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      Systematic analysis of telomere length and somatic alterations in 31 cancer types

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          Abstract

          Cancer cells survive cellular crisis through telomere maintenance mechanisms. We report telomere lengths in 18,430 samples, including tumors and non-neoplastic samples, across 31 cancer types. Tumor telomeres were shorter compared to normal tissues, and longer in sarcomas and gliomas compared to other cancers. Amongst 6,835 cancers, 73% expressed telomerase reverse transcriptase ( TERT), which was associated with TERT point mutations, rearrangements, DNA amplifications, and transcript fusions, and predicted telomerase activity. TERT promoter methylation provided an additional deregulatory TERT expression mechanism. Five percent of cases, mostly with undetectable TERT, harbored ATRX or DAXX alterations, demonstrated elongated telomeres and increased telomeric repeat containing RNA ( TERRA). The remaining 22% of tumors neither expressed TERT, nor harbored alterations in ATRX/DAXX. In this group, telomere length positively correlated with TP53 and RB1 mutations. Our analysis integrates TERT abnormalities, telomerase activity and genomic alterations with telomere length in cancer.

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          Most cited references31

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          Telomeres and human disease: ageing, cancer and beyond.

          Telomere length and telomerase activity are important factors in the pathobiology of human disease. Age-related diseases and premature ageing syndromes are characterized by short telomeres, which can compromise cell viability, whereas tumour cells can prevent telomere loss by aberrantly upregulating telomerase. Altered functioning of both telomerase and telomere-interacting proteins is present in some human premature ageing syndromes and in cancer, and recent findings indicate that alterations that affect telomeres at the level of chromatin structure might also have a role in human disease. These findings have inspired a number of potential therapeutic strategies that are based on telomerase and telomeres.
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            Phaeochromocytoma.

            Phaeochromocytomas are rare neuroendocrine tumours with a highly variable clinical presentation but most commonly presenting with episodes of headaches, sweating, palpitations, and hypertension. The serious and potentially lethal cardiovascular complications of these tumours are due to the potent effects of secreted catecholamines. Biochemical testing for phaeochromocytoma is indicated not only in symptomatic patients, but also in patients with adrenal incidentalomas or identified genetic predispositions (eg, multiple endocrine neoplasia type 2, von Hippel-Lindau syndrome, neurofibromatosis type 1, and mutations of the succinate dehydrogenase genes). Imaging techniques such as CT or MRI and functional ligands such as (123)I-MIBG are used to localise biochemically proven tumours. After the use of appropriate preoperative treatment to block the effects of secreted catecholamines, laparoscopic tumour removal is the preferred procedure. If removal of phaeochromocytoma is timely, prognosis is excellent. However, prognosis is poor in patients with metastases, which especially occur in patients with large, extra-adrenal tumours.
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              The somatic genomic landscape of chromophobe renal cell carcinoma.

              We describe the landscape of somatic genomic alterations of 66 chromophobe renal cell carcinomas (ChRCCs) on the basis of multidimensional and comprehensive characterization, including mtDNA and whole-genome sequencing. The result is consistent that ChRCC originates from the distal nephron compared with other kidney cancers with more proximal origins. Combined mtDNA and gene expression analysis implicates changes in mitochondrial function as a component of the disease biology, while suggesting alternative roles for mtDNA mutations in cancers relying on oxidative phosphorylation. Genomic rearrangements lead to recurrent structural breakpoints within TERT promoter region, which correlates with highly elevated TERT expression and manifestation of kataegis, representing a mechanism of TERT upregulation in cancer distinct from previously observed amplifications and point mutations.
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                Author and article information

                Journal
                9216904
                2419
                Nat Genet
                Nat. Genet.
                Nature genetics
                1061-4036
                1546-1718
                18 July 2017
                30 January 2017
                March 2017
                01 September 2017
                : 49
                : 3
                : 349-357
                Affiliations
                [1 ]The Jackson Laboratory Institute for Genomic Medicine, Farmington, Connecticut, USA
                [2 ]Oncology Graduate School Amsterdam, VU University Medical Center, Amsterdam, The Netherlands
                [3 ]Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                [4 ]Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                [5 ]Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                [6 ]Program in Biostatistics, Bioinformatics, and Systems Biology The University of Texas Graduate School of Biomedical Sciences at Houston, Houston, Texas, USA
                [7 ]Graduate Program in Structural and Computational Biology and Molecular Biophysics, Baylor College of Medicine, Houston, Texas, USA
                [8 ]Institute for Applied Cancer Science, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                [9 ]Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                [10 ]Biopathology Center, Nationwide Children’s Hospital, Columbus, Ohio, USA
                [11 ]Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA
                Author notes
                Correspondence should be addressed to Z.S. ( syzhenger@ 123456gmail.com ), R.G.W.V. ( roel.verhaak@ 123456jax.org )
                Article
                PMC5571729 PMC5571729 5571729 nihpa893058
                10.1038/ng.3781
                5571729
                28135248
                c10c35c0-506a-459a-8ad6-54e8036427be
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