癌睾丸抗原pas1在卵巢癌中的罕见表达

Biomarkers in cancer Pub Date : 2015-08-16 eCollection Date: 2015-01-01 DOI:10.4137/BIC.S28378
Ghazala Khan, Suzanne E Brooks, Ken I Mills, Barbara-Ann Guinn
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引用次数: 11

摘要

卵巢癌在疾病的早期阶段是可以治疗的;然而,它通常在晚期才被发现,此时治疗已不再有效。如果发现得早(第一阶段),有90%的机会存活5年。因此,确定早期生物标志物以提高卵巢癌的早期发现是势在必行的。癌睾丸抗原(cta),如Per ARNT SIM (PAS)结构域1 (PASD1),是独特的,因为它们的表达仅限于免疫受限的部位,如睾丸和胎盘,不表达MHC I类,和癌症,使它们理想地定位为免疫治疗的靶标,以及潜在的生物标志物,用于癌症检测的表达。我们检测了PASD1a和b在许多细胞系、8个健康卵巢样本、8个正常邻近卵巢组织和191个卵巢癌组织中的表达,这些组织主要是I期(n = 164)和II期(n = 14)疾病。我们发现,尽管皮肤癌染色呈阳性,但只有一个i期卵巢癌患者组织表达了可检测水平的PASD1a和b。这可能主要反映了检查的I期卵巢癌样本。为了研究PASD1表达的限制,我们检测了子宫内膜组织阵列,在30例恶性肿瘤组织、23例增生组织和16例正常子宫内膜组织中均未发现PASD1表达。我们的研究表明,寻找能够检测早期卵巢癌的单一癌症-睾丸抗原/生物标志物必须继续下去。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Infrequent Expression of the Cancer-Testis Antigen, PASD1, in Ovarian Cancer.

Infrequent Expression of the Cancer-Testis Antigen, PASD1, in Ovarian Cancer.

Infrequent Expression of the Cancer-Testis Antigen, PASD1, in Ovarian Cancer.

Ovarian cancer is very treatable in the early stages of disease; however, it is usually detected in the later stages, at which time, treatment is no longer as effective. If discovered early (Stage I), there is a 90% chance of five-year survival. Therefore, it is imperative that early-stage biomarkers are identified to enhance the early detection of ovarian cancer. Cancer-testis antigens (CTAs), such as Per ARNT SIM (PAS) domain containing 1 (PASD1), are unique in that their expression is restricted to immunologically restricted sites, such as the testis and placenta, which do not express MHC class I, and cancer, making them ideally positioned to act as targets for immunotherapy as well as potential biomarkers for cancer detection where expressed. We examined the expression of PASD1a and b in a number of cell lines, as well as eight healthy ovary samples, eight normal adjacent ovarian tissues, and 191 ovarian cancer tissues, which were predominantly stage I (n = 164) and stage II (n = 14) disease. We found that despite the positive staining of skin cancer, only one stage Ic ovarian cancer patient tissue expressed PASD1a and b at detectable levels. This may reflect the predominantly stage I ovarian cancer samples examined. To examine the restriction of PASD1 expression, we examined endometrial tissue arrays and found no expression in 30 malignant tumor tissues, 23 cases of hyperplasia, or 16 normal endometrial tissues. Our study suggests that the search for a single cancer-testes antigen/biomarker that can detect early ovarian cancer must continue.

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