Resistência a múltiplas drogas: um problema da clínica oncológica com solução na pesquisa básica

Autores

  • Ludmila S. Medina da Cunha Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.
  • Fernando Medina da Cunha Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.
  • Mary da Silva Thereza Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.
  • Regina A. Martinho Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.
  • André Augusto Jr. G. Moraes Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.
  • Ricardo Lima Zoliner Departamento de Clínica Médica. Universidade estadual de Campinas (UNICAMP). Campinas (SP), Brasil.

DOI:

https://doi.org/10.32635/2176-9745.RBC.1991v37n1/4.3110

Palavras-chave:

Quimioterapia, Resistência a Múltiplas Drogas

Resumo

A resistência que as células neoplásicas apresentam aos agentes quimioterápicos sempre é um grande problema para o oncologista clínico. A descoberta da glicoproteína (170 Pgp) responsável pela resistência a múltiplas drogas (MDR) abriu novas perspectivas de se superar este difícil tipo de resistência. Neste trabalho, apresentamos uma retrospectiva do trabalho de pesquisa realizado até a definição do modelo que hoje rege os trabalhos clínicos no emprego de agentes reversores da MDR.

Downloads

Não há dados estatísticos.

Referências

BIEDLER JL, RIEHM H. Celular resistance to actinomycin D in chinese hamster ccii in vitro: Cross-resistance, radioautographic, and cytogenetic studies. Cancer Res 1970; 30: 1174-1184.

BEcH-HANSON NT, TILL JE, LING V. Pleiotropic phenotype of colchicine-resistant HO ceils: cross resistance and coliateral sensitivity. J Cell Physiol 1976; 88: 23-32. DOI: https://doi.org/10.1002/jcp.1040880104

JULIANO JL, LiNG VA. A surface glycoprotein modulating drug permeabiflty in chinese hamster ovary ceil mutants. Biochem Biophys Acta 1976; 455: 152-162. DOI: https://doi.org/10.1016/0005-2736(76)90160-7

KARTNER N, RIORDAN JR, LING V. Ceil surtace Pgtycoprotein is associated with multidrug resistance in mamalian cell lines. Science 1983; 221: 1285-1288. DOI: https://doi.org/10.1126/science.6137059

UNO V, THOMPSON LH. Reduced permeabiity in CHO cells as a mechanism of resistance to colcine. J Ccii PhysioI 1973; 83: 103-116. DOI: https://doi.org/10.1002/jcp.1040830114

BECK WT. The ccli biology of multipie drug resistance. Pharmacol 1987; 36: 2879-2887. DOI: https://doi.org/10.1016/0006-2952(87)90198-5

BASK1N F, ROSEMBERG RN, DEV V. Correiation of double-minute chromosomes with unstable multidrug cross-resistance in uptake mutants of neurobiastoma celis. Proc Nat Acad Sci (USA) 1981; 78: 3654-3658. DOI: https://doi.org/10.1073/pnas.78.6.3654

GRUND SH, PATIL SR, SHAH HO, PAUW PG, STADLER JK. Correlations of unstable multidrug cross resistance in chinese hamster ovary celis with a homogenously staining region on chromosome. 1. Mol Cell Bioi 1983; 3: 1634-1647. DOI: https://doi.org/10.1128/MCB.3.9.1634

RONINSON iB, ABLESON HT, HOUSMAN DE, HOWELL N, VARSHAVSKU A. Amplification of specific DNA sequences correlates with multidrug resistance in chinese hamster celis. Nature 1984; 309:636-628. DOI: https://doi.org/10.1038/309626a0

SCOTTO KW, BIEDLER JL, MELERA PW. Amplification and expression of genes associated with multidrug resistance in mammahan cells. Science 1986; 232:751. DOI: https://doi.org/10.1126/science.2421411

CROOP JM, GUILD BC, GROS P, HOUSMAN DE. Genetics of multidrug resistance: relationship 01 a cioned gene to the complete multidrug resistance phenotype. Cancer Research 1987; 47: 5982-

UEDA K, CARDARELLI C, GOTTESMANN MM, PASTAN I. Expression of a fui ienght cDNA for human 'MDRi" gene confers resistance to coichicine, doxorubicin and vinbiastine. Proc NatAcad

Sci (USA) 1987; 84: 3004, DOI: https://doi.org/10.1073/pnas.84.9.3004

GUILD BC, MULLIGAN RC, GROS P, HOUSMAN DE. Retroviral transfer of a murine cDNA for multidrug resistance confers pleiotropic drug resistance to celis without prior drug seiection. Proc Nat Acad Sci (USA) 1989; 85:1595-1599. DOI: https://doi.org/10.1073/pnas.85.5.1595

MARX J. Drug resistance olcancer celis probe. Science 1986; 234: 818. DOI: https://doi.org/10.1126/science.2877493

FOJO AT, UEDA K, SLAMON DJ, POPLACK DO, GOTTESMAN MM, PASTAN I. Expression of multidrug resistance gene in human tumors and tissues. Proc Nati Acad Sci (USA) 1987; 84: 265-269. DOI: https://doi.org/10.1073/pnas.84.1.265

SUGAWARA 1, KATACKA 1, MORISHITA Y, HAMADA H, TSU RUO T, ITOYAMA S, MORi S. Tissue distribution of P-giycoprotein encoded by a multidrug resistant gene as revealed by a monocional antibody MRK16. Cancer Res 1988; 48: 1926-1929.

GOLDSTEIN U, GALSKi H, FOJO A etai. Expression of a multidrug resistance gene in human cancers. J Nati Cancer lnst 1989; 81: 116-124. DOI: https://doi.org/10.1093/jnci/81.2.116

CHAN HSL, THORNER PS, HADDAD O, LiNG V. Immunohistochemical detection of P-glycoprotein: prognostic correlation in soft tissue sarcoma of chiidhood. J Clin Oncol 1990; 8: 689-704. DOI: https://doi.org/10.1200/JCO.1990.8.4.689

HAMADA H, TSURUO T. Functional role for the 170-180 kDa glycoprotein specific to drug resistant tumor cells as revealed by morioclonal antibodies. Proc Nati Acad Sci (USA) 1986; 83: 7785-7789. DOI: https://doi.org/10.1073/pnas.83.20.7785

SCHEPER RJ, BUETE JWM, BIROXTERMAN HJ, PINEDO H. Morroclonal antibody JS131 detects a highly conserved epitope on the Pgp associated to multidrug resistance. lntJ Cancer 1988: 42: 389-394. DOI: https://doi.org/10.1002/ijc.2910420314

KATNER N, PORELLE DE, BRADLEYG, LING V. Detection of P-glycoprotein in resistant cell lines by monoclonal antibodies. Nature 1985: 316: 820-824. DOI: https://doi.org/10.1038/316820a0

TSURUO T, LIDA H, NOJILRI M, TSUKAGOSHI 5, SAKUIRAI Y. Circunvention of vincristine and adriamycin resistance in vitro and in vivo by calcium influx blockers. Cancer Res 1983; 43: 2905-2910.

ROGAN AM, HAMILTON TC, VOUNG RC. Reversal of adriamycin resistance by verapamil in human ovarian cancer. Scionce 1984; 224: 994-996. DOI: https://doi.org/10.1126/science.6372095

TSURUO T, LIDA H, KITATANI Y, YOKOTA K, TSUKAGOSHI S, SAKURAI Y. Effects of quinidine and related compounds on cytotoxicity and celularaccumulation of vincristine and adriamycin in drug resistant tumor cells. Cancer Res 1984: 4303-4307.

SLATER LM, SWEET P, STUPECKY M, WETZEL MW, GUPTA S. Cyclosporin A corrects daunorrubicin resistance ir, Ehrlich ascited carcinoma. Br J Cancer 1986: 54: 235-238. DOI: https://doi.org/10.1038/bjc.1986.167

CORWELL MM, PASTAN 1, GOTTESMAN MM. Certain calcium channel blockers bind speciíically to multidrug resistant human KB carcinoma membrane vesicles and inhibit drug binding to P-glycoprotein. J Biol Chem 1987; 262: 2166-2170. DOI: https://doi.org/10.1016/S0021-9258(18)61633-3

SAFA AR, GLOVER CJ, SEWELL JL, MEYERS MB, BIEDLER JL, FELSTED RL. Identification of the multidrug resistance related membrane glycoprotein as an acceptor for calcium channel blockers. J Biol Chem 1987; 262:7884-7888. DOI: https://doi.org/10.1016/S0021-9258(18)47650-8

OZOLS RF, CUNNION RE, KLECKER RW. Verapamil and adriamycin in the treatment of drug resistant ovarian cancer patients. J Clin Oncol 1987:5:641-647. DOI: https://doi.org/10.1200/JCO.1987.5.4.641

SHINIDA H, INABA M, TSURUO T. In vivo circunvention of vincristine resistance in mice with P388 Ieukemia using a novel compound: AHC-52. Cancer Res 1989; 49: 1722-1726.

TWENTYMAN PR. Modification of cytotoxic drug resistance by immunosuppresive cyclosporins. Br J Cancer 1988: 57: 264-268. DOI: https://doi.org/10.1038/bjc.1988.55

KRAMER RA, ZAKHER J, KIM G. Role of the glutathione redox cycle in acquired and de novo multidrug resistance. Science 1988; 241: 694-697. DOI: https://doi.org/10.1126/science.3399900

MCGRATH T, CEUTER MS. Adriamycin resistance in HL-60 cells in the absence of detectable P-glycoprotein. Biochem Biophys Res Com 1987; 145: 1171-1176. DOI: https://doi.org/10.1016/0006-291X(87)91560-9

MIRISKI SEL, GEIRLACH JH, COLE SPC. Multidrug resistance in a human small cell lung cancer une selected in adriamycin. Cancer Res 1987; 47: 2594-2598.

DANKS MK, YALOWISH JC, BECK WT. Atypical multiple drug resistance in a humam leukemic ceil une selocted for resistance to teniposide(VM 26). Cancer Res 1987:47: 1297-1301.

BECI< WT, LIRTAIN MC, DANKS MK. Pharmacological molecular and cytogenetic analysis of atypical multidrug resistant human leukemia cells. Cancer Res 1987:47: 5455-5460.

COWAN KH, BATIST G, TULPULE A, SENHA BK, MEYERS CE. Similar biochemical changes associated with multidrug resistance in human breast cancer celis and carcinogen-induced resistance to xenobiotics in rats. Proc Natl Acad Sci (USA) 1986: 83: 9328-9332. DOI: https://doi.org/10.1073/pnas.83.24.9328

Downloads

Publicado

2023-07-26

Como Citar

1.
Cunha LSM da, Cunha FM da, Thereza M da S, Martinho RA, Moraes AAJG, Zoliner RL. Resistência a múltiplas drogas: um problema da clínica oncológica com solução na pesquisa básica. Rev. Bras. Cancerol. [Internet]. 26º de julho de 2023 [citado 17º de maio de 2024];37(1/4):51-5. Disponível em: https://rbc.inca.gov.br/index.php/revista/article/view/3110

Edição

Seção

ARTIGO ORIGINAL

Artigos mais lidos pelo mesmo(s) autor(es)