Computational Analysis Of Potential Key Genes Associated With Dopamine Neurotransmission In Pheochromocytoma And Paraganglioma

نویسندگان

چکیده

Pheochromocytoma and Paraganglioma (PCPG) are rare potentially lethal neuroendocrine tumors. PCPG that predominantly or exclusively produce secrete DA is rarely seen it has been known dopamine-secreting related with advanced malignant features metastases. Up to the present, little about role of dopamine neurotransmission dopaminergic system in initiation progression PCPG. The genes significant expression differences between normal tissue pheochromocytoma paraganglioma, survival correlation analysis, CpG islands prediction, miRNA-target enrichment analysis were performed by several bioinformatics tools. In present study, was determined COMT gene significantly less expressed than showed a remarkable relationship differential shorter overall among individuals (HR=1, p=0.011). MAOA pair correlated (p=0.012; R=0.19) hsa-miR-5000-5p regulates both (p=0.00215, FDR=0.127). Our findings suppose may be implicated tumor suppressive mechanism. values genes, have potential used genetic evaluation pathogenesis prognosis Further vitro vivo studies required clarify molecular mechanism

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Utility of 123I-MIBG Standardized Uptake Value in Patients with Refractory Pheochromocytoma and Paraganglioma

Objective(s): Single-photon emission computed tomography (SPECT) using metaiodobenzylguanidine (MIBG) is an important diagnostic tool for the treatment of refractory pheochromocytoma and paraganglioma (PPGL). Owing to the difficulty of SPECT quantification, the tumour-to-background ratio (TBR) is used to assess disease activity. However, the utility of TBR is limited o...

متن کامل

Hereditary paraganglioma-pheochromocytoma syndromes associated with SDHD and RET mutations.

BACKGROUND Hereditary paraganglioma-pheochromocytoma syndromes (PGL/PCC) are rare tumors arising from neuroendocrine cells. METHODS AND RESULTS The proband, a 59-year-old white man and his 42-year-old elder son had a medical history of bilateral carotid body PGL and both presented for treatment of abdominal PGLs. His 36-year-old daughter had excision of recurrent malignant carotid body PGL an...

متن کامل

Phenylethanolamine N-methyltransferase downregulation is associated with malignant pheochromocytoma/paraganglioma

Malignant pheochromocytoma/paraganglioma (PCC/PGL) is defined by the presence of metastases at non-chromaffin sites, which makes it difficult to prospectively diagnose malignancy. Here, we performed array CGH (aCGH) and paired gene expression profiling of fresh, frozen PCC/PGL samples (n = 12), including three malignant tumors, to identify genes that distinguish benign from malignant tumors. Mo...

متن کامل

the stady and analysis of rice agroclimatology in lenjan

the west of esfahan province, iran, is one of the most important agricultural areas throughout the country due to the climate variability and life-giving water of zayanderood river. rice is one of the major and economic crops in this area. the most important climatic elements in agricultural activities which should be considered include temperature, relative humidity, precipitation and wind. so...

15 صفحه اول

Primary Cardiac Pheochromocytoma (Paraganglioma)

Pheochromocytomas are catecholamine-producing neuroendocrine tumors arise from primitive neural crest cells. About 90% of these tumors occur as solitary benign tumors of the adrenal medulla, where majority of chromaffin cells are concentrated. Only ten percent originates from extra-adrenal sites with the organ of Zukerkandal (paraganglia along abdominal aorta) being the most common. Chromaffin ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Hitite journal of science and engineering

سال: 2021

ISSN: ['2148-4171', '2149-2123']

DOI: https://doi.org/10.17350/hjse19030000245