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Table 3 Results of FISH, aCGH, Q-PCR analyses of chromosome 17, displayed in relation to NBTs ploidy status

From: Differential expression of genes mapping to recurrently abnormal chromosomal regions characterize neuroblastic tumours with distinct ploidy status

Case Number

Ploidy

MYCN

FISH Chromosome 17

a CGH Chr. 17

Q-PCR Gene copy No. (fold change)

Disease Status

Survival Status

   

Cell % (# DNA probe signals: LSI 17p13.1: CEP 17)

p

cen

q

RUTBC1 (17p13.3)

NME1 (17q21)

  

1

near-3n

NA

n.e

G

G

G

2.3

2.5

NP

A

2

near-3n

NA

45 (2:2), 55 (3:3)

G

G

G

1.5

1.5

NP

A

3

near-3n

NA

45 (2:2), 55 (3:3)

G

G

G

1.3

1.4

NP

A

4

near-3n

NA

30 (2:2), 70 (3:3)

G

G

G

3.6

2.2

NP

A

5

near-3n

NA

50 (2:2), 50 (3:3)

G

G

G

1.6

1.3

NP

A

6

near-3n

NA

50 (2:2), 50 (3:3)

G

G

G

1.4

1.5

NP

A

7

near-2n

NA

5 (1:1), 80 (2:2), 10 (3:3), 5 (4:4)

n.e

n.e

n.e

0.7

1.4

NP

A

8

near-2n

NA

33 (1:1), 66 (2:2)

-

-

-

0.8

0.7

P

D

9

near-2n

A

7 (1:1), 7 (2:1), 60 (2:2), 20 (1:2), 6 (2:3)

-

-

G

1.1

1.4

P

D

10

near-2n

NA

80 (2:2), 15 (2:3), 5 (3:3)

-

-

G

1.2

1.5

NP

A

11

near-2n

NA

28 (1:1); 11 (2:1), 56 (2:2), 5 (3:2)

n.e

n.e

n.e

1.1

0.9

P

D

12

near-4n

A

45 (2:2); 55 (3:3)

-

-

G

1

1.4

P

D

13

near-4n

A

45 (2:2), 45 (3:3), 10 (4:4)

G

G

G

2.2

1.9

P

D

  1. Thirteen representative cases drawn from the HSJD cohort analyzed by FISH, aCGH and Q-PCR of chromosome 17. n.e = not evaluable results. MYCN amplification status: NA = not amplified, A = amplified. Disease status: NP = no disease progression, P = disease progression. Survival status: A = alive, D = dead. FISH: results are displayed as percentage of cells exhibiting the observed number of DNA probe signals, and exact number of signals for the DNA probes used: chromosome 1 (LSI 1p36 and LSI 1q25 DNA probes) and chromosome 17(LSI 17p13.1 and CEP 17 DNA probes). Array CGH: p and q = chromosome arms, cen. = centromeric; G = chromosome gain, L = chromosome loss. Q-PCR: gene copy number fold changes are determined by the ΔΔCT relative quantification method.