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Snail mRNA及E—cadherin mRNA在乳腺癌中的表达及临床意义 被引量:1

The expression of Snail mRNA and E-cadherin mRNA in breast cancer and their clinical significance
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摘要 目的探讨Snail mRNA及E—cadherin mRNA在乳腺浸润性导管癌中的表达及其临床意义。方法应用原位杂交技术测30例乳腺单纯性增生、30例乳腺导管内癌和70例乳腺浸润性导管癌组织中Snail mRNA及E—cadherin mRNA的表达。结果Snail mRNA及E—cadherin mRNA在乳腺单纯性增生、乳腺导管内癌和乳腺浸润性导管癌组织中的阳性率分别为23.3%、46.7%、81.4%和96.7%、66.7%、35.7%,差异有统计学意义(P〈0.01);Snail mRNA及E-cadherin mRNA在同组间表达差异有统计学意义(P〈0.05);Snail mRNA表达与年龄、肿瘤大小和组织学分级无关(P〉0.05),淋巴结转移与否Snail mRNA表达差异有统计学意义(P〈0.01);E-cad mRNA表达与年龄、肿瘤大小无关(P〉0.05),淋巴结转移与否、不同组织学分级E-cad mRNA表达差异有统计学意义(P〈0.01);Snail mRNA与E-cadherin mRNA的表达呈负相关(r=-0.56,P=0.00)。结论Snail mRNA过表达与E-cadherin mRNA低表达可能参与乳腺癌浸润转移的发生,并与淋巴结转移密切相关,因而检测两者的表达对判断乳腺癌预后、转移有重要价值。 Objective To investigate the expressions of Snail mRNA and E-cad mRNA in invasive ductal carcinoma and their clinical significance. Methods The expression of Snail mRNA and E-cad mRNA were detected on mammary gland hyperplasia (30cases), intraductal breast carcinoma (30cases) and invasive ductal carcinoma (70cases)by in situ hybridization. Results The positive expression rate of Snail mRNA and E-cad mRNA in mammary gland hyperplasia, intraductal breast carcinoma and invasive ductal carcinoma were 23.3% ,46. 7% ,81.4% and 96. 7% ,66.7% ,35.7% ,respectively. Therewas significant difference among them( P 〈 0. 01 ). There was difference between Snail mRNA and E-cad mRNA in the same group( P 〈0. 05). Snail mRNA was not related to age, tumor size or histopathological grade ( P 〉 0. 05), but it was related to lymphatic metastasis ( P 〈 0. 01 ). E-cad mRNA was not related to age, tumor size( P 〉 0. 05), but it was related to lymphatic metastasis and histopathological grade( P 〈 0. 01 ). There were positive relationship between Snail mRNA and E-cad mRNA( r = -0. 56, P =0. 00). Conclusions The overexpression of Snail mRNA and low expression of E-cad mRNA were involved in the infiltration and metastasis of breast carcinoma, and they were related to lymphatic metastasis. Therefore, the test of the expression of them were valuable in predicting the prognostic and metastasis of breast carcinoma.
出处 《中国医师杂志》 CAS 2011年第7期912-916,共5页 Journal of Chinese Physician
关键词 钙黏着糖蛋白类/生物合成 转录因子/生物合成 乳腺肿瘤/代谢 Cadherins/BI Transcription factors/BI Breast neoplasms/ME
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  • 1柴丽,康健,谷京城,于广久.喉癌E-钙粘附素蛋白表达[J].中国耳鼻咽喉头颈外科,2004,11(3):189-191. 被引量:2
  • 2张阿丽,王全胜,陈刚,钟亚华,谢丛华,周云峰,马丁.Snail与E-cadherin在上皮性肿瘤中的表达及其临床意义[J].肿瘤,2006,26(5):469-471. 被引量:14
  • 3万进,吴泽宇,林华欢,骆新兰,张威,杜嘉林,姚远,王志度,杨钰.中下段直肠癌E-钙粘附素表达与直肠系膜转移的关系[J].中华消化杂志,2007,27(3):199-200. 被引量:1
  • 4Batlle E, Sancho E, Franci C, et al. The transcription factor snail is a repressor of E2 cadherin gene expression in epithelial tumour cells [ J ]. Nat Cell Biol, 2000, 2 (2) :84-89.
  • 5Miyoshi A, Kitajima Y, Kido S, et al. Snail accelerates cancer invasion by up regulating MMP expression and is associated with poor prognosis of hepatocellular carcinoma [ J ]. Br J Cancer, 2005, 92(2) :252-258.
  • 6Cheng C W, Wu P E, Yu J C, et al. Mechanisms of inactivation of E-cadherin in breast carcinoma: modification of the two-hit hypothesis of tumor suppressor gene [ J ]. Oncogene, 2001, 20 ( 29 ) : 3814-3823.
  • 7Palmer H G, Larriba M J, Carcia J M, et al. The transcription factor SNAIL represses vitamin D receptor expression and responsiveness in human colon cancer [ J ]. Nat Med, 2004, 10(9) :917-919.
  • 8Come C, Amoux V, Bibeau F, et al. Roles of the transcriptionfactors Snail and slug during mammary morphogenesis and breast carcinoma progression [ J ]. J Mammary Gland Biol Neoplasia, 2004, 9(2) : 183-193.
  • 9Cano A, Perez-Moreno M A, Rodrigo L, et al. The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expressi on [J]. Nat Cell Biol, 2000, 2(2) :76-83.
  • 10Wanami L S, Chen H Y, Peiro S, et al. Vascular endothelial growth factor-A stimulates Snail expression in breast tumor cells: Implications for tumor progression [ J]. Exp Cell Res, 2008, 314(13) :2448-2453.

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  • 1Sheng H, Shao J, Townsend CM Jr, et al. Phosphatidylinositol 3-ki- nase mediates proliferative signals in intestinal epithelial ceils [ J ]. Gut,2003, 52(10) :1472-1478.
  • 2van Zijl F, Zulehner G, Petz M, et al. Epithelial-mesenchymal transition in hepatocellular carcinoma [ J ]. Future Oncol, 2009,5 (8) :1169-1179.
  • 3Guarino M, Rubino B, Ballabio G. The role of epithelial-mesen- chymal transition in cancer pathology [ J ]. Pathology, 2007, 39 (3) :305-318.
  • 4Majehrzak A, Witkowska M, Smolewski P. Inhibition of the PI3K/Akt/mTOR signaling pathway in diffuse large B-cell lym- phoma: current knowledge and clinical significance [ J ]. Mole- cules ,2014,19 (9) : 14304-14315.
  • 5Jayasooriya RG, Dilshara MG, Choi YH, et al. Tianeptine sodium salt suppresses TNF-α-induced expression of matrix metalloprotein- ase-9 in human carcinoma cells via suppression of the PI3K/Akt- mediated NF-κB pathway[ J]. Environ Toxicol Pharmacol, 2014, 38(2) :502-509.
  • 6Xue G, Restuccia DF, Lan Q, et al. Akt/PKB-mediated phos- phorylation of Twistl promotes tumor metastasis via mediating cross-talk between PI3K/Akt and TGF-β signaling axes [ J ]. Cancer Discov,2012,2 (3) :248-259.
  • 7Liang W, Hao Z, Han JL, et al. CAV-1 contributes to bladder cancer progression by inducing epithelial-to-mesenchymal transi- tion [ J ]. Urol Oncol,2014,32 ( 6 ) : 855-863.
  • 8Kandil E, Tsumagari K, Ma J, et al. Synergistic inhibition of thy- roid cancer by suppressing MAPK/PI3K,/AKT pathways [ J ]. J Surg Res, 2013,184(2) :898-906.
  • 9Laco J, Ryska A, C6p J, et al. Expression of galectin-3, cytok- eratin 19, neural cell adhesion molecule and E-cadhedrin in cer- tain variants of papillary thyroid carcinoma [ J ]. Cesk Patol, 2008,44 (4) : 103-107.
  • 10胡建兵,刘静,谢文,杨勇,郭华雄,骆骏,郭韦韦,张平,张朋.Twist、E—cadherin及Vimentin在表达及意义宫颈鳞状上皮癌变的[J].中国医师杂志,2012,14(4):473-476. 被引量:5

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