Recombinant Organisms as Source of Cancer Biotherapeutics

作者: Kapil Mehta , Bharat B. Aggarwal

DOI: 10.1007/978-94-009-0029-5_4

关键词:

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

参考文章(259)
Hiroshi Suzuki, Kiyoshi Yasukawa, Takashi Saito, Ryo Goitsuka, Atsuhiko Hasegawa, Yoshiyuki Ohsugi, Tetsuya Taga, Tadamitsu Kishimoto, Anti-human interleukin-6 receptor antibody inhibits human myeloma growth in vivo European Journal of Immunology. ,vol. 22, pp. 1989- 1993 ,(1992) , 10.1002/EJI.1830220806
S. Ramakrishnan, Michael J. Bjorn, L. L. Houston, Recombinant ricin A chain conjugated to monoclonal antibodies: improved tumor cell inhibition in the presence of lysosomotropic compounds. Cancer Research. ,vol. 49, pp. 613- 617 ,(1989)
David M. Goldenberg, Anastasia L. Jones, Hans J. Hansen, David J. P. FitzGerald, Ira Pastan, Robert J. Kreitman, Pseudomonas exotoxin-based immunotoxins containing the antibody LL2 or LL2-Fab' induce regression of subcutaneous human B-cell lymphoma in mice Cancer Research. ,vol. 53, pp. 819- 825 ,(1993)
Stephen L. Briggs, Lynn D. Apelgren, Dianna L. Zimmerman, Thomas F. Bumol, Antitumor activity of the monoclonal antibody-Vinca alkaloid immunoconjugate LY203725 (KS1/4-4-desacetylvinblastine-3-carboxhydrazide) in a nude mouse model of human ovarian cancer. Cancer Research. ,vol. 50, pp. 3540- 3544 ,(1990)
F. Uckun, W. Evans, C. Forsyth, K. Waddick, L. Ahlgren, L. Chelstrom, A. Burkhardt, J. Bolen, D. Myers, Biotherapy of B-cell precursor leukemia by targeting genistein to CD19-associated tyrosine kinases Science. ,vol. 267, pp. 886- 891 ,(1995) , 10.1126/SCIENCE.7531365
Colin J. Sanderson, The biological role of interleukin 5. Stem Cells. ,vol. 8, pp. 147- 154 ,(1990) , 10.1002/STEM.5530080713
S. M. Lippman, D. R. Parkinson, L. M. Itri, R. S. Weber, S. P. Schantz, D. M. Ota, M. A. Schusterman, I. H. Krakoff, J. U. Gutterman, W. K. Hong, 13-cis-Retinoic Acid and Interferon α -2a: Effective Combination. Therapy for Advanced Squamous Cell Carcinoma of the Skin Journal of the National Cancer Institute. ,vol. 84, pp. 235- 241 ,(1992) , 10.1093/JNCI/84.4.235
S. R. Paul, F. Bennett, J. A. Calvetti, K. Kelleher, C. R. Wood, R. M. O'Hara, A. C. Leary, B. Sibley, S. C. Clark, D. A. Williams, Molecular cloning of a cDNA encoding interleukin 11, a stromal cell-derived lymphopoietic and hematopoietic cytokine. Proceedings of the National Academy of Sciences of the United States of America. ,vol. 87, pp. 7512- 7516 ,(1990) , 10.1073/PNAS.87.19.7512
D Novick, H Engelmann, D Wallach, M Rubinstein, Soluble cytokine receptors are present in normal human urine. Journal of Experimental Medicine. ,vol. 170, pp. 1409- 1414 ,(1989) , 10.1084/JEM.170.4.1409
Samuel Broder, Judith E. Karp, New Directions in Molecular Medicine Cancer Research. ,vol. 54, pp. 653- 665 ,(1994)