of collagen fibrils. Metastatic cancer cells appear distinctively well adapted to sense these features using filopodia protrusions to enhance their alignment and migration.

Indexed as

Cell Line, TumorCollagenFluorescent Antibody TechniqueHumansMicroscopy, Electron, ScanningNanotechnologyNeoplasm MetastasisSurface PropertiesUrinary Bladder NeoplasmsCollagenbladder cancercollagen fibrilmetastasisnanotechnologyNanotopography

Identifiers

PMID25465204
PMCPMC4615689

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Registered trials

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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.