Literature DB >> 27677582

Erratum to: Oncolytic virus efficiency inhibited growth of tumour cells with multiple drug resistant phenotype in vivo and in vitro.

Elena P Goncharova1, Julia S Ruzhenkova1, Ivan S Petrov1,2, Sergey N Shchelkunov3, Marina A Zenkova4.   

Abstract

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Year:  2016        PMID: 27677582      PMCID: PMC5039827          DOI: 10.1186/s12967-016-1041-3

Source DB:  PubMed          Journal:  J Transl Med        ISSN: 1479-5876            Impact factor:   5.531


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Erratum to: J Transl Med (2016) 14:241 DOI 10.1186/s12967-016-1002-x

Unfortunately, the original version of this article [1] contained an error. Figures 2 and 7 were the incorrect versions. They have been corrected in the original article and are also included correctly in this erratum.
Fig. 2

Development of LIVP-GFP infection in various tumour cells. Development of LIVP-GFP infection in RLS (green circles), RLS-40 (red circles), KB-3-1 (violet squares), KB-8-5 (black line with open squares) and melanoma B-16 (blue triangles) tumour cells at MOI of 1 (a) and MOI of 10 (b). Cells were incubated with virus for 1 h, washed with PBS and incubated up to the analysis in IMDM supplemented with 2 % FBS. Viral titre was measured by PFU assay. Data of three independent experiments are presented

Fig. 7

Effect of LIVP-GFP treatment on the immune responses of tumour-bearing mice. a Summary data showing a significant increase of the number of IFN-γ-ransecreting splenocytes in LIVP-GFP-treated mice (n = 6) with RLS-40 or with melanoma B-16 tumours. Comparison of immune-related proteins GMC-SF (b) and IL-6 (c) in the blood serum of RLS-40 bearing mice during the treatment with LIVP-GFP (the experimental scheme was shown in Fig. 5a): red circles and blue squares for RLS-40 bearing mice treated with LIVP-GFP and PBS, respectively; black triangles healthy mice receiving PBS. The levels of cytokines in the blood serum were measured by ELISA. For each day, the value of mean ± SEM is shown

Development of LIVP-GFP infection in various tumour cells. Development of LIVP-GFP infection in RLS (green circles), RLS-40 (red circles), KB-3-1 (violet squares), KB-8-5 (black line with open squares) and melanoma B-16 (blue triangles) tumour cells at MOI of 1 (a) and MOI of 10 (b). Cells were incubated with virus for 1 h, washed with PBS and incubated up to the analysis in IMDM supplemented with 2 % FBS. Viral titre was measured by PFU assay. Data of three independent experiments are presented Effect of LIVP-GFP treatment on the immune responses of tumour-bearing mice. a Summary data showing a significant increase of the number of IFN-γ-ransecreting splenocytes in LIVP-GFP-treated mice (n = 6) with RLS-40 or with melanoma B-16 tumours. Comparison of immune-related proteins GMC-SF (b) and IL-6 (c) in the blood serum of RLS-40 bearing mice during the treatment with LIVP-GFP (the experimental scheme was shown in Fig. 5a): red circles and blue squares for RLS-40 bearing mice treated with LIVP-GFP and PBS, respectively; black triangles healthy mice receiving PBS. The levels of cytokines in the blood serum were measured by ELISA. For each day, the value of mean ± SEM is shown
  1 in total

1.  Oncolytic virus efficiency inhibited growth of tumour cells with multiple drug resistant phenotype in vivo and in vitro.

Authors:  Elena P Goncharova; Julia S Ruzhenkova; Ivan S Petrov; Sergey N Shchelkunov; Marina A Zenkova
Journal:  J Transl Med       Date:  2016-08-18       Impact factor: 5.531

  1 in total
  1 in total

1.  Virotherapy of the Malignant U87 Human Glioblastoma in the Orthotopic Xenotransplantation Mouse SCID Model.

Authors:  S N Shchelkunov; I A Razumov; I V Kolosova; A V Romashchenko; E L Zavjalov
Journal:  Dokl Biochem Biophys       Date:  2018-03-14       Impact factor: 0.834

  1 in total

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