诊断病理学杂志
診斷病理學雜誌
진단병이학잡지
CHINESE JOURNAL OF DIAGNOSTIC PATHOLOGY
2009年
5期
337-339
,共3页
大肠肿瘤%磷酸化丝氨酸/苏氨酸激酶%血管内皮生长因子%微血管密度
大腸腫瘤%燐痠化絲氨痠/囌氨痠激酶%血管內皮生長因子%微血管密度
대장종류%린산화사안산/소안산격매%혈관내피생장인자%미혈관밀도
Colorectal neoplasms%pAkt%VEGF%MVD
目的 检测大肠癌组织磷酸化丝氨酸/苏氨酸激酶(pAkt)、血管内皮生长因子(VEGF)的表达和微血管密度(MVD)及其临床意义.方法 应用免疫组化SP法检测76例大肠癌的pAkt、VEGF和MVD.结果 大肠癌pAkt 和VEGF的阳性表达率分别为73.7%(56/76)和85.5%(65/76).pAkt的阳性表达与肿瘤浸润深度、临床分期和淋巴结转移(P<0.05)及其MVD(P<0.01)显著相关.pAkt阳性组的MVD明显高于阴性组.VEGF的阳性表达与大肠癌的临床分期显著相关(P<0.05).pAkt蛋白表达与VEGF蛋白表达密切相关(P<0.05).结论 pAkt和VEGF与大肠癌发生、发展和转移密切相关,提示阻断pI3K/Akt信号传导通路将对大肠癌的治疗提供新的靶点.
目的 檢測大腸癌組織燐痠化絲氨痠/囌氨痠激酶(pAkt)、血管內皮生長因子(VEGF)的錶達和微血管密度(MVD)及其臨床意義.方法 應用免疫組化SP法檢測76例大腸癌的pAkt、VEGF和MVD.結果 大腸癌pAkt 和VEGF的暘性錶達率分彆為73.7%(56/76)和85.5%(65/76).pAkt的暘性錶達與腫瘤浸潤深度、臨床分期和淋巴結轉移(P<0.05)及其MVD(P<0.01)顯著相關.pAkt暘性組的MVD明顯高于陰性組.VEGF的暘性錶達與大腸癌的臨床分期顯著相關(P<0.05).pAkt蛋白錶達與VEGF蛋白錶達密切相關(P<0.05).結論 pAkt和VEGF與大腸癌髮生、髮展和轉移密切相關,提示阻斷pI3K/Akt信號傳導通路將對大腸癌的治療提供新的靶點.
목적 검측대장암조직린산화사안산/소안산격매(pAkt)、혈관내피생장인자(VEGF)적표체화미혈관밀도(MVD)급기림상의의.방법 응용면역조화SP법검측76례대장암적pAkt、VEGF화MVD.결과 대장암pAkt 화VEGF적양성표체솔분별위73.7%(56/76)화85.5%(65/76).pAkt적양성표체여종류침윤심도、림상분기화림파결전이(P<0.05)급기MVD(P<0.01)현저상관.pAkt양성조적MVD명현고우음성조.VEGF적양성표체여대장암적림상분기현저상관(P<0.05).pAkt단백표체여VEGF단백표체밀절상관(P<0.05).결론 pAkt화VEGF여대장암발생、발전화전이밀절상관,제시조단pI3K/Akt신호전도통로장대대장암적치료제공신적파점.
Objective To study effect of the expression of phosphorylated Akt (pAkt), vascular endothelial growth factor (VEGF) and on intratumour microvessel density (MVD)in colorectal carcinoma tissues. Methods Immunohistochemical method was used to detect the expression of pAkt, VEGF and MVD in 76 colorectal carcinomas. Results Hie positive expression rates of pAkt and VEGF of colorectal carcinoma were 73.7% (56/76)and 85.5% (65/76)respectively. The positive expression of pAkt was correlated to the invasive depth, clinical staging, lymph node metastasis and intratumor MVD. The positive expression of VEGF was closely related to clinical staging. The expression of pAkt and VEGF was positively correlation. Conclusion The results shown that pAkt and VEGF might have important significance in the carcinogenesis, progression, and metastasis of colorectal carcinoma, and p13K/Akt might be as a potentially useful target for therapeutic intervention in colorectal carcinoma patients.