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人多药耐药基因(MDR1)在人骨肉瘤中的表达及其预后相关性

Expression of the human multidrug resistance gene (MDR1) and prognostic correlation in human osteogenic sarcoma.

作者信息

Imanishi T, Abe Y, Suto R, Higaki S, Ueyama Y, Nakamura M, Tamaoki N, Fukuda H, Imai N

机构信息

Department of Orthopedic Surgery, Tokai University School of Medicine, Kanagawa, Japan.

出版信息

Tokai J Exp Clin Med. 1994 Sep;19(1-2):39-46.

PMID:7660382
Abstract

The overexpression of P-glycoprotein (P-Gp), encoded by the human multidrug resistant gene (MDRA), decreases lipophilic drug accumulation in multidrug resistant cells in vitro. It is still not clear whether P-Gp contribute to the problem of multidrug resistance (MDR) in osteogenic sarcoma (OS). We examined the MDR1 expression of 20 OS specimens (11 primary tumors, 10 xenografts, 1 overlapping), by Northern blotting and by the reverse transcriptase-polymerase chain reaction (RT-PCR), and evaluated by the relationship between MDR1 expression and patient prognosis. RT-PCR revealed MDR1 expression in 9/20 OS; 5/11 primary tumors and 5/10 OS-xenografts; northern blotting revealed MDR1 expression in only 5/20 OS. One primary OS specimen and its corresponding xenograft had similar levels of MDR1 expression. All 20 patients with OS were treated with chemotherapeutic protocols including doxorubicin, cisplatin, methotrexate and ifosfamide. Eight of 9 OS-patients expressing MDR1 were resistant to chemotherapy and had a poor prognosis. The relationship between MDR1 expression and poor prognosis in the 20 OS-patients was significant (p < 0.01). The results support the assumption that MDR1 expression is related to MDR in human OS.

摘要

由人类多药耐药基因(MDRA)编码的P-糖蛋白(P-Gp)过表达,可降低体外多药耐药细胞中亲脂性药物的蓄积。P-Gp是否导致骨肉瘤(OS)的多药耐药(MDR)问题仍不清楚。我们通过Northern印迹法和逆转录聚合酶链反应(RT-PCR)检测了20例OS标本(11例原发性肿瘤、10例异种移植瘤、1例重叠标本)的MDR1表达,并评估了MDR1表达与患者预后之间的关系。RT-PCR显示20例OS中有9例表达MDR1;11例原发性肿瘤中有5例,10例OS异种移植瘤中有5例;Northern印迹法显示20例OS中只有5例表达MDR1。1例原发性OS标本及其相应的异种移植瘤具有相似水平的MDR1表达。所有20例OS患者均接受了包括阿霉素、顺铂、甲氨蝶呤和异环磷酰胺在内的化疗方案治疗。9例表达MDR1的OS患者中有8例对化疗耐药且预后较差。20例OS患者中MDR1表达与预后不良之间的关系具有显著性(p<0.01)。结果支持MDR1表达与人OS中的MDR相关这一假设。

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