Evidence map›Paper›PMID 30428555›Full record

ArticlePharmaceutics2018

Cisplatin Loaded Multiwalled Carbon Nanotubes Induce Resistance in Triple Negative Breast Cancer Cells.

Madalina Andreea Badea, Mariana Prodana, Anca Dinischiotu, Carmen Crihana, Daniela Ionita, Mihaela Balas

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 47 citations in OpenAlex.

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  11. [Effects of length and chemical modification on the activation of vascular endothelial cells induced by multi walled carbon nanotubes].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2021
    Article
  12. Review
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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

6 authors at 3 institutions in 1 country.

Madalina Andreea BadeaDepartment of Biochemistry and Molecular Biology, Faculty of Biology, University of Bucharest, 91-95 Splaiul Independentei, R-050095 Bucharest, Romania. madalina.andreea.badea@drd.unibuc.ro.
Mariana ProdanaDepartment of General Chemistry, Faculty of Applied Chemistry and Materials Science, Politehnica University of Bucharest, 313 Splaiul Independentei, 060042 Bucharest, Romania. mariana.prodana@upb.ro.
Anca DinischiotuDepartment of Biochemistry and Molecular Biology, Faculty of Biology, University of Bucharest, 91-95 Splaiul Independentei, R-050095 Bucharest, Romania. anca.dinischiotu@bio.unibuc.ro.
Carmen CrihanaCF2 Clinical Hospital Bucharest, 63 Blvd. Marasesti, 011464 Bucharest, Romania. ccrihana@hotmail.com.
Daniela IonitaDepartment of General Chemistry, Faculty of Applied Chemistry and Materials Science, Politehnica University of Bucharest, 313 Splaiul Independentei, 060042 Bucharest, Romania. daniela.ionita@upb.ro.
Mihaela BalasDepartment of Biochemistry and Molecular Biology, Faculty of Biology, University of Bucharest, 91-95 Splaiul Independentei, R-050095 Bucharest, Romania. mihaela.radu@bio.unibuc.ro.ORCID 0000-0001-9522-0118
University of Bucharest · ROUniversitatea Națională de Știință și Tehnologie Politehnica București · ROClinical Emergency Hospital Bucharest · RO

Funding

Romanian Ministry of Education and by Executive Agency for Higher Education, Research, Development and Innovation Funding project 183PED/2017
6 · The paper itself

Abstract

In this paper we developed a method for multiwalled carbon nanotubes (MWCNTs) use as carriers for a drug based on platinum in breast cancer therapy. The method of functionalization involves the carboxyl functionalization of nanotubes and encapsulation of cisplatin (CDDP) into MWCNTs. The biological properties of MWCNTs loaded with CDDP (MWCNT-COOH-CDDP) and of individual components MWCNT-COOH and free CDDP were evaluated on MDA-MB-231 cells. Various concentrations of CDDP (0.316⁻2.52 µg/mL) and MWCNTs (0.5⁻4 µg/mL) were applied on cells for 24 and 48 h. Only at high doses of CDDP (1.26 and 2.52 µg/mL) and MWCNT-COOH-CDDP (2 and 4 µg/mL) cell morphological changes were observed. The cellular viability decreased only with approx. 40% after 48 h of exposure to 2.52 µg/mL CDDP and 4 µg/mL MWCNT-COOH-CDDP despite the high reactive oxygen species (ROS) production induced by MWCNTs starting with 24 h. After 48 h, ROS level dropped as a result of the antioxidant defence activation. We also found a significant decrease of caspase-3 and p53 expression after 48 h, accompanied by a down-regulation of NF-κB in cells exposed to MWCNT-COOH-CDDP system which promotes apoptosis escape and thus failing to overcome the triple negative breast cancer (TNBC) cells resistance.

Indexed as

carbon nanotubescisplatinMDA-MB-231 cellsNrf2reactive oxygen species

Identifiers

PMID30428555
PMCPMC6321179
OpenAlexW2901172773

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.