Oncogenes/Growth Factors & Environment

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Oncogenes/Growth Factors & Environment 8 th Postgraduate Course in Endocrine Surgery Crete, Greece September, 2006 Orlo H. Clark M.D.

Thyroid Cancer Thyroid cancer is the 8 th most common and most rapidly increasing cancer in women An estimated 30,000 cases will occur in the United States in 2006 It frequently affects individuals under 50 years of age There are about 300,000 survivors of thyroid cancer in the USA

Thyroid Cancer There are 5 major types of thyroid cancers: (Papillary 80% / Follicular 9% / Hurthle Cell 3% / Medullary 7% / Anaplastic 1%) Familial thyroid cancer occurs in about 25% of patients with medullary thyroid cancer and 5 % of those with papillary and Hurthle cell cancer Familial Non Medullary thyroid cancer is defined as thyroid cancer affecting at least two first degree relatives (roughly 90% are papillary)

Thyroid Cancer Epidemiology Ron et al (1991): 5 fold increased risk of thyroid cancer when another family member has thyroid cancer Goldgar et al. (1994): 9 fold increase of thyroid cancer in association with breast cancer

Environment and Genetics Genetics Environment Disease

Histogram Occult PTC

Patient with large PTC

CT of PTC

PET Scan

Thyroid Cancer: A Lethal Endocrine Neoplasm (NIH Conference) Although the mortality rate from thyroid cancer is low, it is the highest among cancers affecting the endocrine glands (excluding the ovary). (Robbin J et al. Ann Intern Med 115:133-147, 147, 1991)

Death from Thyroid Cancer UCSF 1965-1995 Patient Characteristics (102 patients) Mean age 58 years (range 12 to 90 years) 31 less than 45 years of age Tumor size ranged from 0.6 to 13.0 cms Metastases in 46% (regional) and 18% distant 50% of patients with PTC & HTC verses 11% of FTC died of locally advanced disease (Wu HS et al, JACS 191:600-606, 2000)

Genes Implicated in Sporadic Papillary Thyroid Cancer BRAF ras TRK MET p53 Gene RET/PTC Comment More frequent in children and after radiation (Tyrosine Kinase) Most common mutation in PTC- Appears to be associated with more aggressive tumors Early in tumor development and more frequent in follicular thyroid cancer Activated in about 15% of PTC (Tyrosine Kinase) Over expressed Tyrosine Kinase Dedifferentiated or undifferentiated tumors

Normal follicular thyroid cell Hyperfunctioning thyroid nodule Occult PTC PTC Poorly differentiated PTC Anaplastic Thyroid Cancer Follicular Adenoma FTC Hürthle Cell Adenoma HCC ras TRK RET/PTC MET myc BRAF ras PTEN fos PAX8 / PPARγ ras myc fos p53 p53 p53 TSH-R Gsα/gsp Normal parafollicular C-cell C-cell hyperplasia RET MTC

Inherited Thyroid Cancer Syndromes Syndrome Multinodular goiter (MNG) Trabecular, oxyphilic & MNG PTC-Renal neoplasia PTC Follicular variant PTC Familial adenomatous polyposis Cowden's Syndrome Chromosome Location 14q31 19p 13.2 1q 21 2q21 5q21-22 22 10q23.3 Gene???? APC* PTE N * > 80% of these thyroid cancers have ret/ptc somatic mutations.

Familial Non-Medullary Thyroid Cancer Familial Hürthle cell (TCO): 19p13.2 1 Familial papillary thyroid cancer with papillary renal neoplasia (fptc/prn): 1q21 2 Familial papillary thyroid cancer in Tas1 (fptc): 2q21 3 fptc/prn fptc TCO 1. Canzian et al. Am J Hum Genet. 63:1743, 1998. 2. Malchoff et al. JCEM. 85(5):1758, 2000. 3. McKay et al. Am J Hum Genet. 69(2):440, 2001

Photo of Thyroid Cancer Cell

TSH Suppression and Thyroid Cancer After 30 years follow-up, we found that there were 25% fewer recurrences in patients treated with T 4 as compared with no adjunctive therapy (p <.01), and there were fewer cancer deaths in the T 4 group (6% versus 12%; p < 0.0001). (Mazzaferri EL, Jhiang, SM: Am J Med 73:424, 1994)

TSH Suppression and Thyroid Cancer Relapse-free survival was longer in patients with TSH <0.05 or < 0.1 than in those with non-suppressed TSH values The level of TSH suppression was an independent prognostic factor using multivariate analysis (Pujol P, et al. JCEM,, 1996)

Outcome of Children Treated for Thyroid Cancer Thyroid stimulating hormone suppression was the only intervention shown to reduce the recurrence rate. (Landau D et al European J Cancer 36: 214-220, 220, 2000)

Thyroid Cancer ret PTC (Tg - PTC - 1) transgenic mice develop develop thyroid cancer are are responsive to TSH suppression (grow slower but still grow) (S. Jhiang, PhD ATA,, 2002)

Thyroid Cancer: Potential New Methods of Therapy Anti-angiogenesis agents Redifferentiation agents Retinoids Aromatic fatty acids (phenylacetate/phenylbutrate) PPAR gamma agonists Histone deacetylase (HDAC) inhibitors (Tricostatin A/Depsipeptide) COX 2 inhibitors Gene therapy P53/TTF 1 /PAX8/NIS Anti invasion (metalloproteinase inhibitors