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The detection of MDR1 gene expression using fluorogenic probe quantitative RT-PCR method

  • Basic Investigation
  • Published:
Chinese Journal of Cancer Research

Abstract

Objective: To establish a fluoregenic probe quantitative RT-PCR (FQ-RT-PCR) method for detection of the expression of MDR1 gene in tumor cells and to investigate the expression of MDR1 gene in patients with lung cancer. Methods: The fluorogenic quantitative RT-PCR method for detection of the expression of MDR1 gene was established. K562/ADM and K562 cell lines or 45 tumor tissues from patients with lung cancer were examined on PE Applied Biosystems 7700 Sequence Detection machine. Results: the average levels of MDR1 gene expression in K562/ADM cells and K562 cells were (6.86±0.65)× 107 copies/µg RNA and (8.49±0.67)×105 copies/µg RNA, respectively. The former was 80.8 times greater than the latter. Each sample was measured 10 times and the coefficient variation (CV) was 9.5% and 7.9%, respectively. Various levels of MDR1 gene expression were detected in 12 of 45 patients with lung cancer. Conclusion: Quantitative detection of MDR1 gene expression in tumor cells was achieved by using FQ-RT-PCR. FQ-RT-PCR is an accurate, and sensitive method and easy to perform. Using this method, low levels of MDR1 gene expression could be detected in 24% of the patients with lung cancer.

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References

  1. Noonan KE, Beck C, Holzmayer TA, et al. Quantitative analysis of MDR1(multidrug resistance) gene expression in human tumors by polymerase chain reaction[J]. Proc Natl Acad Si USA 1990; 87: 7160.

    Article  CAS  Google Scholar 

  2. Cao Liping, Wang Bin, Yu Zhifei. Construction of the internal standard RNA and DNA templates for MDR1 quantitation RT-PCR analysis[J]. J Exp Hematol (Chinese) 1997; 5393.

  3. Heid CA, Steven J, Livak KJ, et al. Real time quantitative PCR[J]. Genome Res 1996; 6: 986.

    Article  PubMed  CAS  Google Scholar 

  4. Gibson UE, Heid CA, Williams PM. A novel method for real time quantitative RT-PCR[J]. Genome Res 1996; 6: 995.

    Article  PubMed  CAS  Google Scholar 

  5. Shen Shiren, Su Yin, Huang Xiuqing, et al. Establishment of K562 cell line resistant to ADM and a preliminary observation on its characteristic biology[J]. Chin J Cancer 1992; 11: 222.

    Google Scholar 

  6. Li XB, Zhao XS, Tian DZ, et al. A new method for PCR products cloning -A-T clone technique[J]. Prog Biochem Biophy (Chin). 1999; 26:187.

    CAS  Google Scholar 

  7. Debuire B, Sol O, Lemoine A, et al. Nonisotopic competitive RT-PCR assay to measure MDR1 gene expression[J]. Clin Chem 1995; 41: 819.

    PubMed  CAS  Google Scholar 

  8. Cross NC P, Feng L, Chase A, et al. Competitive Polymerase chain reaction to estimate the number of bcr-abl transcripts in chronic myeloid leukemia patients after bone marrow transplantation[J]. Blood 1993; 82: 1929.

    PubMed  CAS  Google Scholar 

  9. Shin HJ, Lee JS, Hong WK, et al. Study of multidrug resistance (mdr1) gene in non-small-cell lung cancer[J]. Anticancer Res 1992; 12: 367.

    PubMed  CAS  Google Scholar 

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Correspondence to Gao Jing-song.

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Foundation item: This work was supported by a grant from the National New Technology Program (No. 1998-345).

Biography: Gao Jin-song, (1963–), doctor of medicine, Sun Yat-sen University of Medical Sciences, majors in gene diagnosis of malignant tumor.

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Gao, Js., Ma, G., Tong, M. et al. The detection of MDR1 gene expression using fluorogenic probe quantitative RT-PCR method. Chin. J. Cancer Res. 13, 96–100 (2001). https://doi.org/10.1007/s11670-001-0023-y

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  • DOI: https://doi.org/10.1007/s11670-001-0023-y

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