Altered microRNA Expression Patterns in Hepatoblastoma Patients

被引:66
作者
Magrelli, Armando [1 ]
Azzalin, Gianluca [2 ]
Salvatore, Marco [1 ]
Viganotti, Mara [1 ]
Tosto, Fabrizio [1 ]
Colombo, Teresa [2 ]
Devito, Rita [3 ]
Di Masi, Alessandra [4 ]
Antoccia, Antonio [4 ]
Lorenzetti, Stefano [5 ]
Maranghi, Francesca [5 ]
Mantovani, Alberto [5 ]
Tanzarella, Caterina [4 ]
Macino, Giuseppe [2 ]
Taruscio, Domenica [1 ]
机构
[1] Ist Super Sanita, Natl Ctr Rare Dis, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, Dept Cellular Biotechnol & Hematol, Rome, Italy
[3] Bambino Gesu Pediat Hosp, IRCCS, Rome, Italy
[4] Univ Roma Tre, Dept Biol, Rome, Italy
[5] Ist Super Sanita, Unit Vet & Food Toxicol, Dept Food Safety & Vet Publ Hlth, I-00161 Rome, Italy
来源
TRANSLATIONAL ONCOLOGY | 2009年 / 2卷 / 03期
关键词
HEPATOCELLULAR-CARCINOMA; BIRTH CHARACTERISTICS; SUPPRESSOR GENE; OVARIAN-CANCER; IDENTIFICATION; PROLIFERATION; METHYLATION; PROFILES; CLUSTER; MEMBERS;
D O I
10.1593/tlo.09124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Liver cancers in children are rare representing only 1.1% of malignancies, with an annual incidence rate of 1.5 cases per million. Hepatoblastoma and hepatocellular carcinomas are the most common malignancies of the liver occurring in young people aged 15 years or younger. Molecular basis of both tumors are still unclear, and common markers (i. e., CTNNB1, APC, IGF-2) are not always useful in the characterization of sporadic forms; in this respect, microRNA recently associated with carcinogenesis could play a pivotal role in their onset. CTNNB1 and APC were analyzed by sequencing, and IGF-2 promoter methylation status was assessed by methylation-specific polymerase chain reaction. MicroRNA expression was assayed by microarray and quantitative reverse transcription-polymerase chain reaction in hepatoblastoma samples. Although few genomic alterations were detected in ours samples, an altered expression of some microRNA in hepatoblastoma was observed. Unsupervised clustering shows that microRNA profile can distinguish tumor from nontumor tissues. Further analyses of microRNA contents in hepatoblastoma compared with hepatocellular carcinoma highlighted four upregulated microRNA (miR-214, miR-199a, miR-150 [P <.01], and miR-125a [P < .05]) and one downregulated microRNA (miR-148a [P <.01]). In conclusion, although our samples were poorly informative from a genetic point of view, they showed a peculiar microRNA expression pattern compared with nontumor tissues and hepatocellular carcinoma. MicroRNA could represent valid markers for the classification of pediatric liver tumors.
引用
收藏
页码:157 / 163
页数:7
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