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本文引用的文献

1
Optimized exosome isolation protocol for cell culture supernatant and human plasma.优化的细胞培养上清液和人血浆外泌体分离方案。
J Extracell Vesicles. 2015 Jul 17;4:27031. doi: 10.3402/jev.v4.27031. eCollection 2015.
2
High-grade ovarian cancer secreting effective exosomes in tumor angiogenesis.高级别卵巢癌在肿瘤血管生成中分泌有效的外泌体。
Int J Clin Exp Pathol. 2015 May 1;8(5):5062-70. eCollection 2015.
3
Exosomes in cancer: small particle, big player.癌症中的外泌体:小颗粒,大作用。
J Hematol Oncol. 2015 Jul 10;8:83. doi: 10.1186/s13045-015-0181-x.
4
Exosomes serve as tumour markers for personalized diagnostics owing to their important role in cancer metastasis.外泌体在癌症转移中发挥着重要作用,因此可作为用于个性化诊断的肿瘤标志物。
J Extracell Vesicles. 2015 Jun 19;4:27522. doi: 10.3402/jev.v4.27522. eCollection 2015.
5
Transketolase is upregulated in metastatic peritoneal implants and promotes ovarian cancer cell proliferation.转酮醇酶在转移性腹膜种植体中上调,并促进卵巢癌细胞增殖。
Clin Exp Metastasis. 2015 Jun;32(5):441-55. doi: 10.1007/s10585-015-9718-1. Epub 2015 Apr 21.
6
Cancer exosomes perform cell-independent microRNA biogenesis and promote tumorigenesis.癌症外泌体可进行非细胞依赖的微小RNA生物合成并促进肿瘤发生。
Cancer Cell. 2014 Nov 10;26(5):707-21. doi: 10.1016/j.ccell.2014.09.005. Epub 2014 Oct 23.
7
Metabolic effect of TAp63α: enhanced glycolysis and pentose phosphate pathway, resulting in increased antioxidant defense.TAp63α的代谢效应:增强糖酵解和磷酸戊糖途径,从而增强抗氧化防御能力。
Oncotarget. 2014 Sep 15;5(17):7722-33. doi: 10.18632/oncotarget.2300.
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Stromal fibroblast-derived miR-409 promotes epithelial-to-mesenchymal transition and prostate tumorigenesis.基质成纤维细胞衍生的 miR-409 促进上皮-间充质转化和前列腺肿瘤发生。
Oncogene. 2015 May 21;34(21):2690-9. doi: 10.1038/onc.2014.212. Epub 2014 Jul 28.
9
Regulation of the pentose phosphate pathway in cancer.癌症中磷酸戊糖途径的调控
Protein Cell. 2014;5(8):592-602. doi: 10.1007/s13238-014-0082-8. Epub 2014 Jul 12.
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Methylseleninic acid sensitizes Notch3-activated OVCA429 ovarian cancer cells to carboplatin.甲基亚硒酸使Notch3激活的OVCA429卵巢癌细胞对卡铂敏感。
PLoS One. 2014 Jul 10;9(7):e101664. doi: 10.1371/journal.pone.0101664. eCollection 2014.

外泌体介导的磷酸戊糖途径在卵巢癌转移中的作用:蛋白质组学分析

Exosomes mediated pentose phosphate pathway in ovarian cancer metastasis: a proteomics analysis.

作者信息

Yi Huan, Zheng Xiangqin, Song Jianrong, Shen Rongkai, Su Yanzhao, Lin Danmei

机构信息

Gynecological Oncology, Fujian Maternity and Children Health Hospital Fujian Medical University Teaching Hospital Fuzhou 350005, China.

The First Affiliated Hospital of Fujian Medical University Fuzhou 350005, China.

出版信息

Int J Clin Exp Pathol. 2015 Dec 1;8(12):15719-28. eCollection 2015.

PMID:26884841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4730054/
Abstract

Epithelial ovarian cancer is the most lethal gynecological malignancies for readily metastasis. Exosomes have played an influential role in carcinogenicity and cancer progression. Our aim is to discover exosome-related mechanisms in ovarian cancer progress and explore potential diagnostic biomarkers and therapeutic targets of ovarian cancer. We initially presented the proteomic profiles of exosomes derived from two late-stage ovarian cell lines, OVCA429 and HO8910PM. A total of 2940 exosomal proteins were recorded by MS. FunRich appropriately processed these exosomal proteins, manifesting some superiority in contrast to Blast2go. Moreover, we demonstrated the pentose phosphate pathway was a dominant mechanism in exosome mediated intracellular communication. Glucose-6-phosphate dehydrogenase, transketolase and transaldolase 1, three key enzymes regulated pentose phosphate pathway, were all marked in the same exosomal parts of proteins between two ovarian cell lines. Moreover, these key proteins might become diagnostic, prognostic biomarkers and therapeutic targets of ovarian cancer.

摘要

上皮性卵巢癌是最致命的妇科恶性肿瘤,极易发生转移。外泌体在致癌性和癌症进展中发挥了重要作用。我们的目的是发现卵巢癌进展中与外泌体相关的机制,并探索卵巢癌潜在的诊断生物标志物和治疗靶点。我们最初展示了源自两种晚期卵巢癌细胞系OVCA429和HO8910PM的外泌体的蛋白质组学图谱。通过质谱记录了总共2940种外泌体蛋白。FunRich对这些外泌体蛋白进行了适当处理,与Blast2go相比显示出一些优势。此外,我们证明磷酸戊糖途径是外泌体介导的细胞内通讯的主要机制。葡萄糖-6-磷酸脱氢酶、转酮醇酶和转醛醇酶1这三种调节磷酸戊糖途径的关键酶,在两种卵巢癌细胞系的相同外泌体蛋白部分均有标记。此外,这些关键蛋白可能成为卵巢癌的诊断、预后生物标志物和治疗靶点。