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首页> 外文期刊>Oral oncology >Study of FHIT and WWOX expression in mucoepidermoid carcinoma and adenoid cystic carcinoma of salivary gland.
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Study of FHIT and WWOX expression in mucoepidermoid carcinoma and adenoid cystic carcinoma of salivary gland.

机译:FHIT和WWOX在涎腺粘液表皮样癌和腺样囊性癌中表达的研究。

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摘要

Mucoepidermoid carcinoma (MEC) and adenoid cystic carcinoma (ACC) are salivary gland neoplasms with divergent morphological features and clinical behavior. ACC is a basaloid tumor whereas MEC is a glandular epithelial neoplasm. FHIT and WWOX are tumor suppressor genes that encompass the FRA3B and FRA16D fragile sites at chromosomes 3p14.2 and 16q23.3, respectively. In previous studies, we have shown concordant loss of Fhit and Wwox expression in breast cancer, with significantly more frequent loss in cancers of basal-like phenotype. To determine if there is a similar association in salivary gland neoplasms, we designed a study of MEC and ACC of salivary gland on tissue microarrays (TMA). TMAs were constructed from 25 MEC and 19 ACC of salivary gland. Fhit and Wwox protein expression was assessed by immunohistochemical staining of cores on TMAs. Correlations among immunohistochemical markers and histological type were determined by statistical analyses. Significantly reduced Fhit and Wwox expression was observed in ACC (p=0.002 and p<0.001, respectively). The results suggest that, as for breast cancer, loss of Fhit and Wwox expression might have a role in the pathogenesis of basaloid differentiation in salivary gland neoplasms; alternatively, differences in chromatin structure at chromosome fragile regions might make fragile genes more accessible to DNA damage and rearrangement early during preneoplastic stages of basaloid cancers. Studies of basaloid tumors of other organ systems may show similar results and these findings may have implications for treatment modalities designed for basal-like tumors.
机译:粘液表皮样癌(MEC)和腺样囊性癌(ACC)是唾液腺肿瘤,具有不同的形态学特征和临床行为。 ACC是基底样肿瘤,而MEC是腺上皮肿瘤。 FHIT和WWOX是抑癌基因,分别涵盖3p14.2和16q23.3染色体上的FRA3B和FRA16D脆弱位点。在以前的研究中,我们已经显示乳腺癌中Fhit和Wwox表达的一致减少,而基底样表型癌症的消失频率则更高。为了确定唾液腺肿瘤中是否存在相似的关联,我们设计了组织微阵列(TMA)上的唾液腺MEC和ACC的研究。 TMA由25个MEC和19个ACC唾液腺构建而成。 Fhit和Wwox蛋白表达通过TMA核心的免疫组织化学染色进行评估。通过统计分析确定免疫组织化学标记物与组织学类型之间的相关性。在ACC中观察到Fhit和Wwox表达显着降低(分别为p = 0.002和p​​ <0.001)。结果表明,对于乳腺癌,Fhit和Wwox表达的丧失可能与唾液腺肿瘤中基底突分化的发病机制有关。另外,染色体脆弱区域的染色质结构差异可能使脆弱基因在基底类癌的癌前期早期更容易受到DNA损伤和重排。对其他器官系统的基底类肿瘤的研究可能显示出相似的结果,这些发现可能对针对基底样肿瘤设计的治疗方式产生影响。

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