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金黄地鼠舌癌发生过程中增殖性细胞核抗原的表达及淋巴管密度和面积与淋巴道转移的相关性 被引量:1

Expression of PCNA,lymphatic vessel density,lymphatic vessel area and their relationship with lymphaticmetastasis in the hamster tongue cancer development
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摘要 目的通过观察金黄生鼠舌癌发生过程中增殖细胞核抗原(PCNA)的表达情况,分析淋巴管密度和面积的变化与舌癌恶性程度及淋巴道转移的相关性,探讨淋巴管生成与淋巴道转移的关系。方法用1.5%丙烯酰胺-N,N-二甲基-N-丁基-N-甲基丙烯酸乙酯溴化铵(DMBA)丙酮溶液合并创伤方法,诱导金黄地鼠舌癌模型42只,每2周取材7只。采用HE染色确定舌癌的病理变化,PCNA和桥粒斑蛋白(Desmoplakin)免疫组织化学双标记法显示淋巴管增生情况,并测量肿瘤和淋巴管内皮细胞增殖指数(PI)、淋巴管密度(LVD)和淋巴管面积(LVA)作统计学分析。结果金黄地鼠舌癌的形成经历了非典型增生-原位癌-早期浸润癌的过程;在非典型增生组PI(91.55),LVA(7570.23),LVD(2.50);原位癌组PI(113.36),LVA(12105.45),LVD(3.73);早期浸润癌组PI(124.67),LVA(14524.33),LVD(5.33),各组间LVA,LVD,PI差异显著(P<0.05),且PI与LVA及LVD呈正相关(P<0.05);淋巴结转移组PI(130.50),LVA(15430.67),LVD(6.17),非转移组PI(113.00),LVA(12711.67),LVD(3.67),两组差异显著(P<0.05)。结论舌癌发生过程中存在新生淋巴管,舌癌形成过程中微淋巴管的LVA和LVD值增大,与舌癌的恶性程度呈正相关,与淋巴道转移呈正相关。 Objective To investigate the relationship of the lymphangiogenesis and lymphatic metastasis by observing the expression of proliferating cell nuclear antigen in the hamster tongue cancer development and analyzing the correlations of lymph vessel density (LVD), lymphatic vessel area (LVA) and malignance or lymphatic metastasis of tongue cancer ceils. Methods Forty-two hamster tongue cancer models were induced by painting 1.5% 7, 12-dimethylben (a) anthracene (DMBA) acetone solution after scratching, 7 models were sacrificed every two weeks. The pathological changes of tongue cancer were determined by the HE staining. The lymphatic hyperplasia was determined by PCNA and Desmoplakin( DP I + I] ) Immunohistochemical double staining. The tumors and lymphatic endothelial cell proliferation index (proliferation index, PI), lymphatic vessel density (LVD) and lymphatic vessel area (LVA) were measured and statistically analyzed. Results The oncogenesis of tongue was divided into three stages: atypical hyperplasia, carcinoma in situ and early invasive stage; atypical hyperplasia group: PI (91.55), LVA (7570.23), LVD (2.50); carcinoma in situ group: PI (113.36), LVA (12105.45), LVD (3.73); early invasive group: PI (124.67), LVA (14524.33), LVD (5.33). The PI, LVA and LVD were compared among groups above (P 〈 0.05), and the correlation of PI with LVA and LVD was positive ( P 〈 0.05) ; Lymphatic metastasis group: PI ( 130.50), LVA ( 15430.67), LVD (6.17), non lymphatic metastasis group:PI (113), LVA (1:2711.67), LVD (3.67), the PI, LVA and LVD were compared between the two groups above ( P 〈 0.05 ). Conclusion With the development of hamster tongue cancer, lymphatic endothelial cell proliferation activity increased, suggesting that the lymphangiogenesis existed in the tongue carcinogenesis process; the values of the LVD and LVA increased in the hamster tongue cancer development, which was positively correlated with the cancer cell malignance and lymphatic metastasis.
出处 《解剖学报》 CAS CSCD 北大核心 2009年第6期902-908,共7页 Acta Anatomica Sinica
基金 国家自然科学基金资助项目(305400083) 教育部留学回国启动基金资助项目[教外司留(2007)1108]
关键词 舌癌 增殖细胞核抗原 桥粒斑蛋白 免疫组织化学 金黄地鼠 Tongue cancer PCNA Desmoplakin Immunohistochemistry Hamster
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参考文献18

  • 1Virata MLA, Wagner RM, Parry DAD, et al. Molecular-structure of the human Desmoplakin-I and Desmoplakin-II amino terminus [ J ]. Proc Natl Acad Sci USA, 1992,89(2):544-548.
  • 2Omaehi T, Kawai Y, Mizuno R, et al. Immunohistochemieal demonstration of proliferating lymphatic vessels in eoloreetal carcinoma and its clinicopathological significance[J]. Cancer Lett,2007,246(1- 2) : 167-172.
  • 3Eichten A, Hyun WC, Coussens LM. Distinctive features of angiogenesis and lymphangiogenesis determine their functionality during de novo tumor development [ J]. Cancer Res, 2007, 67 ( 11 ) : 5211- 5220.
  • 4Liang P, Hong JW, Ubukata H, et al. Increased density and diameter of lymphatic microvessels correlate with lymph node metastasis in early stage invasive colorectal carcinoma[J]. Virchows Arch,2006,448(5) : 570-575.
  • 5Raju B, Haug SR, Ibrahim SO, et al. High interstitial fluid pressure in rat tongue cancer is related to increased lymph vessel area, tumor size, invasiveness and decreased body weight[J]. J Oral Pathol Med, 2008,37(3) : 137-144.
  • 6Pathak AP, Artemov D, Neeman M, et al. Lymph node metastasis in breast cancer xenografts is associated with increased regions of extravascular drain, lymphatic vessel area, and invasive phenotype[ J ]. Cancer Res, 2006,66(10) :5151-5155.
  • 7Fujita K, Kaku T, Sasaki M, et al. Experimental production of lingual carcinomas in hamsters by local application of 9, 10-Dimethyl-1, 2- Benzanthracene[J]. J Dent Res, 1973,52(2):327-332.
  • 8Valraktaris E, Spyridonidou S, Papakosta V, et al. The hamster model of sequential oral oneogenesis[J]. Oral Oncol,2008,44(4):315-324.
  • 9Schwartz JL, Gu X, Kitties RA, et al. Experimental oral carcinoma of the tongue and buccal mucosa: possible biologic markers linked to cancers at two anatomic sites[ J]. Oral Orcol,2000,36(2) :225-235.
  • 10于大海,温玉明,李龙江,王昌美,王晓毅,付风华.口腔癌VEGF-C表达和血管及淋巴管生成与淋巴道转移关系的研究[J].临床口腔医学杂志,2001,17(1):6-9. 被引量:12

二级参考文献44

  • 1赵洪伟,李龙江,谢文扬.舌根鳞癌颈淋巴结微转移灶检测对预后的影响[J].中国口腔颌面外科杂志,2004,2(3):162-164. 被引量:8
  • 2[1]Pepper MS. Lymphangiogenesis and tumor metastasis: mythos or reality[J]. Clin. Cancer Res, 2001,7:462-468.
  • 3[2]Fisher B. Role of the lymphatic system in dissemination of tumor,in lymph and the lymphatic system led [M]. Mayerson. H.S.324(Charles C. Thomas. Springfield, Illinois.1968).?
  • 4[3]Skobe M. Structure function and molecular control of the skin lymphatic system.[J]. J.Invest. Dermatol. Symp. Proceed, 2000, 5:14-19.
  • 5[4]Partanen TA. Lack of lymphatic vascular specificity of vascular endothelial growth factor erceeptor 3 in 185 vascular tumors[J].Cancer, 1999,86:2406-2412.
  • 6[5]Valtola R. VEGFR-3 and its ligand VEGF-C are associated with angiogenesis in breast cancer [J]. Am J.Pathol, 1999,154:1381-1390.
  • 7[6]Banerji S. LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan[J]. J. Cell Biol, 1999,144:789-801.
  • 8[7]Prevo R. Mouse LYVE-1 is an endocytic receptor for hyaluronan in lymphatic endothelium[M]. J.Biol. Chem,2001:19420-19430.
  • 9[8]Gale NW and Yancopoulos GD. Growth factors acting via endothelial venules cell-specific receptor tyrosine kinases:VEGFs,angiopoietins and ephrins in vascular development [J].Genes Dev,1999,13:1055-1066.
  • 10[9]Lee FC, Tilghmann RC. Lymph vessels in rabbit carcinoma, with a note on the normal lymph vessel structure of the testis [J].Arch Surg, 1993,26:602-616.

共引文献24

同被引文献9

  • 1谢立平,腾河,刘士龙,郑金华.舌癌鼠舌乳头及结缔组织芯扫描电镜观察[J].解剖科学进展,2007,13(1):1-4. 被引量:1
  • 2Laitakari J, Stenback F. Collagen matrix in development and progression of experimentally induced respiratory neoplasms in the hamster[J]. Toxicol Pathol, 2001, 29(5): 514.
  • 3Ushiki T. Collagen fibers, reticular fibers and elastic fibers. A comprehensive understanding from a morphological viewpoint [J]. Arch Histol Cytol, 2002, 65(2): 109.
  • 4Souza LF, Souza VF, Silva LD, et al. Expression of basement membrane laminin in oral squamous cell carcinomas [J]. Braz J Otorhinolaryngol, 2007, 73(6): 768.
  • 5Firth NA, Reade PC. The prognosis of oral mucosal squamous cell carcinomas: a comparison of clinical and histopathological grading and of laminin and type IV collagen staining [ J ]. Aust Dent J, 1996, 41(2): 83.
  • 6Zheng J, Xie L, Teng H, et al. Morphological changes in the lingual papillae and their connective tissue cores on the 7, 12-dimethylbenz [alpha]anthracene (DMBA) stimulated rat experimental model [J]. Okajimas Folia Anat Jpn, 2009, 85(4): 129.
  • 7三浦 裕士.新染色法のすべて[M].东京:医齿药出版株式会社,1999:10.9.
  • 8Sounni NE, Noel A. Membrane type-matrix metalloproteinases and tumor progression [J]. Biochimie, 2005, 87(3-4): 329.
  • 9Gunduz K, Demireli P, Inanir I, et al. Expression of matrix metalloproteinases (MMP-2, MMP-3, and MMP-9) and fibronectin in lichen planus[J]. J Cutan Pathol, 2006, 33(8): 545.

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