不同亚型的大肠侧向发育型肿瘤的KRAS、APC、p53表达(1)
[摘要]目的 比较不同亚型的大肠侧向发育型腫瘤(LST)、≥10 mm隆起型腺瘤、进展期大肠癌的KRAS、APC、p53的基因表达情况，探讨不同亚型LST的分子发生途径。方法 应用高分辨率溶解曲线法(HRM)分别检测2016年1月～2018年7月我院收治的38例颗粒型LST(LST-G)和13例非颗粒型LST(LST-NG)以及60例隆起型腺瘤、48例进展期大肠癌的KRAS、APC、p53的基因表达情况，应用统计学方法比较四组病变的基因表达差异。结果 LST-G，LST-NG，隆起型腺瘤、进展期大肠癌的KRAS、APC、p53突变率分别为52.6%、7.7%、46.7%和60.4%，15.8%、53.8%、20.0%和58.3%，7.9%、46.2%、11.7%和66.7%。LST-NG组KRAS突变率均低于LST-G组、隆起型腺瘤组和进展期大肠癌组，差异有统计学意义(P<0.05)，而LST-G组和隆起型腺瘤组KRAS突变率比较，差异无统计学意义(P>0.05)；LST-NG组APC和p53突变率高于LST-G组和隆起型腺瘤组，差异有统计学意义(P<0.05)，而LST-G组和隆起型腺瘤组APC和p53突变率比较，差异无统计学意义(P>0.05)，LST-NG组的APC和p53突变率低于进展期大肠癌组，但差异无统计学意义(P>0.05)。结论 LST-G和LST-NG的基因表达不同，2种不同亚型的LST可能存在不同的分子发生途径。
[关键词]大肠侧向发育型肿瘤；亚型；高分辨率溶解曲线法；分子发生机制
[中图分类号] R735.34 [文献标识码] A [文章编号] 1674-4721(2019)5(b)-0060-03
Expression of KRAS， APC and p53 in different subtypes of laterally spreading tumors
ZHONG Xuan-fang HUANG Wen-feng LIU Yu-hui
Department of Gastroenterology， Huizhou First People′s Hospital， Guangdong Province， Huizhou 516001， China.
[Abstract] Objective To compare the gene expression of KRAS， APC and p53 in different subtypes of colorectal lateral developmental tumors (LST)， polypoid colorectal adenomas (≥10 mm) and advanced colorectal cancer， and to investigate the molecular pathogenesis of the different subtypes of colorectal lateral developmental tumors. Methods The gene expression of KRAS， APC and p53 in our hospital from January 2016 to July 2018， 38 cases of granular categories (LST-G)， 13 cases of nongranular categories(LST-NG)， 60 cases of polypoid colorectal adenomas and 48 cases of advanced colorectal cancer were detected by High Resolution Melting(HRM). Results The mutation rate of KRAS， APC and p53 in LST-G group， LST-NG group， polypoid adenoma group and colorectal cancer group were 52.6%， 7.7%， 46.7%and 60.4%， 15.8%； 53.8%， 20.0% and 58.3%， 7.9%， 46.2%， 11.7%， and 6.7% respectively. The KRAS mutation rate of LST-NG group were significantly lower than LST-G group， polypoid adenomas group and advanced colorectal cancer group respectively(P<0.05). But there was no significant difference between LST-G group and polypoid adenomas group (P>0.05). The APC and p53 mutation rate of LST-NG group were significantly higher than LST-G and polypoid adenomas group (P<0.05)， whereas the APC and p53 mutation rate were no significant difference between LST-G group and polypoid adenomas group (P>0.05)， the APC and p53 mutation rate in LST-NG group were lower than the advanced colorectal cancer group， but there were no statistically significant difference (P>0.05). Conclusion The differences of gene expression between LST-G and LST-NG may remind the different molecular pathways., http://www.100md.com(钟选芳 黄文峰 刘宇辉)
[关键词]大肠侧向发育型肿瘤；亚型；高分辨率溶解曲线法；分子发生机制
[中图分类号] R735.34 [文献标识码] A [文章编号] 1674-4721(2019)5(b)-0060-03
Expression of KRAS， APC and p53 in different subtypes of laterally spreading tumors
ZHONG Xuan-fang HUANG Wen-feng LIU Yu-hui
Department of Gastroenterology， Huizhou First People′s Hospital， Guangdong Province， Huizhou 516001， China.
[Abstract] Objective To compare the gene expression of KRAS， APC and p53 in different subtypes of colorectal lateral developmental tumors (LST)， polypoid colorectal adenomas (≥10 mm) and advanced colorectal cancer， and to investigate the molecular pathogenesis of the different subtypes of colorectal lateral developmental tumors. Methods The gene expression of KRAS， APC and p53 in our hospital from January 2016 to July 2018， 38 cases of granular categories (LST-G)， 13 cases of nongranular categories(LST-NG)， 60 cases of polypoid colorectal adenomas and 48 cases of advanced colorectal cancer were detected by High Resolution Melting(HRM). Results The mutation rate of KRAS， APC and p53 in LST-G group， LST-NG group， polypoid adenoma group and colorectal cancer group were 52.6%， 7.7%， 46.7%and 60.4%， 15.8%； 53.8%， 20.0% and 58.3%， 7.9%， 46.2%， 11.7%， and 6.7% respectively. The KRAS mutation rate of LST-NG group were significantly lower than LST-G group， polypoid adenomas group and advanced colorectal cancer group respectively(P<0.05). But there was no significant difference between LST-G group and polypoid adenomas group (P>0.05). The APC and p53 mutation rate of LST-NG group were significantly higher than LST-G and polypoid adenomas group (P<0.05)， whereas the APC and p53 mutation rate were no significant difference between LST-G group and polypoid adenomas group (P>0.05)， the APC and p53 mutation rate in LST-NG group were lower than the advanced colorectal cancer group， but there were no statistically significant difference (P>0.05). Conclusion The differences of gene expression between LST-G and LST-NG may remind the different molecular pathways., http://www.100md.com(钟选芳 黄文峰 刘宇辉)