Musrap Natasha, Karagiannis George S, Saraon Punit, Batruch Ihor, Smith Chris, Diamandis Eleftherios P
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
J Proteomics. 2014 May 30;103:204-15. doi: 10.1016/j.jprot.2014.03.042. Epub 2014 Apr 12.
Ovarian cancer is a highly metastatic disease that is often characterized by widespread abdominal dissemination. A hallmark of ovarian cancer progression is the attachment of malignant cells to the mesothelium and the formation of invasive peritoneal implants. Therefore, delineating factors involved in cancer-peritoneal cell interaction is critical to improving patient survival, as it may lead to the discovery of novel therapeutic targets. As such, we aimed to identify proteins that participate in this interaction by comparing the secreted proteome of a co-culture model containing ovarian cancer (OVCAR-5) and mesothelial cells (LP-9), to their respective monoculture secretomes. In total, 49 proteins were differentially secreted during cancer and mesothelial cell contact. Relative mRNA expression of candidates was performed, which revealed a significant increase in MUC5AC gene expression in cancer cells cultured in three different co-culture models (OVCAR-5 and LP-9; BG-1 and LP-9; OV-90 and LP-9). An increased expression was also observed in LP-9 cells that were co-cultured with OVCAR-5 and OV-90 cancer cells. Further immunocytochemistry analysis also confirmed increased expression of MUC5AC in ovarian cancer and peritoneal co-cultures. Overall, our analysis uncovers novel molecular markers of peritoneal metastasis, which may have potential roles in regulating the progression of the disease.
In this study, our objective was to focus on identifying novel mediators of ovarian cancer and peritoneal interaction using a mass spectrometry-based approach. Our analysis resulted in the discovery of both previously known and novel factors involved this interaction, and as such, these newly discovered proteins might have potential roles in cancer progression, such as invasion and adhesion. We believe that these findings add to our current knowledge and understanding of ovarian cancer progression, and will aid researchers in their future attempts in finding new targets of the disease.
卵巢癌是一种具有高度转移性的疾病,其特征通常是广泛的腹腔播散。卵巢癌进展的一个标志是恶性细胞附着于间皮并形成侵袭性腹膜种植体。因此,阐明参与癌症 - 腹膜细胞相互作用的因素对于提高患者生存率至关重要,因为这可能会导致发现新的治疗靶点。因此,我们旨在通过比较包含卵巢癌(OVCAR - 5)和间皮细胞(LP - 9)的共培养模型与其各自的单培养分泌蛋白组,来鉴定参与这种相互作用的蛋白质。总共,在癌症和间皮细胞接触期间有49种蛋白质差异分泌。对候选蛋白进行了相对mRNA表达分析,结果显示在三种不同的共培养模型(OVCAR - 5和LP - 9;BG - 1和LP - 9;OV - 90和LP - 9)中培养的癌细胞中,MUC5AC基因表达显著增加。在与OVCAR - 5和OV - 90癌细胞共培养的LP - 9细胞中也观察到表达增加。进一步的免疫细胞化学分析也证实了MUC5AC在卵巢癌和腹膜共培养物中的表达增加。总体而言,我们的分析揭示了腹膜转移的新分子标志物,其可能在调节疾病进展中具有潜在作用。
在本研究中,我们的目标是使用基于质谱的方法专注于鉴定卵巢癌与腹膜相互作用的新介质。我们的分析导致发现了参与这种相互作用的已知和新因素,因此,这些新发现的蛋白质可能在癌症进展中具有潜在作用,如侵袭和黏附。我们相信这些发现增加了我们目前对卵巢癌进展的认识和理解,并将有助于研究人员未来寻找该疾病新靶点的尝试。