SBIR/STTR Research Award

Targeted Degradation of PKR mRNA with 2-5A Antisense

Award identifier bd726d1764b81b7efe9e4d348ec4aefe436016c0d85d675bc3088d4753dcb166Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$133,536

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
RIDGEWAY BIOSYSTEMS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Inflammatory diseases represent increasing health care cost to American people. For many chronic inflammatory diseases (asthma, rheumatoid arthritis, bowel inflammatory diseases, etc.), there are no effective treatment. With the increase in the aging population of American society, this problem becomes aggravating. Targeted degradation of important factors (cytokines, cytokine receptors and intracellular mediators) participating in the inflammation signaling is a cost-effective strategy to develop an anti-inflammatory therapeutic measure. PKR is emerging as an important mediator for inflammatory process by transducing signaling activation of NF-kappa B or p38 to activate gene transcription of a number of inflammatory cytokines. Therefore, disruption of PKR activity is a particular attractive means of treating inflammatory diseases. The advantage of selecting PKR as a target also resides in that PKR is nonessential protein for cell survival compared with other targets (TNF-alpha, NF-kappa B, p38, etc.) which are vital for cell survival. Disruption of their activities may lead to undesirable and unexpected side effects. RBI is developing a novel class of chimerical oligonucleotides for use in antisense therapeutic strategies. This chimeras are comprised of an antisense component, which directs the compound to the complementary PKR sequences, and an activator moiety, 2',5'-oligoadenylate (2-5A) that serves to activate a cellular enzyme, ribonuclease L (RNase L), which cleaves the target RNA. Preliminary results demonstrated that 2-5A anti-PKR chimera can efficiently degrade PKR and inhibit PKR activation. The goal of this proposal is to progress this compound toward commercialization by obtaining a lead chimera compound with affinity to both human and murine PKR mRNA, and investigating the anti-inflammatory activity of the lead compound. If successful, the 2-5A anti-PKR compound will have a potential application to the treatment of chronic inflammatory diseases including rheumatoid arthritis, Crohn's diseases etc.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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