Literature DB >> 7891229

Molecular mechanisms of drug resistance in tumours.

D J Harrison1.   

Abstract

Despite advances in the design and use of chemotherapeutic drugs, the majority of human cancers are resistant to therapy at presentation or become resistant after an initial partial response. This suggests that resistance may be inherent in a tumour cell or may evolve under the selection pressure of drug administration. A number of possible molecular explanations for drug resistance exist. There may be exclusion of drug from the cell, failure to activate the prodrug to its active form, increased detoxification, alteration in the drug target, enhanced repair capability of the cell after injury, or failure to engage an appropriate response, leading to apoptosis in the damaged cell. Many of these factors may co-exist in vivo in human tumours; some are a feature of cell lineage whilst others appear de novo during disease progression. Modulation of these mechanisms has been of some value in laboratory studies but widespread clinical application and benefit remain some way off.

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Year:  1995        PMID: 7891229     DOI: 10.1002/path.1711750103

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  11 in total

1.  Involvement of microtubules in the regulation of Bcl2 phosphorylation and apoptosis through cyclic AMP-dependent protein kinase.

Authors:  R K Srivastava; A R Srivastava; S J Korsmeyer; M Nesterova; Y S Cho-Chung; D L Longo
Journal:  Mol Cell Biol       Date:  1998-06       Impact factor: 4.272

2.  Fusion tyrosine kinases induce drug resistance by stimulation of homology-dependent recombination repair, prolongation of G(2)/M phase, and protection from apoptosis.

Authors:  Artur Slupianek; Grazyna Hoser; Ireneusz Majsterek; Agnieszka Bronisz; Maciej Malecki; Janusz Blasiak; Richard Fishel; Tomasz Skorski
Journal:  Mol Cell Biol       Date:  2002-06       Impact factor: 4.272

3.  Method for quantifying expression of functionally active topoisomerase II in patients with leukaemia.

Authors:  A R Cattan; D Levett; E A Douglas; P G Middleton; P R Taylor
Journal:  J Clin Pathol       Date:  1996-10       Impact factor: 3.411

4.  Identification of genetic changes associated with drug resistance by reverse in situ hybridization.

Authors:  S F Hoare; C A Freeman; J C Coutts; J M Varley; L James; W N Keith
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

5.  p53-independent death and p53-induced protection against apoptosis in fibroblasts treated with chemotherapeutic drugs.

Authors:  R D Malcomson; M Oren; A H Wyllie; D J Harrison
Journal:  Br J Cancer       Date:  1995-10       Impact factor: 7.640

6.  Induction of acquired drug resistance in endothelial cells and its involvement in anticancer therapy.

Authors:  Limin Huang; Christelle Perrault; Jennifer Coelho-Martins; Chaoquan Hu; Charlène Dulong; Mariana Varna; Jielin Liu; Jian Jin; Claudine Soria; Lionel Cazin; Anne Janin; Hong Li; Rémi Varin; He Lu
Journal:  J Hematol Oncol       Date:  2013-07-09       Impact factor: 17.388

7.  Multidrug resistance phenotype in the RMS-GR human rhabdomyosarcoma cell line obtained after polychemotherapy.

Authors:  J Prados; C Melguizo; J A Marchal; C Vélez; L Alvarez; A Aránega
Journal:  Jpn J Cancer Res       Date:  1999-07

Review 8.  Interaction of tumor-associated macrophages and cancer chemotherapy.

Authors:  Irina Larionova; Nadezhda Cherdyntseva; Tengfei Liu; Marina Patysheva; Militsa Rakina; Julia Kzhyshkowska
Journal:  Oncoimmunology       Date:  2019-04-13       Impact factor: 8.110

Review 9.  YKL-39 as a Potential New Target for Anti-Angiogenic Therapy in Cancer.

Authors:  Julia Kzhyshkowska; Irina Larionova; Tengfei Liu
Journal:  Front Immunol       Date:  2020-01-22       Impact factor: 7.561

10.  Genome-wide analysis of miRNA signature differentially expressed in doxorubicin-resistant and parental human hepatocellular carcinoma cell lines.

Authors:  Jufeng Zhang; Ying Wang; Pingping Zhen; Xia Luo; Chao Zhang; Lin Zhou; Yanxin Lu; Yang Yang; Wei Zhang; Jun Wan
Journal:  PLoS One       Date:  2013-01-24       Impact factor: 3.240

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