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PMID: 2642869 Published · ppublish English Journal Article Review

Therapeutic opportunities involving cellular oncogenes: novel approaches fostered by biotechnology.

Huber BE

Abstract

Biotechnological processes are having a major impact on many industrial sectors, including the pharmaceutical industry. The contributions of recombinant DNA and hybridoma technologies to modern therapeutics include production of natural and unnatural peptides, subunit vaccines, monoclonal antibodies and nucleic acid hybridization probes for in vitro and in vivo diagnostics and biological imaging, therapeutic monoclonal antibodies as tissue-specific delivery systems or as agents to confer passive immunity, production of therapeutic targets for rational drug design, and the use of cloned enzymes as stereospecific catalysts in large-scale production of small medicinal molecules. Biotechnological advances have led to the identification of a discrete set of genes, oncogenes, which may be essential contributing factors for a great variety and number of human cancers. In addition, biotechnological innovations are fostering the exploitation of oncogenes as novel therapeutic targets for cancer diagnosis, prognosis, and treatment. Because oncogenes are activated in transformation by either qualitative or quantitative mechanisms, however, different biotechnology-based therapeutic approaches are required for each class.

MeSH Terms
Biotechnology Cell Transformation, Neoplastic Drug Industry Gene Expression Regulation Humans Neoplasms/diagnosis,physiopathology,therapy Oncogenes Proto-Oncogene Proteins Proto-Oncogenes
Chemicals
Proto-Oncogene Proteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Huber B E
Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709.
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
0892-6638
Published
1989-01-00
Pages
5-13
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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