Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody: Immunogene approach

Jiabing Chen, Shinobu Gamou, Atsushi Takayanagi, Yuichiro Ohtake, Masafumi Ohtsubo, Nobuyoshi Shimizu

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The 'Fab immunogene' is a novel gene transfer vehicle in which the Fab fragment of anti-human epidermal growth factor (EGF) receptor antibody B4G7 is conjugated with poly-L-lysine to form an affinity complex with DNA. It was developed to target delivery of therapeutic genes into EGF receptor-hyperproducing tumor cells. Various characteristic features of the immunogene have been documented. Here we add further evidence to prove that in vitro transfer of β-galactosidase/Fab immunogene is exclusively to EGF receptor-positive cells and that the herpes simplex virus thymidine kinase (TK)/Fab immunogene induces substantial suicide effects on A431 tumor cells when treated together with ganciclovir. The in vivo specificity of the immunogene transfer was examined using A431 tumor-bearing nude mice. When these nude mice were injected intraperitoneally with the chloramphenicol acetyltransferase (CAT)/Fab immunogene, CAT DNA was detected in the tumors as well as in liver and kidney but not brain, whereas CAT mRNA and enzyme activity were detected only in the tumors. Local and intraperitoneal injection of the TK/Fab immunogene and subsequent administration of ganciclovir effectively suppressed the growth of A431 tumors transplanted on the backs of nude mice. These observations suggest a possible application of the Fab immunogene system in cancer gene therapy.

Original languageEnglish
Pages (from-to)2673-2681
Number of pages9
JournalHuman Gene Therapy
Volume9
Issue number18
Publication statusPublished - 1998 Dec 10

Fingerprint

Epidermal Growth Factor Receptor
Squamous Cell Carcinoma
Chloramphenicol O-Acetyltransferase
Antibodies
Nude Mice
Genes
Neoplasms
Ganciclovir
Thymidine Kinase
Therapeutics
Galactosidases
erbB-1 Genes
Immunoglobulin Fab Fragments
Neoplasm Genes
DNA
Simplexvirus
Intraperitoneal Injections
Genetic Therapy
Suicide
Lysine

ASJC Scopus subject areas

  • Genetics

Cite this

Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody : Immunogene approach. / Chen, Jiabing; Gamou, Shinobu; Takayanagi, Atsushi; Ohtake, Yuichiro; Ohtsubo, Masafumi; Shimizu, Nobuyoshi.

In: Human Gene Therapy, Vol. 9, No. 18, 10.12.1998, p. 2673-2681.

Research output: Contribution to journalArticle

Chen, Jiabing ; Gamou, Shinobu ; Takayanagi, Atsushi ; Ohtake, Yuichiro ; Ohtsubo, Masafumi ; Shimizu, Nobuyoshi. / Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody : Immunogene approach. In: Human Gene Therapy. 1998 ; Vol. 9, No. 18. pp. 2673-2681.
@article{f779419601484da28da5a12d7bdffc6e,
title = "Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody: Immunogene approach",
abstract = "The 'Fab immunogene' is a novel gene transfer vehicle in which the Fab fragment of anti-human epidermal growth factor (EGF) receptor antibody B4G7 is conjugated with poly-L-lysine to form an affinity complex with DNA. It was developed to target delivery of therapeutic genes into EGF receptor-hyperproducing tumor cells. Various characteristic features of the immunogene have been documented. Here we add further evidence to prove that in vitro transfer of β-galactosidase/Fab immunogene is exclusively to EGF receptor-positive cells and that the herpes simplex virus thymidine kinase (TK)/Fab immunogene induces substantial suicide effects on A431 tumor cells when treated together with ganciclovir. The in vivo specificity of the immunogene transfer was examined using A431 tumor-bearing nude mice. When these nude mice were injected intraperitoneally with the chloramphenicol acetyltransferase (CAT)/Fab immunogene, CAT DNA was detected in the tumors as well as in liver and kidney but not brain, whereas CAT mRNA and enzyme activity were detected only in the tumors. Local and intraperitoneal injection of the TK/Fab immunogene and subsequent administration of ganciclovir effectively suppressed the growth of A431 tumors transplanted on the backs of nude mice. These observations suggest a possible application of the Fab immunogene system in cancer gene therapy.",
author = "Jiabing Chen and Shinobu Gamou and Atsushi Takayanagi and Yuichiro Ohtake and Masafumi Ohtsubo and Nobuyoshi Shimizu",
year = "1998",
month = "12",
day = "10",
language = "English",
volume = "9",
pages = "2673--2681",
journal = "Human Gene Therapy",
issn = "1043-0342",
publisher = "Mary Ann Liebert Inc.",
number = "18",

}

TY - JOUR

T1 - Targeted in vivo delivery of therapeutic gene into experimental squamous cell carcinomas using anti-epidermal growth factor receptor antibody

T2 - Immunogene approach

AU - Chen, Jiabing

AU - Gamou, Shinobu

AU - Takayanagi, Atsushi

AU - Ohtake, Yuichiro

AU - Ohtsubo, Masafumi

AU - Shimizu, Nobuyoshi

PY - 1998/12/10

Y1 - 1998/12/10

N2 - The 'Fab immunogene' is a novel gene transfer vehicle in which the Fab fragment of anti-human epidermal growth factor (EGF) receptor antibody B4G7 is conjugated with poly-L-lysine to form an affinity complex with DNA. It was developed to target delivery of therapeutic genes into EGF receptor-hyperproducing tumor cells. Various characteristic features of the immunogene have been documented. Here we add further evidence to prove that in vitro transfer of β-galactosidase/Fab immunogene is exclusively to EGF receptor-positive cells and that the herpes simplex virus thymidine kinase (TK)/Fab immunogene induces substantial suicide effects on A431 tumor cells when treated together with ganciclovir. The in vivo specificity of the immunogene transfer was examined using A431 tumor-bearing nude mice. When these nude mice were injected intraperitoneally with the chloramphenicol acetyltransferase (CAT)/Fab immunogene, CAT DNA was detected in the tumors as well as in liver and kidney but not brain, whereas CAT mRNA and enzyme activity were detected only in the tumors. Local and intraperitoneal injection of the TK/Fab immunogene and subsequent administration of ganciclovir effectively suppressed the growth of A431 tumors transplanted on the backs of nude mice. These observations suggest a possible application of the Fab immunogene system in cancer gene therapy.

AB - The 'Fab immunogene' is a novel gene transfer vehicle in which the Fab fragment of anti-human epidermal growth factor (EGF) receptor antibody B4G7 is conjugated with poly-L-lysine to form an affinity complex with DNA. It was developed to target delivery of therapeutic genes into EGF receptor-hyperproducing tumor cells. Various characteristic features of the immunogene have been documented. Here we add further evidence to prove that in vitro transfer of β-galactosidase/Fab immunogene is exclusively to EGF receptor-positive cells and that the herpes simplex virus thymidine kinase (TK)/Fab immunogene induces substantial suicide effects on A431 tumor cells when treated together with ganciclovir. The in vivo specificity of the immunogene transfer was examined using A431 tumor-bearing nude mice. When these nude mice were injected intraperitoneally with the chloramphenicol acetyltransferase (CAT)/Fab immunogene, CAT DNA was detected in the tumors as well as in liver and kidney but not brain, whereas CAT mRNA and enzyme activity were detected only in the tumors. Local and intraperitoneal injection of the TK/Fab immunogene and subsequent administration of ganciclovir effectively suppressed the growth of A431 tumors transplanted on the backs of nude mice. These observations suggest a possible application of the Fab immunogene system in cancer gene therapy.

UR - http://www.scopus.com/inward/record.url?scp=0032506793&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0032506793&partnerID=8YFLogxK

M3 - Article

C2 - 9874265

AN - SCOPUS:0032506793

VL - 9

SP - 2673

EP - 2681

JO - Human Gene Therapy

JF - Human Gene Therapy

SN - 1043-0342

IS - 18

ER -