Abstract

According to the epidemiological studies, about 4.4% of American general elderly population has a pronounced hypothyroidism and relies on thyroid hormone supplements daily. The prevalence of hypothyroidism in our patients with pancreatic cancer was much higher, 14.1%. A retrospective analysis was performed on patients who underwent pancreaticoduodenectomy (Whipple procedure) or distal pancreatectomy and splenectomy (DPS) at Thomas Jefferson University Hospital, Philadelphia, from 2005 to 2012. The diagnosis of hypothyroidism was correlated with clinicopathologic parameters including tumor stage, grade, and survival. To further understand how thyroid hormone affects pancreatic cancer behavior, functional studies including wound-induced cell migration, proliferation, and invasion were performed on pancreatic cancer cell lines, MiaPaCa-2 and AsPC-1. We found that hypothyroid patients taking exogenous thyroid hormone were more than three times likely to have perineural invasion, and about twice as likely to have higher T stage, nodal spread, and overall poorer prognostic stage (P < 0.05). Pancreatic cancer cell line studies demonstrated that exogenous thyroid hormone treatment increased cell proliferation, migration, and invasion (P < 0.05). We conclude that exogenous thyroid hormone may contribute to the progression of pancreatic cancer.

Highlights

  • Invasive pancreatic cancer is the fourth leading cause of cancer death in the United States

  • body mass index (BMI) was not significantly different in the hypothyroid group when compared to the euthyroid group (27.9 versus 26.3, resp.)

  • This study demonstrates that there may be an association between thyroid hormone supplementation and pancreatic cancer invasion

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Summary

Introduction

Invasive pancreatic cancer is the fourth leading cause of cancer death in the United States. Despite many advances in cancer biology over the past years, pancreatic cancer remains an elusive disease process that requires further studies to understand its molecular biology and investigate possible therapeutic targets. The major product of the thyroid is T4, most of it is converted to more biologically active T3 that binds to nuclear thyroid receptors and modulates the expression of proteins traditionally known to increase basal metabolic rate and enhance growth [3]. The prevalence of thyroid disorders increases with age (up to 4.4% for 60 years and Journal of Thyroid Research older) and is consistent with females having higher rates of hypothyroidism than men [5,6,7,8]

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