Pathogenesis (development of disease)
Thyroid carcinomas arise from either thyrocytes (follicular epithelial cells of the thyroid gland; papillary and follicular carcinoma) or parafollicular C cells (medullary carcinoma). They arise from genetic alterations of these cells.
The reason for this genetic alteration is unclear in many cases.
Etiology (causes)
Biographic causes
- Genetic burden from parents, grandparents, especially in medullary thyroid carcinoma and familial syndromes e.g., MEN 2
- Genetic risk depending on gene polymorphisms:
- Genes/SNPs (single nucleotide polymorphism):
- Genes: FOXE1
- SNP: rs965513 in an intergenic region.
- Allele constellation: AG (1.77-fold).
- Allele constellation: AA (3.1-fold)
- SNP: rs1867277 in the gene FOXE1
- Allele constellation: AG (1.5-fold).
- Allele constellation: AA (2.0-fold)
- SNP: rs944289 in an intergenic region.
- Allele constellation: CT (1.3-fold).
- Allele constellation: TT (1.69-fold)
- Genes/SNPs (single nucleotide polymorphism):
- Genetic risk depending on gene polymorphisms:
- Ethnic origin – Asian and African ancestry [US study!, 1].
- Birth weight of female children: at birth weight 2,500-3,999 grams for reference:
- <2,500 grams: thyroid carcinoma risk 13% lowered.
- > 4,000 grams: thyroid carcinoma risk 11% increased
Probably insulin-like growth factor 1 (IGF-1)-related.
Behavioral causes
- Diet – iodine deficiency
- Overweight (BMI ≥ 25; obesity); there is a clear association between obesity, diabetes mellitus and differentiated thyroid carcinoma; bes. strong predictor was BMI
Disease-related causes
- Hashimoto’s thyroiditis
Radiation
- Condition after radiotherapy (radiotherapy) of the neck region or mediastinum (mediastinum, this is a vertically running tissue space in the chest cavity); after a CT in the head and neck region, the risk of tumors is increased for children. This is especially true for thyroid carcinomas (increased by 78%) and brain tumors (increased by 60%). The overall cancer incidence is increased by 13%.
- Ionizing radiation