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与高级别浆液性卵巢癌输卵管起源相关的候选基因的鉴定

Identification of candidate genes associated with tubal origin of high-grade serous ovarian cancer.

作者信息

Xiang Li, Rong Guohua, Zhao Jing, Wang Zhenyan, Shi Fengfeng

机构信息

Department of Gynecology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.

Department of Breast Surgery, Qingdao Municipal Hospital (Group), Qingdao, Shandong 266000, P.R. China.

出版信息

Oncol Lett. 2018 May;15(5):7769-7775. doi: 10.3892/ol.2018.8346. Epub 2018 Mar 26.

Abstract

Evidence indicates that high-grade serous ovarian carcinoma arises from the fallopian tube, rather than ovarian surface epithelium. This is termed the 'tubal origin' theory. The aim of the present study was to compare the immunophenotype and gene expression profiling among high-grade serous ovarian carcinoma (HGSOC), fallopian tube epithelium (FTE) and ovarian surface epithelium (OSE) based on tubal origin theory, and identify the differential genes associated with ovarian carcinogenesis. A total of 61 cases of fresh tissue samples including 21 cases of HGSOC, 20 cases of OSE, and 20 cases of FTE were obtained following surgical resection. Immunostaining was performed to detect the expression of PAX8, which has been considered as a potential immunophenotype marker of Müllerian origin. Illumina BeadChip was applied for gene expression profiling. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was performed to confirm the differential expression of candidate genes between HGSOC and FTE. The results of the present study demonstrated that PAX8 was highly expressed in HGSOC (19/21, 90.4%) and FTE (20/20, 100%), but not in OSE (3/20, 14.3%). A dendrogram generated by cluster analysis indicated a higher similarity of gene expression profile between HGSOC and FTE than OSE. A total of 2,412 differentially expressed genes were identified (absolute fold change >2) between HGSOC and FTE, including 822 upregulated genes in cancer and 1,590 downregulated genes. S100 calcium binding protein P, Ras-interacting protein 1, Wnt family member 5A, tumor-associated calcium signal transducer 2, Dickkopf Wnt signaling pathway inhibitor 3 and tumor suppressor candidate 3 genes were identified as candidate markers, of which the differential gene expression in HGSOC and FTE was confirmed by RT-qPCR (P<0.05). The results indicate the presence of a greater similarity in the immunophenotype and gene expression profile of HGSOC and FTE, when compared with OSE, which was consistent with the tubal origin theory of HGSOC.

摘要

有证据表明,高级别浆液性卵巢癌起源于输卵管,而非卵巢表面上皮。这被称为“输卵管起源”理论。本研究的目的是基于输卵管起源理论,比较高级别浆液性卵巢癌(HGSOC)、输卵管上皮(FTE)和卵巢表面上皮(OSE)的免疫表型和基因表达谱,并鉴定与卵巢癌发生相关的差异基因。手术切除后共获得61例新鲜组织样本,其中包括21例HGSOC、20例OSE和20例FTE。进行免疫染色以检测PAX8的表达,PAX8被认为是苗勒氏起源的潜在免疫表型标志物。应用Illumina BeadChip进行基因表达谱分析。进行逆转录定量聚合酶链反应(RT-qPCR)以证实HGSOC和FTE之间候选基因的差异表达。本研究结果表明,PAX8在HGSOC(19/21,90.4%)和FTE(20/20,100%)中高表达,但在OSE(3/20,14.3%)中不表达。聚类分析生成的树状图表明,HGSOC和FTE之间的基因表达谱比与OSE更相似。在HGSOC和FTE之间共鉴定出2412个差异表达基因(绝对倍数变化>2),其中包括癌症中上调的822个基因和下调的1590个基因。S100钙结合蛋白P、Ras相互作用蛋白1、Wnt家族成员5A、肿瘤相关钙信号转导蛋白2、Dickkopf Wnt信号通路抑制剂3和肿瘤抑制候选3基因被鉴定为候选标志物,其中HGSOC和FTE中的差异基因表达通过RT-qPCR得到证实(P<0.05)。结果表明,与OSE相比,HGSOC和FTE在免疫表型和基因表达谱上存在更大的相似性,这与HGSOC的输卵管起源理论一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02a4/5920857/b3ee85f99f47/ol-15-05-7769-g00.jpg

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