Ishida Masaharu, Sunamura Makoto, Furukawa Toru, Akada Masanori, Fujimura Hiroko, Shibuya Emiko, Egawa Shinichi, Unno Michiaki, Horii Akira
Department of Molecular Pathology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Sendai, Japan.
World J Gastroenterol. 2007 Sep 14;13(34):4593-7. doi: 10.3748/wjg.v13.i34.4593.
To evaluate the significance of BNIP3 in the pathogenesis of pancreatic cancer, we analyzed the relationship between the expression of BNIP3 and survival rate of the patients with pancreatic cancer, or chemosensitivities in pancreatic cancer cell lines, particularly for gemcitabine, the first-line anti-tumor drug for pancreatic cancer.
To compare the expression level of BNIP3 with the resistance to gemcitabine, eight pancreatic cancer cell lines were subjected to gemcitabine treatment and the quantitative real-time RT-PCR method was used to evaluate BNIP3 expression. Immunohistochemical analysis was also performed using 22 pancreatic cancer specimens to study relationship between BNIP3 expression and survival rate.
Although no significantly positive association between BNIP3 mRNA level and gemcitabine chemosensitivity was observed, pancreatic cancer cell lines that were sensitive to gemcitabine treatment tended to show high levels of BNIP3 expression. The converse, an absence of BNIP3 expression, was not correlated with gemcitabine resistance. We further compared the BNIP3 expression profiles of resected primary pancreatic cancer specimens with the prognosis of the patients, and found a tendency of favorable prognosis and low BNIP3 expression.
High levels of BNIP3 expression cannot be used as one of the predicting factors for gemcitabine chemosensitivity, and some yet to be known factors will have to fill the gap for the accurate prediction of pancreatic cancer chemosensitivity to gemcitabine. However, BNIP3 expression may have an impact on prediction of prognosis of patients with pancreatic cancer.
为了评估BNIP3在胰腺癌发病机制中的意义,我们分析了BNIP3表达与胰腺癌患者生存率之间的关系,以及其与胰腺癌细胞系化疗敏感性的关系,特别是对于胰腺癌一线抗肿瘤药物吉西他滨的敏感性。
为了比较BNIP3的表达水平与对吉西他滨的耐药性,对8个胰腺癌细胞系进行吉西他滨处理,并采用定量实时逆转录聚合酶链反应(RT-PCR)方法评估BNIP3的表达。还使用22个胰腺癌标本进行免疫组织化学分析,以研究BNIP3表达与生存率之间的关系。
虽然未观察到BNIP3 mRNA水平与吉西他滨化疗敏感性之间存在显著正相关,但对吉西他滨治疗敏感的胰腺癌细胞系往往显示出较高水平的BNIP3表达。相反,BNIP3表达缺失与吉西他滨耐药性无关。我们进一步比较了切除的原发性胰腺癌标本的BNIP3表达谱与患者的预后,发现预后良好且BNIP3表达较低的趋势。
BNIP3高表达不能作为吉西他滨化疗敏感性的预测因素之一,一些未知因素必须填补这一空白,以准确预测胰腺癌对吉西他滨的化疗敏感性。然而,BNIP3表达可能对胰腺癌患者的预后预测有影响。