首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Hyaluronidases and hyaluronan synthases expression is inversely correlated with malignancy in lung/bronchial pre-neoplastic and neoplastic lesions, affecting prognosis
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Hyaluronidases and hyaluronan synthases expression is inversely correlated with malignancy in lung/bronchial pre-neoplastic and neoplastic lesions, affecting prognosis

机译:透明质酸酶和透明质酸合酶的表达与肺/支气管癌前病变和肿瘤病变的恶性程度呈负相关,影响预后

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We collected a series of 136 lung/bronchial and 56 matched lung parenchyma tissue samples from patients who underwent lung/bronchial biopsies and presented invasive carcinoma after lung surgery. The lung/bronchial samples included basal cell hyperplasia, squamous metaplasia, moderate dysplasia, adenomatous hyperplasia, severe dysplasia, squamous cell carcinoma and adenocarcinoma. Matched lung parenchyma tissue samples included 25 squamous cell carcinomas and 31 adenocarcinomas. Immunohistochemistry was performed to analyze for the distribution of hyaluronidase (Hyal)-1 and −3, and hyaluronan synthases (HAS)-1, −2, and −3. Hyal-1 showed significantly higher expression in basal cell hyperplasia than in moderate dysplasia (P=0.01), atypical adenomatous hyperplasia (P=0.0001), or severe dysplasia (P=0.03). Lower expression of Hyal-3 was found in atypical adenomatous hyperplasia than in basal cell hyperplasia (P=0.01) or moderate dysplasia (P=0.02). HAS-2 was significantly higher in severe dysplasia (P=0.002) and in squamous metaplasia (P=0.04) compared with basal cell hyperplasia. HAS-3 was significantly expressed in basal cell hyperplasia compared with atypical adenomatous hyperplasia (P=0.05) and severe dysplasia (P=0.02). Lower expression of HAS-3 was found in severe dysplasia compared with squamous metaplasia (P=0.01) and moderate dysplasia (P=0.01). Epithelial Hyal-1 and −3 and HAS-1, −2, and −3 expressions were significantly higher in pre-neoplastic lesions than in neoplastic lesions. Comparative Cox multivariate analysis controlled by N stage and histologic tumor type showed that patients with high HAS-3 expression in pre-neoplastic cells obtained by lung/bronchial biopsy presented a significantly higher risk of death (HR=1.19; P=0.04). We concluded that localization of Hyal and HAS in lung/bronchial pre-neoplastic and neoplastic lesions was inversely related to malignancy, which implied that visualizing these factors could be a useful diagnostic procedure for suspected lung cancer. Finalizing this conclusion will require a wider study in a randomized and prospective trial.
机译:我们从接受肺/支气管活检并在肺癌手术后呈浸润性癌的患者中收集了136份肺/支气管和56份匹配的肺实质组织样本。肺/支气管样本包括基底细胞增生,鳞状上皮化生,中度发育不良,腺瘤性增生,重度不典型增生,鳞状细胞癌和腺癌。匹配的肺实质组织样本包括25例鳞状细胞癌和31例腺癌。进行免疫组织化学以分析透明质酸酶(Hyal)-1和-3以及透明质酸合酶(HAS)-1,-2和-3的分布。 Hyal-1在基底细胞增生中的表达明显高于中度不典型增生(P = 0.01),非典型腺瘤性增生(P = 0.0001)或严重不典型增生(P = 0.03)。在非典型腺瘤增生中发现Hyal-3的表达低于基底细胞增生(P = 0.01)或中度不典型增生(P = 0.02)。与基底细胞增生相比,重度不典型增生(P = 0.002)和鳞状化生(P = 0.04)中的HAS-2显着更高。与非典型腺瘤样增生(P = 0.05)和严重不典型增生(P = 0.02)相比,HAS-3在基底细胞增生中表达明显。与鳞状上皮化生(P = 0.01)和中度不典型增生(P = 0.01)相比,重度不典型增生发现HAS-3表达较低。肿瘤前病变中的上皮Hyal-1和-3以及HAS-1,-2和-3的表达显着高于肿瘤病变。由N期和组织学肿瘤类型控制的比较Cox多变量分析表明,通过肺/支气管活检获得的肿瘤前细胞中高HAS-3表达的患者死亡风险显着更高(HR = 1.19; P = 0.04)。我们得出的结论是,Hyal和HAS在肺癌/支气管癌前病变和赘生性病变中的定位与恶性程度呈负相关,这意味着可视化这些因素可能是可疑肺癌的有用诊断方法。要最终得出结论,需要在一项随机和前瞻性试验中进行更广泛的研究。

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