首页> 外文期刊>Histopathology: Official Journal of the British Division of the International Academy of Pathology >Reg IV expression is associated with cell growth and prognosis of adenoid cystic carcinoma in the salivary gland.
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Reg IV expression is associated with cell growth and prognosis of adenoid cystic carcinoma in the salivary gland.

机译:Reg IV表达与唾液腺腺样囊性癌的细胞生长和预后有关。

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摘要

AIMS: Regenerating islet-derived family, member 4 (Reg IV) is associated with the progression of various cancers. The aim was to examine Reg IV expression in adenoid cystic carcinomas (ACCs) in salivary glands. METHODS AND RESULTS: Reg IV expression was detected by immunohistochemistry and compared with clinicopathological parameters. Expression of phosphorylated epidermal growth factor receptor (pEGFR), phosphorylated AKT (pAKT) and MUC2 was examined by immunohistochemistry. Reg IV function was assessed with Reg IV antisense S-oligodeoxynucleotides (AS) in ACC3 human ACC cells. Reg IV was expressed by salivary duct epithelia and acinus myoepithelia, but not in squamous epithelia. Reg IV expression was found in 41% (17/41) of ACCs, but in none of 40 oral squamous cell carcinomas (OSCCs) and was associated with nodal metastasis (P = 0.047) and poor prognosis (P = 0.012) in ACCs. Reg IV expression was associated with pEGFR (14/17, 82%) in Reg IV+ ACCs, but had no relationship with pAKT or MUC2 expressionin ACCs. Cell growth was inhibited by AS treatment in Reg IV+ ACC3 cells, but not in HSC-4 OSCC cells, whereas in vitro invasion of neither cell types was affected by AS treatment. CONCLUSIONS: These results suggest that Reg IV might accelerate cell growth and disease progression of ACCs.
机译:目的:再生的胰岛衍生家族成员4(Reg IV)与各种癌症的进展有关。目的是研究唾液腺中腺样囊性癌(ACC)中Reg IV的表达。方法与结果:采用免疫组织化学方法检测Reg IV的表达,并与临床病理参数进行比较。通过免疫组织化学检查磷酸化的表皮生长因子受体(pEGFR),磷酸化的AKT(pAKT)和MUC2的表达。使用Reg IV反义S-寡脱氧核苷酸(AS)在ACC3人ACC细胞中评估Reg IV功能。 Reg IV由唾液管上皮和腺泡肌上皮表达,但在鳞状上皮中不表达。在41%(17/41)的ACC中发现Reg IV表达,但在40例口腔鳞状细胞癌(OSCC)中均未发现Reg IV的表达,并且与ACC的淋巴结转移(P = 0.047)和不良预后相关(P = 0.012)。 Reg IV + ACC中Reg IV的表达与pEGFR(14/17,82%)相关,但与ACC中pAKT或MUC2的表达无关。在Reg IV + ACC3细胞中,AS处理可抑制细胞生长,而在HSC-4 OSCC细胞中,AS处理可抑制细胞生长,而AS处理对两种细胞类型的体外侵袭均无影响。结论:这些结果表明Reg IV可能加速ACC的细胞生长和疾病进展。

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