The Curious Case of the HepG2 Cell Line: 40 Years of Expertise

被引:172
作者
Arzumanian, Viktoriia A. [1 ]
Kiseleva, Olga I. [1 ]
Poverennaya, Ekaterina V. [1 ]
机构
[1] Inst Biomed Chem, Moscow 119121, Russia
基金
俄罗斯科学基金会;
关键词
HepG2 cell line; mutations; hepatocellular carcinoma; hepatoblastoma; hepatocytes; HEPATOCELLULAR-CARCINOMA CELLS; PRIMARY HUMAN HEPATOCYTES; GENE-EXPRESSION ANALYSIS; HEPATITIS-B; PROFILING REVEALS; HISTOLOGIC SUBTYPES; SIGNALING PATHWAYS; PROMOTER MUTATIONS; GENOMIC ANALYSIS; DOWN-REGULATION;
D O I
10.3390/ijms222313135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver cancer is the third leading cause of cancer death worldwide. Representing such a dramatic impact on our lives, liver cancer is a significant public health concern. Sustainable and reliable methods for preventing and treating liver cancer require fundamental research on its molecular mechanisms. Cell lines are treated as in vitro equivalents of tumor tissues, making them a must-have for basic research on the nature of cancer. According to recent discoveries, certified cell lines retain most genetic properties of the original tumor and mimic its microenvironment. On the other hand, modern technologies allowing the deepest level of detail in omics landscapes have shown significant differences even between samples of the same cell line due to cross- and mycoplasma infection. This and other observations suggest that, in some cases, cell cultures are not suitable as cancer models, with limited predictive value for the effectiveness of new treatments. HepG2 is a popular hepatic cell line. It is used in a wide range of studies, from the oncogenesis to the cytotoxicity of substances on the liver. In this regard, we set out to collect up-to-date information on the HepG2 cell line to assess whether the level of heterogeneity of the cell line allows in vitro biomedical studies as a model with guaranteed production and quality.
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页数:19
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共 189 条
  • [81] Hep G2 is a hepatoblastoma-derived cell line
    Lopez-Terrada, Dolores
    Cheung, Sau Wai
    Finegold, Milton J.
    Knowles, Barbara B.
    [J]. HUMAN PATHOLOGY, 2009, 40 (10) : 1512 - 1515
  • [82] Histologic subtypes of hepatoblastoma are characterized by differential canonical Wnt and Notch pathway activation in DLK plus precursors
    Lopez-Terrada, Dolores
    Gunaratne, Preethi H.
    Adesina, Adekunle M.
    Pulliam, Joseph
    Hoang, David M.
    Nguyen, Yummy
    Mistretta, Toni-Ann
    Margolin, Judith
    Finegold, Milton J.
    [J]. HUMAN PATHOLOGY, 2009, 40 (06) : 783 - 794
  • [83] Drug-Metabolizing Activity, Protein and Gene Expression of UDP-Glucuronosyltransferases Are Significantly Altered in Hepatocellular Carcinoma Patients
    Lu, Linlin
    Zhou, Juan
    Shi, Jian
    Peng, Xiao-juan
    Qi, Xiao-xiao
    Wang, Ying
    Li, Fang-yuan
    Zhou, Fu-Yuan
    Liu, Liang
    Liu, Zhong-Qiu
    [J]. PLOS ONE, 2015, 10 (05):
  • [84] Transcriptomic and genomic analysis of human hepatocellular carcinomas and hepatoblastomas
    Luo, Jian-Hua
    Ren, Baoguo
    Keryanov, Sergei
    Tseng, George C.
    Rao, Uma N. M.
    Monga, Satdarshan P.
    Strom, Steven
    Demetris, Anthony J.
    Nalesnik, Michael
    Yu, Yan P.
    Ranganathan, Sarangarajan
    Michalopoulos, George K.
    [J]. HEPATOLOGY, 2006, 44 (04) : 1012 - 1024
  • [85] Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity:: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH)
    Luquet, I.
    Lai, J. L.
    Barin, C.
    Baranger, L.
    Bilhou-Nabera, C.
    Lippert, E.
    Gervais, C.
    Talmant, P.
    Cornillet-Lefebvre, P.
    Perot, C.
    Nadal, N.
    Mozziconacci, M. J.
    Lafage-Pochitaloff, M.
    Eclache, V.
    Mugneret, F.
    Lefebvre, C.
    Herens, C.
    Speleman, F.
    Poirel, H.
    Tigaud, I.
    Cabrol, C.
    Rousselot, P.
    Daliphard, S.
    Imbert, M.
    Garand, R.
    Genevieve, F.
    Berger, R.
    Terre, C.
    [J]. LEUKEMIA, 2008, 22 (01) : 132 - 137
  • [86] Microarray-Based Gene Expression Analysis of Hepatocellular Carcinoma
    Maass, Thorsten
    Sfakianakis, Ioannis
    Staib, Frank
    Krupp, Markus
    Galle, Peter R.
    Teufel, Andreas
    [J]. CURRENT GENOMICS, 2010, 11 (04) : 261 - 268
  • [87] Insights Into the Somatic Mutation Burden of Hepatoblastomas From Brazilian Patients
    Marques Aguiar, Talita Ferreira
    Rivas, Maria Prates
    Costa, Silvia
    Maschietto, Mariana
    Rodrigues, Tatiane
    de Barros, Juliana Sobral
    Barbosa, Anne Caroline
    Valieris, Renan
    Fernandes, Gustavo R.
    Bertola, Debora R.
    Cypriano, Monica
    Caminada de Toledo, Silvia Regina
    Major, Angela
    Tojal, Israel
    de Pinho Apezzato, Maria Lucia
    Carraro, Dirce Maria
    Rosenberg, Carla
    Lima da Costa, Cecilia Maria
    Cunha, Isabela W.
    Sarabia, Stephen Frederick
    Terrada, Dolores-Lopez
    Victorino Krepischi, Ana Cristina
    [J]. FRONTIERS IN ONCOLOGY, 2020, 10
  • [88] IGF2 Is Up-regulated by Epigenetic Mechanisms in Hepatocellular Carcinomas and Is an Actionable Oncogene Product in Experimental Models
    Martinez-Quetglas, Iris
    Pinyol, Roser
    Dauch, Daniel
    Torrecilla, Sara
    Tovar, Victoria
    Moeini, Agrin
    Alsinet, Clara
    Portela, Anna
    Rodriguez-Carunchio, Leonardo
    Sole, Manel
    Lujambio, Amaia
    Villanueva, Augusto
    Thung, Swan
    Esteller, Manel
    Zender, Lars
    Llovet, Josep M.
    [J]. GASTROENTEROLOGY, 2016, 151 (06) : 1192 - 1205
  • [89] GREB1 induced by Wnt signaling promotes development of hepatoblastoma by suppressing TGFβ signaling
    Matsumoto, Shinji
    Yamamichi, Taku
    Shinzawa, Koei
    Kasahara, Yuuya
    Nojima, Satoshi
    Kodama, Takahiro
    Obika, Satoshi
    Takehara, Tetsuo
    Morii, Eiichi
    Okuyama, Hiroomi
    Kikuchi, Akira
    [J]. NATURE COMMUNICATIONS, 2019, 10 (1)
  • [90] Taurine and liver diseases: a focus on the heterogeneous protective properties of taurine
    Miyazaki, Teruo
    Matsuzaki, Yasushi
    [J]. AMINO ACIDS, 2014, 46 (01) : 101 - 110