Evidence map›Paper›PMID 26254295›Full record

ArticleOncotarget2015

Nanovehicles as a novel target strategy for hyperthermic intraperitoneal chemotherapy: a multidisciplinary study of peritoneal carcinomatosis.

Maciej Nowacki, Marek Wisniewski, Karolina Werengowska-Ciecwierz, Katarzyna Roszek, Joanna Czarnecka, I Łakomska, Tomasz Kloskowski, Dominik Tyloch, Robert Debski, Katarzyna Pietkun and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

19 authors at 5 institutions in 2 countries.

Maciej NowackiChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Marek WisniewskiPhysicochemistry of Carbon Materials Research Group, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Poland.
Karolina Werengowska-CiecwierzPhysicochemistry of Carbon Materials Research Group, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Poland.
Katarzyna RoszekDepartment of Biochemistry, Faculty of Biology and Environment Protection, Nicolaus Copernicus University in Toruń, Poland.
Joanna CzarneckaDepartment of Biochemistry, Faculty of Biology and Environment Protection, Nicolaus Copernicus University in Toruń, Poland.
I ŁakomskaFaculty of Chemistry, Nicolaus Copernicus University in Toruń, Poland.
Tomasz KloskowskiChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Dominik TylochChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Robert DebskiDepartment of Pediatric Hematology and Oncology, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Katarzyna PietkunChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Marta PokrywczynskaChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Dariusz GrzankaChair of Dermatology Department, Faculty of Medicine, Nicolaus Copernicus University, Toruń, Sexually Transmitted Diseases and Immunodermatology, Bydgoszcz, Poland.
Rafał CzajkowskiChair of Dermatology Department, Faculty of Medicine, Nicolaus Copernicus University, Toruń, Sexually Transmitted Diseases and Immunodermatology, Bydgoszcz, Poland.
Gerard DrewaDepartment of Medical Biology, University of Bydgoszcz, Poland.
A JundziłłChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Joseph K AgyinDepartment of Biochemistry, The University of Texas Health Science Center, San Antonio, TX, USA.
Samy L HabibDepartment of Cellular and Structural Biology, The University of Texas Health Science Center, San Antonio, TX, USA.
Artur P TerzykPhysicochemistry of Carbon Materials Research Group, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Poland.
Tomasz DrewaChair of Regenerative Medicine, Tissue Engineering Department, Ludwik Rydygier's Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, Poland.
Nicolaus Copernicus University · PLCollegium Medicum in Bydgoszcz · PLThe University of Texas Health Science Center · USThe University of Texas Health Science Center at San Antonio · USUniversity of Bydgoszcz · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In general, detection of peritoneal carcinomatosis (PC) occurs at the late stage when there is no treatment option. In the present study, we designed novel drug delivery systems that are functionalized with anti-CD133 antibodies. The C1, C2 and C3 complexes with cisplatin were introduced into nanotubes, either physically or chemically. The complexes were reacted with anti-CD133 antibody to form the labeled product of A0-o-CX-chem-CD133. Cytotoxicity screening of all the complexes was performed on CHO cells. Data showed that both C2 and C3 Pt-complexes are more cytotoxic than C1. Flow-cytometry analysis showed that nanotubes conjugated to CD133 antibody have the ability to target cells expressing the CD133 antigen which is responsible for the emergence of resistance to chemotherapy and disease recurrence. The shortest survival rate was observed in the control mice group (K3) where no hyperthermic intraperitoneal chemotherapy procedures were used. On the other hand, the longest median survival rate was observed in the group treated with A0-o-C1-chem-CD133. In summary, we designed a novel drug delivery system based on carbon nanotubes loaded with Pt-prodrugs and functionalized with anti-CD133 antibodies. Our data demonstrates the effectiveness of the new drug delivery system and provides a novel therapeutic modality in the treatment of melanoma.

Indexed as

AC133 AntigenAnimalsAntibodiesAntigens, CDCisplatinCombined Modality TherapyDisease Models, AnimalDrug Delivery SystemsGlycoproteinsHyperthermia, InducedImmunotoxinsInjections, IntraperitonealMelanoma, ExperimentalMiceMice, Inbred C57BLNanotubes, CarbonAC133 AntigenAntibodiesAntigens, CDCisplatinGlycoproteinsImmunotoxinsNanotubes, CarbonPeptidesProm1 protein, mousecarcinomatosishyperthermic intraperitoneal chemotherapyintraperitoneal perfusion and nanovehiclespalliative

Identifiers

PMID26254295
PMCPMC4673199
OpenAlexW1516495355

What OpenQuestion 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 OpenQuestion graph.