Evidence map›Paper›PMID 29147947›Full record

ArticleProgress in biomaterials2017

Biocompatibility of vertically aligned multi-walled carbon nanotube scaffolds for human breast cancer cell line MDA-MB-231.

E M Akinoglu, K Ozbilgin, P Kilicaslan Sonmez, M M Ozkut, M Giersig, S Inan, E Gumustepe, C Kurtman

Abstract read
In one paragraph

Article in Progress in biomaterials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Past, Present, and Future of Anticancer Nanomedicine.International journal of nanomedicine · 2020
    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

8 authors.

E M AkinogluInternational Academy of Optoelectronics at Zhaoqing, South China Normal University, Zhaoqing, Guangdong, China.
K OzbilginDepartment of Histology and Embryology, Faculty of Medicine, Celal Bayar University, Uncubozköy, Manisa, Turkey. kemalozbilgin@yahoo.com.
P Kilicaslan SonmezDepartment of Histology and Embryology, Faculty of Medicine, Celal Bayar University, Uncubozköy, Manisa, Turkey.
M M OzkutDepartment of Histology and Embryology, Faculty of Medicine, Celal Bayar University, Uncubozköy, Manisa, Turkey.
M GiersigInternational Academy of Optoelectronics at Zhaoqing, South China Normal University, Zhaoqing, Guangdong, China.
S InanDepartment of Histology and Embryology, Faculty of Medicine, Izmir University of Economy, Izmir, Turkey.
E GumustepeDepartment of Radiation Oncology, Faculty of Medicine, Ankara University, Ankara, Turkey.
C KurtmanDepartment of Radiation Oncology, Faculty of Medicine, Ankara University, Ankara, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the current study was to determine whether the MWCNT-based scaffold has a suitable structure for cell growth and provides a biocompatible environment for human MDA-MB-231 cell lines. MWCNT-based nanostructured scaffolds were produced by plasma-enhanced chemical vapor deposition (PECVD) technique. MDA-MB-231 cells were seeded on MWCNTs-textured silicon scaffolds and on pristine silicon surfaces. After 1 week of culturing, the scaffolds were prepared for SEM analysis and immunocytochemical staining was performed for the two groups (MWCNT scaffold and pristine silicon surface), using MMP-2, MMP-9, PI3K, AKT and NF-κB primary antibodies. SEM analyses showed that the MDA-MB-231 cells better adhered to the MWCNT-based nanostructured scaffold than the pristine silicon surface. Immunohistochemical activity of the MDA-MB-231 cells on both materials has similar staining with anti-AKT MMP-2, MMP-9 and NF-κB primary antibodies. Therefore, the results of the present study suggest that the MWCNT-based scaffolds enhanced cell adhesion to the scaffold and exhibited more biomimetic properties and physiological adaptation with the potential to be used for in vitro metastasis studies of BrCa cell lines.

Indexed as

BiocompatibilityBreast cancerImmunohistochemistryMDA-MB-231MWCNTs

Identifiers

PMID29147947
PMCPMC5700912

What OpenQuestion holds

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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.