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mRNAs of tyrosine hydroxylase and dopa decarboxylase but not of GD2 synthase are specific for neuroblastoma minimal disease and predicts outcome for children with high-risk disease when measured at diagnosis

Trager, Catarina (författare)
Karolinska Institutet
Vernby, Asa (författare)
Karolinska University Hospital, Sweden
Kullman, Anita (författare)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet
visa fler...
Øra, Ingrid (författare)
Lund University,Lunds universitet,Pediatrik, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Paediatrics (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund University Hospital, Sweden
Kogner, Per (författare)
Karolinska Institutet
Kågedal, Bertil (författare)
Östergötlands Läns Landsting,Linköpings universitet,Klinisk kemi,Hälsouniversitetet
visa färre...
 (creator_code:org_t)
Wiley, 2008
2008
Engelska.
Ingår i: International Journal of Cancer. - : Wiley. - 0020-7136 .- 1097-0215. ; 123:12, s. 2849-2855
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Several transcripts have been claimed to be clinically valuable for detecting minimal disease in neuroblastoma, but they have not been prospectively compared in a standardized manner. Tyrosine hydroxylase (TH), dopa decarboxylase (DDC) and GD2 synthase (GD2S) mRNAs were analyzed in 554 blood (PB) and bone marrow (BM) samples from 58 children with neuroblastoma. Samples from 44 children with other diseases served as controls. High transcript concentrations of TH, GD2S or DDC in PB or BM at diagnosis were associated with poor prognosis. TH in BM above median indicated worse outcome for a homogenous cohort with high-risk neuroblastoma (survival probability 91% for TH below median versus 33% for TH above median, p = 0.009). The number of children with localized neuroblastoma with increased results in PB did not differ between the three transcripts. In these children, all without morphologically detectable neuroblastoma in BM, the number of patients with elevated GD2S in BM at diagnosis was significantly higher than for the other transcripts (10/16 elevated, P = 0.012). GD2S was elevated in PB from 10/28 controls without neuroblastoma compared to 1/28 for TH and DDC (p < 0.001). In BM from these children GD2S was significantly elevated. We conclude that high expression of TH and DDC both in Ill and BM corresponds to metastatic neuroblastoma at diagnosis, residual disease, and poor outcome. Children with high-risk neuroblastoma and low levels of TH in BM at diagnosis may be cured by current therapy. GD2S is less specific than TH and DDC mRNA for neuroblastoma detection in PB and BM.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

neuroblastoma
qRT-PCR tyrosine hydroxylase mRNA
dopa decarboxylase mRNA
GD2 Synthase mRNA
high-risk neuroblastoma
MEDICINE
MEDICIN
mRNA
dopa decarboxylase
neuroblastoma
qRT-PCR tyrosine hydroxylase mRNA
GD2 Synthase mRNA
high-risk neuroblastoma

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