首页> 外文期刊>Journal of Ovarian Research >Kallikrein family proteases KLK6 and KLK7 are potential early detection and diagnostic biomarkers for serous and papillary serous ovarian cancer subtypes
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Kallikrein family proteases KLK6 and KLK7 are potential early detection and diagnostic biomarkers for serous and papillary serous ovarian cancer subtypes

机译:激肽释放酶家族蛋白酶KLK6和KLK7是浆液性和乳头状浆液性卵巢癌亚型的潜在早期检测和诊断生物标志物

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Background Early detection of ovarian cancer remains a challenge due to widespread metastases and a lack of biomarkers for early-stage disease. This study was conducted to identify relevant biomarkers for both laparoscopic and serum diagnostics in ovarian cancer. Methods Bioinformatics analysis and expression screening in ovarian cancer cell lines were employed. Selected biomarkers were further validated in bio-specimens of diverse cancer types and ovarian cancer subtypes. For non-invasive detection, biomarker proteins were evaluated in serum samples from ovarian cancer patients. Results Two kallikrein (KLK) serine protease family members (KLK6 and KLK7) were found to be significantly overexpressed relative to normal controls in most of the ovarian cancer cell lines examined. Overexpression of KLK6 and KLK7 mRNA was specific to ovarian cancer, in particular to serous and papillary serous subtypes. In situ hybridization and histopathology further confirmed significantly elevated levels of KLK6 and KLK7 mRNA and proteins in tissue epithelium and a lack of expression in neighboring stroma. Lastly, KLK6 and KLK7 protein levels were significantly elevated in serum samples from serous and papillary serous subtypes in the early stages of ovarian cancer, and therefore could potentially decrease the high “false negative” rates found in the same patients with the common ovarian cancer biomarkers human epididymis protein 4 (HE4) and cancer antigen 125 (CA-125). Conclusion KLK6 and KLK7 mRNA and protein overexpression is directly associated with early-stage ovarian tumors and can be measured in patient tissue and serum samples. Assays based on KLK6 and KLK7 expression may provide specific and sensitive information for early detection of ovarian cancer.
机译:背景技术由于广泛的转移和早期疾病的生物标志物的缺乏,早期检测卵巢癌仍然是一个挑战。进行该研究以鉴定用于卵巢癌的腹腔镜和血清诊断的相关生物标志物。方法采用卵巢癌细胞系的生物信息学分析和表达筛选方法。所选的生物标志物已在多种癌症类型和卵巢癌亚型的生物样本中得到进一步验证。对于非侵入性检测,在卵巢癌患者的血清样品中评估了生物标志物蛋白。结果发现在大多数受检卵巢癌细胞系中,激肽释放酶(KLK)丝氨酸蛋白酶家族成员(KLK6和KLK7)相对于正常对照明显过表达。 KLK6和KLK7 mRNA的过度表达是卵巢癌特有的,特别是浆液性和乳头状浆液性亚型。原位杂交和组织病理学进一步证实组织上皮细胞中KLK6和KLK7 mRNA和蛋白的水平显着升高,并且在相邻基质中缺乏表达。最后,在卵巢癌的早期,浆液和乳头浆液性亚型血清样品中的KLK6和KLK7蛋白水平显着升高,因此有可能降低在具有常见卵巢癌生物标志物的同一患者中发现的高“假阴性”率人附睾蛋白4(HE4)和癌症抗原125(CA-125)。结论KLK6和KLK7 mRNA和蛋白的过度表达与早期卵巢肿瘤直接相关,可在患者组织和血清样本中检测到。基于KLK6和KLK7表达的测定可为卵巢癌的早期检测提供特异性和敏感信息。

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