Endocrine-Related Cancer ( 2012 ) 19 L 15 – L 18 The effect of the ATG 16 L 1 Thr 300 Ala polymorphism on susceptibility and outcome of patients with epithelial cell-derived thyroid carcinoma

Epithelial cell-derived thyroid carcinoma (TC) is the most common endocrine malignancy. Increasing evidence suggests that autophagy, a complex process of autodigestion in conditions of cellular stress, plays an important role in the pathophysiology of the TC malignant process. One of the main mammalian autophagy proteins is autophagy related 16-like 1 (ATG16L1), which is essential for autophagosome formation, induction of autophagy, and modulation of inflammation (Saitoh et al. 2008). Subsequently, defective autophagy in ATG16L1 knockout mice results in an increased production of the proinflammatory cytokine interleukin 1b (IL1b; Saitoh et al. 2008) that is also known to affect the growth and differentiation of different malignant cell types (Apte & Voronov 2002). Considering the potential role of both autophagy and IL1b in the pathology of TC, we hypothesized that genetic variation in ATG16L1 influences the susceptibility for and the outcome of TC. One single nucleotide polymorphism of the ATG16L1 gene (c.898AOG, Thr300Ala, rs2241880) has been shown to affect the autophagy process (Cooney et al. 2010) and also to modulate production of IL1b in human cells (Plantinga et al. 2011). We investigated whether this ATG16L1 polymorphism is associated with the susceptibility or clinical outcome of TC. One hundred and thirty nine patients (75% women, mean age 39G13 (S.D.) years) with histologically confirmed TC (papillary (70%), follicular TC (24%), or both (6%)), who visited the outpatient clinic at the Department of Endocrinology of our centre, were included. Primary treatment consisted of (near-) total thyroidectomy in all patients and modified radical neck dissections in patients with confirmed nodal metastases, followed by ablation with radioactive iodine (I, RAI) of residual thyroid tissue. Initial cure is

[1]  M. Oosting,et al.  Crohn's disease-associated ATG16L1 polymorphism modulates pro-inflammatory cytokine responses selectively upon activation of NOD2 , 2011, Gut.

[2]  D. Jewell,et al.  NOD2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presentation , 2010, Nature Medicine.

[3]  L. Duntas,et al.  The ‘rings of fire’ and thyroid cancer , 2009, Hormones.

[4]  Kari Stefansson,et al.  Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations , 2009, Nature Genetics.

[5]  Nathaniel Rothman,et al.  International patterns and trends in thyroid cancer incidence, 1973–2002 , 2009, Cancer Causes & Control.

[6]  S. Akira,et al.  Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1β production , 2008, Nature.

[7]  K. Aben,et al.  Trends in incidence and mortality of thyroid carcinoma in The Netherlands between 1989 and 2003: Correlation with thyroid fine‐needle aspiration cytology and thyroid surgery , 2008, International journal of cancer.

[8]  E. Voronov,et al.  Interleukin-1--a major pleiotropic cytokine in tumor-host interactions. , 2002, Seminars in cancer biology.

[9]  J. Hershman,et al.  Antitumor actions of cytokines on new human papillary thyroid carcinoma cell lines. , 1996, The Journal of clinical endocrinology and metabolism.

[10]  S. Nagataki,et al.  Interleukin-1 inhibits human thyroid carcinoma cell growth. , 1992, The Journal of clinical endocrinology and metabolism.