Oncology, School of Biosciences and Medicine, FHMS, University of Surrey, Leggett Building, Daphne Jackson Road, Guildford, GU2 7WG, UK.
Present Address: The Royal Marsden NHS Foundation Trust, Downs Rd, Sutton, London, SM2 5PT, UK.
BMC Cancer. 2018 Oct 3;18(1):943. doi: 10.1186/s12885-018-4816-5.
Epithelial ovarian cancer is a common malignancy, with no clinically approved diagnostic biomarker. Engrailed-2 (EN2) is a homeodomain-containing transcription factor, essential during embryological neural development, which is dysregulated in several cancer types. We evaluated the expression of EN2 in Epithelial ovarian cancer, and reviewed its role as a biomarker.
We evaluated 8 Epithelial ovarian cancer cell lines, along with > 100 surgical specimens from the Royal Surrey County Hospital (2009-2014). In total, 108 tumours and 5 normal tissue specimens were collected. En2 mRNA was evaluated by semi-quantitative RT-PCR. Histological sub-type, and platinum-sensitive/-resistant status were compared. Protein expression was assessed in cell lines (immunofluorescence), and in > 150 tumours (immunohistochemistry).
En2 mRNA expression was elevated in serous ovarian tumours compared with normal ovary (p < 0.001), particularly in high-grade serous ovarian cancer (p < 0.0001) and in platinum-resistant tumours (p = 0.0232). Median Overall Survival and Progression-free Survival were reduced with high En2 expression (OS = 28 vs 42 months, p = 0.0329; PFS = 8 vs 27 months; p = 0.0004). Positive cytoplasmic EN2 staining was demonstrated in 78% of Epithelial ovarian cancers, with absence in normal ovary. EN2 positive high-grade serous ovarian cancer patients had a shorter PFS (10 vs 17.5 months; p = 0.0103).
The EN2 transcription factor is a novel ovarian cancer biomarker. It demonstrates prognostic value, correlating with worse Overall Survival and Progression-free Survival. It is hoped that further work will validate its use as a biomarker, and provide insight into the role of EN2 in the development, progression and spread of ovarian cancer.
上皮性卵巢癌是一种常见的恶性肿瘤,目前尚无临床认可的诊断生物标志物。Engrailed-2(EN2)是一种含有同源域的转录因子,在胚胎神经发育过程中必不可少,在多种癌症类型中失调。我们评估了上皮性卵巢癌中 EN2 的表达,并回顾了其作为生物标志物的作用。
我们评估了 8 种上皮性卵巢癌细胞系,以及来自皇家萨里郡医院(2009-2014 年)的 >100 例手术标本。共收集了 108 个肿瘤和 5 个正常组织标本。通过半定量 RT-PCR 评估 En2 mRNA 的表达。比较组织学亚型和铂类敏感/耐药状态。在细胞系中(免疫荧光)和 >150 个肿瘤中评估蛋白表达(免疫组化)。
与正常卵巢相比,浆液性卵巢肿瘤中 En2 mRNA 的表达升高(p<0.001),尤其是高级别浆液性卵巢癌(p<0.0001)和铂类耐药肿瘤(p=0.0232)。高 En2 表达组的总生存(OS)和无进展生存(PFS)时间均缩短(OS=28 与 42 个月,p=0.0329;PFS=8 与 27 个月,p=0.0004)。在 78%的上皮性卵巢癌中检测到细胞质 EN2 染色阳性,而在正常卵巢中则没有。EN2 阳性的高级别浆液性卵巢癌患者的 PFS 更短(10 与 17.5 个月,p=0.0103)。
EN2 转录因子是一种新的卵巢癌生物标志物。它具有预后价值,与总生存和无进展生存较差相关。希望进一步的工作能够验证其作为生物标志物的用途,并深入了解 EN2 在卵巢癌的发生、发展和扩散中的作用。