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生长激素受体、桥粒斑珠蛋白和NEDD9蛋白的表达与人类乳腺癌的肿瘤进展和转移的关系

Expression of growth hormone receptor, plakoglobin and NEDD9 protein in association with tumour progression and metastasis in human breast cancer.

作者信息

Štajduhar Emil, Sedić Mirela, Leniček Tanja, Radulović Petra, Kerenji Aleksandar, Krušlin Božo, Pavelić Krešimir, Kraljević Pavelić Sandra

机构信息

Sestre Milosrdnice Clinical Hospital Center, Vinogradska 29, 10000, Zagreb, Croatia.

出版信息

Tumour Biol. 2014 Jul;35(7):6425-34. doi: 10.1007/s13277-014-1827-y. Epub 2014 Mar 28.

Abstract

Breast cancer is the most frequently diagnosed cancer and the leading cause of cancer-related deaths among female population worldwide. Metastases are the common cause of morbidity and mortality in breast cancer and can remain latent for several years after surgical removal of the primary tumour. Thus, the identification and functional characterisation of molecular factors that promote oncogenic signalling in mammary tumour development and progression could provide new entry points for designing targeted therapeutic strategies for metastatic breast cancer. In the present study, we investigated the expression of proteins involved in cell signalling (growth hormone receptor (GHR) and NEDD9) and cell-cell adhesion (plakoglobin) in epithelial and stromal compartments of primary ductal invasive breast carcinomas and their axillary lymph node metastases versus non-metastatic tumours. Obtained data revealed remarkable increase in the expression levels of GHR and NEDD9 proteins in both epithelial and stromal components of axillary lymph node metastases in comparison with those of non-metastatic tumours, suggesting that the expression of these two proteins may provide biomarkers for tumour aggressiveness.

摘要

乳腺癌是全球女性中最常被诊断出的癌症,也是癌症相关死亡的主要原因。转移是乳腺癌发病和死亡的常见原因,在原发性肿瘤手术切除后可能潜伏数年。因此,鉴定和功能表征促进乳腺肿瘤发生发展和进展过程中致癌信号传导的分子因子,可为设计转移性乳腺癌的靶向治疗策略提供新的切入点。在本研究中,我们调查了原发性导管浸润性乳腺癌及其腋窝淋巴结转移灶与非转移性肿瘤的上皮和基质成分中参与细胞信号传导(生长激素受体(GHR)和NEDD9)和细胞间粘附(桥粒斑蛋白)的蛋白质表达情况。获得的数据显示,与非转移性肿瘤相比,腋窝淋巴结转移灶的上皮和基质成分中GHR和NEDD9蛋白的表达水平显著增加,表明这两种蛋白质的表达可能为肿瘤侵袭性提供生物标志物。

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