نتایج جستجو برای: associated domain family 1 rassf1a

تعداد نتایج: 4419053  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Yu-Jing Zhang Hui-Chen Wu Jing Shen Habibul Ahsan Wei Yann Tsai Hwai-I Yang Li-Yu Wang Shu-Yuan Chen Chien-Jen Chen Regina M Santella

PURPOSE Most hepatocellular carcinomas (HCC) are diagnosed at an advanced stage. Hypermethylation of CpG islands in promoter regions is now recognized as an important early event in carcinogenesis and detection of methylated DNA has been suggested as a potential biomarker for early detection of cancer. There are no studies on epigenetic changes in samples from HCC patients before diagnosis. We ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Ivy H N Wong Jacqueline Chan Joyce Wong Paul K H Tam

PURPOSE AND EXPERIMENTAL DESIGN The role of RASSF1A has been elucidated recently in regulating apoptosis and cell cycle progression by inhibiting cyclin D1 accumulation. Aberrant RASSF1A promoter methylation has been found frequently in multiple adult cancer types. Using methylation-specific PCR and reverse transcription-PCR, we investigated epigenetic deregulation of RASSF1A in primary tumors,...

Journal: :Cancer research 2006
Frederic J Reu Douglas W Leaman Ratan R Maitra Soo In Bae Leonid Cherkassky Mark W Fox Donald R Rempinski Normand Beaulieu A Robert MacLeod Ernest C Borden

Resistance of human renal cell carcinoma (RCC) and melanoma to the apoptosis-inducing effects of IFNs was postulated to result from epigenetic silencing of genes by DNA methylation, a common feature of human cancers. To reverse silencing, 5-AZA-deoxycytidine (5-AZA-dC) or selective depletion of DNA methyltransferase 1 (DNMT1) by phosphorothioate oligonucleotide antisense (DNMT1 AS) were employe...

Journal: :Cancer research 2003
Tamotsu Kuroki Francesco Trapasso Sai Yendamuri Ayumi Matsuyama Hansjuerg Alder Masaki Mori Carlo M Croce

Promoter hypermethylation is an alternative way to inactivate tumor suppressor genes in cancer. Alterations of chromosome 3p are frequently involved in many types of cancer, including esophageal squamous cell carcinoma. Here, we investigated the methylation status and loss of heterozygosity (LOH) of 3p tumor suppressor genes. We examined the promoter methylation status of von Hippel-Lindau dise...

Journal: Vaccine Research 2015
F Badmasti, F Shahcheraghi, H Nemati, O Nasiri, S Bouzari, SD Siadat,

Introduction: Acinetobacter baumannii is associated with hospital-acquired infections. Outer membrane protein A of A.baumannii (AbOmpA) is a well-characterized virulence factor which has important roles in pathogenesis of this bacterium. Methods: Based on our PCR-sequencing of ompA gene in the clinical isolates, AbOmpA protein can be categorized into two types, named here type-1 and type-2. We ...

2017
Fang Liu Ming Gong Li Gao Xiaoping Cai Hui Zhang Yigai Ma

OBJECTIVE The purpose of this study was to evaluate the frequency of RASSF1A hypermethylation in patients with acute myeloid leukemia (AML), in an attempt to modify the current molecular model for disease prognosis. MATERIALS AND METHODS Aberrant RASSF1A promoter methylation levels were assessed in 226 newly diagnosed non-M3 AML patients and 30 apparently healthy controls, by quantitative met...

Journal: :Cancer research 2002
Meryl E Lusher Janet C Lindsey Farida Latif Andrew D J Pearson David W Ellison Steven C Clifford

Epigenetic inactivation of the RASSF1A tumor suppressor gene (TSG) at chromosome 3p21.3 was examined in medulloblastoma, the most common malignant brain tumor of childhood. Seventy-nine % (27 of 34) of primary tumors and 100% (8 of 8) of medulloblastoma cell lines displayed extensive tumor-specific DNA hypermethylation across the RASSF1A promoter-associated CpG island. Hypermethylation was asso...

Journal: :Cancer research 2001
C Morrissey A Martinez M Zatyka A Agathanggelou S Honorio D Astuti N V Morgan H Moch F M Richards T Kishida M Yao P Schraml F Latif E R Maher

Renal cell carcinoma (RCC), the most common adult kidney neoplasm, is histopathologically heterogeneous, with most sporadic RCCs ( approximately 80%) classified as clear cell (CC) tumors. Chromosome 3p allele loss is the most frequent genetic alteration in RCC but is associated specifically with sporadic and hereditary forms of clear cell RCC (CC-RCC) and is not a feature of non-CC-RCC, such as...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شاهد - دانشکده علوم پایه 1391

به دنبال کشف و جداسازی dna جنینی از خون مادر اخیرأ مشخص شده است که امکان تشخیص تفاوت های اپی ژنتیکی بین dna آزاد جنینی و مادری وجود دارد. هدف این مطالعه تشخیص تعداد نسخه کروموزوم 21 جنین با استفاده از تفاوت متیلاسیون dna جنین جدا شده از خون مادر بود که منجر به تشخیص پیش از تولد غیرتهاجمی تریزومی 21 می شود. جهت تشخیص تعداد نسخه کروموزوم 21 جنین از مارکرهای اپی ژنتیکی hlcs و rassf1a که به ترتیب ر...

2016
Natalia Volodko Mohamed Salla Alaa Zare El-Arbi Abulghasem Krista Vincent Matthew G.K. Benesch Todd P.W. McMullen Oliver F. Bathe Lynne Postovit Shairaz Baksh

Epigenetic silencing of RASSF1A is frequently observed in numerous cancers and has been previously reported. The promoter region of RASSF1A is predicted to have 75 CpG sites, and very few studies demonstrate how the methylation of these sites affects expression. In addition, the expression relationship between RASSF1A and its downstream target, modulator of apoptosis 1 (MOAP-1), is poorly under...

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