Literature DB >> 12353234

Gene therapy for intraperitoneally disseminated pancreatic cancers by Escherichia coli uracil phosphoribosiltransferase (UPRT) gene mediated by restricted replication-competent adenoviral vectors.

Masaru Oonuma1, Makoto Sunamura, Fuyuhiko Motoi, Shouji Fukuyama, Hiromune Shimamura, Jun-Ichiro Yamauchi, Kazuhiko Shibuya, Shin-Ichi Egawa, Hirofumi Hamada, Kazunori Takeda, Seiki Matsuno.   

Abstract

Although patients with unresectable pancreatic tumors have been treated with 5-fluorouracil (5FU)-based combination chemotherapy, the drug resistance of cancer cells presents a crucial therapeutic problem. It was reported that UPRT overcomes 5FU resistance. UPRT catalyzes the synthesis of 5-fluorouridine monophosphate (FUMP) from Uracil and phosphoribosylpyrophosphate (PRPP). The antitumor effect of 5FU is enhanced by augmenting 5-fluorodeoxyuridine monophosphate (FdUMP) converted from FUMP, which inhibits thymidylate synthetase (TS). We first demonstrated that injecting an E1-deficient adenoviral vector (Adv) expressing UPRT (AxCAUPRT) followed by 5-FU treatment resulted in a volume reduction of xenotransplanted human tumors. In examining the therapeutic effect of AxCAUPRT/5-FU against peritoneal dissemination, we found that non-selective gene transduction of AxCAUPRT caused severe adverse effects arising from the increase of F-dUMP in normal intestine. Because the therapeutic gene delivered by a restricted replication-competent Adv lacking 55 kDa E1B protein (AxE1AdB) is speculated to be expressed selectively in tumors, mice with established tumors were injected with AxE1AdB and E1-deleted Adv expressing the lacZ reporter gene (AxCAlacZ). The expression of the reporter gene (lacZ) was selectively enhanced in disseminated tumors. The therapeutic advantage of restricted replication competent Adv that expresses UPRT (AxE1AdB-UPRT) was evaluated in an intraperitoneal disseminated tumor model. To study the anti-tumor effect of AxE1AdB-UPRT/5FU, mice with disseminated AsPC-1 tumors were administered the Adv, followed by the 5FU treatment. It was shown that the treatment with AxE1AdB-UPRT/5FU caused a dramatic reduction of the disseminated tumor burden without toxicity in normal tissues. Our results showed that the AxE1AdB-UPRT/5FU system is a promising tool for intraperitoneal disseminated pancreatic cancer. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12353234     DOI: 10.1002/ijc.10650

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  4 in total

Review 1.  Gene therapy for pancreatic cancer targeting the genomic alterations of tumor suppressor genes using replication-selective oncolytic adenovirus.

Authors:  Makoto Sunamura; Masaru Oonuma; Fuyuhiko Motoi; Hisashi Abe; Yukoh Saitoh; Toru Hoshida; Shigeru Ottomo; Akira Horii; Seiki Matsuno
Journal:  Hum Cell       Date:  2002-09       Impact factor: 4.174

2.  Adenoviral p53 gene transfer and gemcitabine in three patients with liver metastases due to advanced pancreatic carcinoma.

Authors:  Gernot W Wolkersdörfer; Christian Thiede; Rainer Fischer; Gerhard Ehninger; Cornelie Haag
Journal:  HPB (Oxford)       Date:  2007       Impact factor: 3.647

3.  Imaging intratumoral convection: pressure-dependent enhancement in chemotherapeutic delivery to solid tumors.

Authors:  Terence P F Gade; Ian M Buchanan; Matthew W Motley; Yousef Mazaheri; William M Spees; Jason A Koutcher
Journal:  Clin Cancer Res       Date:  2009-01-01       Impact factor: 12.531

4.  Signalling pathway impact analysis based on the strength of interaction between genes.

Authors:  Zhenshen Bao; Xianbin Li; Xiangzhen Zan; Liangzhong Shen; Runnian Ma; Wenbin Liu
Journal:  IET Syst Biol       Date:  2016-08       Impact factor: 1.615

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.