gms | German Medical Science

83. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

16.05. - 20.05.2012, Mainz

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Identification of genes associated with laryngeal squamous cell carcinoma by cDNA microarray

Meeting Abstract

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  • corresponding author Xiaohui Shen - Dept. of ORL, HNS, Drum Tower Hospital, Nanjing, China
  • Ni Rongshen - Dept. of ORL, HNS, BenQ Medical Center, Nanjing, China

Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie. 83. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie. Mainz, 16.-20.05.2012. Düsseldorf: German Medical Science GMS Publishing House; 2012. Doc12hnod309

doi: 10.3205/12hnod309, urn:nbn:de:0183-12hnod3092

Veröffentlicht: 4. April 2012

© 2012 Shen et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.

Gliederung

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Objective: In order to identify genes involved in tumorigenesis and development of laryngeal squamous cell carcinoma (LSCC), we compared the gene expression profile between matched adjacent normal tissues and LSCC tissues by cDNA microarray.

Methods: Gene expression profiles were screened using cDNA microarrays which contained the whole human being genome in related adjacent normal tissues and matched LSCC tissues from the same patients. Positive findings within the groups of seven genes invloved in cell cycle/adhesion/motility were verified with Reverse transcription-PCR (RT-PCR) and Western blot.

Results: Expression of 349 genes was significantly different between cases and controls. 112 genes were up-regulated; 237 genes were down-regulated. The results of RT-PCR and Western blot supported the reliability of our microarray analysis.

Conclusion: Our study provides the first evidence that SENP1,CD109,CKS2,Lamininα3,IntegrinαV, Integrinβ8 are up-regulated and Lamininα2 are down-regulated in LSCC. These findings provide a large body of information regarding gene expression profiles associated with LSCC, and also represent a source of potential targets for LSCC therapeutics.

Supported by: Nanjing Health Bureau Foundation