Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

The defining feature of the Quantitative Multiplex Methylation-Specific PCR (QM-MSP) method to sensitively quantify DNA methylation is the two-step PCR approach for a multiplexed analysis of a panel of up to 12 genes in clinical samples with minimal quantities of DNA. In the first step, for up to 12 genes tested, one pair of gene-specific primers (forward and reverse) amplifies the methylated and unmethylated copies of the same gene simultaneously and in multiplex, in one PCR reaction. This methylation-independent amplification step produces amplicons of up to 109 copies per μL after 36 cycles of PCR. In the second step, the amplicons of the first reaction (STEP 1) are quantified with a standard curve using real-time PCR and two independent fluorophores to detect methylated/unmethylated DNA of each gene in the same well (e.g., 6FAM and VIC). One methylated copy is detectable in 100,000 reference gene copies. Methylation is reported on a continuous scale. For the gene panel, the highest level of normal DNA methylation above which a sample would be called positive is derived by using Receiver Operating Characteristic (ROC), maximizing assay specificity and sensitivity to distinguish between normal/benign versus tumor DNA. QM-MSP can be applied to clinical samples of fresh or fixed ductal cells, ductal fluid, nipple fluid, fine needle aspirates, core biopsies, and tumor tissue sections.

Original languageEnglish (US)
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages473-496
Number of pages24
Volume1708
DOIs
StatePublished - Jan 1 2018

Publication series

NameMethods in Molecular Biology
Volume1708
ISSN (Print)1064-3745

Fingerprint

DNA Methylation
Methylation
Polymerase Chain Reaction
Genes
DNA
Large-Core Needle Biopsy
Nipples
ROC Curve
Real-Time Polymerase Chain Reaction
Neoplasms
Sensitivity and Specificity

Keywords

  • Bisulfite
  • Cells
  • DNA methylation
  • Methylation-specific PCR
  • QM-MSP
  • Quantitation
  • Tissue

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

Cite this

Fackler, M. J., & Sukumar, S. (2018). Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay. In Methods in Molecular Biology (Vol. 1708, pp. 473-496). (Methods in Molecular Biology; Vol. 1708). Humana Press Inc.. https://doi.org/10.1007/978-1-4939-7481-8_24

Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay. / Fackler, Mary Jo; Sukumar, Saraswati.

Methods in Molecular Biology. Vol. 1708 Humana Press Inc., 2018. p. 473-496 (Methods in Molecular Biology; Vol. 1708).

Research output: Chapter in Book/Report/Conference proceedingChapter

Fackler, MJ & Sukumar, S 2018, Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay. in Methods in Molecular Biology. vol. 1708, Methods in Molecular Biology, vol. 1708, Humana Press Inc., pp. 473-496. https://doi.org/10.1007/978-1-4939-7481-8_24
Fackler MJ, Sukumar S. Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay. In Methods in Molecular Biology. Vol. 1708. Humana Press Inc. 2018. p. 473-496. (Methods in Molecular Biology). https://doi.org/10.1007/978-1-4939-7481-8_24
Fackler, Mary Jo ; Sukumar, Saraswati. / Quantitation of DNA methylation by quantitative multiplex methylation-specific PCR (QM-MSP) assay. Methods in Molecular Biology. Vol. 1708 Humana Press Inc., 2018. pp. 473-496 (Methods in Molecular Biology).
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