PMID- 20044941 OWN - NLM STAT- MEDLINE DCOM- 20100617 LR - 20211020 IS - 1756-9966 (Electronic) IS - 0392-9078 (Print) IS - 0392-9078 (Linking) VI - 29 IP - 1 DP - 2010 Jan 4 TI - Evaluation of biodistribution and safety of adenovirus vector containing MDR1 in mice. PG - 1 LID - 10.1186/1756-9966-29-1 [doi] AB - BACKGROUND: The aim of this study is to examine the safety and distribution of Ad-EGFP-MDR1, an adenovirus encoding human multidurg resistance gene (human MDR1), in the mice colon carcinoma model. METHODS: After bone marrow cells (BMCs) were infected with Ad-EGFP-MDR1, they were administered by intra bone marrow-bone marrow transplantation (IBM-BMT). Total adenovirus antibody and serum adenovirus neutralizing factor (SNF) were determined. Biodistribution of Ad-EGFP-MDR1 was detected by in situ hybridization and immunohistochemistry. The peripheral hematocyte white blood cell (WBC), haemoglobin (Hb), red blood cell (RBC) and platelet (Plt) counts were analyzed. RESULTS: Neither total adenovirus antibody nor SNF increased weeks after BMT. In situ hybridization and immunohistochemistry demonstrated concordant expression of human MDR1 and P-gp which were found in lung, intestine, kidney and BMCs after BMT, but not detected in liver, spleen, brain and tumor. No significant abnormality of the recovery hematocyte was observed on Day 30 after treatment. CONCLUSION: The results indicate that IBM-BMT administration of a replication defective adenovirus is a feasible mode of delivery, allowing exogenous transference. The findings in this study are conducted for the future long-term studies of safety assessment of Ad-EGFP-MDR1. FAU - Zhao, ZhenZhen AU - Zhao Z AD - Surgery and Oncology Laboratory, Pediatric Research Institution, Children's Hospital of ChongQing Medical University, ChongQing, China. FAU - Liu, Wei AU - Liu W FAU - Su, Yuxi AU - Su Y FAU - Zhu, Jin AU - Zhu J FAU - Zheng, GaiHuan AU - Zheng G FAU - Luo, Qing AU - Luo Q FAU - Jin, XianQing AU - Jin X LA - eng PT - Evaluation Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100104 PL - England TA - J Exp Clin Cancer Res JT - Journal of experimental & clinical cancer research : CR JID - 8308647 RN - 0 (ABCB1 protein, human) RN - 0 (ATP Binding Cassette Transporter, Subfamily B) RN - 0 (ATP Binding Cassette Transporter, Subfamily B, Member 1) RN - 0 (Antibodies, Viral) SB - IM MH - ATP Binding Cassette Transporter, Subfamily B MH - ATP Binding Cassette Transporter, Subfamily B, Member 1/*genetics MH - Adenoviridae/*genetics MH - Animals MH - Antibodies, Viral/analysis MH - Bone Marrow Transplantation/methods MH - Cell Line, Tumor MH - Defective Viruses/genetics MH - Female MH - Gene Transfer Techniques MH - *Genetic Vectors/administration & dosage/adverse effects MH - Male MH - Mice MH - Mice, Inbred BALB C MH - Transfection PMC - PMC2819043 EDAT- 2010/01/05 06:00 MHDA- 2010/06/18 06:00 PMCR- 2010/01/04 CRDT- 2010/01/05 06:00 PHST- 2009/08/29 00:00 [received] PHST- 2010/01/04 00:00 [accepted] PHST- 2010/01/05 06:00 [entrez] PHST- 2010/01/05 06:00 [pubmed] PHST- 2010/06/18 06:00 [medline] PHST- 2010/01/04 00:00 [pmc-release] AID - 1756-9966-29-1 [pii] AID - 10.1186/1756-9966-29-1 [doi] PST - epublish SO - J Exp Clin Cancer Res. 2010 Jan 4;29(1):1. doi: 10.1186/1756-9966-29-1.