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新型S-腺苷甲硫氨酸脱羧酶抑制剂4-脒基茚满-1-(2'-脒基)腙的全身给药可使无胸腺裸鼠体内的人前列腺癌产生细胞生长停滞。

Systemic administration of 4-amidinoindanon-1-(2'-amidino)-hydrazone, a new inhibitor of s-adenosylmethionine decarboxylase, produces cytostasis of human prostate-cancer in athymic nude-mice.

作者信息

Delworth M, Nishioka K, Pettaway C, Gutman M, Killion J, Voneschenbach A, Fidler I

机构信息

UNIV TEXAS,MD ANDERSON CANC CTR,DEPT CELL BIOL,HOUSTON,TX 77030. UNIV TEXAS,MD ANDERSON CANC CTR,DEPT UROL,HOUSTON,TX 77030. UNIV TEXAS,MD ANDERSON CANC CTR,DEPT SURG ONCOL,HOUSTON,TX 77030.

出版信息

Int J Oncol. 1995 Feb;6(2):293-9. doi: 10.3892/ijo.6.2.293.

Abstract

CGP 48664A, a new S-adenosylmethionine decarboxylase inhibitor, blocks the production of spermidine and spermine, two polyamines that play critical roles in cellular proliferation. Under in vitro conditions, CGP 48664A produced cytostasis of the human prostate cancer cell lines LNCaP, LNCaP-LN3, PC-3M, and PC-3M-MM2 in a dose-dependent manner. This cytostasis was reversed by the addition of exogenous polyamines to the culture medium. LNCaP-LN3 cells or PC-3M-MM2 cells were implanted into the prostate of nude mice. Daily administration of CGP 48664A significantly inhibited tumor size and serum levels of prostate-specific antigen in mice implanted with LNCaP-LN3 cells. The therapeutic effect was related to the time the treatment was initiated, the volume of disease, and the length of treatment. CGP 48664A was not effective against the fast-growing PC-3M-MM2 tumor. These data suggest that to broaden its effectiveness, CGP 48664A should be combined with other cytoreductive agents.

摘要

CGP 48664A是一种新型S-腺苷甲硫氨酸脱羧酶抑制剂,可阻断亚精胺和精胺的生成,这两种多胺在细胞增殖中发挥关键作用。在体外条件下,CGP 48664A以剂量依赖的方式使人类前列腺癌细胞系LNCaP、LNCaP-LN3、PC-3M和PC-3M-MM2产生细胞生长停滞。向培养基中添加外源性多胺可逆转这种细胞生长停滞。将LNCaP-LN3细胞或PC-3M-MM2细胞植入裸鼠前列腺。每日给予CGP 48664A可显著抑制植入LNCaP-LN3细胞的小鼠的肿瘤大小和前列腺特异性抗原的血清水平。治疗效果与开始治疗的时间、疾病体积和治疗时长有关。CGP 48664A对快速生长的PC-3M-MM2肿瘤无效。这些数据表明,为扩大其有效性,CGP 48664A应与其他细胞减灭剂联合使用。

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