Interleukin-6 as an enhancer of anti-angiogenic therapy for ovarian clear cell carcinoma

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作者
Toshiyuki Seki
Nozomu Yanaihara
Jason Solomon Shapiro
Misato Saito
Junya Tabata
Ryo Yokomizo
Daito Noguchi
Takafumi Kuroda
Ayako Kawabata
Jiro Suzuki
Kazuaki Takahashi
Haruka Matsuzawa
Misayo Miyake
Masataka Takenaka
Yasushi Iida
Satoshi Yanagida
Aikou Okamoto
机构
[1] The Jikei University School of Medicine,Department of Obstetrics and Gynecology
[2] Northwestern University,Feinberg Cardiovascular Research Institute
[3] The Jikei University School of Medicine,Department of Pathology
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Ovarian clear cell carcinoma (OCCC) is a subtype of epithelial ovarian cancer (EOC) that is associated with elevated interleukin-6 (IL-6) expression, resistance to chemotherapy, and increased mortality. Although bevacizumab (Bev) is a widely used anti-angiogenic agent for EOC, the efficacy of Bev and the role of IL-6 in modulating angiogenesis in OCCC are unknown. We performed tube formation assays using human umbilical vein endothelial cells (HUVEC) cultured in OCCC cell-conditioned medium and using cells directly co-cultured with OCCC cells. We observed that IL-6 inhibition significantly mitigated the ability of Bev to impede tube formation in both cases. Furthermore, IL-6 blockade disrupted the anti-angiogenic efficacy of Bev and its concomitant anti-tumor activity. In addition, IL-6 inhibition resulted in a significant increase in angiopoietin-1 (Ang1) secretion and decreased vascular endothelial growth factor (VEGF) expression. Clinical specimens also exhibited this reciprocal relationship between IL-6 and Ang1 expression. Finally, depletion of Ang1 abrogated the effects of IL-6 inhibition on Bev activity, demonstrating that IL-6 supports the anti-angiogenic activity of Bev by suppressing Ang1 expression and promoting dependence on VEGF for angiogenesis. Altogether, our data suggest that OCCC tumors with high IL-6 levels are candidates for Bev therapy.
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