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血管紧张素Ⅱ及其受体1在断端正常鳞状上皮及食管鳞癌中的表达及其差异 被引量:1

Expressions of angiotensin Ⅱ and angiotensin Ⅱ type 1 receptor in normal squamous epithelium and esophageal squamous cell carcinoma and their difference
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摘要 目的:观察食管断端正常鳞状上皮与鳞癌组织中血管紧张素Ⅱ及血管紧张素Ⅱ受体1的表达。方法:实验于2005-07/10在河南省肿瘤重点实验室完成。采用免疫组织化学SP法检测49例食管断端正常鳞状上皮及53例食管鳞癌组织中血管紧张素Ⅱ及血管紧张素Ⅱ受体1的表达。在高倍镜下选取阳性细胞最多的区域,记录5个高倍视野中血管紧张素Ⅱ、血管紧张素Ⅱ受体1阳性细胞的百分比,计算其平均值。阳性细胞<10%为穴-雪;10%~30%为穴+雪;30%~50%为穴誒雪;>50%为穴誔雪。结果:血管紧张素Ⅱ和血管紧张素Ⅱ受体1定位于胞浆和胞膜。血管紧张素Ⅱ主要为弥漫性表达,在正常鳞状上皮和鳞癌组织中的阳性表达率分别是51.02%(25/49)和86.79%(46/53)。血管紧张素Ⅱ受体1在46.94%(23/49)的正常鳞状上皮的扁平细胞层和棘层细胞表达,在77.36%(41/53)的鳞癌组织中主要呈弥漫性表达,部分癌巢可见“阴性外围”表达模式。血管紧张素Ⅱ、血管紧张素Ⅱ受体1在鳞癌组织中的表达均显著高于正常鳞状上皮穴均P<0.01雪。血管紧张素Ⅱ在各级鳞癌组织中的表达差异无显著性穴P>0.05雪;血管紧张素Ⅱ受体1在I级鳞癌组织中的表达显著高于Ⅱ、Ⅲ级鳞癌组织穴分别P<0.05,P<0.01雪,在Ⅱ、Ⅲ级鳞癌组织中的表达差异无显著性穴P>0.05雪。血管紧张素Ⅱ、血管紧张素Ⅱ受体1在鳞癌侵及食管深层和浅层、有淋巴结转移和无淋巴结转移的表达差异均无显著性(P>0.05)。结论:血管紧张素Ⅱ受体1可能与食管鳞癌的分化有关,血管紧张素Ⅱ及其血管紧张素Ⅱ受体1可能参与食管鳞癌的发生发展,但与食管鳞癌的浸润和淋巴结转移无明显关系。 AIM: To observe the expressions of angiotensin Ⅱ (Ang Ⅱ ) and Ang Ⅱ type 1 receptor (AT1R) in the normal squamous epithelium and esophageal squamous cell carcinoma (ESCC). METHODS: The experiment was undertaken in the Henan Key Laboratory for Tumor Pathology from July to October 2005. SP immunohistochemical method was performed to detect the expressions of Ang Ⅱ and AT1R in the ESCC tissues of 53 cases and normal esophageal squamous epithelium of 49 cases. The percentages and average value of Ang Ⅱ and AT1R positive cells were estimated in five high-power fields which comprised the most positive cells, and graded into one of four categories: (-),〈10%; (+),10%-30%; (++),30%-50%; (+++),〉50%. RESULTS: Ang Ⅱ and AT1R were localized in the cytoplasm and membrane of cells, and Ang Ⅱ .was mostly expressed diffusely. The rates of positive expression of Ang Ⅱ in normal esophageal squamous epithelium and ESCC tissues were 51.02% (25/49) and 86.79% (46/53) respectively. AT1R were expressed in the stratum spinosum and pinacocyte layer of 46.94% (23/49) normal esophageal squamous epithelia, and diffusely expressed in 77.36% (41/53) ESCC tissues, with the "negative periphery" pattern was observed in some cancer nests. The expressions of Ang Ⅱ and AT1R were significantly higher in ESCC tissues than in normal esophageal squamous epithelia (P 〈 0.01). There was no significant difference in the expressions of Ang Ⅱ in ESCC tissues of different grades (P 〉 0.05); The expression of AT1R was significantly higher in grade Ⅰ than in grade Ⅱ and grade Ⅲ of ESCC tissues (P 〈 0.05, P 〈 0.01), with no significant difference between grade Ⅱ and grade Ⅲ of ESCC tissues (P 〉 0.05). Differences were also insignificant in the expressions of Ang Ⅱ and AT1R not only between the superficial layer and deep layer of esophagus invaded by ESCC but also between the lymph node metastasis group and non-lymph node metastasis group (P 〉 0.05). CONCLUSION: AT1R may be associated with the differentiation of ESCC. Ang Ⅱ and AT1R are possibly involved in the occurrence and development of ESCC, but unrelated with the infiltration and lymph node metastasis of ESCC.
出处 《中国临床康复》 CAS CSCD 北大核心 2006年第20期101-103,i0004,共4页 Chinese Journal of Clinical Rehabilitation
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  • 1Kikkawa F,Mizuno M,Shibata K,et al.Activation of invasiveness of cervical carcinoma cells by angiotensin-Ⅱ.Am J Obstet Gynecol 2004; 190:1258-63
  • 2Fujimoto Y,Sasaki T,Tsuchida A,et al.Angiotensin-Ⅱ typelreceptor expression in human pancreatic cancer and growth inhibition by angiotensin-Ⅱ type 1 receptor antagonist.FEBS Lett 2001 ;495:197-200
  • 3Suganuma T,Ino K,Shibata K,et al.Functional expression of the angiotensin Ⅱ type 1 receptor in human ovarian carcinoma cells and its blockade therapy resulting in suppression of tumor invasion,angiogenesis,and peritoneal dissemination.Clin Cancer Res 2005; 11:2686-94
  • 4De Nuccio I,Salvati G,Genovesi G,et al.Physiopathology of the reninangiotensin system in the ovary.Minerva Endocrinol 1999;24:77-81
  • 5Ando H,Nagasaka T,Nomura M,et al.Premenstrual disappearance of aminopeptidase A in endometrial stromal cells around endometrial spiralarteries/arterioles during the decidual change.J Clin Endocrinol Metab 2002;87:2303-9
  • 6Inwang ER,Puddefoot JR,Brown CL,et al..Angiotensin Ⅱ type1receptor expression in human breast tissues.Br J Cancer 1997;75:1279-83
  • 7Takeda H,Kondo S.Differences between squamous cell carcinoma and keratoacanthoma in angiotensin type-1 receptor expression.A m J Pathol 2001;158:1633-7
  • 8Nishizuka Y.The molecular heterogeneity of protein kinase C and its implications for cellular regulation.Nature 1988;334:661-5
  • 9Duff JL,Berk BC,Corson MA.Angiotensin Ⅱ stimulates the pp44 and pp42mitogen-activated protein kinases in cultured rat aortic smooth muscle cells.Biochem Biophys Res Commun 1992; 188:257-64
  • 10Nouet S,Nahmias C.Signal transduction from the angiotensin Ⅱ AT2receptor.Trends Endocrinol Metab 2000; 11:1-6

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