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[喉鳞状细胞癌瘤内淋巴管生成与淋巴转移关系的研究]

[Study on relationship between intratumoral lymphangiogenesis of laryngeal squamous cell carcinoma and lymphatic metastasis].

作者信息

Huangfu Hui, Kong Weijia, Gong Shusheng, Wang Binquan, Zhang Chunming

机构信息

Department of Otorhinolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

出版信息

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 May;22(9):385-8.

Abstract

OBJECTIVE

To elucidate the relationship between the intratumoral lymphangiogenesis and lymphatic metastasis, and provide some theoretic evidence for the judgement of lymph node metastasis and prognosis of laryngeal squamous cell carcinoma (LSCC), also for the treatment.

METHOD

Immunohistochemical analysis was performed to 50 specimens of LSCC with lymphatic endothelial marker (Lymphatic vessel endothelial hyaluronan receptor-1 LYVE-1), the vascular endothelial marker CD34 and the pKi67 proliferation marker to record lymphatic vessel density (LVD). Quantitation of lymphangiogenesis growth factor VEGF-C by RT- PCR was performed to 30 specimens of LSCC. Finally the correlation between LVD and tumor TNM grade, VEGF-C mRNA, grade of diffraction was analyzed with statistics methods.

RESULT

Newly proliferating lymphatic vessel were observed in all LSCC. The median copy number of VEGF-c mRNA was 4-5-fold higher in LSCC than in adjacent normal tissue. There was correlation between tumor VEGF-C mRNA copy number and intratumoral LVD (n =30, P <0.05), there was no significant association between LVD and sex, T stage and grade of diffraction (n =50, P >0.05) but N stage (n = 50, P <0.05).

CONCLUSION

Newly proliferating lymphatic vessels existed in LSCC. There was correlation between high levels of LVD in LSCC than in normal tissue. And the high level of VEGF-C may accelerate the lymphatic metastasis by promoting the proliferation of intratumoral lymphatic.

摘要

目的

阐明喉鳞状细胞癌(LSCC)瘤内淋巴管生成与淋巴转移之间的关系,为判断喉鳞状细胞癌的淋巴结转移及预后,以及治疗提供理论依据。

方法

对50例LSCC标本采用淋巴管内皮标志物(淋巴管内皮透明质酸受体-1,LYVE-1)、血管内皮标志物CD34及pKi67增殖标志物进行免疫组化分析,记录淋巴管密度(LVD)。对30例LSCC标本采用逆转录-聚合酶链反应(RT-PCR)定量检测淋巴管生成生长因子VEGF-C。最后采用统计学方法分析LVD与肿瘤TNM分级、VEGF-C mRNA、分化程度之间的相关性。

结果

在所有LSCC中均观察到新生淋巴管。LSCC中VEGF-c mRNA的中位拷贝数比癌旁正常组织高4-5倍。肿瘤VEGF-C mRNA拷贝数与瘤内LVD之间存在相关性(n = 30,P < 0.05),LVD与性别、T分期及分化程度之间无显著相关性(n = 50,P > 0.05),但与N分期相关(n = 50,P < 0.05)。

结论

LSCC中存在新生淋巴管。LSCC中LVD水平高于正常组织,两者存在相关性。高水平的VEGF-C可能通过促进瘤内淋巴管增殖加速淋巴转移。

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