中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2008年
7期
911-914
,共4页
程艳丽%林静%张明奎%王付增%程存拴
程豔麗%林靜%張明奎%王付增%程存拴
정염려%림정%장명규%왕부증%정존전
食管肿瘤%细胞凋亡%血管内皮生长因子类%淋巴转移%预后
食管腫瘤%細胞凋亡%血管內皮生長因子類%淋巴轉移%預後
식관종류%세포조망%혈관내피생장인자류%림파전이%예후
Esophageal neoplasms%Apoptosis%Vascular endothelial growth factors%Lymphatic metastasis%Prognosis
目的 探讨食管鳞癌组织中细胞凋亡、血管内皮生长因于(VEGF)的表达与临床病理及预后的关系.方法 采用原位DNA末端标记(TUNEL法)、免疫组化(S-P法)及组织病理学等方法,检测61例原发性食管鳞癌组织中细胞凋亡、VEGF的表达.计算出凋亡指数(AI)并测出VEGF的平均吸光度,进行单因素和多因素COX分析.结果 AI和VEGF吸光度(A)与肿瘤的分化程度、TNM分期有关.低分化程度组和高TNM分期组VEGF吸光度明显高于高分化程度组及低TNM分期组(P<0.01),而其AI值明显低于高分化程度组及低TNM分期组(P<0.01).浸润深度超过肌层组及有淋巴结转移组VEGF明显高于浸润深度未超过肌层及无淋巴结转移组(P<0.01),而AI与浸润深度无关(P>0.05).单因素分析结果显示患者生存率降低与AI、VEGF、TNM分期、淋巴结转移、分化程度和浸润深度有关.将上述指标进行多因素COX分析,结果显示AI、VEGF是独立的预后因素.结论 细胞凋亡和血管形成参与了食管鳞癌的形成;VEGF与食管鳞癌的血管形成密切相关,其表达增高与食管鳞癌的浸润及淋巴结转移有关;AI、VEGF是食管鳞癌独立的预后因素.
目的 探討食管鱗癌組織中細胞凋亡、血管內皮生長因于(VEGF)的錶達與臨床病理及預後的關繫.方法 採用原位DNA末耑標記(TUNEL法)、免疫組化(S-P法)及組織病理學等方法,檢測61例原髮性食管鱗癌組織中細胞凋亡、VEGF的錶達.計算齣凋亡指數(AI)併測齣VEGF的平均吸光度,進行單因素和多因素COX分析.結果 AI和VEGF吸光度(A)與腫瘤的分化程度、TNM分期有關.低分化程度組和高TNM分期組VEGF吸光度明顯高于高分化程度組及低TNM分期組(P<0.01),而其AI值明顯低于高分化程度組及低TNM分期組(P<0.01).浸潤深度超過肌層組及有淋巴結轉移組VEGF明顯高于浸潤深度未超過肌層及無淋巴結轉移組(P<0.01),而AI與浸潤深度無關(P>0.05).單因素分析結果顯示患者生存率降低與AI、VEGF、TNM分期、淋巴結轉移、分化程度和浸潤深度有關.將上述指標進行多因素COX分析,結果顯示AI、VEGF是獨立的預後因素.結論 細胞凋亡和血管形成參與瞭食管鱗癌的形成;VEGF與食管鱗癌的血管形成密切相關,其錶達增高與食管鱗癌的浸潤及淋巴結轉移有關;AI、VEGF是食管鱗癌獨立的預後因素.
목적 탐토식관린암조직중세포조망、혈관내피생장인우(VEGF)적표체여림상병리급예후적관계.방법 채용원위DNA말단표기(TUNEL법)、면역조화(S-P법)급조직병이학등방법,검측61례원발성식관린암조직중세포조망、VEGF적표체.계산출조망지수(AI)병측출VEGF적평균흡광도,진행단인소화다인소COX분석.결과 AI화VEGF흡광도(A)여종류적분화정도、TNM분기유관.저분화정도조화고TNM분기조VEGF흡광도명현고우고분화정도조급저TNM분기조(P<0.01),이기AI치명현저우고분화정도조급저TNM분기조(P<0.01).침윤심도초과기층조급유림파결전이조VEGF명현고우침윤심도미초과기층급무림파결전이조(P<0.01),이AI여침윤심도무관(P>0.05).단인소분석결과현시환자생존솔강저여AI、VEGF、TNM분기、림파결전이、분화정도화침윤심도유관.장상술지표진행다인소COX분석,결과현시AI、VEGF시독립적예후인소.결론 세포조망화혈관형성삼여료식관린암적형성;VEGF여식관린암적혈관형성밀절상관,기표체증고여식관린암적침윤급림파결전이유관;AI、VEGF시식관린암독립적예후인소.
Objective To investigate the relationship between apoptcsis, expressions of VEGF and clinicopathological characteris- tics, and prognosis in esophageal squamous cell carcinoma (ESCC). Methods Sixty-one surgical specimens of primary esophageal squa- mous cell carcinomas were examined for VEGF by immunohistochemical staining (S-P). Apoptcsis was determined by TUNEL (TdT media- ting dUTP-biotin nick end-labeling) method. Clinicopathologic features were examined by histopathology. The prognostic impacts of these pa- rameters were analyzed by univariate and survival analysis. Results AI and VEGF were well correlated with differentiation, TNM stage. Lower tumor differentiation and higher TNM stage were related to decreasing AI and VEGF. In addition, VEGF in the groups of invasion be- yond muscularis and lymph node metastasis is significant higher than that in invasion reaching muacularis and no lymph node metastasis (P <0.01). But there were no significant correlation between AI and invasion( P>0.05). The simple-factor analysis results showed that the decrease of AI, VEGF, lymph node metastases, lower tumor differentiation, and invasion reaching muscularis were related to decrease of sur- vival rate. However, multivariate Cox analysis demonstrated that only AI and VEGF were the significant prognostic factors. Conclusions Apoptosis and angiagenesis participate in ESCC and promote its growth. VEGF is related to angiogenesis of ESCC. The increase of VEGF may promote invasion and lymph node metastasis. AI and VEGF are significant prognostic factors in ESCC.