Use of Formalin-fixed Paraffin-embedded Tumor Tissue as a DNA Source in Molecular Epidemiological Studies of Pediatric CNS Tumors

被引:3
作者
Ferguson, Anthea Elizabeth [1 ]
Cohn, Richard Julian [1 ]
Ashton, Lesley Jayne [1 ]
机构
[1] Childrens Canc Inst Australia, Mol Epidemiol Grp, Randwick, NSW, Australia
关键词
formalin-fixed; paraffin-embedded; DNA; childhood; cancer; brain; COMPARATIVE GENOMIC HYBRIDIZATION; REAL-TIME-PCR; CANCER SUSCEPTIBILITY GENES; POLYMERASE-CHAIN-REACTION; NUCLEIC-ACIDS; EXTRACTION METHODS; FRESH-FROZEN; DEGRADED DNA; COPY NUMBER; AMPLIFICATION;
D O I
10.1097/PDM.0b013e3182340a78
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Formalin-fixed paraffin-embedded tissue (FFPET) samples are a potential source of DNA for molecular epidemiological studies. However, the use of FFPET samples can be restricted by the yield and quality of DNA isolated. The aim of this study was to examine whether FFPET biopsies from pediatric central nervous system tumors were a feasible alternative to archival frozen tissue when characterizing common gene polymorphisms. DNA was isolated from 50 frozen pediatric central nervous system tumor biopsies and matched FFPET samples. Real-time polymerase chain reaction (PCR) was used to quantify DNA and characterize GSTT1, GSTM1, GSTP1, and MTHFR gene polymorphisms. The use of whole-genome amplification (WGA) to increase DNA yields was also investigated. The results showed that DNA isolated from FFPET samples was more fragmented and provided smaller yields than DNA isolated from frozen samples. Attempts to increase the DNA yield from FFPET using WGA were unsuccessful. DNA from FFPET samples was successfully genotyped for the GSTP1 Ile105Val and MTHFR 677 C > T polymorphisms in 98% of samples and was 100% concordant with the results from frozen tissue. However, DNA from FFPET performed poorly in real-time PCR assays for GSTM1 and GSTT1 deletion polymorphisms. Our investigations show that DNA extracted from FFPET is substantially fragmented and not readily amplified using WGA. In addition, careful validation of PCR assays should be carried out due to the variable amplification of fragmented FFPET DNA.
引用
收藏
页码:105 / 113
页数:9
相关论文
共 54 条
  • [41] DNA extraction from archival formalin-fixed, paraffin-embedded tissue sections based on the antigen retrieval principle: Heating under the influence of pH
    Shi, SR
    Cote, RJ
    Wu, L
    Liu, C
    Datar, R
    Shi, Y
    Liu, DX
    Lim, H
    Taylor, CR
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2002, 50 (08) : 1005 - 1011
  • [42] Sjöholm MIL, 2005, CANCER EPIDEM BIOMAR, V14, P251
  • [43] Effect of fixatives and tissue processing on the content and integrity of nucleic acids
    Srinivasan, M
    Sedmak, D
    Jewell, S
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (06) : 1961 - 1971
  • [44] DNA banking for epidemiologic studies: A review of current practices
    Steinberg, K
    Beck, J
    Nickerson, D
    Garcia-Closas, M
    Gallagher, M
    Caggana, M
    Reid, Y
    Cosentino, M
    Ji, J
    Johnson, D
    Hayes, RB
    Earley, M
    Lorey, F
    Hannon, H
    Khoury, MJ
    Sampson, E
    [J]. EPIDEMIOLOGY, 2002, 13 (03) : 246 - 254
  • [45] New approaches for genotyping paraffin wax embedded breast tissue from patients with cancer: the Iowa women's health study
    Thyagarajan, B
    Anderson, KE
    Kong, F
    Selk, FR
    Lynch, CF
    Gross, MD
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 2005, 58 (09) : 955 - 961
  • [46] A multiplex PCR predictor for aCGH success of FFPE samples
    van Beers, EH
    Joosse, SA
    Ligtenberg, MJ
    Fles, R
    Hogervorst, FBL
    Verhoef, S
    Nederlof, PM
    [J]. BRITISH JOURNAL OF CANCER, 2006, 94 (02) : 333 - 337
  • [47] Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations:: Report of the BIOMED-2 Concerted Action BMH4-CT98-3936
    van Dongen, JJM
    Langerak, AW
    Brüggemann, M
    Evans, PAS
    Hummel, M
    Lavender, FL
    Delabesse, E
    Davi, F
    Schuuring, E
    García-Sanz, R
    van Krieken, JHJM
    Droese, J
    González, D
    Bastard, C
    White, HE
    Spaargaren, M
    González, M
    Parreira, A
    Smith, JL
    Morgan, GJ
    Kneba, M
    Macintyre, EA
    [J]. LEUKEMIA, 2003, 17 (12) : 2257 - 2317
  • [48] DNA extraction and stability for epidemiological studies
    Visvikis, S
    Schlenck, A
    Maurice, M
    [J]. CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 1998, 36 (08) : 551 - 555
  • [49] Amplification of PCR products in excess of 600 base pairs using DNA extracted from decalcified, paraffin wax embedded bone marrow trephine biopsies
    Wickham, CL
    Boyce, M
    Joyner, MV
    Sarsfield, P
    Wilkins, BS
    Jones, DB
    Ellard, S
    [J]. JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY, 2000, 53 (01): : 19 - 23
  • [50] A high frequency of sequence alterations is due to formalin fixation of archival specimens
    Williams, C
    Pontén, F
    Moberg, C
    Söderkvist, P
    Uhlén, M
    Pontén, J
    Sitbon, G
    Lundeberg, J
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (05) : 1467 - 1471