广东医学
廣東醫學
엄동의학
Guangdong Medical Journal
2015年
14期
2161-2164
,共4页
罗玉龙%葛全兴%聂玉强%王红%杜艳蕾%沈波%李瑜元
囉玉龍%葛全興%聶玉彊%王紅%杜豔蕾%瀋波%李瑜元
라옥룡%갈전흥%섭옥강%왕홍%두염뢰%침파%리유원
具核梭杆菌%结直肠癌%荧光定量PCR%荧光原位杂交
具覈梭桿菌%結直腸癌%熒光定量PCR%熒光原位雜交
구핵사간균%결직장암%형광정량PCR%형광원위잡교
Fusobacterium nucleatum%colorectal cancer%FQ-PCR%FISH
目的:探讨具核梭杆菌( Fn)感染与结直肠癌( CRC)的相关性。方法对手术切除、经病理证实的101例CRC组织和配对正常组织进行实时荧光定量PCR(FQ-PCR)检测组织中Fn丰度。随机抽选其中22例CRC和配对正常组织进行荧光原位杂交,验证FQ-PCR的结果,分析Fn的富集度与临床病理指标的相关性。结果两检测方法均证实Fn在CRC组织中富集,CRC组织中Fn丰度显著高于配对正常组织者占87.1%(88/101),CRC组织Fn丰度归一化值为0.242±0.034,显著高于配对正常组织的0.050±0.017(P=0.000)。 Fn的高丰度与患者的性别、年龄、肿瘤位置、分化程度、浸润程度、Dukes分期等临床病理指标均无显著相关性( P>0.05),而与淋巴转移密切相关( P<0.05)。结论 Fn在CRC组织中富集,并有可能促进淋巴结转移。
目的:探討具覈梭桿菌( Fn)感染與結直腸癌( CRC)的相關性。方法對手術切除、經病理證實的101例CRC組織和配對正常組織進行實時熒光定量PCR(FQ-PCR)檢測組織中Fn豐度。隨機抽選其中22例CRC和配對正常組織進行熒光原位雜交,驗證FQ-PCR的結果,分析Fn的富集度與臨床病理指標的相關性。結果兩檢測方法均證實Fn在CRC組織中富集,CRC組織中Fn豐度顯著高于配對正常組織者佔87.1%(88/101),CRC組織Fn豐度歸一化值為0.242±0.034,顯著高于配對正常組織的0.050±0.017(P=0.000)。 Fn的高豐度與患者的性彆、年齡、腫瘤位置、分化程度、浸潤程度、Dukes分期等臨床病理指標均無顯著相關性( P>0.05),而與淋巴轉移密切相關( P<0.05)。結論 Fn在CRC組織中富集,併有可能促進淋巴結轉移。
목적:탐토구핵사간균( Fn)감염여결직장암( CRC)적상관성。방법대수술절제、경병리증실적101례CRC조직화배대정상조직진행실시형광정량PCR(FQ-PCR)검측조직중Fn봉도。수궤추선기중22례CRC화배대정상조직진행형광원위잡교,험증FQ-PCR적결과,분석Fn적부집도여림상병리지표적상관성。결과량검측방법균증실Fn재CRC조직중부집,CRC조직중Fn봉도현저고우배대정상조직자점87.1%(88/101),CRC조직Fn봉도귀일화치위0.242±0.034,현저고우배대정상조직적0.050±0.017(P=0.000)。 Fn적고봉도여환자적성별、년령、종류위치、분화정도、침윤정도、Dukes분기등림상병리지표균무현저상관성( P>0.05),이여림파전이밀절상관( P<0.05)。결론 Fn재CRC조직중부집,병유가능촉진림파결전이。
Objective To investigate whether Fusobacterium nucleatum ( Fn) infection is associated with colorec-tal cancer ( CRC) .Methods The resected CRC ( pathologically confirmed) mass and matched normal samples from 101 patients were collected.Quantitative fluorescent polymerase chain reaction ( FQ-PCR) was applied to detect Fn in CRC versus matched normal tissues.Fluorescence in situ hybridization ( FISH) analysis was performed on 22 randomly selected CRC and matched samples to confirm FQ-PCR results.Abundance of Fn was analyzed for association with clinicopatho-logical parameters.Results Both analyses demonstrated that Fn was significantly over-represented in CRC.The rate of Fn over-abundance in CRC tissues versus that in matched normal tissues was 87.1%(88/101).The abundance of Fn was significantly greater in tumor tissues ( 0.242 ±0.034 ) than in matched normal tissues ( 0.050 ±0.017 ) ( P =0.000) .No significant association of Fn load with patients′gender, age, cancer location, stages and infiltration ( P>0.05) but with lymph node metastases (P=0.000) was observed.Conclusion Fn is enriched in the CRC tissues, which may be associated with CRC development and promote lymph node metastasis.