Abstract A086: Omental fat in ovarian cancer induces lymphangiogenesis

B. Lenoir, D. Ferber, V. Starrach, M. Suarez-Carmona, S. Schott, I. Zoernig, D. Jäger, N. Halama
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Abstract

Ovarian cancer metastasis occurs by direct multifocal seeding into the peritoneum as well as by migration through the lymphatic system. High-grade ovarian carcinoma patients often present with distant metastases. Significant risk factors for the development of those are stage, grade, and lymph node involvement. The increase of the number of lymphatic vessels seems to be implicated in ovarian tumor progression. While the tropism of ovarian cancer cells for fat is well described, the potential impact of an adipose-rich microenvironment on the dissemination of metastasis via lymphatic vessels has never been investigated. So far, in this study, we examined the effect of omental fat on lymphangiogenesis in ovarian carcinoma. For that we used a cohort of 80 ovarian cancer specimens. We observed a higher number of tumor-associated vessels and principally lymphatic vessels in ovarian cancer in contact with the omentum. These lymphatic vessels are predominantly localized along the fat tissue. A higher secretion of VEGF-C is observed in ovarian tissues containing fat compared to the ones without fat, giving a potential explanation to the observed increase of lymphatic vessels in fatty tissues. We also developed a healthy fat tissue explant culture model and treated whole tissue explants with ascites. Herein, we saw an increase of the number of adipose-derived stem cells (ADSCs). These ADSCs express lymphatic markers such as D2-40 and Lyve-1. We also observed an impact of fat supernatant on the proliferation, migration and tube formation of lymphatic endothelial cells in vitro. In conclusion, we can say that omental fat in ovarian cancer seems to have an impact on lymphangiogenesis. The close contact of ascites with fat tissue seems to lead to a differentiation of adipose-derived stem cells into lymphatic endothelial cells. Further investigations must be performed to understand the exact mechanisms underlying this phenomenon. Citation Format: Benedicte M.A. Lenoir, Dyke Ferber, Victor Starrach, Meggy Suarez-Carmona, Sarah Schott, Inka Zoernig, Dirk Jager, Niels Halama. Omental fat in ovarian cancer induces lymphangiogenesis [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A086.
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A086:卵巢癌大网膜脂肪诱导淋巴管生成
卵巢癌转移发生直接多灶播种到腹膜以及通过淋巴系统迁移。高级别卵巢癌患者常伴有远处转移。这些疾病发展的重要危险因素是分期、分级和淋巴结受累。淋巴管数量的增加似乎与卵巢肿瘤的进展有关。虽然卵巢癌细胞对脂肪的趋向性得到了很好的描述,但富含脂肪的微环境对通过淋巴管传播转移的潜在影响从未被研究过。到目前为止,在本研究中,我们研究了大网膜脂肪对卵巢癌淋巴管生成的影响。为此,我们使用了一组80个卵巢癌样本。我们观察到卵巢癌中与网膜接触的肿瘤相关血管数量较多,主要是淋巴管。这些淋巴管主要沿脂肪组织分布。与不含脂肪的卵巢组织相比,在含脂肪的卵巢组织中观察到更高的VEGF-C分泌,这可能解释了脂肪组织中观察到的淋巴管增加。我们还建立了健康脂肪组织外植体培养模型,并用腹水处理整个组织外植体。在这里,我们看到脂肪来源的干细胞(ADSCs)数量的增加。这些ADSCs表达淋巴标记物,如D2-40和Lyve-1。我们还观察了脂肪上清对体外淋巴内皮细胞增殖、迁移和成管的影响。总之,我们可以说卵巢癌的网膜脂肪似乎对淋巴管生成有影响。腹水与脂肪组织的密切接触似乎导致脂肪来源的干细胞分化为淋巴内皮细胞。必须进行进一步的调查,以了解这一现象背后的确切机制。引文格式:Benedicte M.A. Lenoir, Dyke Ferber, Victor Starrach, Meggy Suarez-Carmona, Sarah Schott, Inka zoerning, Dirk Jager, Niels Halama。卵巢癌大网膜脂肪诱导淋巴管生成[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志2019;7(2增刊):摘要nr A086。
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