Oblimersen bcl-2 antisense: Facilitating apoptosis in anticancer treatment

被引:241
作者
Klasa, RJ
Gillum, AM
Klem, RE
Frankel, SR
机构
[1] Genta Inc, Med Operat, Berkeley Hts, NJ 07922 USA
[2] British Columbia Canc Agcy, Div Med Oncol, Vancouver, BC V5Z 4E6, Canada
[3] British Columbia Canc Agcy, Dept Adv Therapeut, Vancouver, BC V5Z 4E6, Canada
来源
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT | 2002年 / 12卷 / 03期
关键词
D O I
10.1089/108729002760220798
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The components of the apoptotic program are targets for anticancer therapy. Bcl-2 protein inhibits apoptosis and confers resistance to treatment with traditional cytotoxic chemotherapy, radiotherapy, and monoclonal antibodies (mAb). Oblimersen sodium (G3139, Genasense(TM), Genta Inc., Berkeley Heights, NJ) is an antisense oligonucleotide (AS-ON) compound designed to specifically bind to the first 6 codons of the human bcl-2 mRNA sequence, resulting in degradation of bcl-2 mRNA and subsequent decrease in Bcl-2 protein translation. Oblimersen is the first oligonucleotide to demonstrate proof of principle of an antisense effect in human tumors by the documented downregulation of the target Bcl-2 protein. A growing body of preclinical and clinical evidence suggests that oblimersen synergizes with many cytotoxic and biologic/immunotherapeutic agents against a variety of hematologic malignancies and solid tumors. Randomized clinical trials are currently underway to evaluate the efficacy and tolerability of oblimersen in combination with cytotoxic chemotherapy in chronic lymphocytic leukemia, multiple myeloma, malignant melanoma, and non-small cell lung cancer. In addition, nonrandomized trials are under way to evaluate oblimersen in non-Hodgkin's lymphoma, acute myeloid leukemia, and hormone-refractory prostate cancer. Preclinical data also support the clinical evaluation of oblimersen in additional tumor types, including chronic myelogenous; leukemia and breast, small cell lung, gastric, colon, bladder, and Merkel cell cancers. Enhancement of the efficacy of anticancer treatments with oblimersen Bcl-2 antisense therapy represents a promising new apoptosis-modulating strategy, and ongoing clinical trials will test this therapeutic approach.
引用
收藏
页码:193 / 213
页数:21
相关论文
共 125 条
  • [1] PHARMACOKINETICS, BIODISTRIBUTION, AND STABILITY OF OLIGODEOXYNUCLEOTIDE PHOSPHOROTHIOATES IN MICE
    AGRAWAL, S
    TEMSAMANI, J
    TANG, JY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) : 7595 - 7599
  • [2] Auer RL, 2001, BLOOD, V98, p808A
  • [3] Baba M, 2000, INT J CANCER, V85, P260, DOI 10.1002/(SICI)1097-0215(20000115)85:2<260::AID-IJC18>3.0.CO
  • [4] 2-R
  • [5] Ballas ZK, 1996, J IMMUNOL, V157, P1840
  • [6] HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC ANALYSIS OF PHOSPHOROTHIOATE ANALOGS OF OLIGODEOXYNUCLEOTIDES IN BIOLOGICAL-FLUIDS
    BIGELOW, JC
    CHRIN, LR
    MATHEWS, LA
    MCCORMACK, JJ
    [J]. JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1990, 533 : 133 - 140
  • [7] Caspase involved synergistic cytotoxicity of bcl-2 antisense oligonucleotides and Adriamycin on transitional cell cancer cells
    Bilim, V
    Kasahara, T
    Noboru, H
    Takahashi, K
    Tomita, Y
    [J]. CANCER LETTERS, 2000, 155 (02) : 191 - 198
  • [8] Growth inhibition of DU-145 prostate cancer cells by a Bcl-2 antisense oligonucleotide is enhanced by N-(2-hydroxyphenyl)all-trans retinamide
    Campbell, MJ
    Dawson, M
    Koeffler, HP
    [J]. BRITISH JOURNAL OF CANCER, 1998, 77 (05) : 739 - 744
  • [9] BCL-2 PROTEIN EXPRESSION IN CUTANEOUS MALIGNANT-MELANOMA AND BENIGN MELANOCYTIC NEVI
    CERRONI, L
    SOYER, HP
    KERL, H
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1995, 17 (01) : 7 - 11
  • [10] Phase III multicenter randomized trial of the dartmouth regimen versus dacarbazine in patients with metastatic melanoma
    Chapman, PB
    Einhorn, LH
    Meyers, ML
    Saxman, S
    Destro, AN
    Panageas, KS
    Begg, CB
    Agarwala, SS
    Schuchter, LM
    Ernstoff, MS
    Houghton, AN
    Kirkwood, JM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) : 2745 - 2751