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喉鳞状细胞癌Paxillin表达的临床意义 被引量:1

Clinical implications of paxillin expressing in laryngeal squamous cell carcinoma
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摘要 目的探讨喉鳞状细胞癌Paxillin蛋白表达的临床意义。方法运用免疫组化S-P法检测石蜡包埋喉鳞癌标本74例,以及癌旁正常组织70例,癌旁轻度、中度、重度不典型增生黏膜上皮组织65、697、2例,分析比较Paxillin蛋白表达水平与患者各类临床资料的相关性及其临床意义。结果喉鳞癌组织Paxillin阳性率明显高于正常组织标本(P<0.05),不同分化程度癌组织的Paxillin阳性率也存在显著性差异,低分化者阳性率明显高于高和中分化组(P=0.001),伴有颈部淋巴结转移者阳性率明显高于无转移者(P=0.000),而且临床Ⅳ期病例阳性率又明显高于其他各期患者(P=0.000)。结论Paxillin的阳性表达水平与喉鳞状细胞癌的分化程度、颈淋巴结转移、临床分期有明显相关性,对其病理过程具有一定影响。 Objective To investigate the clinical implications of paxillin expressing in laryngeal squamous cell carcinoma (LSCC). Methods Included in this study were 74 samples of LSCC, 70 samples of paraeanceous healthy tissue, and 65, 69 and 72 eases of paracanceous dysplastic tissue samples at mild, moderate and severe degrees respectively. The expression of paxillin in them was detected by means of immunohistoehemieal S-P procedures. Then, comparative analysis was made to explore the association of paxillin expressing With various kinds of clinical data and to see its clinical implications of paxillin. Results The positive expressing rate of paxillin in LSCC was significantly higher than that in healthy tissue samples (P〈0.05). Furthermore, such a difference was also seen among the samples with differently differentiating levels, seen with very higher positive expressing rate of paxillin in poorly differentiated cancerous tissues (P 〈 0. 001), very higher positive rate among the eases with neck lymph node metastasis (P 〈 0. 000), and vexy higher positive rate among the eas- es at IV clinical staging (P 〈 0. 000). Conclusions There are significant associations of paxillin expressing with differentiating levels, neck metastasis and clinical staging of LSCC, and the activity of paxiiin expression holds significant implications in the developing course of this tumor.
出处 《中国中西医结合耳鼻咽喉科杂志》 2006年第6期351-353,共3页 Chinese Journal of Otorhinolaryngology in Integrative Medicine
基金 广东省科技厅基金资助项目(2002C30403 2005B10401048)
关键词 喉鳞状细胞癌 PAXILLIN 临床意义 Laryngeal squamous cell carcinoma Paxillin Clinical implications
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  • 1Schwartz MA,Schaller MD,Ginsberg MH.Integrins:emerging paradigms of signal transduction.Ann Rev Cell Dev Biol,1995,11:549-559. 被引量:1
  • 2Richardson A,Malik RK,Hildebrand JD,et al.Inhibition of cell spreading by expression of C-terminal domain of focal adhesion kinase(FAK) is rescued by coexpression of Src or catalytically inactive FAK:arole for paxillin tyrosine phosphorylation.Mol Boil Cell,1997,17:6906-6914. 被引量:1
  • 3Nakamura K,Yano H,Uchida H,et al.Tyrosine phosphorylation of paxillin alpha is involved in temporospatial regulation of paxillin-containing focal adhesion formation and F-actin organization in motile cells.J Biol Chem,2000,275:27155-27164. 被引量:1
  • 4Imamura F,Mukai M,Ayaki M,et al.Y-27632,an inhibitor of rho-associated protein kinase,suppresses tumor cell invation via regulation of focal adhesion and focal adhesion kinase.Jpn J Cancer Res,2000,91:811-816. 被引量:1
  • 5Even RSC,Maoz M,Pokroy E,et al.Tumor cell invasion is promoted by actlvasion of protease activated receptor-1 in cooperation with the alpha beta 5 integrin.J Biol Chem,2001,276:10952-10962. 被引量:1
  • 6李莹,药立波,刘新平,王立峰,韩月恒,林树新,俞强.RNAi引起的Paxillin和p130Cas下调抑制胃癌细胞失巢性生长[J].中国生物化学与分子生物学报,2005,21(3):408-414. 被引量:11
  • 7Lu Z,Jiang G,Blume-jensen P,et al.Epidermal growth factor-induced tumor cell invasion and metastasis initiated by dephosphorylation and downregulatlon of focal adhesion kinase.Mol Cell Biol,2001,21:4016-4031. 被引量:1
  • 8李海刚,谢德荣,黎洪浩,曾弘,曾韵洁,沈溪明.肝细胞癌Paxillin和VEGF的表达及其临床意义[J].中国肿瘤临床,2004,31(7):412-413. 被引量:10

二级参考文献19

  • 1李晓明.血管内皮细胞生长因子及其受体与肿瘤血管形成[J].国外医学(肿瘤学分册),1997,24(1):11-13. 被引量:54
  • 2Sattler M, Pisick E, Morrison PT, et al. Role of the cytoskeletal protein paxillin in oncogenesis [J]. Crit Rev Oncog, 2000, 11 (1):63-76 被引量:1
  • 3Turner CE. Paxillin interactions [J]. J Cell Sci, 2000, 113 (Pt 23):4139-4140 被引量:1
  • 4Inoue K, Ozeki Y, Suganuma T, et al. Vascular endothelial growth factor expression in primary esophageal squamous cell carcinoma. Association with angiogenesis and tumor progression [J]. Cancer, 1997, 79(2): 206~213 被引量:1
  • 5Imamura F, Mukai M, Ayaki M, et al. Y-27632, an inhibitor of rho-associated protein kinase, suppresses tumor cell invasion via regulation of focal adhesion and focal adhesion kinase [J]. Jpn J Cancer Res, 2000, 91(8): 811~816 被引量:1
  • 6Tu LC, Chou CK, Chen HC, et al. Protein kinase C-mediated tyrosine phosphorylation of paxillin and focal adhesion kinase requires cytoskeletal integrity and is uncoupled to mitogen-activated protein kinase activation in human hepatoma cells[J]. J Biomed S 被引量:1
  • 7Munshi N, GroopmanJE, Gill PS, et al. c-Src mediates mitogenic signals and associates with cytoskeletal proteins upon vascular endothelial growth factor stimulation in Kaposi's sarcoma cells [J]. J Immunol, 2000, 164(3): 1169~1174 被引量:1
  • 8Frisch S M, Francis H. Disruption of epithelial cell-matrix interactions induces apoptasis. J Cell Biol, 1994, 124:619-626. 被引量:1
  • 9Schlaepfer D D, Hauck C R, Sieg D J. Signaling through focal adhesion kinase. Prog Biophys Mol Biol , 1999, 71(3-4):435-478. 被引量:1
  • 10Wei L, Yang Y, Yu Q. Tyrosine kinase-dependent,phosphatidylinositol 3'-kinase, and mitogen-activated protein kinase-independent signaling pathways prevent lung adenocarcinoma cells from anoikis. Cancer Res,2001, 61(6) : 2439 - 2444. 被引量:1

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