宁波大学学报(理工版)
寧波大學學報(理工版)
저파대학학보(리공판)
JOURNAL OF NINGBO UNIVERSITY (NSEE)
2001年
1期
96-99
,共4页
胃肠道肿瘤/端粒酶%胃肠道肿瘤/c-myc%分子切缘
胃腸道腫瘤/耑粒酶%胃腸道腫瘤/c-myc%分子切緣
위장도종류/단립매%위장도종류/c-myc%분자절연
目的:探讨胃肠道恶性肿瘤及其切缘组织中c-myc基因mRNA和端粒酶活性表达与手术切缘的安全性关系。方法:用RT-PCR和TRAP方法检测12例胃癌和18例肠癌标本和切缘组织中c-myc基因mRNA和端粒酶活性的表达。结果:(1)胃肠道恶性肿瘤组织中c-myc基因mRNA和端粒酶活性有很高的表达率。(2)肿瘤的上下切缘组织中c-myc基因mRNA和端粒酶活性表达无明显差异。(3)在中心表达阳性的肿瘤中,距中心4 cm以上端粒酶均为阴性表达,而c-myc基因mRNA在距4 cm处仍有小部分呈阳性表达,5 cm处则呈阴性。结论:就c-myc基因mRNA表达和端粒酶活性表达而言,距离肿瘤5 cm可定为肿瘤的分子切缘。
目的:探討胃腸道噁性腫瘤及其切緣組織中c-myc基因mRNA和耑粒酶活性錶達與手術切緣的安全性關繫。方法:用RT-PCR和TRAP方法檢測12例胃癌和18例腸癌標本和切緣組織中c-myc基因mRNA和耑粒酶活性的錶達。結果:(1)胃腸道噁性腫瘤組織中c-myc基因mRNA和耑粒酶活性有很高的錶達率。(2)腫瘤的上下切緣組織中c-myc基因mRNA和耑粒酶活性錶達無明顯差異。(3)在中心錶達暘性的腫瘤中,距中心4 cm以上耑粒酶均為陰性錶達,而c-myc基因mRNA在距4 cm處仍有小部分呈暘性錶達,5 cm處則呈陰性。結論:就c-myc基因mRNA錶達和耑粒酶活性錶達而言,距離腫瘤5 cm可定為腫瘤的分子切緣。
목적:탐토위장도악성종류급기절연조직중c-myc기인mRNA화단립매활성표체여수술절연적안전성관계。방법:용RT-PCR화TRAP방법검측12례위암화18례장암표본화절연조직중c-myc기인mRNA화단립매활성적표체。결과:(1)위장도악성종류조직중c-myc기인mRNA화단립매활성유흔고적표체솔。(2)종류적상하절연조직중c-myc기인mRNA화단립매활성표체무명현차이。(3)재중심표체양성적종류중,거중심4 cm이상단립매균위음성표체,이c-myc기인mRNA재거4 cm처잉유소부분정양성표체,5 cm처칙정음성。결론:취c-myc기인mRNA표체화단립매활성표체이언,거리종류5 cm가정위종류적분자절연。
Objective: To detect the c-myc mRNA and telomerase activity(TA) expression in the tumor center and peripheral tissues of patients with gastrointestinal cancers, and to explore the security of tumor surgical margins. Methods: To detect the expression of c-myc mRNA and TA in tumor tissues ,the approximal and distal peripheral tissues, every lcm away from the tumor margin of 12 gastric and 18 colorectal carcinomas with RT-PCR and TRAP methods respectively.Results: (1)The expression rates of c-myc mRNA and TA in tumor tissues are high. (2)There are no remarkable differences of c-myc mRNA and TA expressions between higher or lower tumor surgical margins. (3)C-myc mRNA and TA can′t be detected in 5-cm away peripheral tissues. Conclusion: Considering C-myc mRNA and TA expression, 5 cm can be defined as molecular margin.