Evidence map›Paper›PMID 21575255›Full record

ArticleBMC medical genomics2011

Comprehensive expressional analyses of antisense transcripts in colon cancer tissues using artificial antisense probes.

Rintaro Saito, Keisuke Kohno, Yuki Okada, Yuko Osada, Koji Numata, Chihiro Kohama, Kazufumi Watanabe, Hajime Nakaoka, Naoyuki Yamamoto, Akio Kanai and 6 more

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Article in BMC medical genomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

16 authors.

Rintaro SaitoInstitute for Advanced Biosciences, Keio University, Tsuruoka 997-0017, Japan.
Keisuke Kohno
Yuki Okada
Yuko Osada
Koji Numata
Chihiro Kohama
Kazufumi Watanabe
Hajime Nakaoka
Naoyuki Yamamoto
Akio Kanai
Hiroshi Yasue
Soichiro Murata
Kuniya Abe
Masaru Tomita
Nobuhiro Ohkohchi
Hidenori Kiyosawa

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have identified thousands of sense-antisense gene pairs across different genomes by computational mapping of cDNA sequences. These studies have shown that approximately 25% of all transcriptional units in the human and mouse genomes are involved in cis-sense-antisense pairs. However, the number of known sense-antisense pairs remains limited because currently available cDNA sequences represent only a fraction of the total number of transcripts comprising the transcriptome of each cell type.

methodsTo discover novel antisense transcripts encoded in the antisense strand of important genes, such as cancer-related genes, we conducted expression analyses of antisense transcripts using our custom microarray platform along with 2376 probes designed specifically to detect the potential antisense transcripts of 501 well-known genes suitable for cancer research.

resultsUsing colon cancer tissue and normal tissue surrounding the cancer tissue obtained from 6 patients, we found that antisense transcripts without poly(A) tails are expressed from approximately 80% of these well-known genes. This observation is consistent with our previous finding that many antisense transcripts expressed in a cell are poly(A)-. We also identified 101 and 71 antisense probes displaying a high level of expression specifically in normal and cancer tissues respectively.

conclusionOur microarray analysis identified novel antisense transcripts with expression profiles specific to cancer tissue, some of which might play a role in the regulatory networks underlying oncogenesis and thus are potential targets for further experimental validation. Our microarray data are available at http://www.brc.riken.go.jp/ncrna2007/viewer-Saito-01/index.html.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCluster AnalysisColonic NeoplasmsDNA, ComplementaryDown-RegulationGene Expression ProfilingGenes, NeoplasmHumansMiceOligonucleotide Array Sequence AnalysisPoly AReverse Transcriptase Polymerase Chain ReactionRNA, AntisenseRNA, MessengerRNA ProbesDNA, ComplementaryPoly ARNA, AntisenseRNA, MessengerRNA Probes

Identifiers

PMID21575255
PMCPMC3125192

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.