Discovery and development of anticancer aptamers

被引:388
|
作者
Ireson, Christopher R. [1 ]
Kelland, Lloyd R. [1 ]
机构
[1] Antisoma Res Labs, London, England
关键词
D O I
10.1158/1535-7163.MCT-06-0172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aptamers, also termed as decoys or "chemical antibodies," represent an emerging class of therapeutics. They are short DNA or RNA oligonucleotides or peptides that assume a specific and stable three-dimensional shape in vivo, thereby providing specific tight binding to protein targets. In some cases and as opposed to antisense oligonucleotides, effects can be mediated against extracellular targets, thereby preventing a need for intracellular transportation. The first aptamer approved for use in man is a RNA-based molecule (Macugen, pegaptanib) that is administered locally (intravitreally) to treat age-related macular degeneration by targeting vascular endothelial growth factor. The most advanced aptamer in the cancer setting is AS 1411, formerly known as AGRO 100, which is being administered systemically in clinical trials. AS1411 is a 26-mer unmodified guanosine-rich oligonucleotide, which induces growth inhibition in vitro, and has shown activity against human tumor xenografts in vivo. The mechanism underlying its antiproliferative effects in cancer cells seems to involve initial binding to cell surface nucleolin and internalization, leading to an inhibition of DNA replication. In contrast to other unmodified oligonucleotides, AS 1411 is relatively stable in serum-containing medium, probably as a result of the formation of dimers and a quartet structure. In a dose escalation phase I study in patients with advanced solid tumors, doses up to 10 mg/kg/d (using a four or seven continuous infusion regime) have been studied. Promising signs of activity have been reported (multiple cases of stable disease and one near complete response in a patient with renal cancer) in the absence of any significant adverse effects. Further trials are ongoing in renal and non-small cell lung cancers. In preclinical studies, additional aptamers have been described against several cancer targets, such as tenascin-C, the transcription factor signal transducer and activator of transcription 3, and antiapoptotic and Ku proteins.
引用
收藏
页码:2957 / 2962
页数:6
相关论文
共 50 条
  • [1] Discovery and Development of Therapeutic Aptamers
    Bouchard, P. R.
    Hutabarat, R. M.
    Thompson, K. M.
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2010, 50 : 237 - 257
  • [2] Development of anticancer aptamers targeting cancer stem cells
    Chen, Yuh-Ling
    Hsieh, I-Shan
    Hsu, Keng-Fu
    Hong, Tse-Ming
    [J]. CANCER RESEARCH, 2017, 77
  • [3] Anticancer drug discovery and development
    Colotta, Francesco
    [J]. TARGETED THERAPIES IN CANCER: MYTH OR REALITY?, 2008, 610 : 19 - 42
  • [4] Discovery of Aptamers and the Acceleration of the Development of Targeting Research in Ophthalmology
    Cao, Jiamin
    Zhang, Feng
    Xiong, Wei
    [J]. INTERNATIONAL JOURNAL OF NANOMEDICINE, 2023, 18 : 4421 - 4430
  • [5] Discovery and Development of Macrolides as Anticancer Agents
    Liu, Rongli
    Hou, Yani
    Gu, Yijun
    [J]. CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2021, 21 (18) : 1657 - 1673
  • [6] Discovery and development of azasteroids as anticancer agents
    Birudukota, Nagaraju
    Mudgal, Mukesh Madan
    Shanbhag, Venkatesh
    [J]. STEROIDS, 2019, 152
  • [7] Discovery and development of SAHA as an anticancer agent
    Marks, P. A.
    [J]. ONCOGENE, 2007, 26 (09) : 1351 - 1356
  • [8] Discovery and development of SAHA as an anticancer agent
    P A Marks
    [J]. Oncogene, 2007, 26 : 1351 - 1356
  • [9] Discovery and development of novel anticancer drug capecitabine
    Ishitsuka, H
    Shimma, N
    Horii, I
    [J]. YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1999, 119 (12): : 881 - 897
  • [10] Anticancer drug discovery and development throughout the world
    Schwartsmann, G
    Ratain, MJ
    Cragg, GM
    Wong, JE
    Saijo, N
    Parkinson, DR
    Fujiwara, Y
    Pazdur, R
    Newman, DJ
    Dagher, R
    Di Leone, L
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (18) : 47S - 59S