中华病理学杂志
中華病理學雜誌
중화병이학잡지
Chinese Journal of Pathology
2012年
10期
667-670
,共4页
徐晨%刘亚岚%黄洁%何德明%侯英勇%纪元%侯君%卢韶华%许建芳%胡沁%石园%赵丽君%谭云山
徐晨%劉亞嵐%黃潔%何德明%侯英勇%紀元%侯君%盧韶華%許建芳%鬍沁%石園%趙麗君%譚雲山
서신%류아람%황길%하덕명%후영용%기원%후군%로소화%허건방%호심%석완%조려군%담운산
结直肠肿瘤%DNA突变分析%聚合酶链反应%序列分析
結直腸腫瘤%DNA突變分析%聚閤酶鏈反應%序列分析
결직장종류%DNA돌변분석%취합매련반응%서렬분석
Colorectal neoplasms%DNA mutational analysis%Polymerase chain reaction%Sequence analysis
目的 探讨结直肠腺癌KRAS基因突变的检测及其临床意义.方法 应用PCR直接测序法检测440例结直肠腺癌患者中KRAS基因第2号外显子突变状况,分析KRAS基因突变与患者性别、年龄、组织学分级及临床分期的关系.结果 440例中男性257例,女性183例,年龄22 ~ 88岁,中位年龄60岁.414例为手术标本,15例为肠镜活检组织,11例为肝转移灶穿刺组织.其中146例检测到KRAS基因第2号外显子突变,突变率为33.2% (146/440).146例中,第12位密码子突变118例,包括突变类型有35G>A(Gly12Asp) 62例、35G>T(Gly12Val) 35例、34G>T(Gly12Cys)9例、34G> A(Gly12Ser)6例、35G> C(Gly12Ala)5例、34G> C(Gly12Arg)1例,第13位密码子突变27例,包括突变类型有38G> A(Gly13Asp) 25例、38G> C(Gly13 Val)1例、37G> T(Gly13Cys)1例,另发现1例第14位密码子突变,40G> A(Val14lle).KRAS基因或第12位密码子突变与患者性别有一定的关系,女性突变率高(P值分别为0.021和0.030),KRAS基因或第12位密码子突变与患者性别的差异在临床分期Ⅲ期患者中仍存在(P值分别为0.007和0.003),但在临床分期Ⅰ期、Ⅱ期和Ⅳ期的患者中差异不明显.KRAS基因或第12位密码子突变与临床特征有一定的关系.临床Ⅱ期和临床Ⅳ期之间KRAS突变率或第12位密码子的突变率差异有统计学意义,P值分别为0.028和0.034.Ⅲ、Ⅳ期之间第12位密码子突变率差异有统计学意义(P=0.011).第13位密码子突变与临床分期无关.结论 结直肠腺癌中约三分之一的患者存在KRAS基因第2号外显子突变,KRAS基因突变可能与患者性别有一定的关系,PCR直接测序可稳定地检测KRAS基因突变状况.
目的 探討結直腸腺癌KRAS基因突變的檢測及其臨床意義.方法 應用PCR直接測序法檢測440例結直腸腺癌患者中KRAS基因第2號外顯子突變狀況,分析KRAS基因突變與患者性彆、年齡、組織學分級及臨床分期的關繫.結果 440例中男性257例,女性183例,年齡22 ~ 88歲,中位年齡60歲.414例為手術標本,15例為腸鏡活檢組織,11例為肝轉移竈穿刺組織.其中146例檢測到KRAS基因第2號外顯子突變,突變率為33.2% (146/440).146例中,第12位密碼子突變118例,包括突變類型有35G>A(Gly12Asp) 62例、35G>T(Gly12Val) 35例、34G>T(Gly12Cys)9例、34G> A(Gly12Ser)6例、35G> C(Gly12Ala)5例、34G> C(Gly12Arg)1例,第13位密碼子突變27例,包括突變類型有38G> A(Gly13Asp) 25例、38G> C(Gly13 Val)1例、37G> T(Gly13Cys)1例,另髮現1例第14位密碼子突變,40G> A(Val14lle).KRAS基因或第12位密碼子突變與患者性彆有一定的關繫,女性突變率高(P值分彆為0.021和0.030),KRAS基因或第12位密碼子突變與患者性彆的差異在臨床分期Ⅲ期患者中仍存在(P值分彆為0.007和0.003),但在臨床分期Ⅰ期、Ⅱ期和Ⅳ期的患者中差異不明顯.KRAS基因或第12位密碼子突變與臨床特徵有一定的關繫.臨床Ⅱ期和臨床Ⅳ期之間KRAS突變率或第12位密碼子的突變率差異有統計學意義,P值分彆為0.028和0.034.Ⅲ、Ⅳ期之間第12位密碼子突變率差異有統計學意義(P=0.011).第13位密碼子突變與臨床分期無關.結論 結直腸腺癌中約三分之一的患者存在KRAS基因第2號外顯子突變,KRAS基因突變可能與患者性彆有一定的關繫,PCR直接測序可穩定地檢測KRAS基因突變狀況.
목적 탐토결직장선암KRAS기인돌변적검측급기림상의의.방법 응용PCR직접측서법검측440례결직장선암환자중KRAS기인제2호외현자돌변상황,분석KRAS기인돌변여환자성별、년령、조직학분급급림상분기적관계.결과 440례중남성257례,녀성183례,년령22 ~ 88세,중위년령60세.414례위수술표본,15례위장경활검조직,11례위간전이조천자조직.기중146례검측도KRAS기인제2호외현자돌변,돌변솔위33.2% (146/440).146례중,제12위밀마자돌변118례,포괄돌변류형유35G>A(Gly12Asp) 62례、35G>T(Gly12Val) 35례、34G>T(Gly12Cys)9례、34G> A(Gly12Ser)6례、35G> C(Gly12Ala)5례、34G> C(Gly12Arg)1례,제13위밀마자돌변27례,포괄돌변류형유38G> A(Gly13Asp) 25례、38G> C(Gly13 Val)1례、37G> T(Gly13Cys)1례,령발현1례제14위밀마자돌변,40G> A(Val14lle).KRAS기인혹제12위밀마자돌변여환자성별유일정적관계,녀성돌변솔고(P치분별위0.021화0.030),KRAS기인혹제12위밀마자돌변여환자성별적차이재림상분기Ⅲ기환자중잉존재(P치분별위0.007화0.003),단재림상분기Ⅰ기、Ⅱ기화Ⅳ기적환자중차이불명현.KRAS기인혹제12위밀마자돌변여림상특정유일정적관계.림상Ⅱ기화림상Ⅳ기지간KRAS돌변솔혹제12위밀마자적돌변솔차이유통계학의의,P치분별위0.028화0.034.Ⅲ、Ⅳ기지간제12위밀마자돌변솔차이유통계학의의(P=0.011).제13위밀마자돌변여림상분기무관.결론 결직장선암중약삼분지일적환자존재KRAS기인제2호외현자돌변,KRAS기인돌변가능여환자성별유일정적관계,PCR직접측서가은정지검측KRAS기인돌변상황.
Objective To explore the clinical significance of KRAS mutation detection in colorectal adenocarcinoma.Methods Paraffin-embedded tissue specimens were obtained from 440 patients with colorectal adenocarcinoma.The genomic DNA was extracted.Mutations of exon 2 of KRAS gene were examined by PCR and direct seqaencing.Results Somatic mutations of KRAS gene were identified in 146 cases,with the mutation rate of 33.2% (146/440).Among these 146 patients,KRAS mutation involved codon 12 in 118 patients,including 35G > A (Gly12Asp,62 cases),35G > T (Gly12Val,35 cases),34G > T (Gly12Cys,9 cases),34G > A (Gly12Ser,6 cases),35G > C (Gly12Ala,5 cases),and 34G> C (Gly12Arg,1 case); in 27 patients the mutation involved codon 13,including 38G > A (Gly13Asp,25 cases),38G > C (Gly13 Val,1 case) and 37G > T (Gly13 Cys,1 case) ; and in one patient,the mutation involved codon 14 with 40G > A (Val14Ile).The status of KRAS or codon 12 mutations in colorectal adenocarcinoma was related to patients' gender (P =0.021 and P =0.030,respectively),and this significant correlation to females was conserved in clinical stage Ⅲ (P =0.007 and P =0.003,respectively),but not in stages Ⅰ,Ⅱ,and Ⅳ.The statns of KRAS or codon 12 mutations was also related to tumor stage.Between stage Ⅱ and stage Ⅳ,the mutation rate of KRAS and codon 12 showed significant difference (P =0.028 and 0.034,respectively).Between stage Ⅲ and stage Ⅳ,only the codon 12 mutation rate showed significant difference (P =O.011).Codon 13 mutation was not related to tumor stage.Conclusion About one third of patients with colorectal adenocarcinoma have KRAS gene mutation,which might be related to patients' gender; and could be consistently detected by PCR and direct sequencing.