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外泌体介导的高转移卵巢癌细胞 CD44 的转移促进低转移卵巢癌细胞的迁移和侵袭。

Exosome-mediated transfer of CD44 from high-metastatic ovarian cancer cells promotes migration and invasion of low-metastatic ovarian cancer cells.

机构信息

Department of Gynecologic Oncology, Women's Hospital School of Medicine Zhejiang University, No. 1 Xueshi Road, Hangzhou, 310006, China.

Women's Reproductive Health Research Laboratory of Zhejiang Province, Women's Hospital School of Medicine Zhejiang University, Hangzhou, China.

出版信息

J Ovarian Res. 2021 Feb 24;14(1):38. doi: 10.1186/s13048-021-00776-2.

DOI:10.1186/s13048-021-00776-2
PMID:33627162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7905574/
Abstract

OBJECTIVE

To investigate the detailed roles and mechanisms of tumor-derived exosomes in progression and metastasis of ovarian cancer in vitro.

METHODS

Exosomes were isolated by differential centrifugation method; the morphology, size and biological markers of exosomes were separately defined by transmission electron microscopy, nanoS90 and Western blotting; Trans-well chambers assay was used to assess the ability of migration and invasion of recipient cells uptaking the exosomes from HO8910PM cells. The downstream molecule was screened by mass spectrometry.CD44 was identified by western blotting and the function of CD44 was identified by trans-well chambers assay and CCK8 assay.

RESULTS

Exosomes derived from HO8910PM cells could be transferred to HO8910 cells and promote cell migration and invasion in the recipient cells of ovarian cancer. And CD44 could be transferred to the HO8910 cells through exosomes from HO8910PM cells and influence the migration and invasion ability of HO8910 cells.

CONCLUSION

The more aggressive subpopulation can transfer a metastatic phenotype to the less one via secreting exosomes within a heterogeneous tumor. CD44 may be a potential therapeutic approach for ovarian cancer.

摘要

目的

探讨肿瘤来源的外泌体在卵巢癌细胞体外进展和转移中的详细作用和机制。

方法

采用差速离心法分离外泌体;透射电子显微镜、纳米 S90 和 Western blot 分别鉴定外泌体的形态、大小和生物标志物;Trans-well 室试验评估摄取 HO8910PM 细胞来源的外泌体的受体细胞的迁移和侵袭能力。通过质谱筛选下游分子。Western blot 鉴定 CD44,Trans-well 室试验和 CCK8 试验鉴定 CD44 的功能。

结果

HO8910PM 细胞来源的外泌体可转移至 HO8910 细胞,并促进卵巢癌细胞中受体细胞的迁移和侵袭。并且 CD44 可以通过 HO8910PM 细胞来源的外泌体转移到 HO8910 细胞,并影响 HO8910 细胞的迁移和侵袭能力。

结论

在异质性肿瘤中,侵袭性较强的亚群可以通过分泌外泌体将转移表型转移到侵袭性较弱的亚群。CD44 可能是治疗卵巢癌的潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/700c661fbf55/13048_2021_776_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/c17709ee15a8/13048_2021_776_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/a8a0632efbf2/13048_2021_776_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/1c6dd292abf4/13048_2021_776_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/700c661fbf55/13048_2021_776_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/c17709ee15a8/13048_2021_776_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/a8a0632efbf2/13048_2021_776_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/1c6dd292abf4/13048_2021_776_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de25/7905574/700c661fbf55/13048_2021_776_Fig4_HTML.jpg

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本文引用的文献

1
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CA Cancer J Clin. 2018 Jul;68(4):284-296. doi: 10.3322/caac.21456. Epub 2018 May 29.
2
Tumor-derived exosomal lnc-Sox2ot promotes EMT and stemness by acting as a ceRNA in pancreatic ductal adenocarcinoma.肿瘤来源的外泌体 lnc-Sox2ot 通过作为 ceRNA 在胰腺导管腺癌中发挥作用促进 EMT 和干性。
Oncogene. 2018 Jul;37(28):3822-3838. doi: 10.1038/s41388-018-0237-9. Epub 2018 Apr 12.
3
New Technologies for Analysis of Extracellular Vesicles.新型细胞外囊泡分析技术。
小细胞外囊泡的研究进展:在肿瘤微环境及上皮性卵巢癌诊断与治疗中的作用
Front Oncol. 2025 Feb 11;15:1526944. doi: 10.3389/fonc.2025.1526944. eCollection 2025.
4
Extracellular vesicles in tumor immunity: mechanisms and novel insights.肿瘤免疫中的细胞外囊泡:机制与新见解
Mol Cancer. 2025 Feb 14;24(1):45. doi: 10.1186/s12943-025-02233-w.
5
Impacts of Hyaluronan on Extracellular Vesicle Production and Signaling.透明质酸对细胞外囊泡产生及信号传导的影响
Cells. 2025 Jan 18;14(2):139. doi: 10.3390/cells14020139.
6
Unraveling the extracellular vesicle network: insights into ovarian cancer metastasis and chemoresistance.解析细胞外囊泡网络:揭示卵巢癌转移和化疗耐药的机制。
Mol Cancer. 2024 Sep 16;23(1):201. doi: 10.1186/s12943-024-02103-x.
7
Role of CD44-Positive Extracellular Vesicles Derived from Highly Metastatic Mouse Mammary Carcinoma Cells in Pre-Metastatic Niche Formation.CD44+ 阳性细胞外囊泡在高转移性小鼠乳腺癌细胞前转移龛形成中的作用。
Int J Mol Sci. 2024 Sep 9;25(17):9742. doi: 10.3390/ijms25179742.
8
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J Zhejiang Univ Sci B. 2024 Jul 15;25(7):581-593. doi: 10.1631/jzus.B2300154.
9
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10
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Int J Mol Sci. 2024 Mar 19;25(6):3449. doi: 10.3390/ijms25063449.
Chem Rev. 2018 Feb 28;118(4):1917-1950. doi: 10.1021/acs.chemrev.7b00534. Epub 2018 Jan 31.
4
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5
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Philos Trans R Soc Lond B Biol Sci. 2018 Jan 5;373(1737). doi: 10.1098/rstb.2017.0065.
6
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7
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Mol Cancer Res. 2017 Jan;15(1):78-92. doi: 10.1158/1541-7786.MCR-16-0191. Epub 2016 Oct 6.
8
Extracellular vesicles secreted by highly metastatic clonal variants of osteosarcoma preferentially localize to the lungs and induce metastatic behaviour in poorly metastatic clones.骨肉瘤高转移克隆变体分泌的细胞外囊泡优先定位于肺部,并在低转移克隆中诱导转移行为。
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9
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Cancer Cell. 2016 May 9;29(5):653-668. doi: 10.1016/j.ccell.2016.03.004. Epub 2016 Apr 21.
10
Tumor-Derived Exosomes and Their Role in Cancer Progression.肿瘤来源的外泌体及其在癌症进展中的作用。
Adv Clin Chem. 2016;74:103-41. doi: 10.1016/bs.acc.2015.12.005. Epub 2016 Apr 7.