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纸质出版:2009
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常志伟,王立东,秦艳茹,李苹娟,郭涛,李吉林,常志军,范宗民,何欣,王苒,宋昕.贲门癌家族史阳性患者比较基因组杂交变化特征[J].陆军军医大学学报(原第三军医大学学报),2009,31(09):847-849.
CHANG Zhi-wei,WANG Li-dong,QIN Yan-ru,LI Ping-juan,GUO Tao,LI Ji-ling,CHANG Zhi-jun,FAN Zong-min,HE Xin,WANG Ran,SONG Xin.Characteristics of variation in comparative genomic hybridization from gastric cardia adenocarcinoma patients with family history[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(09):847-849.
常志伟,王立东,秦艳茹,李苹娟,郭涛,李吉林,常志军,范宗民,何欣,王苒,宋昕.贲门癌家族史阳性患者比较基因组杂交变化特征[J].陆军军医大学学报(原第三军医大学学报),2009,31(09):847-849. DOI:
CHANG Zhi-wei,WANG Li-dong,QIN Yan-ru,LI Ping-juan,GUO Tao,LI Ji-ling,CHANG Zhi-jun,FAN Zong-min,HE Xin,WANG Ran,SONG Xin.Characteristics of variation in comparative genomic hybridization from gastric cardia adenocarcinoma patients with family history[J].J Amry Med Univ (J Third Mil Med Univ),2009,31(09):847-849. DOI:
目的 探讨河南食管贲门癌高发区贲门癌肿瘤家族史阳性/阴性患者基因组变化特征。 方法 应用比较基因组杂交技术分析14例贲门癌家族史阳性和28例贲门癌肿瘤家族史阴性患者染色体基因组变化。 结果 贲门癌家族史阳性患者DNA拷贝数扩增高于阴性(>20%)者的染色体部位为20p(FH+ 50% 与 FH- 21%),5p(FH+ 50% 与 FH- 18%),6q(FH+ 43% 与 FH- 18%),16q(FH+ 36% 与 FH- 14%);贲门癌家族史阳性患者DNA拷贝数丢失高于阴性(>20%)者为4q(FH+ 43% 与 FH- 14%)(P>0.05)。1q、3q、6q/p、7p、8q、13q/p、20q/p染色体部位DNA拷贝数扩增和1p、17q/p、19p染色体部位DNA拷贝数丢失在贲门癌家族史阳性和阴性患者中均超过20%(P>0.05)。 结论 20p、5p、6q、16q、4q、17q、 18q、9p、 22q可能存在与贲门癌遗传高易感性相关的关键基因;而1q/p、3q、6q/p、7p、8q、13q/p、20q/p、17q/p、19p可能存在与环境因素相关的贲门癌关键基因。
Objective To characterize the profile of chromosomal imbalances in gastric cardia adenocarcinoma (GCA) with or without family history (GCA FH+ or GCA FH-) in Linzhou
Henan province
and to provide molecular basis to identify the related genes to GCA hereditary susceptibility. Methods Comparative genomic hybridization (CGH) was used to examine 14 cases with GCA FH+ and 28 cases with GCA FH-. Results More frequent DNA copy number gains were observed in GCA FH+ than in GCA FH-. Those with the frequency over 20% were as follows: 20p (FH+ 50% vs FH- 21%)
5p (FH+ 50% vs FH- 18%)
6q (FH+ 43% vs FH- 18%)
16q (FH+ 36% vs FH- 14%
P0.05). More frequent DNA copy number losses were seen in GCA FH+ than in GCA FH-. Those 20% were as follows: 4q (FH+ 43% vs FH- 14%
P0.05). Frequent DNA copy number gains in 1q
3q
6q/p
7p
8q
13q/p
20q/p and frequent DNA copy number losses in 1p
17q/p
19p were both frequent in GCA FH+ and GCA FH- (20%
P0.05). Conclusion Frequent DNA copy number gains on chromosome 20p
5p
6q
and 16q and losses on chromosome 15q in GCA FH+ indicate that these chromosome sites may harbor the genes related with GCA high susceptibility. The similar frequent DNA copy number gains or losses on chromosome 1q/p
3q
6q/p
7p
8q
13q/p
20q/p
17q/p and 19p in GCA FH+ and GCA FH- suggest that genes located in these chromosome sites may be related with environmental risk factors in gastric cardia carcinogenesis.
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