Gene expression profiling of human hepatoblastoma using archived formalin-fixed and paraffin-embedded tissues

We elucidated the genetic profile of hepatoblastomas (HBLs) to identify diagnostic and prognostic markers. RNA was extracted from 32 formalin-fixed, paraffin-embedded HBLs and corresponding nonneoplastic liver (NNL) tissues, and cDNA-mediated annealing, selection, extension, and ligation (DASL) chip...

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Veröffentlicht in:Virchows Archiv : an international journal of pathology 2011-04, Vol.458 (4), p.453-465
Hauptverfasser: Shin, Eun, Lee, Kyoung-Bun, Park, Soo-Young, Kim, Soo-Hee, Ryu, Han-Suk, Park, Young-Nyun, Yu, Eunsil, Jang, Ja-June
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container_title Virchows Archiv : an international journal of pathology
container_volume 458
creator Shin, Eun
Lee, Kyoung-Bun
Park, Soo-Young
Kim, Soo-Hee
Ryu, Han-Suk
Park, Young-Nyun
Yu, Eunsil
Jang, Ja-June
description We elucidated the genetic profile of hepatoblastomas (HBLs) to identify diagnostic and prognostic markers. RNA was extracted from 32 formalin-fixed, paraffin-embedded HBLs and corresponding nonneoplastic liver (NNL) tissues, and cDNA-mediated annealing, selection, extension, and ligation (DASL) chip assays were performed. Immunohistochemistry was performed to confirm the expression of Yin Yang 1 ( YY1 ) protein in HBL. Twenty-four genes that were associated with signal transduction, cell–cell adhesion, cell cycle regulation, and apoptosis were differentially expressed in HBL and NNL tissues. Two apoptosis-associated genes, MYCN and BIRC5 , were highly upregulated in HBL. Eight genes, including YY1 and IGF1 , were upregulated in HBL cases that had a poor prognosis. Thirty-eight genes, including YY1 , were differentially expressed according to histologic differentiation of HBL, and the immunohistochemical expression of YY1 was correlated with poor HBL differentiation. Thus, using DASL chip assays, we report the gene expression profiles of HBL, which suggest new candidate prognostic and diagnostic genetic markers and putative therapeutic targets for HBL.
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RNA was extracted from 32 formalin-fixed, paraffin-embedded HBLs and corresponding nonneoplastic liver (NNL) tissues, and cDNA-mediated annealing, selection, extension, and ligation (DASL) chip assays were performed. Immunohistochemistry was performed to confirm the expression of Yin Yang 1 ( YY1 ) protein in HBL. Twenty-four genes that were associated with signal transduction, cell–cell adhesion, cell cycle regulation, and apoptosis were differentially expressed in HBL and NNL tissues. Two apoptosis-associated genes, MYCN and BIRC5 , were highly upregulated in HBL. Eight genes, including YY1 and IGF1 , were upregulated in HBL cases that had a poor prognosis. Thirty-eight genes, including YY1 , were differentially expressed according to histologic differentiation of HBL, and the immunohistochemical expression of YY1 was correlated with poor HBL differentiation. 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RNA was extracted from 32 formalin-fixed, paraffin-embedded HBLs and corresponding nonneoplastic liver (NNL) tissues, and cDNA-mediated annealing, selection, extension, and ligation (DASL) chip assays were performed. Immunohistochemistry was performed to confirm the expression of Yin Yang 1 ( YY1 ) protein in HBL. Twenty-four genes that were associated with signal transduction, cell–cell adhesion, cell cycle regulation, and apoptosis were differentially expressed in HBL and NNL tissues. Two apoptosis-associated genes, MYCN and BIRC5 , were highly upregulated in HBL. Eight genes, including YY1 and IGF1 , were upregulated in HBL cases that had a poor prognosis. Thirty-eight genes, including YY1 , were differentially expressed according to histologic differentiation of HBL, and the immunohistochemical expression of YY1 was correlated with poor HBL differentiation. 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RNA was extracted from 32 formalin-fixed, paraffin-embedded HBLs and corresponding nonneoplastic liver (NNL) tissues, and cDNA-mediated annealing, selection, extension, and ligation (DASL) chip assays were performed. Immunohistochemistry was performed to confirm the expression of Yin Yang 1 ( YY1 ) protein in HBL. Twenty-four genes that were associated with signal transduction, cell–cell adhesion, cell cycle regulation, and apoptosis were differentially expressed in HBL and NNL tissues. Two apoptosis-associated genes, MYCN and BIRC5 , were highly upregulated in HBL. Eight genes, including YY1 and IGF1 , were upregulated in HBL cases that had a poor prognosis. Thirty-eight genes, including YY1 , were differentially expressed according to histologic differentiation of HBL, and the immunohistochemical expression of YY1 was correlated with poor HBL differentiation. Thus, using DASL chip assays, we report the gene expression profiles of HBL, which suggest new candidate prognostic and diagnostic genetic markers and putative therapeutic targets for HBL.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21369802</pmid><doi>10.1007/s00428-011-1043-8</doi><tpages>13</tpages></addata></record>
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subjects Adolescent
Biological and medical sciences
Biomarkers, Tumor - analysis
Biomarkers, Tumor - genetics
Child
Child, Preschool
Female
Formaldehyde
Gastroenterology. Liver. Pancreas. Abdomen
Gene Expression
Gene Expression Profiling - methods
Genetic markers
Hepatoblastoma - genetics
Hepatoblastoma - mortality
Hepatoblastoma - pathology
Humans
Immunohistochemistry
Infant
Investigative techniques, diagnostic techniques (general aspects)
Kaplan-Meier Estimate
Liver Neoplasms - genetics
Liver Neoplasms - mortality
Liver Neoplasms - pathology
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Medicine
Medicine & Public Health
Oligonucleotide Array Sequence Analysis
Original Article
Other diseases. Semiology
Paraffin Embedding
Pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Prognosis
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - analysis
RNA, Messenger - isolation & purification
Tissue Fixation
title Gene expression profiling of human hepatoblastoma using archived formalin-fixed and paraffin-embedded tissues
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