Research output: Contribution to journal › Article › peer-review
Oncolytic effect of wild-type Newcastle disease virus isolates in cancer cell lines in vitro and in vivo on xenograft model. / Yurchenko, Kseniya S.; Zhou, Peipei; Kovner, Anna V. et al.
In: PLoS ONE, Vol. 13, No. 4, e0195425, 05.04.2018.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Oncolytic effect of wild-type Newcastle disease virus isolates in cancer cell lines in vitro and in vivo on xenograft model
AU - Yurchenko, Kseniya S.
AU - Zhou, Peipei
AU - Kovner, Anna V.
AU - Zavjalov, Evgenii L.
AU - Shestopalova, Lidiya V.
AU - Shestopalov, Alexander M.
PY - 2018/4/5
Y1 - 2018/4/5
N2 - Oncolyic virotherapy is one of the modern experimental techniques to treat human cancers. Here we studied the antitumor activity of wild-type Newcastle disease virus (NDV) isolates from Russian migratory birds. We showed that NDV could selectively kill malignant cells without affecting healthy cells. We evaluated the oncolytic effect of 44 NDV isolates in 4 his-togenetically different human cell lines (HCT116, HeLa, A549, MCF7). The safety of the isolates was also tested in normal peripheral blood mononuclear (PBMC) cells. The viability of tumor cell lines after incubation with NDV isolates was evaluated by MTT. All cell lines, except for normal PBMC primary cells, had different degrees of susceptibility to NDV infection. Seven NDV strains had the highest oncolytic activity, and some NDV strains demonstrated oncolytic selectivity for different cell lines. In vivo, we described the intratumoral activity of NDV/Altai/pigeon/770/2011 against subcutaneous non-small cell lung carcinoma using xenograft SCID mice model. All animals were responsive to therapy. Histology confirmed therapy-induced destructive changes and growing necrotic bulk density in tumor tissue. Our findings indicate that wild-type NDV strains selectively kill tumor cells with no effect on healthy PBMC cells, and intratumoral virotherapy with NDV suppresses the subcutaneous tumor growth in SCID mice.
AB - Oncolyic virotherapy is one of the modern experimental techniques to treat human cancers. Here we studied the antitumor activity of wild-type Newcastle disease virus (NDV) isolates from Russian migratory birds. We showed that NDV could selectively kill malignant cells without affecting healthy cells. We evaluated the oncolytic effect of 44 NDV isolates in 4 his-togenetically different human cell lines (HCT116, HeLa, A549, MCF7). The safety of the isolates was also tested in normal peripheral blood mononuclear (PBMC) cells. The viability of tumor cell lines after incubation with NDV isolates was evaluated by MTT. All cell lines, except for normal PBMC primary cells, had different degrees of susceptibility to NDV infection. Seven NDV strains had the highest oncolytic activity, and some NDV strains demonstrated oncolytic selectivity for different cell lines. In vivo, we described the intratumoral activity of NDV/Altai/pigeon/770/2011 against subcutaneous non-small cell lung carcinoma using xenograft SCID mice model. All animals were responsive to therapy. Histology confirmed therapy-induced destructive changes and growing necrotic bulk density in tumor tissue. Our findings indicate that wild-type NDV strains selectively kill tumor cells with no effect on healthy PBMC cells, and intratumoral virotherapy with NDV suppresses the subcutaneous tumor growth in SCID mice.
KW - A549 Cells
KW - Animals
KW - Bird Diseases/virology
KW - Birds
KW - Carcinoma, Non-Small-Cell Lung/therapy
KW - Cell Line, Tumor
KW - HCT116 Cells
KW - HeLa Cells
KW - Humans
KW - Lung Neoplasms/therapy
KW - MCF-7 Cells
KW - Mice
KW - Mice, SCID
KW - Neoplasm Transplantation
KW - Newcastle disease virus/growth & development
KW - Oncolytic Virotherapy/methods
KW - Russia
KW - Siberia
KW - Transplantation, Heterologous
KW - APOPTOSIS
KW - DEATH
KW - PANCREATIC ADENOCARCINOMA
KW - VIROTHERAPY
KW - REPLICATION
KW - INFECTION
KW - GLIOMA
KW - TRIAL
KW - MTH-68/H
KW - RESPONSES
UR - http://www.scopus.com/inward/record.url?scp=85045037225&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0195425
DO - 10.1371/journal.pone.0195425
M3 - Article
C2 - 29621357
AN - SCOPUS:85045037225
VL - 13
JO - PLoS ONE
JF - PLoS ONE
SN - 1932-6203
IS - 4
M1 - e0195425
ER -
ID: 12419287