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

被引:19
|
作者
Seki, Toshiyuki [1 ]
Yanaihara, Nozomu [1 ]
Shapiro, Jason Solomon [1 ,2 ]
Saito, Misato [1 ]
Tabata, Junya [1 ]
Yokomizo, Ryo [1 ]
Noguchi, Daito [1 ]
Kuroda, Takafumi [1 ]
Kawabata, Ayako [1 ]
Suzuki, Jiro [1 ]
Takahashi, Kazuaki [1 ]
Matsuzawa, Haruka [3 ]
Miyake, Misayo [3 ]
Takenaka, Masataka [1 ]
Iida, Yasushi [1 ]
Yanagida, Satoshi [1 ]
Okamoto, Aikou [1 ]
机构
[1] Jikei Univ, Dept Obstet & Gynecol, Sch Med, Minato Ku, 3-25-8 Nishi Shinbashi, Tokyo 1058461, Japan
[2] Northwestern Univ, Feinberg Cardiovasc Res Inst, Chicago, IL 60611 USA
[3] Jikei Univ, Dept Pathol, Sch Med, Tokyo, Japan
基金
日本学术振兴会;
关键词
ENDOTHELIAL GROWTH-FACTOR; EXPRESSION; CANCER; BEVACIZUMAB; BIOMARKERS; OVEREXPRESSION; IDENTIFICATION; RESISTANCE; SIGNATURE; EFFICACY;
D O I
10.1038/s41598-021-86913-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:9
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