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Table 1 MMP2 genotypes vs clinical, pathological and epidemiological variables

From: Functional polymorphisms in the promoter regions of MMP2 and MMP3 are not associated with melanoma progression

Variables

MMP2

 

-1306 C/T

p-value*

-735 C/T

p-value*

 

CC

CT

TT

 

CC

CT

TT

 

Stage at Diagnosis

        

   0

34 (59%)

19 (33%)

5 (9%)

 

48 (83%)

10 (17%)

0 (0%)

 

   I

320 (64%)

159 (32%)

23 (5%)

 

365 (73%)

123 (25%)

13 (3%)

 

   II

152 (65%)

72 (31%)

9 (4%)

 

184 (78%)

49 (21%)

2 (1%)

 

   III

105 (63%)

54 (32%)

9 (5%)

 

131 (79%)

32 (19%)

3 (2%)

 

   IV

6 (67%)

3 (33%)

0 (0%)

0.92

4 (44%)

5 (56%)

0 (0%)

0.08

Primary Clark Level

        

   I

34 (59%)

19 (33%)

5 (9%)

 

48 (83%)

10 (17%)

0 (0%)

 

   II

70 (65%)

36 (33%)

2 (2%)

 

79 (74%)

23 (22%)

5 (5%)

 

   III

89 (60%)

48 (32%)

12 (8%)

 

115 (77%)

32 (21%)

3 (2%)

 

   IV

308 (64%)

155 (32%)

22 (5%)

 

358 (74%)

116 (24%)

10 (2%)

 

   V

51 (74%)

14 (20%)

4 (6%)

0.20

54 (78%)

15 (22%)

0 (0%)

0.44

Thickness (mm)

        

   In situ

34 (59%)

19 (33%)

5 (9%)

 

48 (83%)

10 (17%)

0 (0%)

 

   < 1.01

201 (63%)

107 (33%)

12 (4%)

 

237 (74%)

72 (23%)

10 (3%)

 

   1.01 – 2.00

174 (64%)

81 (30%)

15 (6%)

 

199 (73%)

68 (25%)

4 (2%)

 

   2.01 – 4.00

100 (63%)

50 (31%)

10 (6%)

 

124 (78%)

33 (21%)

2 (1%)

 

   > 4.00

81 (68%)

35 (29%)

4 (3%)

0.72

94 (78%)

25 (21%)

1 (1%)

0.44

TILs

        

   Absent

129 (63%)

67 (33%)

9 (4%)

 

161 (79%)

40 (20%)

3 (2%)

 

   Non-brisk

262 (67%)

111 (28%)

21 (5%)

 

289 (73%)

95 (24%)

10 (3%)

 

   Brisk

19 (63%)

9 (30%)

2 (7%)

0.80

21 (68%)

10 (32%)

0 (0%)

0.32

Distant Metastasis

        

   Yes

86 (67%)

39 (30%)

4 (3%)

 

97 (76%)

29 (23%)

2 (2%)

 

   No

543 (63%)

281 (32%)

42 (5%)

0.28

653 (75%)

196 (23%)

17 (2%)

0.88

Intransit Metastasis

        

   No

590 (63%)

302 (32%)

46 (5%)

 

705 (75%)

216 (23%)

16 (2%)

 

   Yes

18 (67%)

9 (33%)

0 (0%)

0.44

22 (82%)

3 (11%)

2 (7%)

0.96

Number of Moles

        

   None

161 (62%)

84 (33%)

13 (5%)

 

201 (77%)

54 (21%)

5 (2%)

 

   Few

311 (63%)

166 (33%)

20 (4%)

 

380 (77%)

105 (21%)

11 (2%)

 

   Moderate

112 (67%)

51 (30%)

5 (3%)

 

115 (69%)

49 (30%)

2 (1%)

 

   Many

22 (55%)

11 (28%)

7 (18%)

< 0.01

29 (73%)

10 (25%)

1 (3%)

0.40

Phenotypic Index

        

   1 (low risk)

26 (68%)

11 (29%)

1 (3%)

 

31 (82%)

6 (16%)

1 (3%)

 

   2

132 (63%)

66 (32%)

11 (5%)

 

156 (75%)

47 (23%)

4 (2%)

 

   3

206 (65%)

93 (29%)

18 (6%)

 

231 (73%)

76 (24%)

10 (3%)

 

   4

191 (59%)

122 (38%)

11 (3%)

 

254 (78%)

68 (21%)

4 (1%)

 

   5 (high risk)

73 (70%)

27 (26%)

5 (5%)

0.28

76 (73%)

28 (27%)

0 (0%)

0.36

  1. * The associations were examined in three different ways (see statistical methods for a detailed explanation). The p-values shown refer to the analysis of the three individual genotypes, and appear in bold font if ≤ 0.05. The significance was lost after adjustment for age, sex, phenotypic index, moles, freckles, and race.