Literature DB >> 7104990

Has the well gone dry? The First Cain Memorial Award Lecture.

J A Montgomery.   

Abstract

Contrary to a recent suggestion, new and useful drugs for the treatment of human cancer continue to be developed although clinical trials today are more difficult and the chances for success are diminished. In the past, research at Southern Research Institute led to the development of two new classes of clinically useful anticancer agents, the nitrosoureas and the imidazole triazines. More recently, we have developed an interesting family of cytotoxic compounds, the haloadenine nucleosides, that are resistant to deamination and show biological activity comparable to the corresponding adenine nucleosides given in combination with 2'-deoxycoformycin, a potent inhibitor of adenosine deaminase. Among them, the 2-haloadenine arabinonucleosides and 2'-deoxyribonucleosides appear to have the necessary selectivity for neoplastic cells to be useful anticancer agents.

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Year:  1982        PMID: 7104990

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

1.  Effects of 2-chloroadenine substitution in DNA on restriction endonuclease cleavage reactions.

Authors:  P Hentosh; J C McCastlain
Journal:  Nucleic Acids Res       Date:  1991-06-11       Impact factor: 16.971

Review 2.  Membrane transport and the antineoplastic action of nucleoside analogues.

Authors:  F M Sirotnak; J R Barrueco
Journal:  Cancer Metastasis Rev       Date:  1987       Impact factor: 9.264

3.  Phase I clinical trial of fludarabine phosphate (F-ara-AMP).

Authors:  E S Casper; A Mittelman; D Kelson; C W Young
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

4.  Antileukemic and immunosuppressive activity of 2-chloro-2'-deoxyadenosine.

Authors:  D A Carson; D B Wasson; E Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

5.  Lack of cross-resistance between cytosine arabinoside and a new halogenated nucleoside analogue, 2-bromo-2'-deoxyadenosine in human acute myeloid leukaemia cells.

Authors:  L B Pemble; M G Lihou; R L Blakley; G P Jamieson; P J Smith
Journal:  Cancer Chemother Pharmacol       Date:  1987       Impact factor: 3.333

6.  2-Chloro-2'-deoxyadenosine monophosphate residues in DNA enhance susceptibility to 3'-->5' exonucleases.

Authors:  P Hentosh; P Grippo
Journal:  Biochem J       Date:  1994-09-01       Impact factor: 3.857

7.  Synthesis of 5-chloroformycin A, 5-chloro-2'-deoxyformycin A and certain related 5,7-disubstituted 3-beta-D-ribofuranosylpyrazolo[4,3-d] pyrimidines from formycin A.

Authors:  K G Upadhya; Y S Sanghvi; R K Robins; G R Revankar; B G Ugarkar
Journal:  Nucleic Acids Res       Date:  1986-02-25       Impact factor: 16.971

8.  Phase II study of fludarabine phosphate in patients with advanced colorectal carcinoma.

Authors:  J A Ajani; J L Abbruzzese; J S Faintuch; R Blackburn; B Levin; B M Boman
Journal:  Invest New Drugs       Date:  1988-04       Impact factor: 3.850

Review 9.  Fludarabine phosphate. A new anticancer drug with significant activity in patients with chronic lymphocytic leukemia and in patients with lymphoma.

Authors:  G Rodriguez
Journal:  Invest New Drugs       Date:  1994       Impact factor: 3.850

  9 in total

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