4 research outputs found
Methylation profiling of twenty promoter-CpG islands of genes which may contribute to hepatocellular carcinogenesis
- Author
- A Agathanggelou
- A Feinberg
- A Feninberg
- A HJ Merlo
- AK Gupta
- B Quesnel
- Baomei Gao
- C Sherr
- CH Lin
- CJ Chen
- CT Nguyen
- DJ Simpson
- DJ Wong
- EP NY Xing
- GJ Hannon
- Hongyu Zhang
- IH Wong
- IH Wong
- J Bian
- JD Zhu
- JG Herman
- Jian Xu
- Jian Yu
- Jianguo Chen
- Jianren Gu
- Jingde Zhu
- JK Wiencke
- JR Graff
- KO TS Toyooka
- KW Lo
- LCSGo Japan
- Lisheng Zhang
- M Esteller
- M Hattori
- M Paulsen
- Mengchao Wu
- Min Ni
- MS Soengas
- PA Jones
- R Dammann
- RL Baldwin
- RZ Chen
- S DP Stone
- S Zochbauer-Muller
- SA Foster
- SB Baylin
- SF Hoare
- SL Rosas
- Sushen Zhen
- T Teitz
- WB Chung
- YW Lin
- Publication venue
- BioMed Central
- Publication date
- 01/11/2002
- Field of study
BACKGROUND: Hepatocellular carcinoma (HCC) presents one of the major health threats in China today. A better understanding of the molecular genetics underlying malignant transformation of hepatocytes is critical to success in the battle against this disease. The methylation state of C5 of the cytosine in the CpG di-nucleotide that is enriched within or near the promoter region of over 50 % of the polymerase II genes has a drastic effect on transcription of these genes. Changes in the methylation profile of the promoters represent an alternative to genetic lesions as causative factors for the tumor-specific aberrant expression of the genes. METHODS: We have used the methylation specific PCR method in conjunction with DNA sequencing to assess the methylation state of the promoter CpG islands of twenty genes. Aberrant expression of these genes have been attributed to the abnormal methylation profile of the corresponding promoter CpG islands in human tumors. RESULTS: While the following sixteen genes remained the unmethylated in all tumor and normal tissues: CDH1, APAF1, hMLH1, BRCA1, hTERC, VHL, RARβ, TIMP3, DAPK1, SURVIVIN, p14(ARF), RB1, p15(INK4b), APC, RASSF1c and PTEN, varying degrees of tumor specific hypermethylation were associated with the p16(INK4a ), RASSF1a, CASP8 and CDH13 genes. For instance, the p16(INK4a )was highly methylated in HCC (17/29, 58.6%) and less significantly methylated in non-cancerous tissue (4/29. 13.79%). The RASSF1a was fully methylated in all tumor tissues (29/29, 100%), and less frequently methylated in corresponding non-cancerous tissue (24/29, 82.75%). CONCLUSIONS: Furthermore, co-existence of methylated with unmethylated DNA in some cases suggested that both genetic and epigenetic (CpG methylation) mechanisms may act in concert to inactivate the p16(INK4a )and RASSF1a in HCC. Finally, we found a significant association of cirrhosis with hypermethylation of the p16(INK4a )and hypomethylation of the CDH13 genes. For the first time, the survey was carried out on such an extent that it would not only provide new insights into the molecular mechanisms underscoring the aberrant expression of the genes in this study in HCC, but also offer essential information required for a good methylation-based diagnosis of HCC
The muon system of the Daya Bay Reactor antineutrino experiment
- Author
- An EP
- Arcos JD
- Balantekin AB
- Band HR
- Beriguete W
- Bishai M
- Blyth S
- Brown RE
- Butorov I
- Cao GF
- Cao J
- Carr R
- Chan YL
- Chang JF
- Chang L
- Chang Y
- Chasman C
- Chen HS
- Chen HY
- Chen QY
- Chen SJ
- Chen SM
- Chen XC
- Chen XH
- Chen Y
- Chen YX
- Cheng YP
- Cherwinka JJ
- Chu MC
- Cummings JP
- Dale E
- Deng ZY
- Ding YY
- Diwan MV
- Draeger E
- Du XF
- Dwyer DA
- Edwards WR
- Ely SR
- Fu JY
- Ge LQ
- Gill R
- Goett J
- Gonchar M
- Gong GH
- Gong H
- Gu WQ
- Guan MY
- Guo XH
- Hackenburg RW
- Han GH
- Hans S
- He M
- He Q
- Heeger KM
- Heng YK
- Hinrichs P
- Hor YK
- Hsiung YB
- Hu BZ
- Hu LJ
- Hu LM
- Hu T
- Hu W
- Huang EC
- Huang HX
- Huang HZ
- Huang XT
- Huber P
- Hussain G
- Isvan Z
- Jaffe DE
- Jaffke P
- Jetter S
- Ji XL
- Ji XP
- Jiang HJ
- Jiao JB
- Johnson RA
- Kang L
- Kebwaro JM
- Kettell SH
- Kramer M
- Kwan KK
- Kwok MW
- Kwok T
- Lai WC
- Lai WH
- Lau K
- Lebanowski L
- Lee J
- Lei RT
- Leitner R
- Leung JKC
- Leung KY
- Lewis CA
- Li DJ
- Li F
- Li GS
- Li QJ
- Li WD
- Li XN
- Li XQ
- Li YZB
- Liang H
- Lin CJ
- Lin GL
- Lin PY
- Lin SK
- Link JM
- Littenberg L
- Littlejohn BR
- Liu DW
- Liu H
- Liu JC
- Liu JL
- LIU S
- Liu YB
- Lu C
- Lu HQ
- Luk KB
- Ma QM
- Ma XB
- Ma XY
- Ma YQ
- McDonald KT
- McFarlane MC
- McKeown RD
- Meng Y
- Mitchell I
- Mohapatra D
- Morgan JE
- Nakajima Y
- Napolitano J
- Naumov D
- Naumova E
- Nemchenok I
- Newsom C
- Ngai HY
- Ngai WK
- Ning Z
- Ochoa-Ricoux JP
- Olshevski A
- Patton S
- Pearson CE
- Pec V
- Peng JC
- Piilonen LE
- Pinsky L
- Pun JCS
- Qi FZ
- Qi M
- Qian X
- Raper N
- Ren B
- Ren J
- Rosero R
- Roskovec B
- Ruan XC
- Shao BB
- Steiner H
- Sun GX
- Sun JL
- Tam YH
- Tang X
- Themann H
- Tsang KV
- Tsang RHM
- Tull CE
- Tung YC
- Viren B
- Virostek S
- Vorobel V
- Wang CH
- Wang LS
- Wang LY
- Wang LZ
- Wang M
- Wang NY
- Wang RG
- Wang W
- Wang WW
- Wang X
- Wang YF
- Wang Z
- Wang Z
- Wang ZM
- Webber DM
- Wei HY
- Wei YD
- Wen LJ
- Whisnant K
- White CG
- Whitehead L
- Wilhelmi J
- Wise T
- Wong HLH
- Wong SCF
- Worcester E
- Wu Q
- Xia DM
- Xia JK
- Xia X
- Xing ZZ
- Xu GH
- Xu J
- Xu JL
- Xu JY
- Xu Y
- Xue T
- Yan J
- Yang CG
- Yang L
- Yang MS
- Yang MT
- Ye M
- Yeh M
- Yeh YS
- Young BL
- Yu GY
- Yu JY
- Yu ZY
- Zang SL
- Zhan L
- Zhang C
- Zhang FH
- Zhang JW
- Zhang K
- Zhang QM
- Zhang SH
- Zhang YH
- Zhang YM
- Zhang YX
- Zhang ZJ
- Zhang ZP
- Zhang ZY
- Zhao J
- Zhao QW
- Zhao Y
- Zhao YB
- Zheng L
- Zhong WL
- Zhou L
- Zhou ZY
- Zhuang HL
- Zou JH
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2015
- Field of study
postprin
Pan-cancer analysis of whole genomes
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- The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium View Correspondence (jump link)
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- Publication venue
- Publication date
- 11/12/2019
- Field of study
Cancer is driven by genetic change, and the advent of massively parallel sequencing has enabled systematic documentation of this variation at the whole-genome scale(1-3). Here we report the integrative analysis of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types from the Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium of the International Cancer Genome Consortium (ICGC) and The Cancer Genome Atlas (TCGA). We describe the generation of the PCAWG resource, facilitated by international data sharing using compute clouds. On average, cancer genomes contained 4-5 driver mutations when combining coding and non-coding genomic elements; however, in around 5% of cases no drivers were identified, suggesting that cancer driver discovery is not yet complete. Chromothripsis, in which many clustered structural variants arise in a single catastrophic event, is frequently an early event in tumour evolution; in acral melanoma, for example, these events precede most somatic point mutations and affect several cancer-associated genes simultaneously. Cancers with abnormal telomere maintenance often originate from tissues with low replicative activity and show several mechanisms of preventing telomere attrition to critical levels. Common and rare germline variants affect patterns of somatic mutation, including point mutations, structural variants and somatic retrotransposition. A collection of papers from the PCAWG Consortium describes non-coding mutations that drive cancer beyond those in the TERT promoter(4); identifies new signatures of mutational processes that cause base substitutions, small insertions and deletions and structural variation(5,6); analyses timings and patterns of tumour evolution(7); describes the diverse transcriptional consequences of somatic mutation on splicing, expression levels, fusion genes and promoter activity(8,9); and evaluates a range of more-specialized features of cancer genomes(8,10-18).Peer reviewe
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- Y Nishio
- Y Nishio
- Y Nishio
- Y Pan
- Y Pan
- Y Pan
- Y Shi
- Y Takagi
- Y Tang
- Y Tsujita
- Y Tsujita
- Y Tsukahara
- Y Wang
- Y Wang
- Y Ward
- Y Xu
- Y Yuan
- Y Zhao
- Y Zhao
- Y Zhao
- YC Tseng
- YF Chong
- YF Chong
- YF Chong
- YF Chong
- YF Chong
- YF Chong
- YF Chong
- YF Chong
- YF Shutilin
- YG Lei
- YG Lin
- YH Ha
- YH Kao
- YH Kuo
- YH Kuo
- YH Mariam
- YH Na
- YJ Shur
- YJ Shur
- YJ Tong
- YK Dai
- YM Lee
- YP Chen
- YP Huang
- YQ Guo
- YS Chun
- YS Chun
- YS Chun
- YS Lu
- YT Cha
- YT Hsieh
- YT Hsieh
- YT Yeo
- YT Yeo
- YT Yeo
- YT Yeo
- YT Yeo
- YT Yeo
- YW Cheung
- YW Cheung
- YW Cheung
- YW Cheung
- YW Cho
- YY Chien
- YY Wang
- YZ Meng
- Z Benabdelghani
- Z Benabdelghani
- Z Benabdelghani
- Z Benabdelghani
- Z Chai
- Z Chai
- Z Chai
- Z Chai
- Z Chai
- Z Sun
- Z Zhang
- Z Zhang
- Z Zhong
- Z Zhong
- ZB Qiu
- ZB Qiu
- ZB Qiu
- ZB Qiu
- ZB Qiu
- ZG Gardlund
- ZH Ping
- ZH Ping
- ZL Zhou
- ZS Nurkeeva
- ZX Zhang
- ZY Yang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study