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鉴定血浆 hsa_circ_0008673 表达作为乳腺癌的潜在生物标志物和肿瘤调控因子。

Identification of plasma hsa_circ_0008673 expression as a potential biomarker and tumor regulator of breast cancer.

机构信息

Department of Breast and Thyroid Surgery, Wuhan Integrated TCM & Western Medicine Hospital, Hubei, China.

出版信息

J Clin Lab Anal. 2020 Sep;34(9):e23393. doi: 10.1002/jcla.23393. Epub 2020 Aug 18.

DOI:10.1002/jcla.23393
PMID:32808350
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7521290/
Abstract

OBJECTIVE

Cell-free circular RNAs (circRNAs) are stable and abundantly exist in body fluids. In this study, we aimed to investigate plasma cell-free circRNAs as a novel class of biomarkers for the diagnosis of breast cancer (BC).

METHODS

Differentially expressed circRNAs from 6 normal and 6 BC plasma samples were detected by microarray. Hsa_circ_0008673 was then screened and validated in the plasma of 102 normal and 378 BC samples. A receiver operating characteristic (ROC) curve was used to evaluate the diagnostic value. The correlations between hsa_circ_0008673 expression and demographic characteristics, tumor features, and prognosis were analyzed. The effects of hsa_circ_0008673 on BC cell proliferation and metastasis were also measured.

RESULTS

Of the top ten up-regulated (hsa_circ_0008673, hsa_circ_0008500, hsa_circ_0005260, hsa_circ_0003423, hsa_circ_0119881, hsa_circ_0000987, hsa_circ_0007386, hsa_circ_0000091, hsa_circ_0016601, and hsa_circ_0008549) and top ten down-regulated (hsa_circ_0000826, hsa_circ_0072697, hsa_circ_0004587, hsa_circ_0000471, hsa_circ_0007786, hsa_circ_0001417, hsa_circ_0005982, hsa_circ_0001566, hsa_circ_0003823, and hsa_circ_0003823) circRNAs from microarray, hsa_circ_0008673 was the most significantly up-regulated circRNA in BC, and represented a good diagnostic value. Hsa_circ_0008673 was remarkably down-regulated after breast mastectomy. Hsa_circ_0008673 expression was associated with larger tumor size, distant metastasis, positive estrogen receptor (ER) status, and positive progesterone receptor (PR) status. Additionally, hsa_circ_0008673 could serve as a prognostic predicator of overall survival (OS) and disease-specific survival (DSS). Cell assays proved that hsa_circ_0008673 knockdown contributed to inhibition of tumor cell proliferation and migration.

CONCLUSION

Plasma cell-free hsa_circ_0008673 was up-regulated in BC, which was associated with poorer prognosis and promoted tumor proliferation and metastasis. Hsa_circ_0008673 is a promising biomarker for tumor diagnosis and prognostic assessment of BC patients.

摘要

目的

无细胞循环 RNA(circRNAs)在体液中稳定且大量存在。本研究旨在探讨血浆无细胞 circRNAs 是否可作为乳腺癌(BC)诊断的新型生物标志物。

方法

采用微阵列检测 6 例正常和 6 例 BC 血浆样本中的差异表达 circRNAs。然后在 102 例正常和 378 例 BC 样本中筛选和验证 hsa_circ_0008673。使用受试者工作特征(ROC)曲线评估诊断价值。分析 hsa_circ_0008673 表达与人口统计学特征、肿瘤特征和预后的相关性。还测量了 hsa_circ_0008673 对 BC 细胞增殖和转移的影响。

结果

在微阵列中,十大上调(hsa_circ_0008673、hsa_circ_0008500、hsa_circ_0005260、hsa_circ_0003423、hsa_circ_0119881、hsa_circ_0000987、hsa_circ_0007386、hsa_circ_0000091、hsa_circ_0016601 和 hsa_circ_0008549)和十大下调(hsa_circ_0000826、hsa_circ_0072697、hsa_circ_0004587、hsa_circ_0000471、hsa_circ_0007786、hsa_circ_0001417、hsa_circ_0005982、hsa_circ_0001566、hsa_circ_0003823 和 hsa_circ_0003823)circRNAs 中,hsa_circ_0008673 在 BC 中上调最显著,具有良好的诊断价值。hsa_circ_0008673 在乳房切除术后显著下调。hsa_circ_0008673 的表达与肿瘤体积较大、远处转移、雌激素受体(ER)阳性和孕激素受体(PR)阳性有关。此外,hsa_circ_0008673 可作为总生存(OS)和疾病特异性生存(DSS)的预后预测因子。细胞试验证明 hsa_circ_0008673 敲低有助于抑制肿瘤细胞增殖和迁移。

结论

BC 患者血浆无细胞 hsa_circ_0008673 上调,与预后不良相关,并促进肿瘤增殖和转移。hsa_circ_0008673 是一种有前途的肿瘤诊断和 BC 患者预后评估的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/d6ad490aec10/JCLA-34-e23393-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/6643a369ce2b/JCLA-34-e23393-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/a5e06482d143/JCLA-34-e23393-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/288492b9258c/JCLA-34-e23393-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/57bd482f37ff/JCLA-34-e23393-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/d6ad490aec10/JCLA-34-e23393-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/6643a369ce2b/JCLA-34-e23393-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/a5e06482d143/JCLA-34-e23393-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/288492b9258c/JCLA-34-e23393-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/57bd482f37ff/JCLA-34-e23393-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c3/7521290/d6ad490aec10/JCLA-34-e23393-g005.jpg

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