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Study on STK15 gene abnormality and centrosomal amplification in laryngeal carcinoma / 中华医学遗传学杂志
Article de Zh | WPRIM | ID: wpr-328909
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate STK15 gene abnormality and centrosomal amplification in laryngeal carcinoma.</p><p><b>METHODS</b>STK15 gene mRNA expressional level was tested in 62 cases of laryngeal squamous cell carcinoma and laryngeal squamous cell carcinoma cell line Hep-2 by reverse transcription-polymerase chain reaction(RT-PCR); the mutation of STK15 gene exon 6 and exon 7 in the same tissues and cells was detected by PCR-single strand conformation polymorphism. Immunofluorescent antibodies were used to test centrosomal amplification in Hep-2 cell line as an example.</p><p><b>RESULTS</b>STK15 gene overexpressed in 39 cases of laryngeal carcinoma (63%) and Hep-2 cell line. No mutation was found in exon 6 and exon 7 of STK15 gene in the above tissues and cells. Centrosomal amplification was apparent in Hep-2 cell line. The number of centrosome in a single cell changed from 1 to 7, and Hep-2 cells with amplified centrosomes (more than 2 in one cell) were 11%-23%.</p><p><b>CONCLUSION</b>STK15 gene overexpression and centrosomal amplification were first found in human laryngeal squamous cell carcinoma, which indicated that STK15 gene overexpression leading to centrosomal amplification might occur in the early stage of human laryngeal carcinogenesis and be one of the key mechanisms for the occurrence of laryngeal carcinoma.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Anatomopathologie / ARN messager / Tumeurs du larynx / Exons / Protein-Serine-Threonine Kinases / Centrosome / Aurora kinases / Aurora kinase A / Génétique / Mutation Limites du sujet: Humans langue: Zh Texte intégral: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Année: 2004 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Anatomopathologie / ARN messager / Tumeurs du larynx / Exons / Protein-Serine-Threonine Kinases / Centrosome / Aurora kinases / Aurora kinase A / Génétique / Mutation Limites du sujet: Humans langue: Zh Texte intégral: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Année: 2004 Type: Article