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Cross-species hybridization of microarrays for studying tumor transcriptome of brain metastasis

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dc.contributor.authorPark, ES-
dc.contributor.authorKim, SJ-
dc.contributor.authorKim, SW-
dc.contributor.authorYoon, SL-
dc.contributor.authorLeem, SH-
dc.contributor.authorKim, SB-
dc.contributor.authorKim, SM-
dc.contributor.authorPark, YY-
dc.contributor.authorCheong, JH-
dc.contributor.authorWoo, HG-
dc.contributor.authorMills, GB-
dc.contributor.authorFidler, IJ-
dc.contributor.authorLee, JS-
dc.date.accessioned2012-03-28T05:31:00Z-
dc.date.available2012-03-28T05:31:00Z-
dc.date.issued2011-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/6340-
dc.description.abstractAlthough the importance of the cellular microenvironment (soil) during invasion and metastasis of cancer cells (seed) has been well-recognized, technical challenges have limited the ability to assess the influence of the microenvironment on cancer cells at the molecular level. Here, we show that an experimental strategy, competitive cross-species hybridization of microarray experiments, can characterize the influence of different microenvironments on cancer cells by independently extracting gene expression data of cancer and host cells when human cancer cells were xenografted into different organ sites of immunocompromised mice. Surprisingly, the analysis of gene expression data showed that the brain microenvironment induces complete reprogramming of metastasized cancer cells, resulting in a gain of neuronal cell characteristics and mimicking neurogenesis during development. We also show that epigenetic changes coincide with transcriptional reprogramming in cancer cells. These observations provide proof of principle for competitive cross-species hybridization of microarray experiments to characterize the effect of the microenvironment on tumor cell behavior.-
dc.language.isoen-
dc.subject.MESHAnimals-
dc.subject.MESHAstrocytes-
dc.subject.MESHBase Sequence-
dc.subject.MESHBrain Neoplasms-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCoculture Techniques-
dc.subject.MESHDNA Methylation-
dc.subject.MESHDNA Primers-
dc.subject.MESHDNA, Neoplasm-
dc.subject.MESHEpigenesis, Genetic-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMice-
dc.subject.MESHMice, Inbred BALB C-
dc.subject.MESHMice, Nude-
dc.subject.MESHNeoplasm Transplantation-
dc.subject.MESHNeurons-
dc.subject.MESHNucleic Acid Hybridization-
dc.subject.MESHOligonucleotide Array Sequence Analysis-
dc.subject.MESHSpecies Specificity-
dc.subject.MESHTranscriptome-
dc.subject.MESHTransplantation, Heterologous-
dc.subject.MESHTumor Microenvironment-
dc.titleCross-species hybridization of microarrays for studying tumor transcriptome of brain metastasis-
dc.typeArticle-
dc.identifier.pmid21987811-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198333/-
dc.contributor.affiliatedAuthor우, 현구-
dc.type.localJournal Papers-
dc.identifier.doi10.1073/pnas.1114210108-
dc.citation.titleProceedings of the National Academy of Sciences of the United States of America-
dc.citation.volume108-
dc.citation.number42-
dc.citation.date2011-
dc.citation.startPage17456-
dc.citation.endPage17461-
dc.identifier.bibliographicCitationProceedings of the National Academy of Sciences of the United States of America, 108(42). : 17456-17461, 2011-
dc.identifier.eissn1091-6490-
dc.relation.journalidJ000278424-
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Journal Papers > School of Medicine / Graduate School of Medicine > Physiology
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