رسالة جامعية

Biomarkers in pheochromocytomas and paragangliomas

التفاصيل البيبلوغرافية
العنوان: Biomarkers in pheochromocytomas and paragangliomas
المؤلفون: Leijon, Helena
المساهمون: Kujala, Paula, University of Helsinki, Faculty of Medicine, Department of Pathology, Doctoral Programme in Biomedicin, Helsingin yliopisto, lääketieteellinen tiedekunta, Biolääketieteellinen tohtoriohjelma, Helsingfors universitet, medicinska fakulteten, Doktorandprogrammet i biomedicin, Arola, Johanna, Haglund, Caj, Salmenkivi, Kaisa
بيانات النشر: Helsingin yliopisto
Helsingfors universitet
University of Helsinki
سنة النشر: 2018
المجموعة: Helsingfors Universitet: HELDA – Helsingin yliopiston digitaalinen arkisto
مصطلحات موضوعية: Lääketiede
الوصف: Pheochromocytomas (PHEOs) derived from adrenal medulla and paragangliomas (PGLs) from sympathetic or parasympathetic paraganglia are rare neuroendocrine tumors. Incidence of PHEOs and PGLs is between 0.4–9.5 cases per one million people per year. In Finland about 10–15 PHEOs are diagnosed per year, but the incidence is rising. PHEOs and sympathetic PGLs can secrete catecholamines, often in bouts, which makes the symptoms associated with these tumors very diverse, with high blood pressure being the leading symptom. During recent years, knowledge of the variable genetic background and pathogenesis of PGLs and PHEOs has increased, and about 30-40% of these tumors are known to be hereditary. However, prognosis and aggressiveness of an individual tumor cannot be unequivocally predicted histologically or with any biomarkers. The aim of this thesis was to find biomarkers in PHEOs and PGLs for diagnostic, prognostic, and predictive purposes. The study cohort consisted of 153 consecutive PHEOs or PGLs operated from 147 patients during the years 1973–2009 at Helsinki University Hospital. Tissue microarray blocks were constructed for immunohistochemistry studies. Matrix-assisted laser desorption/ionization time of flight mass spectrometric profiling of 16 tissue samples was used to analyze N-glycan structures in eight metastasized and eight nonmetastasized tumors. In addition, five thyroid PGLs originating from the population-based European-American-Head-and-Neck-Paraganglioma-Registry (European-American-HNPGL-Registry, Freiburg, Germany) were investigated. Metastasized PHEOs and PGLs expressed significantly more intracytoplasmic human antigen R (HuR) protein immunohistochemically than nonmetastasized tumors. The metastatic potential was also associated with higher proliferation and tumor necrosis. Five somatostatin receptors (SSTR1–5) showed individual and varying SSTR profiles in PHEOs and PGLs. The most abundant SSTRs were SSTR2 and SSTR3. Between metastatic PHEOs and PGLs the SSTR2 expression varied – all PGLs were ...
نوع الوثيقة: doctoral or postdoctoral thesis
وصف الملف: application/pdf
اللغة: English
ردمك: 978-951-51-4750-9
978-951-51-4751-6
951-51-4750-6
951-51-4751-4
العلاقة: URN:ISBN:978-951-51-4750-9; Helsinki: Unigrafia, 2018; http://hdl.handle.net/10138/266764Test; URN:ISBN:978-951-51-4751-6
الإتاحة: http://hdl.handle.net/10138/266764Test
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رقم الانضمام: edsbas.D973D3C0
قاعدة البيانات: BASE
الوصف
ردمك:9789515147509
9789515147516
9515147506
9515147514