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肿瘤相关巨噬细胞通过 CCL18-ZEB1-M-CSF 反馈环诱导球体形成,促进卵巢癌的腹腔转移。

Tumor-associated macrophages induced spheroid formation by CCL18-ZEB1-M-CSF feedback loop to promote transcoelomic metastasis of ovarian cancer.

机构信息

Translation Medicine Center, Sun Yat-sen University First Affiliated Hospital, Guangzhou, China

Translation Medicine Center, Sun Yat-sen University First Affiliated Hospital, Guangzhou, China.

出版信息

J Immunother Cancer. 2021 Dec;9(12). doi: 10.1136/jitc-2021-003973.

Abstract

BACKGROUND

Ovarian cancer (OvCa)-tumor-associated macrophages (TAMs) spheroids are abundantly present within ascites of high malignant patients. This study investigated the mutual interaction of OvCa cells and TAMs in the spheroids.

METHODS

Three-dimensional coculture system and transwell coculture system were created to mimic the OvCa and TAMs in spheroids and in disassociated state. Transwell-migration assay and scratch wound healing assay were used to measure the invasive and migratory capacity. Western blot, quantitative reverse transcription-PCR and immunostaining were used to measure the mesenchymal and epithelial markers. Flow cytometry was used to assess the polarization of TAMs. Also, the differential gene expression profile of OvCa cells and OvCa cells from spheroids were tested by RNA-sequence. Finally, the ovarian mice models were constructed by intraperitoneal injection of ID8 or OvCa-TAMs spheroids.

RESULTS

Our results indicated that the formation of OvCa-TAMs spheroids was positive related to the malignancy of OvCa cells. M2-TAMs induced the epithelial-mesenchymal transition of OvCa cells by releasing chemokine (C-C motif) ligand 18 (CCL18) in the spheroids. While, CCL18 induced macrophage colony-stimulating factor (M-CSF) transcription in OvCa cells through zinc finger E-box-binding homeobox 1 (ZEB1). This study further indicated that M-CSF secreted by OvCa cells drived the polarization of M2-TAMs. Therefore, a CCL18-ZEB1-M-CSF interacting loop between OvCa cells and TAMs in the spheroids was identified. Moreover, with blocking the expression of ZEB1 in the OvCa cell, the formation of OvCa-TAMs spheroids was impeded. In the ovarian mice models, the formation of OvCa-TAMs spheroids in the ascites was promoted by overexpressing of ZEB1 in OvCa cells, which resulted in faster and earlier transcoelomic metastasis.

CONCLUSION

These findings suggested that the formation of OvCa-TAMs spheroids resulted in aggressive phenotype of OvCa cells, as a specific feedback loop CCL18-ZEB1-M-CSF in it. Inhibition of ZEB1 reduced OvCa-TAMs spheroids in the ascites, impeding the transcoelomic metastasis and improving the outcome of ovarian patients.

摘要

背景

卵巢癌(OvCa)-肿瘤相关巨噬细胞(TAMs)球体在高恶性患者的腹水中大量存在。本研究调查了 OvCa 细胞与球体中 TAMs 之间的相互作用。

方法

建立了三维共培养系统和 Transwell 共培养系统,以模拟球体中和分离状态下的 OvCa 和 TAMs。Transwell 迁移实验和划痕愈合实验用于测量侵袭和迁移能力。Western blot、定量逆转录-PCR 和免疫染色用于测量间充质和上皮标志物。流式细胞术用于评估 TAMs 的极化。此外,通过 RNA 测序测试了 OvCa 细胞和球体中的 OvCa 细胞的差异基因表达谱。最后,通过腹腔注射 ID8 或 OvCa-TAMs 球体构建卵巢小鼠模型。

结果

我们的结果表明,OvCa-TAMs 球体的形成与 OvCa 细胞的恶性程度呈正相关。M2-TAMs 在球体中通过释放趋化因子(C-C 基序)配体 18(CCL18)诱导 OvCa 细胞的上皮-间充质转化。然而,CCL18 通过锌指 E 盒结合同源框 1(ZEB1)诱导 OvCa 细胞中巨噬细胞集落刺激因子(M-CSF)的转录。本研究进一步表明,OvCa 细胞分泌的 M-CSF 驱动了 M2-TAMs 的极化。因此,鉴定了球体中 OvCa 细胞和 TAMs 之间的 CCL18-ZEB1-M-CSF 相互作用环。此外,通过阻断 OvCa 细胞中 ZEB1 的表达,阻碍了 OvCa-TAMs 球体的形成。在卵巢小鼠模型中,通过过表达 OvCa 细胞中的 ZEB1,促进了腹水中 OvCa-TAMs 球体的形成,导致更快和更早的体腔转移。

结论

这些发现表明,OvCa-TAMs 球体的形成导致了 OvCa 细胞的侵袭表型,这是其中特定的反馈环 CCL18-ZEB1-M-CSF 的结果。抑制 ZEB1 减少了腹水中的 OvCa-TAMs 球体,阻碍了体腔转移,改善了卵巢患者的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ec0/8718465/2aa79e0db8d2/jitc-2021-003973f01.jpg

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