Genetics and epigenetics of liver cancer

Research output: Contribution to journalReviewResearchpeer-review

Standard

Genetics and epigenetics of liver cancer. / Ozen, Cigdem; Yildiz, Gokhan; Dagcan, Alper Tunga; Cevik, Dilek; Ors, Aysegul; Keles, Umur; Topel, Hande; Ozturk, Mehmet.

In: New Biotechnology, Vol. 30, No. 4, 25.05.2013, p. 381-4.

Research output: Contribution to journalReviewResearchpeer-review

Harvard

Ozen, C, Yildiz, G, Dagcan, AT, Cevik, D, Ors, A, Keles, U, Topel, H & Ozturk, M 2013, 'Genetics and epigenetics of liver cancer', New Biotechnology, vol. 30, no. 4, pp. 381-4. https://doi.org/10.1016/j.nbt.2013.01.007

APA

Ozen, C., Yildiz, G., Dagcan, A. T., Cevik, D., Ors, A., Keles, U., Topel, H., & Ozturk, M. (2013). Genetics and epigenetics of liver cancer. New Biotechnology, 30(4), 381-4. https://doi.org/10.1016/j.nbt.2013.01.007

Vancouver

Ozen C, Yildiz G, Dagcan AT, Cevik D, Ors A, Keles U et al. Genetics and epigenetics of liver cancer. New Biotechnology. 2013 May 25;30(4):381-4. https://doi.org/10.1016/j.nbt.2013.01.007

Author

Ozen, Cigdem ; Yildiz, Gokhan ; Dagcan, Alper Tunga ; Cevik, Dilek ; Ors, Aysegul ; Keles, Umur ; Topel, Hande ; Ozturk, Mehmet. / Genetics and epigenetics of liver cancer. In: New Biotechnology. 2013 ; Vol. 30, No. 4. pp. 381-4.

Bibtex

@article{c0c0cfd35d1f45e6ac598fc8c8ab507d,
title = "Genetics and epigenetics of liver cancer",
abstract = "Hepatocellular carcinoma (HCC) represents a major form of primary liver cancer in adults. Chronic infections with hepatitis B (HBV) and C (HCV) viruses and alcohol abuse are the major factors leading to HCC. This deadly cancer affects more than 500,000 people worldwide and it is quite resistant to conventional chemo- and radiotherapy. Genetic and epigenetic studies on HCC may help to understand better its mechanisms and provide new tools for early diagnosis and therapy. Recent literature on whole genome analysis of HCC indicated a high number of mutated genes in addition to well-known genes such as TP53, CTNNB1, AXIN1 and CDKN2A, but their frequencies are much lower. Apart from CTNNB1 mutations, most of the other mutations appear to result in loss-of-function. Thus, HCC-associated mutations cannot be easily targeted for therapy. Epigenetic aberrations that appear to occur quite frequently may serve as new targets. Global DNA hypomethylation, promoter methylation, aberrant expression of non-coding RNAs and dysregulated expression of other epigenetic regulatory genes such as EZH2 are the best-known epigenetic abnormalities. Future research in this direction may help to identify novel biomarkers and therapeutic targets for HCC.",
keywords = "Carcinoma, Hepatocellular/genetics, Epigenesis, Genetic, Epigenomics, Humans, Liver Neoplasms/genetics",
author = "Cigdem Ozen and Gokhan Yildiz and Dagcan, {Alper Tunga} and Dilek Cevik and Aysegul Ors and Umur Keles and Hande Topel and Mehmet Ozturk",
note = "Copyright {\textcopyright} 2013 Elsevier B.V. All rights reserved.",
year = "2013",
month = may,
day = "25",
doi = "10.1016/j.nbt.2013.01.007",
language = "English",
volume = "30",
pages = "381--4",
journal = "New Biotechnology",
issn = "1871-6784",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - Genetics and epigenetics of liver cancer

AU - Ozen, Cigdem

AU - Yildiz, Gokhan

AU - Dagcan, Alper Tunga

AU - Cevik, Dilek

AU - Ors, Aysegul

AU - Keles, Umur

AU - Topel, Hande

AU - Ozturk, Mehmet

N1 - Copyright © 2013 Elsevier B.V. All rights reserved.

PY - 2013/5/25

Y1 - 2013/5/25

N2 - Hepatocellular carcinoma (HCC) represents a major form of primary liver cancer in adults. Chronic infections with hepatitis B (HBV) and C (HCV) viruses and alcohol abuse are the major factors leading to HCC. This deadly cancer affects more than 500,000 people worldwide and it is quite resistant to conventional chemo- and radiotherapy. Genetic and epigenetic studies on HCC may help to understand better its mechanisms and provide new tools for early diagnosis and therapy. Recent literature on whole genome analysis of HCC indicated a high number of mutated genes in addition to well-known genes such as TP53, CTNNB1, AXIN1 and CDKN2A, but their frequencies are much lower. Apart from CTNNB1 mutations, most of the other mutations appear to result in loss-of-function. Thus, HCC-associated mutations cannot be easily targeted for therapy. Epigenetic aberrations that appear to occur quite frequently may serve as new targets. Global DNA hypomethylation, promoter methylation, aberrant expression of non-coding RNAs and dysregulated expression of other epigenetic regulatory genes such as EZH2 are the best-known epigenetic abnormalities. Future research in this direction may help to identify novel biomarkers and therapeutic targets for HCC.

AB - Hepatocellular carcinoma (HCC) represents a major form of primary liver cancer in adults. Chronic infections with hepatitis B (HBV) and C (HCV) viruses and alcohol abuse are the major factors leading to HCC. This deadly cancer affects more than 500,000 people worldwide and it is quite resistant to conventional chemo- and radiotherapy. Genetic and epigenetic studies on HCC may help to understand better its mechanisms and provide new tools for early diagnosis and therapy. Recent literature on whole genome analysis of HCC indicated a high number of mutated genes in addition to well-known genes such as TP53, CTNNB1, AXIN1 and CDKN2A, but their frequencies are much lower. Apart from CTNNB1 mutations, most of the other mutations appear to result in loss-of-function. Thus, HCC-associated mutations cannot be easily targeted for therapy. Epigenetic aberrations that appear to occur quite frequently may serve as new targets. Global DNA hypomethylation, promoter methylation, aberrant expression of non-coding RNAs and dysregulated expression of other epigenetic regulatory genes such as EZH2 are the best-known epigenetic abnormalities. Future research in this direction may help to identify novel biomarkers and therapeutic targets for HCC.

KW - Carcinoma, Hepatocellular/genetics

KW - Epigenesis, Genetic

KW - Epigenomics

KW - Humans

KW - Liver Neoplasms/genetics

U2 - 10.1016/j.nbt.2013.01.007

DO - 10.1016/j.nbt.2013.01.007

M3 - Review

C2 - 23392071

VL - 30

SP - 381

EP - 384

JO - New Biotechnology

JF - New Biotechnology

SN - 1871-6784

IS - 4

ER -

ID: 389913877