Department of Oncological Science (Surgery II), Oita University Faculty of Medicine, Oita, Japan.
Eur J Cardiothorac Surg. 2010 Feb;37(2):440-5. doi: 10.1016/j.ejcts.2009.05.056. Epub 2009 Aug 20.
The present study examined the clinicopathological impact of survivin expression in oesophageal squamous cell carcinoma (ESCC). In addition, the biological role of anti-apoptosis parameter in ESCC was examined immunohistochemically.
Subjects comprised 71 patients followed up for 5 years after surgery for ESCC and analysed immunohistochemically to examine the clinicopathological impact of survivin expression. Separately, 37 fresh frozen samples of ESCC obtained recently were examined concerning splicing variant expression of survivin using reverse-transcription polymerase chain reaction (RT-PCR).
Immunohistochemical survivin expression was detected in the nuclei of 10 ESCC specimens (14.1%) and cytoplasm of 22 specimens (31.0%). Nuclear expression displayed no clinicopathological implications, but cytoplasmic expression correlated with histological differentiation (p=0.002) and tumour invasion (p=0.073) and showed prognostic impacts in univariate (p=0.0184) and multivariate (p=0.0299) analyses. Survivin, survivin-2B and survivin-deltaEx3 mRNA were amplified in 31 (83.8%), 23 (62.2%) and 26 (70.3%) specimens, respectively, by RT-PCR. Survivin-2B level related significantly with histological differentiation (p=0.038), but no other significant implication was identified between any mRNA and clinicopathological factors.
As a molecular biological anti-apoptotic factor, survivin expression was of use in assessing prognosis in ESCC. Inhibition of survivin may be useful as a molecular biological therapy in ESCC.
本研究检测了生存素在食管鳞状细胞癌(ESCC)中的临床病理影响。此外,还通过免疫组织化学检测了 ESCC 中抗凋亡参数的生物学作用。
本研究共纳入 71 例接受手术治疗的 ESCC 患者,对其进行了 5 年的随访,并通过免疫组织化学检测了生存素表达的临床病理影响。此外,还使用逆转录聚合酶链反应(RT-PCR)检测了最近获得的 37 例 ESCC 新鲜冷冻样本中生存素剪接变异体的表达。
10 例 ESCC 标本(14.1%)的细胞核中检测到生存素的免疫组化表达,22 例标本(31.0%)的细胞质中检测到生存素的免疫组化表达。核表达与临床病理无关,但细胞质表达与组织学分化(p=0.002)和肿瘤侵袭(p=0.073)相关,且在单因素(p=0.0184)和多因素(p=0.0299)分析中具有预后意义。通过 RT-PCR,在 31 例(83.8%)、23 例(62.2%)和 26 例(70.3%)标本中扩增了生存素、生存素-2B 和生存素-deltaEx3 mRNA。生存素-2B 水平与组织学分化显著相关(p=0.038),但其他 mRNA 与临床病理因素之间未发现其他显著相关性。
作为一种分子生物学抗凋亡因子,生存素表达可用于评估 ESCC 的预后。抑制生存素可能对 ESCC 的分子生物学治疗有用。