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      • Predisposition to Cancer Caused by Genetic and Functional Defects of Mammalian <i>Atad5</i>

        Bell, Daphne W.,Sikdar, Nilabja,Lee, Kyoo-young,Price, Jessica C.,Chatterjee, Raghunath,Park, Hee-Dong,Fox, Jennifer,Ishiai, Masamichi,Rudd, Meghan L.,Pollock, Lana M.,Fogoros, Sarah K.,Mohamed, Hassa Public Library of Science 2011 PLoS genetics Vol.7 No.8

        <▼1><P>ATAD5, the human ortholog of yeast Elg1, plays a role in PCNA deubiquitination. Since PCNA modification is important to regulate DNA damage bypass, ATAD5 may be important for suppression of genomic instability in mammals <I>in vivo</I>. To test this hypothesis, we generated heterozygous (<I>Atad5<SUP>+/m</SUP></I>) mice that were haploinsuffficient for Atad5. <I>Atad5<SUP>+/m</SUP></I> mice displayed high levels of genomic instability <I>in vivo</I>, and <I>Atad5<SUP>+/m</SUP></I> mouse embryonic fibroblasts (MEFs) exhibited molecular defects in PCNA deubiquitination in response to DNA damage, as well as DNA damage hypersensitivity and high levels of genomic instability, apoptosis, and aneuploidy. Importantly, 90% of haploinsufficient <I>Atad5<SUP>+/m</SUP></I> mice developed tumors, including sarcomas, carcinomas, and adenocarcinomas, between 11 and 20 months of age. High levels of genomic alterations were evident in tumors that arose in the <I>Atad5<SUP>+/m</SUP></I> mice. Consistent with a role for <I>Atad5</I> in suppressing tumorigenesis, we also identified somatic mutations of <I>ATAD5</I> in 4.6% of sporadic human endometrial tumors, including two nonsense mutations that resulted in loss of proper ATAD5 function. Taken together, our findings indicate that loss-of-function mutations in mammalian <I>Atad5</I> are sufficient to cause genomic instability and tumorigenesis.</P></▼1><▼2><P><B>Author Summary</B></P><P>Genomic instability is a hallmark of tumorigenesis, suggesting that mutations in genes suppressing genomic instability contribute to this phenotype. In this study, we demonstrate for the first time that haploinsufficiency for Atad5, a protein that is important in stabilizing stalled DNA replication forks by regulating PCNA ubiquitination during DNA damage bypass, predisposes >90% of mice to tumorigenesis in multiple organs. In heterozygous <I>Atad5</I> mice, both somatic cells and the spontaneous tumors showed high levels of genomic instability. In a subset of sporadic human endometrial tumors, we identified heterozygous loss-of-function somatic mutations in the <I>ATAD5</I> gene, consistent with the role of mouse <I>Atad5</I> in suppressing tumorigenesis. Collectively, our findings suggest that <I>ATAD5</I> may be a novel tumor suppressor gene.</P></▼2>

      • How Our Practice of Histopathology, Especially Tumour Pathology has Changed in the Last Two Decades: Reflections from a Major Referral Center in Pakistan

        Ahmad, Zubair,Idrees, Romana,Fatima, Saira,Arshad, Huma,Din, Nasir-Ud,Memon, Aisha,Minhas, Khurram,Ahmed, Arsalan,Fatima, Syeda Samia,Arif, Muhammad,Ahmed, Rashida,Haroon, Saroona,Pervez, Shahid,Hassa Asian Pacific Journal of Cancer Prevention 2014 Asian Pacific journal of cancer prevention Vol.15 No.9

        Continued advances in the field of histo pathology (and cyto pathology) over the past two decades have resulted in dramatic changes in the manner in which these disciplines are now practiced. This is especially true in the setting of a large university hospital where the role of pathologists as clinicians (diagnosticians), undergraduate and postgraduate educators, and researchers has evolved considerably. The world around us has changed significantly during this period bringing about a considerable change in our lifestyles and the way we live. This is the world of the internet and the world-wide web, the world of Google and Wikipedia, of Youtube and Facebook where anyone can obtain any information one desires at the push of a button. The practice of histo (and cyto) pathology has also evolved in line with these changes. For those practicing this discipline in a poor, developing country these changes have been breathtaking. This is an attempt to document these changes as experienced by histo (and cyto) pathologists practicing in the biggest center for Histopathology in Pakistan, a developing country in South Asia with a large (180 million) and ever growing population. The Section of Histopathology, Department of Pathology and Microbiology at the Aga Khan University Hospital (AKUH) in Karachi, Pakistan's largest city has since its inception in the mid-1980s transformed the way histopathology is practiced in Pakistan by incorporating modern methods and rescuing histopathology in Pakistan from the primitive and outdated groove in which it was stuck for decades. It set histopathology in Pakistan firmly on the path of modernity and change which are essential for better patient management and care through accurate and complete diagnosis and more recently prognostic and predictive information as well.

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