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Destruction of Bystander Cells by Tumor Cells Transfected With Inducible Nitric Oxide (NO) Synthase Gene
Author(s) -
Keping Xie,
Shuang Huang,
Zhongyun Dong,
ShinHun Juang,
Ya Wang,
Isaiah J. Fidler
Publication year - 1997
Publication title -
jnci journal of the national cancer institute
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.797
H-Index - 356
eISSN - 1460-2105
pISSN - 0027-8874
DOI - 10.1093/jnci/89.6.421
Subject(s) - bystander effect , transfection , nitric oxide synthase , nitric oxide , tumor cells , microbiology and biotechnology , chemistry , gene , cancer research , biology , immunology , biochemistry , organic chemistry
The activation of an enzyme, inducible nitric oxide synthase (iNOS), catalyzes the production of endogenous nitric oxide (NO). NO, in turn, is associated with cell death, suppression of tumor development, and inhibition of metastasis of murine melanoma cells. Moreover, the in vivo induction of iNOS is associated with regression of established hepatic metastases. Whether this regression required the activation of the iNOS gene in every tumor cell or whether NO-producing tumor cells can also kill bystander (neighboring) cells has been previously unknown.

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