Literature DB >> 28793330

Correction: Potential therapeutic impact of CD13 expression in non-small cell lung cancer.

Lars Henning Schmidt, Caroline Brand, Janine Stucke-Ring, Christoph Schliemann, Torsten Kessler, Saliha Harrach, Michael Mohr, Dennis Görlich, Alessandro Marra, Ludger Hillejan, Carsten Müller-Tidow, Georg Lenz, Eva Wardelmann, Rainer Wiewrodt, Wolfgang E Berdel, Christian Schwöppe, Wolfgang Hartmann.   

Abstract

[This corrects the article DOI: 10.1371/journal.pone.0177146.].

Entities:  

Year:  2017        PMID: 28793330      PMCID: PMC5549952          DOI: 10.1371/journal.pone.0183201

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Fig 3 appears incorrectly. Please see the complete, correct Fig 3 here.
Fig 3

In vivo therapeutic activity of systemic tTF-NGR against CD13+ A549 tumor xenografts.

To investigate CD13 expression flow cytometry was performed with a monoclonal PE-labeled anti-CD13 antibody. CD13 expression was found in 47% of the A549 lung cancer cells (green, control; purple, CD13) (Fig 3A). Following treatment with tTF-NGR (1 mg tTF-NGR/kg x5 (arrows); i.v.; n = 4 CD-1 nude mice) tumor growth of subcutaneous A549 xenotransplants was reduced as compared to the saline control group (n = 6) CD-1 nude mice (Fig 3B). The CD13 expression in subcutaneous A549 xenotransplant is demonstrated by immunofluorescence; since the antibodies used for CD13 and CD31 staining are speciesspecific for human CD13 and CD31, vascular and perivascular staining were not assayed in the xenografts (Fig 3C).

In vivo therapeutic activity of systemic tTF-NGR against CD13+ A549 tumor xenografts.

To investigate CD13 expression flow cytometry was performed with a monoclonal PE-labeled anti-CD13 antibody. CD13 expression was found in 47% of the A549 lung cancer cells (green, control; purple, CD13) (Fig 3A). Following treatment with tTF-NGR (1 mg tTF-NGR/kg x5 (arrows); i.v.; n = 4 CD-1 nude mice) tumor growth of subcutaneous A549 xenotransplants was reduced as compared to the saline control group (n = 6) CD-1 nude mice (Fig 3B). The CD13 expression in subcutaneous A549 xenotransplant is demonstrated by immunofluorescence; since the antibodies used for CD13 and CD31 staining are speciesspecific for human CD13 and CD31, vascular and perivascular staining were not assayed in the xenografts (Fig 3C).
  1 in total

1.  Potential therapeutic impact of CD13 expression in non-small cell lung cancer.

Authors:  Lars Henning Schmidt; Caroline Brand; Janine Stucke-Ring; Christoph Schliemann; Torsten Kessler; Saliha Harrach; Michael Mohr; Dennis Görlich; Alessandro Marra; Ludger Hillejan; Carsten Müller-Tidow; Georg Lenz; Eva Wardelmann; Rainer Wiewrodt; Wolfgang E Berdel; Christian Schwöppe; Wolfgang Hartmann
Journal:  PLoS One       Date:  2017-06-12       Impact factor: 3.240

  1 in total
  2 in total

1.  Aminopeptidase N (CD13): Expression, Prognostic Impact, and Use as Therapeutic Target for Tissue Factor Induced Tumor Vascular Infarction in Soft Tissue Sarcoma.

Authors:  Torsten Kessler; Ariane Baumeier; Caroline Brand; Michael Grau; Linus Angenendt; Saliha Harrach; Ursula Stalmann; Lars Henning Schmidt; Georg Gosheger; Jendrik Hardes; Dimosthenis Andreou; Johannes Dreischalück; Georg Lenz; Eva Wardelmann; Rolf M Mesters; Christian Schwöppe; Wolfgang E Berdel; Wolfgang Hartmann; Christoph Schliemann
Journal:  Transl Oncol       Date:  2018-08-17       Impact factor: 4.243

2.  Identification of potential target genes of non-small cell lung cancer in response to resveratrol treatment by bioinformatics analysis.

Authors:  Peng Gao; Guanghui Ren
Journal:  Aging (Albany NY)       Date:  2021-10-11       Impact factor: 5.682

  2 in total

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