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Recombinant Organisms as Source of Cancer Biotherapeutics

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Book cover Principles of Cancer Biotherapy

Abstract

The last fifteen years have witnessed a tremendous rise in new biological treatments for cancer. These treatments, collectively referred to as ’biological therapy,’are primarily based on stimulating the natural host immune response against the cancerous cells. Biological therapies in combination with chemotherapy, surgery, or radiation therapy have started showing promise as effective means for treating cancer. New approaches in biological therapy have been possible mainly because of increased knowledge of the cellular immune system and especially to new developments in biotechnology. Recombinant DNA technology, for example, has made it possible to generate large amounts of many biological compounds for the first time. The novelty of recombinant technology is the precision and efficiency with which scientists can manipulate genes. The ability to isolate human genes and insert them into microorganisms which then produce human proteins, thereby serving as biological factories, has revolutionized the field of biological therapy. Interferons have special significance to recombinant DNA technology as paradigm modifiers of immune response. The interest in the therapeutic potential of interferon against cancer and viral diseases has served as catalyst to the emerging recombinant DNA industry. Despite its great promise as an antiviral agent, the clinical application of interferon has been rather slow, mainly because of the lack of methods for producing adequate amounts of the protein. Interest in interferon beyond the field of virology began in the early 1960s, when workers began to recognize its growth-inhibitory and immuneactivation properties. During the 1960s and early 1970s, reports of interferon’s antiviral and antitumor activity in laboratory animals and humans stirred up this interest and several groups decided to purify human interferon for clinical use.

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Abbreviations

ADA:

adenosine deaminase

AML:

acute myeloid leukemia

bFGF:

basic fibroblast growth factor

CML:

chronic mylogenous leukemia

CSF:

colonystimulating factor

EGF:

epidermal growth factor

EPO:

erythropoietin

FDA:

Food and Drug Administration

HIV:

human immunodeficiency virus

IFN:

interferon

IL:

interleukin

LIF:

leukemia inhibitory factor

MAb:

monclonal antibody

PDGF:

platelet-derived growth factor

PE:

Pseudomonas exotoxin

PEG:

polyethylene glycol

TGF:

transforming growth factor

TNF:

tumor necrosis factor

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© 1998 Springer-Verlag Berlin Heidelberg

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Mehta, K., Aggarwal, B.B. (1998). Recombinant Organisms as Source of Cancer Biotherapeutics. In: Oldham, R.K. (eds) Principles of Cancer Biotherapy. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-0029-5_4

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