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多发性骨髓瘤细胞系及临床标本中mdr1 mRNA的定量聚合酶链反应分析

Quantitative polymerase chain reaction analysis of mdr1 mRNA in multiple myeloma cell lines and clinical specimens.

作者信息

Futscher B W, Blake L L, Gerlach J H, Grogan T M, Dalton W S

机构信息

Arizona Cancer Center, Bone Marrow Transplant Program, Tucson 85724.

出版信息

Anal Biochem. 1993 Sep;213(2):414-21. doi: 10.1006/abio.1993.1440.

Abstract

We have designed a new polymerase chain reaction (PCR) protocol for the quantitation of mdr1 mRNA in cell lines and clinical specimens. This protocol uses an in vitro-generated RNA molecule as an internal standard. This synthetic RNA contains the same mdr1 primer sequences as the cellular mRNA, but yields a different-sized PCR product after amplification. Since a single primer set is used in quantitation, differences in primer efficiency are not a concern. We have used this assay to measure mdr1 expression in a multiple myeloma cell line, 8226/S, its drug resistant variants 8226/dox6 and 8226/dox40, and tumor samples from 10 patients with B-cell malignancies (9 multiple myeloma, 1 chronic lymphocytic leukemia). 8226/S does not express mdr1 mRNA. 8226/dox6 is 10-fold resistant to doxorubicin, and expresses 32 mdr1 mRNA/10 pg cellular RNA. 8226/dox40 is 140-fold resistant to doxorubicin, and expresses 890 mdr1 mRNA/10 pg cellular RNA. Seven of the 10 patients had levels of mdr1 mRNA expression below that seen in the multidrug-resistant, human multiple myeloma cell line, 8226/dox6. Three patients had levels of mdr1 expression comparable to those seen in 8226/dox6. No patient had levels of mdr1 expression close to that seen in 8226/dox40. Sample RNA integrity is assured by PCR analysis of a different, ubiquitous, cell cycle independent, histone variant, H3.3. This assay will be useful for studying low level mdr1 expression in cell lines and clinical specimens.

摘要

我们设计了一种新的聚合酶链反应(PCR)方案,用于定量细胞系和临床标本中的mdr1 mRNA。该方案使用体外生成的RNA分子作为内标。这种合成RNA包含与细胞mRNA相同的mdr1引物序列,但扩增后产生大小不同的PCR产物。由于定量时使用单一引物组,因此无需担心引物效率差异。我们已使用该检测方法来测量多发性骨髓瘤细胞系8226/S、其耐药变体8226/dox6和8226/dox40以及10例B细胞恶性肿瘤患者(9例多发性骨髓瘤,1例慢性淋巴细胞白血病)的肿瘤样本中mdr1的表达。8226/S不表达mdr1 mRNA。8226/dox6对阿霉素耐药10倍,每10 pg细胞RNA表达32个mdr1 mRNA。8226/dox40对阿霉素耐药140倍,每10 pg细胞RNA表达890个mdr1 mRNA。10例患者中有7例mdr1 mRNA表达水平低于多药耐药的人多发性骨髓瘤细胞系8,226/dox6中的水平。3例患者的mdr1表达水平与8226/dox6中的水平相当。没有患者的mdr1表达水平接近8226/dox40中的水平。通过对另一种普遍存在的、与细胞周期无关的组蛋白变体H3.3进行PCR分析,确保样本RNA的完整性。该检测方法将有助于研究细胞系和临床标本中低水平的mdr1表达。

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