Literature DB >> 6392302

Clinical implications of current studies in carcinogenesis.

B A Ponder.   

Abstract

Carcinogenesis probably proceeds through a succession of cellular events. Understanding of these events may provide a rational basis for the development of anticarcinogenic treatments. These will be designed to reverse or delay the evolution of a tumor before the stage at which invasion develops. The design and conduct of trials of such agents will be easiest if they are aimed at relatively late stages in the carcinogenic process. Recent research on viral and cellular oncogenes, growth factors, and the cellular mechanism of action of phorbol ester tumor promoters raises the hope that each will be understood and related to the others by their effects on different components of a set of central controls for cellular growth and differentiation. This may ultimately provide a means for rational design of anticarcinogenic treatment. Understanding is still very far from complete, however, and we are still a long way from potential clinical application. An immediate alternative to the long-term rational approach is an empirical one based, for example, on the use of retinoids. The design and interpretation of empirically based trials of anticarcinogenic agents requires careful thought.

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Year:  1984        PMID: 6392302     DOI: 10.1007/BF00390456

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  47 in total

1.  Activation of mouse genes in transformed cells.

Authors:  M R Scott; K H Westphal; P W Rigby
Journal:  Cell       Date:  1983-09       Impact factor: 41.582

2.  The secrets of cancer.

Authors:  J Logan; J Cairns
Journal:  Nature       Date:  1982-11-11       Impact factor: 49.962

Review 3.  Inhibition of cell-cell communication by tumor promoters.

Authors:  J E Trosko; L P Yotti; S T Warren; G Tsushimoto; C Chang
Journal:  Carcinog Compr Surv       Date:  1982

Review 4.  In vitro studies on the mode of action of the phorbol esters, potent tumor promoters, part 2.

Authors:  P M Blumberg
Journal:  Crit Rev Toxicol       Date:  1981-06       Impact factor: 5.635

5.  An organ culture of adult mouse skin: an in vitro model for studying the molecular mechanism of skin tumor promotion.

Authors:  A K Verma; R K Boutwell
Journal:  Biochem Biophys Res Commun       Date:  1980-09-30       Impact factor: 3.575

6.  Angiogenic activity as a marker of neoplastic and preneoplastic lesions of the human bladder.

Authors:  G W Chodak; C Haudenschild; R F Gittes; J Folkman
Journal:  Ann Surg       Date:  1980-12       Impact factor: 12.969

7.  Multistage models and primary prevention of cancer.

Authors:  N E Day; C C Brown
Journal:  J Natl Cancer Inst       Date:  1980-04       Impact factor: 13.506

8.  c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association.

Authors:  C Huerre; S Despoisse; S Gilgenkrantz; G M Lenoir; C Junien
Journal:  Nature       Date:  1983 Oct 13-19       Impact factor: 49.962

9.  The c-Ha-ras1, insulin and beta-globin loci map outside the deletion associated with aniridia-Wilms' tumour.

Authors:  B de Martinville; U Francke
Journal:  Nature       Date:  1983 Oct 13-19       Impact factor: 49.962

10.  Studies on the mechanism of skin tumor promotion: evidence for several stages in promotion.

Authors:  T J Slaga; S M Fischer; K Nelson; G L Gleason
Journal:  Proc Natl Acad Sci U S A       Date:  1980-06       Impact factor: 11.205

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