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자료유형
학술저널
저자정보
Gyu-Seok Cho (Soonchunhyang University) Tae Sung Ahn (Soonchunhyang University) Dongjun Jeong (Soonchunhyang University) Jae-Jun Kim (Soonchunhyang University) Chang-Jin Kim (Soonchunhyang University) Hyun-Deuk Cho (Soonchunhyang University) Dong-Kook Park (Dankook University) Moo-Jun Baek (Soonchunhyang University)
저널정보
대한외과학회 Annals of Surgical Treatment and Research 대한외과학회지 Vol.80 No.6
발행연도
2011.6
수록면
404 - 411 (8page)

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Purpose: Recently, two alternatively spliced survivin variants, survivin-ΔEx3 and survivin-2B, were identified in a single copy of the survivin gene. It has been reported that the expressions of survivin splice variants significantly correlates with the clinical results in many types of human carcinoma. We investigated the transcription levels of survivin and its splice variants in human colorectal carcinomas, and analyzed correlations between survivin expression levels and clinicopathologic features. Methods: We used Western blot and real-time quantitative reverse transcription polymerase chain reaction (RT-PCR) to analyze the protein and mRNA expression levels of survivin variants in 51 colorectal carcinomas. The quantitative RT-PCR was performed using primer pairs specific for survivin and each of its splice variants, then normalized for the gene that encodes glyceraldehydes-3-phosphate dehydrogenase. Results: In Western blotting, the protein levels of survivin were higher in the tumor tissue than in normal tissue. The expression of survivin, survivin-2B and survivin-ΔEx3 mRNA was present in 96%, 64.7%, and 82.4% of the samples, respectively. When the pathologic parameters were compared, colorectal cancers of advanced pT stages showed significant decrease in survivin-2B mRNA expression by the quantitative RT-PCR (P < 0.001). Conclusion: The decreased expression of survivin-2B might be related to tumor progression in colorectal cancers. This finding indicates that alternatively spliced variants of survivin may be involved in refining the functions of survivin during tumor progression.

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UCI(KEPA) : I410-ECN-0101-2013-514-002684064