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乳腺癌组织中Tuberin和磷酸化Girdin蛋白的表达及临床意义 被引量:1

Expressions of Tuberin and phosphorylated Girdin in breast cancer and their clinical significances
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摘要 目的探讨乳腺癌组织中Tuberin和磷酸化Girdin(p-Girdin)蛋白的表达及其与乳腺癌临床病理特征和分子分型的关系。方法应用免疫组化Envision法检测102例乳腺非特殊型浸润性导管癌、52例乳腺导管原位癌、31例乳腺纤维腺瘤组织中Tuberin及p-Girdin蛋白的表达情况。结果 Tuberin在乳腺非特殊型浸润性导管癌、乳腺导管原位癌、乳腺纤维腺瘤组织中的阳性表达率分别为33.3%、59.6%和77.4%,差异有统计学意义(P<0.05)。Tuberin与乳腺非特殊型浸润性导管癌患者年龄、病理学分期、组织学分级、肿瘤大小、淋巴结转移、雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体(HER-2)无关(P>0.05)。Tuberin在管腔A型、管腔B型、HER-2(+)型和三阴性乳腺非特殊浸润性导管癌中的阳性表达率分别为34.0%、40.0%、31.3%和21.4%,差异无统计学意义(P>0.05)。p-Girdin在乳腺非特殊型浸润性导管癌、乳腺导管原位癌和乳腺纤维腺瘤组织中的阳性表达率分别为64.7%、38.4%和22.6%,差异有统计学意义(P<0.05)。p-Girdin与乳腺非特殊型浸润性导管癌的病理学分期、淋巴结转移数及HER-2状态呈正相关(P<0.05),与患者年龄、组织学分级、肿瘤大小、ER、PR无相关性(P>0.05)。p-Girdin在乳腺非特殊浸润性导管癌的四种分子分型中的阳性表达率分别为57.4%、92.0%、62.5%和42.9%,差异有统计学意义(P>0.05)。Tuberin与p-Girdin在乳腺非特殊浸润性导管癌中的表达无关(P>0.05)。结论乳腺癌组织中Tuberin的表达明显降低,可能具有抑制乳腺癌增殖、侵袭、转移的作用,而p-Girdin的表达可能与乳腺癌的恶性进展密切相关。 Objective To detect the expressions of Tuberin and phosphorylated Girdin( p-Girdin)in breast cancer and its association with pathological characteristics and molecular subtypes of breast cancer.Methods Immunohistochemical Envision chemical method was used to investigate the expression of Tuberin and phosphorylated Girdin( p-Girdin) in 102 cases of non-special type invasive carcinoma( IDCNOS) of breast,52 cases of ductal carcinoma in situ( DCIS),and 31 cases of breast fibroad-noma.Results The expression of Tuberin protein positive expresstion rate was 33.3%,59.6%,77.4%,respectively.There was significant difference among IDC-NOS,DCIS and breast fibroadnoma( P〉 0.05).The expression rate of Tuberin was not related to age,pathologic stage,histological grade,tumor size,lymph node metastasis,estrogen receptor( ER),progesterone receptor( PR) of the patients with IDC-NOS( P〈 0.05).The expression of Tuberin in luminal A,luminal B,human epidermal growth factor receptor 2( HER-2)( +)type and triple negative were 34.0%,40.0%,31.3%,21.4%,respectively.There was no statistically significant difference( P〈 0.05).The expression of p-Girdin protein positive expresstion rate were 64.7%,38.4%,22.6%,respectively.There was statistically significant difference among IDC-NOS,DCIS and breast fibroadnoma( P〈 0.05).The expression of p-Girdin was positively associated with pathologic stage,lymph node metastasis and HER-2( P〈 0.05).But no significant association was identified between p-Girdin expresstion and age of patients,histological grade,tumor size,ER,PR( P〈 0.05).The expression of p-Girdin in luminal A,luminal B,HER-2( +) type and triple negative were 57.4%,92.0%,62.5%,42.9%,the difference was statistically significant( P〈 0.05).The expression of Tuberin and p-Girdin among the IDC-NOS patient has no relevance( P〉 0.05).Conclusion The expression of Tuberin in breast cancer tissues was reduced significantly,and may have inhibition on breast cancer tissues' s proliferation,invasion,metastasis.The expression of phosphorylated Girdin may have relationship with deterioration of breast cancer.
出处 《中国肿瘤临床与康复》 2014年第10期1153-1157,共5页 Chinese Journal of Clinical Oncology and Rehabilitation
关键词 乳腺肿瘤 TUBERIN 磷酸化Girdin 免疫组织化学 Breast neoplasms Tuberin Phosphorylated Girdin Immunohistochemistry
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  • 1Mise J, Dembitz V, Banfic H,et al. Combined inhibition of PI3K and roTOR exerts synergistic antiproliferative effect, but dimini- shes differentiative properties of rapamycin in acute myeloid leu- kemia cells [ J ]. Pathol Oncol Res, 2011, 17:645-656.
  • 2Tamburini J, Chapuis N, Bardet V, et al. Mammol/Lalian target of rapamycin (mTOR) inhibition activates phosphatidylinositol 3 kinase/Akt by up-regulating insulin-like growth factor receptor signaling in acute myeloid leckemia: Rationale for therapeutic inhibition of both pathways [ J ]. Blood, 2008, 111:379-382.
  • 3Liu J, Stevens PD, Gao 3". mTOR dependent regulation of PHLPP expression controls the rapamycin sensitivity in cancer cells [J]. J Biol Chem, 2011,286:6510-6520.
  • 4Han JM,Sahin M. TSC1/TSC2 signaling in the CNS[JI. FEBSLett, 2011, 585:973-980.
  • 5Jiang WG, Sampson J, Martin TA, et al. Tuberin and hamartin are aberrantly expressed and linked to clinical outcome in human breast cancer the role of promoter methylation of TSC genes [ J ]. Eur J Cancer, 2005, 11:1628-1636.
  • 6Dressler AC, Hudelist G, Fink-Retter A, et al. Tuberin and p27 expression in breast cancer patients with or without BRCA germ- line mutations [ J ]. Cancer Res Clin Oncol, 2013, 139: 1349-55.
  • 7Jiang P, Enomoto A,Jijiwa M,et al. An actin-binding protein Girdin regulates the motility of breast cancer ceils [ J ]. Cancer Res, 2008, 68:1310-1318.
  • 8Ghosh P, Garcia-Marcos M, Bomheimer SJ, et al. Activation of Galphai3 triggers cell migrate- on via regulation of GIV[J]. Cell Biol, 2008, 182:381-393.
  • 9陈秀华,林洁,李璐蓉,等.消化系统肿瘤中Girdin基因的表达分析[J].医学信息,2013,26:6-8.
  • 10Miyake H, Maeda K, Asai N,et al. The actin-binding protein Girdin and its Akt-mediated phos- phory lation regulate neointi- ma formation after vascular injury [ J]. Circ Res, 2011, 108 : 1170-1179.

同被引文献23

  • 1Dowling EC, Klabunde C, Patnick J, et al. Breast and cervical cancer screening programme implementation in 16 countries[J], J Med Screen,2010,17(3):139 -146.
  • 2Garcia - Marcos M, Ghosh P, Farquhar MG. GIV/Girdin transmits signals from multiple receptors by triggering trimerit G protein activation [J]. J Biol Chem, 2015,290 ( 11 ) : 6697 - 6704.
  • 3Cao K, Lu C, Han S, et al. Expression of Girdin in primary hepatocellular carcinoma and its effect on cell proliferation and invasion[J]. Int J Clin Exp Pathol,2015,8( 1 ) :551 - 559.
  • 4Wang C, Lin J, Li L, et al. Expression and clinical significance of girdin in gastric cancer[J]. Mol Clin Oncol,2014, 2(3) :425 -428.
  • 5Enomoto A, Ping J, Takahashi M. Girdin, a novel actin - binding protein, and its family of proteins possess versatile functions in the Akt and Wnt signaling pathways [ J ]. Ann N Y Acad Sci,2006,1086( 1 ) : 169 - 184.
  • 6Ha A, Polyanovsky A, Avidor - Reiss T. Drosophila hook - related protein(girdin)is essential for sensory dendrite formation [ J ]. Genetics,2015,200 (4) : 1149 - 1159.
  • 7Jin F, Liu C, Guo Y, et al. Clinical implications of Girdin and PI3K protein expression in breast cancer [ J ]. Oncol Lett,2013,5(5) :1549 - 1553.
  • 8Ghosh P, Garcia - Marcos M, Farquhar MG. GIV/Girdin is a rheostat that fine - tunes growth factor signals during tumor progression [ J ]. Cell Adh Migr, 2011,5 ( 3 ) : 237 - 248.
  • 9Yamamura Y, Asai N, Enomoto A, et al. Akt - Girdin signaling in cancer - associated fibroblasts contributes to tumor progression [ J ]. Cancer Res, 2015,75 ( 5 ) : 813 - 823.
  • 10Jin SY, Lee HS, Kim EK, et al. Reactive oxygen species and PI3K/Akt signaling in cancer [ J ]. Free Radic Biol Med,2014,75 (1) :34 - 35.

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