梁军①, 苗蕊①, 邢慧敏②. 血管生成拟态在子宫内膜癌组织中的表达及意义[J]. 中国肿瘤临床, 2015, 42(23): 1124-1127. DOI: 10.3969/j.issn.1000-8179.2015.23.050
引用本文: 梁军①, 苗蕊①, 邢慧敏②. 血管生成拟态在子宫内膜癌组织中的表达及意义[J]. 中国肿瘤临床, 2015, 42(23): 1124-1127. DOI: 10.3969/j.issn.1000-8179.2015.23.050
Jun LIANG1, Rui MIAO1, Huimin XING2. Expression and significance of vasculogenic mimicry in endometrial carcinoma tissues[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2015, 42(23): 1124-1127. DOI: 10.3969/j.issn.1000-8179.2015.23.050
Citation: Jun LIANG1, Rui MIAO1, Huimin XING2. Expression and significance of vasculogenic mimicry in endometrial carcinoma tissues[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2015, 42(23): 1124-1127. DOI: 10.3969/j.issn.1000-8179.2015.23.050

血管生成拟态在子宫内膜癌组织中的表达及意义

Expression and significance of vasculogenic mimicry in endometrial carcinoma tissues

  • 摘要: 目的:探讨血管生成拟态(v asculogenic mimicry,VM)在子宫内膜癌中的表达及其与临床病理特征和预后的关系。方法:收集解放军白求恩国际和平医院2005年1 月至2014年6 月术后随访资料完整的子宫内膜癌标本267 例,采用CD31/PAS双重染色鉴定VM结构,分为VM阳性组与VM阴性组,免疫组织化学SP法检测CD133 的表达。结果:267 例子宫内膜癌患者中65例(24.3%)存在VM。VM的形成与子宫内膜癌FIGO分期(χ2= 9.987 ,P = 0.002),组织学分级(χ2= 11.795 ,P = 0.001),肌层浸润深度(χ2= 5.499,P = 0.019),脉管内有无癌栓(χ2= 22.599,P < 0.001)及淋巴结有无转移(χ2= 7.848,P = 0.005)密切相关。Kaplan-Mei er法生存分析发现VM阳性组生存时间(中位生存时间为51个月)明显低于VM阴性组(中位生存时间为100 个月),二者比较差异具有统计学意义(χ2= 70.973,P < 0.001)。 CD133 在VM阳性组的表达率为75.4%(49/ 65),较VM阴性组58.9%(119/ 202)高,二者比较差异具有统计学意义(χ2= 5.720,P = 0.017)。 结论:VM与子宫内膜癌的发生、发展及恶性度密切相关,是影响患者预后的重要指标,CD133 表达阳性的肿瘤干细胞可能参与子宫内膜癌VM的形成。

     

    Abstract: Objective:To investigate the expression of vasculogenic mimicry (VM) in endometrial carcinoma tissues and its rela -tionship with the clinicopathologic features and prognosis of the disease. Methods:A total of 267 paraffin-embedded endometrial carci -noma specimens of patients with complete follow-up data were collected from the Shijiazhuang Bethune International Peace Hospital between January 2005and June 2014. CD 31-PAS dual staining was performed to identify the VM structure. Tissue samples were then divided into VM-positive and VM-negative groups. CD 133 expression was detected by immunohistochemical streptavidin peroxidase method.Results:Among the 267 endometrial carcinoma patients, 65cases ( 24.3%) were VM positive. VM formation was closely corre-lated with the International Federation of Gynecology and Obstetrics Staging ( χ2=9.987, P=0.002), histodifferentiation grade (χ2=11 .795, P=0.001), myometrial invasion depth (χ2=5.499, P=0.019), vascular cancer embolus (χ2=22.599, P<0.001), and lymph node me -tastasis ( χ2=7.848, P=0.005). Kaplan-Meier survival curve analysis showed that survival time was significantly shorter in the VM-posi -tive group (median survival time was 51months) than in the VM-negative group (median survival time was 100 months) ( χ2=70.973, P<0.001). Moreover, CD 133 expression was significantly higher in the VM-positive group 75.4% (49/65) than in the VM-negative group 58.9% (119/202) (χ2=5.720, P=0.017). Conclusion:VM is closely correlated with the pathogenesis, development, and malignancy of endometrial carcinoma. Furthermore, VM is one of the important indexes influencing the prognosis of this disease. Therefore, CD 133-positive cells may contribute to VM formation.

     

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