Boylan Kristin L M, Afiuni-Zadeh Somaieh, Geller Melissa A, Argenta Peter A, Griffin Timothy J, Skubitz Amy P N
Department of Laboratory Medicine & Pathology, University of Minnesota Medical School, MMC 395, 420 Delaware St. SE, Minneapolis, MN, 55455, USA.
Ovarian Cancer Early Detection Program, University of Minnesota Medical School, Minneapolis, MN, USA.
Clin Proteomics. 2021 Jan 7;18(1):4. doi: 10.1186/s12014-020-09309-3.
The purpose of this study was to determine whether the residual fixative from a liquid-based Pap test or a swab of the cervix contained proteins that were also found in the primary tumor of a woman with high grade serous ovarian cancer. This study is the first step in determining the feasibility of using the liquid-based Pap test or a cervical swab for the detection of ovarian cancer protein biomarkers.
Proteins were concentrated by acetone precipitation from the cell-free supernatant of the liquid-based Pap test fixative or eluted from the cervical swab. Protein was also extracted from the patient's tumor tissue. The protein samples were digested into peptides with trypsin, then the peptides were run on 2D-liquid chromatography mass spectrometry (2D-LCMS). The data was searched against a human protein database for the identification of peptides and proteins in each biospecimen. The proteins that were identified were classified for cellular localization and molecular function by bioinformatics integration.
We identified almost 5000 proteins total in the three matched biospecimens. More than 2000 proteins were expressed in each of the three biospecimens, including several known ovarian cancer biomarkers such as CA125, HE4, and mesothelin. By Scaffold analysis of the protein Gene Ontology categories and functional analysis using PANTHER, the proteins were classified by cellular localization and molecular function, demonstrating that the Pap test fluid and cervical swab proteins are similar to each other, and also to the tumor extract.
Our results suggest that Pap test fixatives and cervical swabs are a rich source of tumor-specific biomarkers for ovarian cancer, which could be developed as a test for ovarian cancer detection.
本研究的目的是确定液基巴氏试验的残留固定剂或宫颈拭子中含有的蛋白质,是否也存在于高级别浆液性卵巢癌女性的原发肿瘤中。本研究是确定使用液基巴氏试验或宫颈拭子检测卵巢癌蛋白质生物标志物可行性的第一步。
通过丙酮沉淀从液基巴氏试验固定剂的无细胞上清液中浓缩蛋白质,或从宫颈拭子中洗脱蛋白质。还从患者的肿瘤组织中提取蛋白质。蛋白质样品用胰蛋白酶消化成肽段,然后将肽段进行二维液相色谱质谱分析(2D-LCMS)。将数据与人类蛋白质数据库进行比对,以鉴定每个生物样本中的肽段和蛋白质。通过生物信息学整合,对鉴定出的蛋白质进行细胞定位和分子功能分类。
我们在三个匹配的生物样本中共鉴定出近5000种蛋白质。三种生物样本中每种都表达了2000多种蛋白质,包括几种已知的卵巢癌生物标志物,如CA125、HE4和间皮素。通过对蛋白质基因本体类别进行支架分析,并使用PANTHER进行功能分析,根据细胞定位和分子功能对蛋白质进行分类,结果表明巴氏试验液和宫颈拭子中的蛋白质彼此相似,也与肿瘤提取物相似。
我们的结果表明,巴氏试验固定剂和宫颈拭子是卵巢癌肿瘤特异性生物标志物的丰富来源,可开发成一种卵巢癌检测试验。