Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches | Proceedings of the 18th Annual Detroit Cancer Symposium Detroit, Michigan, USA - June 13-14, 1986

Frederick A. Valeriote (u. a.)

ISBN 10: 1461294320 / ISBN 13: 9781461294320

Published by Springer, 2011

About this Item

Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches | Proceedings of the 18th Annual Detroit Cancer Symposium Detroit, Michigan, USA - June 13-14, 1986 | Frederick A. Valeriote (u. a.) | Taschenbuch | xviii | Englisch | 2011 | Springer | EAN 9781461294320 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.

Seller Inventory # 105629446

Bibliographic Details

• Title: Biochemical Modulation of Anticancer Agents: Experimental and Clinical Approaches | Proceedings of the 18th Annual Detroit Cancer Symposium Detroit, Michigan, USA - June 13-14, 1986
• Publisher: Springer
• Publication Date: 2011
• Language: English
• ISBN 10: 1461294320
• ISBN 13: 9781461294320
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 235W x 155H x 21D millimeters 235 millimeters width by 155 millimeters height by 21 millimeters depth
• Weight: 563 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

Biochemical Modulation at the present time defines an area of study in which the intracellular metabolism of a given anti­ cancer agent is modulated (usually by a noncytotoxic agent or a cytotoxic agent at sufficiently low dosage to make it non­ cytotoxic) in order to either increase the effectiveness of the particular agent against tumor cells or decrease its cytotox­ icity against normal cells. The major focus of modulation has been the agents 5-fluorouracil (FUra), arabinofuranosylcytosine (ara-C), methotrexate (MTX) and a few alkylating agents. The major thrust of the studies has been to increase the flow of the anticancer agent along the pathway responsible for the formation of the cytotoxic species: for example, FUra to FUTP or ara-C to ara-CTP. While in most cases the application of research re­ sults to clinical trials does not require the subsequent exper­ tise of the laboratory researchers, application of biochemical modulatory schemes to clinical protocols necessitate a dramatic break with the past procedures. As shown in the laboratory­ clinical loop below, close collaboration between the laboratory and clinical investigator is essential. While the laboratory REDEFINE TECHNOLOGY, TESTS OR QUESTIONS FOR FURTHER THERAPEUTIC ADVANCE CLINICAL EXPERIMENTAL PROTOCOL (LABORATORY) RESEARCH STUDIES DEFINE AND TEST APPROPRIATE SCIENTIFIC PARAMETERS results define rationally-based regimens, it is essential that the clinical protocols contain the requirement that clinical material (either tumor or normal tissues) be sampled to deter­ mine whether the biochemical modulation being proposed is in fact beinq accomplished.

Review

`As a whole this book is a useful reference in a relatively new field of cancer research that may eventually expand the scope of cancer chemotherapy.'
Adverse Drug Reaction, Vol. 7, No. 1, Spring 1988