Drug resistance in ovarian cancer: From the laboratory to the clinic

被引:32
作者
Sood, AK
Buller, RE
机构
[1] Univ Iowa Hosp & Clin, Dept Obstet & Gynecol, Div Gynecol Oncol, Iowa City, IA 52242 USA
[2] Univ Iowa Hosp & Clin, Dept Pharmacol, Iowa City, IA 52242 USA
关键词
D O I
10.1016/S0029-7844(98)00184-7
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To provide a review of the basic mechanisms of drug resistance in ovarian cancer and novel strategies to modulate drug resistance for the general obstetrician-gynecologist. Data Sources: Relevant articles published through December 1996 were identified using the MEDLINE data base. Additional sources were found by cross-referencing. Methods of Study Selection: Publications identified by the search were reviewed and evaluated critically for their relevance to drug resistance in ovarian cancer. Tabulation, Integration, and Results: Each reference was reviewed for its contribution to the knowledge regarding mechanisms of chemotherapy resistance in ovarian cancer or strategies to modulate resistance. Conclusion: Ovarian cancer patients have high response rates to initial chemotherapy after cytoreductive surgery. However, most will develop resistance to chemotherapy during the course of their treatment. There are multiple mechanisms resulting in drug resistance. Strategies to modulate drug resistance include dose intensity, various pharmacologic agents, and gene therapy. (Obstet Gynecol 1998; 92:312-9. (C) 1998 by The American College of Obstetricians and Gynecologists.).
引用
收藏
页码:312 / 319
页数:8
相关论文
共 65 条
  • [1] HORMONAL PALLIATION OF CHEMORESISTANT OVARIAN-CANCER - 3 CONSECUTIVE PHASE-II TRIALS OF THE MID-ATLANTIC ONCOLOGY PROGRAM
    AHLGREN, JD
    ELLISON, NM
    GOTTLIEB, RJ
    LALUNA, F
    LOKICH, JJ
    SINCLAIR, PR
    UENO, W
    WAMPLER, GL
    YEUNG, KY
    ALT, D
    FRYER, JG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (10) : 1957 - 1968
  • [2] In vitro and in vivo liposome-mediated gene transfer leads to human MDR1 expression in mouse bone marrow progenitor cells
    Aksentijevich, I
    Pastan, I
    LunardiIskandar, Y
    Gallo, RC
    Gottesman, MM
    Thierry, AR
    [J]. HUMAN GENE THERAPY, 1996, 7 (09) : 1111 - 1122
  • [3] HIGH-DOSE CHEMOTHERAPY IN SOLID TUMORS
    ANTMAN, KH
    SOUHAMI, RL
    [J]. ANNALS OF ONCOLOGY, 1993, 4 : S29 - S44
  • [4] BERMAN E, 1995, LEUKEMIA, V9, P1631
  • [5] EXTENT AND PERSISTENCE OF P-GLYCOPROTEIN INHIBITION IN MULTIDRUG-RESISTANT P388 CELLS AFTER EXPOSURE TO RESISTANCE-MODIFYING AGENTS
    BOESCH, D
    LOOR, F
    [J]. ANTI-CANCER DRUGS, 1994, 5 (02) : 229 - 238
  • [6] BOESCH D, 1991, CANCER RES, V51, P4226
  • [7] SYNERGY IS DOCUMENTED INVITRO WITH LOW-DOSE RECOMBINANT TUMOR-NECROSIS-FACTOR, CISPLATIN, AND DOXORUBICIN IN OVARIAN-CANCER CELLS
    BONAVIDA, B
    TSUCHITANI, T
    ZIGHELBOIM, J
    BEREK, JS
    [J]. GYNECOLOGIC ONCOLOGY, 1990, 38 (03) : 333 - 339
  • [8] Buller RE, 1996, AM J OBSTET GYNECOL, V174, P1241, DOI 10.1016/S0002-9378(96)70667-1
  • [9] Chambers SK, 1996, CLIN CANCER RES, V2, P1693
  • [10] MULTIDRUG-RESISTANCE GENE (P-GLYCOPROTEIN) IS EXPRESSED BY ENDOTHELIAL-CELLS AT BLOOD-BRAIN BARRIER SITES
    CORDONCARDO, C
    OBRIEN, JP
    CASALS, D
    RITTMANGRAUER, L
    BIEDLER, JL
    MELAMED, MR
    BERTINO, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) : 695 - 698