HER2 Support Group Forums - View Single Post - immunomodulatoryoligonuceotides plus herceptin decrease breast cancer growth by 96%!!

Lani · 08-25-2006, 07:18 AM

Mol Cancer Ther. 2006;5:2106-2114
© 2006 American Association for Cancer Research
Research Articles: Therapeutics
Immunomodulatory oligonucleotides as novel therapy for breast cancer: pharmacokinetics, in vitro and in vivo anticancer activity, and potentiation of antibody therapy

Hui Wang1,2, Elizabeth R. Rayburn1, Wei Wang1, Ekambar R. Kandimalla4, Sudhir Agrawal4 and Ruiwen Zhang1,2,3

1 Department of Pharmacology and Toxicology, Division of Clinical Pharmacology; 2 Comprehensive Cancer Center; and 3 Gene Therapy Center, University of Alabama at Birmingham, Birmingham, Alabama; and 4 Idera Pharmaceuticals, Inc., Cambridge, Massachusetts

Requests for reprints: Ruiwen Zhang, Department of Pharmacology and Toxicology, University of Alabama at Birmingham, 1670 University Boulevard, 113 Volker Hall, Birmingham, AL 35294. Phone: 205-934-8558; Fax: 205-975-9330. E-mail: Ruiwen.Zhang@ccc.uab.edu

Oligonucleotides containing CpG motifs and immunomodulatory oligonucleotides (IMO) containing a synthetic immunostimulatory dinucleotide and a novel DNA structure have been suggested to have potential for the treatment of various human diseases. In the present study, a newly designed IMO was evaluated in several models of human (MCF-7 and BT474 xenograft) and murine (4T1 syngeneic) breast cancer. Pharmacokinetics studies of the IMO administered by s.c., i.v., p.o., or i.p. routes were also accomplished. The IMO was widely distributed to various tissues by all four routes, with s.c. administration yielding the highest concentration in tumor tissue. The IMO inhibited the growth of tumors in all three models of breast cancer, with the lowest dose of the IMO inhibiting MCF-7 xenograft tumor growth by >40%. Combining the IMO with the anticancer antibody, Herceptin, led to potent antitumor effects, resulting in >96% inhibition of tumor growth. The IMO also exerted in vitro antitumor activity, as measured by cell growth, apoptosis, and proliferation assays in the presence of Lipofectin. This is the first report of the pharmacokinetics of this agent in normal and tumor-bearing mice. Based on the present results, we believe that the IMO is a good candidate for clinical development for breast cancer therapy used either alone or in combination with conventional cancer therapeutic agents. [Mol Cancer Ther 2006;5(8):2106–14]

08-25-2006, 07:18 AM	#1
Lani Senior Member Join Date: Mar 2006 Posts: 4,778	immunomodulatoryoligonuceotides plus herceptin decrease breast cancer growth by 96%!! Mol Cancer Ther. 2006;5:2106-2114 © 2006 American Association for Cancer Research Research Articles: Therapeutics Immunomodulatory oligonucleotides as novel therapy for breast cancer: pharmacokinetics, in vitro and in vivo anticancer activity, and potentiation of antibody therapy Hui Wang1,2, Elizabeth R. Rayburn1, Wei Wang1, Ekambar R. Kandimalla4, Sudhir Agrawal4 and Ruiwen Zhang1,2,3 1 Department of Pharmacology and Toxicology, Division of Clinical Pharmacology; 2 Comprehensive Cancer Center; and 3 Gene Therapy Center, University of Alabama at Birmingham, Birmingham, Alabama; and 4 Idera Pharmaceuticals, Inc., Cambridge, Massachusetts Requests for reprints: Ruiwen Zhang, Department of Pharmacology and Toxicology, University of Alabama at Birmingham, 1670 University Boulevard, 113 Volker Hall, Birmingham, AL 35294. Phone: 205-934-8558; Fax: 205-975-9330. E-mail: Ruiwen.Zhang@ccc.uab.edu Oligonucleotides containing CpG motifs and immunomodulatory oligonucleotides (IMO) containing a synthetic immunostimulatory dinucleotide and a novel DNA structure have been suggested to have potential for the treatment of various human diseases. In the present study, a newly designed IMO was evaluated in several models of human (MCF-7 and BT474 xenograft) and murine (4T1 syngeneic) breast cancer. Pharmacokinetics studies of the IMO administered by s.c., i.v., p.o., or i.p. routes were also accomplished. The IMO was widely distributed to various tissues by all four routes, with s.c. administration yielding the highest concentration in tumor tissue. The IMO inhibited the growth of tumors in all three models of breast cancer, with the lowest dose of the IMO inhibiting MCF-7 xenograft tumor growth by >40%. Combining the IMO with the anticancer antibody, Herceptin, led to potent antitumor effects, resulting in >96% inhibition of tumor growth. The IMO also exerted in vitro antitumor activity, as measured by cell growth, apoptosis, and proliferation assays in the presence of Lipofectin. This is the first report of the pharmacokinetics of this agent in normal and tumor-bearing mice. Based on the present results, we believe that the IMO is a good candidate for clinical development for breast cancer therapy used either alone or in combination with conventional cancer therapeutic agents. [Mol Cancer Ther 2006;5(8):2106–14]