Skip to main content

Table 3 Characteristic collected from included studies

From: CpG island status as an epigenetic alteration for NIS promoter in thyroid neoplasms; a cross-sectional study with a systematic review

Studies

Method

Studied groups

Methylation status

Potential Clinical Value

NT

BTLs

DTCs

Venkataraman et al. (1999)

MSP

NT (5), PTC (16), FTC (2)

2/5

–

8/18

Chemical demethylation therapy

Neuman et al. (2004)

MSP

ST (14), CTN (14)

0/14

–

6/14

Could be a regulatory mechanism of NIS transcription

Smith et al. (2007)

MSP

Controls (FA (10), goiters (15), normal thyroids (2)), PTC (32)

0

0

7/32

Marker of virulence

Stephen et al. (2011)

MSP

NT (5), hyperthyroid (3), PTC (11), FTC (2)

1/5

1/3

7/13

Early event

Galrão et al. (2013)

SQ-MSP

BTLs (10), PTC (18), FTC (2)

–

2.23

1.92

Very frequent event

Galrão et al. (2014)

BSP

BTLs (10), PTC (18), FTC (2)

–

23.2%

66.1%

Early event

Choi et al. (2014)

BSP and MSP

NT (24), PTC (24)

29%

–

58%

Related to BRAF (V600E) mutation

Stephen et al. (2015)

QMSP

ANT (24), FTC-Hurthle (26), FTC-Classic (27)

 > 0.0

–

 > 0.0

Early changes in thyroid tumorigenesis regardless of cell type

Stephen et al. (2018)

QMSP

NT (71), FA (83), PTC (85), FTC (90)

0.001(0.002)

0.014

(0.041)

PTC (0.009(0.027))

FTC (0.02(0.07))

–

  1. Methylation status of NIS gene promoter: MSP, SQ-MSP, BSP, and QMSP results were expressed as methylated/total samples, arbitrary unit (AU), percentage, and mean (SD), respectively
  2. MSP methylation-specific PCR, SQ-MSP semi-quantitative MSP, QMSP quantitative MSP, BSP Bisulfite-sequencing PCR, ST surrounding tissue, CTN cold thyroid nodules, NT normal thyroid, FA follicular adenoma, BTLs benign thyroid lesions, TC thyroid cancer, FTC follicular thyroid cancer, PTC papillary thyroid cancer, DTC differentiated thyroid cancer, ANT adjacent normal tissue