Ichikawa Wataru, Takahashi Takehiro, Suto Kenichi, Nihei Zenro, Shirota Yoshinori, Shimizu Michio, Sasaki Yasutsuna, Hirayama Renzo
Second Department of Surgery, Saitama Medical School, Saitama, Japan.
Int J Cancer. 2004 Dec 20;112(6):967-73. doi: 10.1002/ijc.20511.
Thymidylate synthase (TS) and dihydropyrimidine dehydrogenase (DPD) are important enzymes of DNA de novo synthesis and the salvage pathway in cancer cells, respectively. Intratumoral TS and DPD gene expressions were evaluated to determine the correlation between the expression of the 2 genes in both normal stromal tissues and tissues with different degrees of malignant differentiation in primary gastric cancer. The study population consisted of 78 consecutive patients with advanced gastric cancer who underwent surgical treatment. Laser-captured microdissection of malignant or normal stromal tissues was performed in formalin-fixed, paraffin-embedded specimens. After extraction of RNA, TS and DPD gene expressions were measured by the real-time reverse transcriptional PCR method. Apart from degree of differentiation, TS and DPD in malignant tissue showed no correlation with clinicopathologic factors. TS in malignant tissue was higher in differentiated type cases than undifferentiated type cases (p < 0.01). However, DPD in malignant tissue of undifferentiated type cases was statistically higher than that of differentiated type cases (p < 0.05). In normal stromal tissue, neither TS nor DPD had any correlation with clinicopathologic factors. TS in malignant tissue was statistically higher than in normal stromal tissue in both differentiated and undifferentiated types (p < 0.0001). DPD in differentiated type malignant tissue was statistically lower than in normal stromal tissue (p < 0.001), but no difference was seen in undifferentiated type cases. TS and DPD gene expressions in primary gastric cancer differ according to degree of differentiation and between malignant and normal stromal tissue.
胸苷酸合成酶(TS)和二氢嘧啶脱氢酶(DPD)分别是癌细胞中DNA从头合成和补救途径的重要酶。评估肿瘤内TS和DPD基因表达,以确定这两种基因在原发性胃癌正常基质组织和不同程度恶性分化组织中的表达相关性。研究人群包括78例连续接受手术治疗的晚期胃癌患者。在福尔马林固定、石蜡包埋的标本中对恶性或正常基质组织进行激光捕获显微切割。提取RNA后,采用实时逆转录PCR法检测TS和DPD基因表达。除分化程度外,恶性组织中的TS和DPD与临床病理因素无相关性。分化型病例恶性组织中的TS高于未分化型病例(p<0.01)。然而,未分化型病例恶性组织中的DPD在统计学上高于分化型病例(p<0.05)。在正常基质组织中,TS和DPD均与临床病理因素无相关性。分化型和未分化型恶性组织中的TS在统计学上均高于正常基质组织(p<0.0001)。分化型恶性组织中的DPD在统计学上低于正常基质组织(p<0.001),但未分化型病例中未见差异。原发性胃癌中TS和DPD基因表达因分化程度以及恶性和正常基质组织的不同而存在差异。