A certified plasmid reference material for the standardisation of BCR–ABL1 mRNA quantification by real-time quantitative PCR

被引:0
|
作者
H White
L Deprez
P Corbisier
V Hall
F Lin
S Mazoua
S Trapmann
A Aggerholm
H Andrikovics
S Akiki
G Barbany
N Boeckx
A Bench
M Catherwood
J-M Cayuela
S Chudleigh
T Clench
D Colomer
F Daraio
S Dulucq
J Farrugia
L Fletcher
L Foroni
R Ganderton
G Gerrard
E Gineikienė
S Hayette
H El Housni
B Izzo
M Jansson
P Johnels
T Jurcek
V Kairisto
A Kizilors
D-W Kim
T Lange
T Lion
K M Polakova
G Martinelli
S McCarron
P A Merle
B Milner
G Mitterbauer-Hohendanner
M Nagar
G Nickless
J Nomdedéu
D A Nymoen
E O Leibundgut
U Ozbek
T Pajič
机构
[1] National Genetics Reference Laboratory (Wessex),Department of Haematology
[2] Salisbury District Hospital,Department of Molecular Medicine and Surgery
[3] Faculty of Medicine,Department of Oncology
[4] University of Southampton,Haematology Department
[5] European Commission,Department of Molecular Haematology
[6] Joint Research Centre,Department of Clinical and Biological Science
[7] Institute for Reference Materials and Measurements,Department of Genetics and Molecular Pathology
[8] Aarhus University Hospital,Medical Genetics Department
[9] Hungarian National Blood Transfusion Service,Department of Clinical Medicine and Surgery
[10] Regional Genetics Laboratory,Department of Immunology
[11] Birmingham Women’s NHS Foundation Trust,Department of Clinical Genetics
[12] Clinical Genetics Karolinska Institutet,Department of Internal Medicine
[13] Department of Laboratory Medicine,Hematology and Oncology
[14] KU,Abteilung für Hämatologie und internistische Onkologie
[15] Molecular Malignancy Laboratory and Haemato-Oncology Diagnostic Service,Department of Experimental
[16] Cambridge University Hospitals NHS Foundation Trust,Department of Haematology
[17] Belfast City Hospital,Department of Medical Genetics
[18] Haematology Laboratory and EA3518,Department of Laboratory Medicine
[19] University Hospital Saint-Louis,Division of Pathology
[20] AP-HP,Department of Hematology
[21] University Paris Diderot,Genetics Department
[22] Yorkhill NHS Trust,Division of Internal Medicine, Department of Haematology
[23] Molecular Haematology,Department of Internal Medicine
[24] Bristol Royal Infirmary,Hematology Department
[25] Bristol,Hematology Department
[26] UK,Hematology Department and HCT Unit
[27] Hematopathology Unit,Department of Immunology
[28] Hospital Clinic,Department of Haematology
[29] IDIBAPS,Department of Laboratory Diagnostics
[30] Barcelona,Department of Hematology/Oncology
[31] Spain,undefined
[32] University of Turin,undefined
[33] Turin,undefined
[34] Italy,undefined
[35] Laboratoire Hematologie,undefined
[36] CHU Bordeaux,undefined
[37] Hematopoiese Leucemique et Cibles Therapeutiques,undefined
[38] INSERM U1035,undefined
[39] Universite Bordeaux,undefined
[40] Bordeaux,undefined
[41] France,undefined
[42] Combined Laboratories,undefined
[43] Derriford Hospital,undefined
[44] Plymouth,undefined
[45] UK,undefined
[46] SA Pathology,undefined
[47] Adelaide,undefined
[48] SA,undefined
[49] Australia,undefined
[50] Imperial Molecular Pathology,undefined
来源
Leukemia | 2015年 / 29卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Serial quantification of BCR–ABL1 mRNA is an important therapeutic indicator in chronic myeloid leukaemia, but there is a substantial variation in results reported by different laboratories. To improve comparability, an internationally accepted plasmid certified reference material (CRM) was developed according to ISO Guide 34:2009. Fragments of BCR–ABL1 (e14a2 mRNA fusion), BCR and GUSB transcripts were amplified and cloned into pUC18 to yield plasmid pIRMM0099. Six different linearised plasmid solutions were produced with the following copy number concentrations, assigned by digital PCR, and expanded uncertainties: 1.08±0.13 × 106, 1.08±0.11 × 105, 1.03±0.10 × 104, 1.02±0.09 × 103, 1.04±0.10 × 102 and 10.0±1.5 copies/μl. The certification of the material for the number of specific DNA fragments per plasmid, copy number concentration of the plasmid solutions and the assessment of inter-unit heterogeneity and stability were performed according to ISO Guide 35:2006. Two suitability studies performed by 63 BCR–ABL1 testing laboratories demonstrated that this set of 6 plasmid CRMs can help to standardise a number of measured transcripts of e14a2 BCR–ABL1 and three control genes (ABL1, BCR and GUSB). The set of six plasmid CRMs is distributed worldwide by the Institute for Reference Materials and Measurements (Belgium) and its authorised distributors (https://ec.europa.eu/jrc/en/reference-materials/catalogue/; CRM code ERM-AD623a-f).
引用
收藏
页码:369 / 376
页数:7
相关论文
共 50 条
  • [41] Exogenous reference RNA for normalization of real-time quantitative PCR
    Smith, RD
    Brown, B
    Ikonomi, P
    Schechter, AN
    BIOTECHNIQUES, 2003, 34 (01) : 88 - 91
  • [42] Guideline to reference gene selection for quantitative real-time PCR
    Radonic, A
    Thulke, S
    Mackay, IM
    Landt, O
    Siegert, W
    Nitsche, A
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 313 (04) : 856 - 862
  • [43] ITALIAN STANDARDIZATION OF QUANTITATIVE REAL-TIME RT-PCR FOR BCR-ABL ON BEHALF OF LABNET GIMEMA CML WP
    Quarantelli, F.
    Martinelli, G.
    Rosti, G.
    Saglio, G.
    Baccarani, M.
    Pane, F.
    HAEMATOLOGICA, 2008, 93 : S75 - S75
  • [44] Selection and Validation of Reference Genes for mRNA Expression by Quantitative Real-Time PCR Analysis in Neolamarckia cadamba
    Huang, Tian
    Long, Jianmei
    Liu, Si-Wen
    Yang, Zi-Wei
    Zhu, Qi-Jin
    Zhao, Xiao-Lan
    Peng, Changcao
    SCIENTIFIC REPORTS, 2018, 8
  • [45] Quantitative assessment of PML-RARa and BCR-ABL by two real-time PCR instruments:: Multiinstitutional laboratory trial
    Bolufer, P
    Colomer, D
    Gomez, MT
    Martínez, J
    Gonzalez, SM
    Gonzalez, M
    Nomdedeu, J
    Bellosillo, B
    Barragán, E
    Lo-Coco, F
    Diverio, D
    Hermosin, L
    García-Marco, J
    de Juan, MD
    Barros, F
    Romero, R
    Sanz, MA
    CLINICAL CHEMISTRY, 2004, 50 (06) : 1088 - 1092
  • [46] Selection and Validation of Reference Genes for mRNA Expression by Quantitative Real-Time PCR Analysis in Neolamarckia cadamba
    Tian Huang
    Jianmei Long
    Si-Wen Liu
    Zi-Wei Yang
    Qi-Jin Zhu
    Xiao-Lan Zhao
    Changcao Peng
    Scientific Reports, 8
  • [47] Comparison of digital PCR with real-time PCR calibrated to the International Scale for BCR-ABL monitoring.
    Shah, Parth
    Cossor, Furha Iram
    Murarka, Shiva
    Dixit, Hemangi
    JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [48] Establishment of quantitative assay for cellular HIV-1 mRNA by real-time PCR
    Nagai, H
    Wada, K
    Tawada, Y
    Morishita, T
    Utsumi, M
    Nishiyama, Y
    Kaneda, T
    XIV INTERNATIONAL AIDS CONFERENCE: BASIC SCIENCES, 2002, : 65 - 68
  • [49] Real-time quantification of different types of bcr-abl transcript in chronic myeloid leukemia
    Amabile, M
    Gannini, B
    Testoni, N
    Montefusco, V
    Rosti, G
    Zardini, C
    Terragna, C
    Buonamici, S
    Ottaviani, E
    Soverini, S
    Fiacchini, M
    Bassi, S
    de Vivo, A
    Trabacchi, E
    Saglio, G
    Pane, F
    Baccarani, M
    Tura, S
    Martinelli, G
    HAEMATOLOGICA, 2001, 86 (03) : 252 - 259
  • [50] Control genes in international standardization of real-time RT-PCR for BCR-ABL
    Moravcova, Jana
    Rulcova, Jana
    Polakova, Katerina Machova
    Klamova, Hana
    LEUKEMIA RESEARCH, 2009, 33 (04) : 582 - 584