相关多药耐药基因产物在胃癌个体化治疗中的临床意义.pdf
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参见附件(167kb)。
splice acceptor site within an exon of the human biotinidase gene [J ] .
Hum Mol Genet ,1997 ,6(5) :7392745.
[13 ] Pomponio RJ ,Narasimhan V , Reynolds TR , et al . DeletionP insertion
mutation that causes biotinidase deficiency may result from the forma2
tion of a quasipalindromic structure[J ] . HumMol Genet ,1996 ,5 (10) :
165721661.
[14 ] Wolf B ,Pomponio RJ ,Norrgard KJ , et al . Delayed2 onset profound bi2
otinidase deficiency[J ] . J Pediatr ,1998 ,132(2) :3622365.
[15 ] Wolf B ,Norrgard K,Pomponio RJ , et al . Profound biotinidase deficien2
cy in two asymptomatic adults[J ] . AmJ Med Genet ,1997 ,73 (1) :529.
[16 ] Xue Y,Yoko A ,Xue L , et al . Haplotype analysis suggests that the two
predominant mutations in Japanese patients with holocarboxylase syn2
thetase deficiency are founder mutations [ J ] . J Hum Genet ,2000 ,45
(6) :3582362.
[17 ] 杨艳玲,山口清次,田上泰子,等.生物素酶缺乏症的诊断与治
疗六例分析[J ] .中华儿科杂志,2003 ,41(4) :2492251.
[18 ] Tang NL ,Hui J ,Yong CK, et al . A genomic approach to mutation anal2
ysis of holocarboxylase synthetase gene in three Chinese patients with
late 2 onset holocarboxylase synthetase deficiency [ J ] . Clin Biochem,2003 ,36 (2) :1452149.
[19 ] Hwu WL , Suzuki Y, Yang X, et al . Late2 onset holocarboxylase syn2
thetase deficiency with homologous R508Wmutation[J ] . J Formos Med
Assoc ,2000 ,99(2) :1742177.
[20 ] Hou JW.Biotin responsive multiple carboxylase deficiency presenting as
diabetic ketoacidosis[J ] . Chang Gung Med J ,2004 ,27(2) :1292133.
收稿日期:2006205202 修回日期:2007203206
相关多药耐药基因产物在胃癌个体化治疗中的临床意义
陶 春1
,罗明慧2
,季加孚3
,林 琳1
,郭 岩2
,张喜才4
,赵静华4
,强 欣1
,张 娟1
(1.内蒙古民族大学医学院,内蒙古 通辽 028000 ; 2.呼伦贝尔市人民医院,内蒙古 海拉尔 021008 ;
3.北京大学临床肿瘤学院,北京 100036 ; 4.内蒙古海拉尔农垦总医院,内蒙古 海拉尔 021000)
中图分类号:R735. 2 ; R969. 3 文献标识码:A 文章编号:100622084(2007) 0720483203
基金项目:内蒙古高等学校科学研究项目(NJ03170)
摘要:为了解胃癌多药耐药基因及其产物表达对化疗效果的影响,应用现代信息技术,收集新近
的有关文献进行综合分析,提出:联合检测 P2糖蛋白、 谷胱苷肽2S 2转移酶、 拓扑异构酶、 肺耐药相关蛋
白等基因及基因产物,对化疗方案的制定及药物的选择意义重大,为开展个体化治疗提供依据。
关键词:胃肿瘤;多药耐药基因产物;检测;个体化治疗
Clinical Signif icance of Products Related to Multidrug Resistance Gene in Individualized Treatment for
Stomach Cancer TAO Chun1
,LUO Ming2hui
2
, JI Jia2 fu3
, et al . (1. Medical College , Inner Mongolia Universi2
ty for Nationalities , Tongliao 028000 , China ; 2. People′ s Hospital in Hulunber City , Hailaer 021008 , China ; 3.
Clinical Tumor College , Beijing University , Beijing 100036 , China ; 4. Hailaer General Hospital of Land Cultiva2
tion , Hailaer 021000 , China)
Abstract : In order to understand the effect of multidrug resistance genes and their gene products on chemo2
therapy for the treatment of stomach cancer ,we collected and analyzed recent articles by using modern information
technology as well as drew a conclution that detection of P2gp、 GST 2 π、 Topo Ⅱ、 LRP and their gene products in
combination not only has an important significance in designing chems and drug selection ,but also provide basis for
individulized treatment .
Key words :Stomach cancer ; Product of multidrug resistance gene ; Detection ; Individualized treatment
肿瘤细胞产生耐药性的原因是多方面的 ,其中以多药耐
药(multi drug resistance ,MDR)最为常见。MDR 是指抗某种细
胞毒药物的耐药细胞对许多结构上无关和作用机制上不同的
其他细胞毒药物产生的交叉耐药。一般可以分为两种 ,一种
为天然性耐药(initial resistance) ,即化疗前已有耐药;另一种为
获得性耐药(acquired resistance ) ,即化疗过程中产生的耐药 ......
Hum Mol Genet ,1997 ,6(5) :7392745.
[13 ] Pomponio RJ ,Narasimhan V , Reynolds TR , et al . DeletionP insertion
mutation that causes biotinidase deficiency may result from the forma2
tion of a quasipalindromic structure[J ] . HumMol Genet ,1996 ,5 (10) :
165721661.
[14 ] Wolf B ,Pomponio RJ ,Norrgard KJ , et al . Delayed2 onset profound bi2
otinidase deficiency[J ] . J Pediatr ,1998 ,132(2) :3622365.
[15 ] Wolf B ,Norrgard K,Pomponio RJ , et al . Profound biotinidase deficien2
cy in two asymptomatic adults[J ] . AmJ Med Genet ,1997 ,73 (1) :529.
[16 ] Xue Y,Yoko A ,Xue L , et al . Haplotype analysis suggests that the two
predominant mutations in Japanese patients with holocarboxylase syn2
thetase deficiency are founder mutations [ J ] . J Hum Genet ,2000 ,45
(6) :3582362.
[17 ] 杨艳玲,山口清次,田上泰子,等.生物素酶缺乏症的诊断与治
疗六例分析[J ] .中华儿科杂志,2003 ,41(4) :2492251.
[18 ] Tang NL ,Hui J ,Yong CK, et al . A genomic approach to mutation anal2
ysis of holocarboxylase synthetase gene in three Chinese patients with
late 2 onset holocarboxylase synthetase deficiency [ J ] . Clin Biochem,2003 ,36 (2) :1452149.
[19 ] Hwu WL , Suzuki Y, Yang X, et al . Late2 onset holocarboxylase syn2
thetase deficiency with homologous R508Wmutation[J ] . J Formos Med
Assoc ,2000 ,99(2) :1742177.
[20 ] Hou JW.Biotin responsive multiple carboxylase deficiency presenting as
diabetic ketoacidosis[J ] . Chang Gung Med J ,2004 ,27(2) :1292133.
收稿日期:2006205202 修回日期:2007203206
相关多药耐药基因产物在胃癌个体化治疗中的临床意义
陶 春1
,罗明慧2
,季加孚3
,林 琳1
,郭 岩2
,张喜才4
,赵静华4
,强 欣1
,张 娟1
(1.内蒙古民族大学医学院,内蒙古 通辽 028000 ; 2.呼伦贝尔市人民医院,内蒙古 海拉尔 021008 ;
3.北京大学临床肿瘤学院,北京 100036 ; 4.内蒙古海拉尔农垦总医院,内蒙古 海拉尔 021000)
中图分类号:R735. 2 ; R969. 3 文献标识码:A 文章编号:100622084(2007) 0720483203
基金项目:内蒙古高等学校科学研究项目(NJ03170)
摘要:为了解胃癌多药耐药基因及其产物表达对化疗效果的影响,应用现代信息技术,收集新近
的有关文献进行综合分析,提出:联合检测 P2糖蛋白、 谷胱苷肽2S 2转移酶、 拓扑异构酶、 肺耐药相关蛋
白等基因及基因产物,对化疗方案的制定及药物的选择意义重大,为开展个体化治疗提供依据。
关键词:胃肿瘤;多药耐药基因产物;检测;个体化治疗
Clinical Signif icance of Products Related to Multidrug Resistance Gene in Individualized Treatment for
Stomach Cancer TAO Chun1
,LUO Ming2hui
2
, JI Jia2 fu3
, et al . (1. Medical College , Inner Mongolia Universi2
ty for Nationalities , Tongliao 028000 , China ; 2. People′ s Hospital in Hulunber City , Hailaer 021008 , China ; 3.
Clinical Tumor College , Beijing University , Beijing 100036 , China ; 4. Hailaer General Hospital of Land Cultiva2
tion , Hailaer 021000 , China)
Abstract : In order to understand the effect of multidrug resistance genes and their gene products on chemo2
therapy for the treatment of stomach cancer ,we collected and analyzed recent articles by using modern information
technology as well as drew a conclution that detection of P2gp、 GST 2 π、 Topo Ⅱ、 LRP and their gene products in
combination not only has an important significance in designing chems and drug selection ,but also provide basis for
individulized treatment .
Key words :Stomach cancer ; Product of multidrug resistance gene ; Detection ; Individualized treatment
肿瘤细胞产生耐药性的原因是多方面的 ,其中以多药耐
药(multi drug resistance ,MDR)最为常见。MDR 是指抗某种细
胞毒药物的耐药细胞对许多结构上无关和作用机制上不同的
其他细胞毒药物产生的交叉耐药。一般可以分为两种 ,一种
为天然性耐药(initial resistance) ,即化疗前已有耐药;另一种为
获得性耐药(acquired resistance ) ,即化疗过程中产生的耐药 ......
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