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信号素7a是产后乳腺癌复发的生物标志物。

Semaphorin 7a is a biomarker for recurrence in postpartum breast cancer.

作者信息

Borges Virginia F, Hu Junxiao, Young Chloe, Maggard Jaron, Parris Hannah J, Gao Dexiang, Lyons Traci R

机构信息

Young Women's Breast Cancer Translational Program, University of Colorado Cancer Center, Aurora, CO USA.

Division of Medical Oncology, University of Colorado, Anschutz Medical Center, Aurora, CO USA.

出版信息

NPJ Breast Cancer. 2020 Oct 19;6:56. doi: 10.1038/s41523-020-00198-1. eCollection 2020.

DOI:10.1038/s41523-020-00198-1
PMID:33088913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7572422/
Abstract

Breast cancer is a global health threat and cases diagnosed in women during the years after childbirth, or postpartum breast cancers (PPBCs), have high risk for metastasis. In preclinical murine models, semaphorin 7a (SEMA7A) drives the metastatic potential of postpartum mammary tumors. Thus, we hypothesize that SEMA7A may drive metastasis of PPBC in women. We report that SEMA7A protein expression is increased in PPBCs compared to their nulliparous counterparts in our University of Colorado cohort. Additionally, tumors from PPBC patients with involved lymph nodes and lymphovascular invasion were higher on average suggesting a potential role for SEMA7A as a prognostic biomarker. Consistent with this hypothesis we identify a level of SEMA7A expression in tumors that can predict for recurrence. We propose SEMA7A as a potential biomarker and therapeutic target for PPBC patients, who currently lack strong predictors of outcome and unique targeted therapy options.

摘要

乳腺癌是一种全球性的健康威胁,在产后几年被诊断出的女性乳腺癌病例,即产后乳腺癌(PPBC),具有很高的转移风险。在临床前小鼠模型中,信号素7a(SEMA7A)驱动产后乳腺肿瘤的转移潜能。因此,我们假设SEMA7A可能驱动女性PPBC的转移。我们报告称,在科罗拉多大学队列中,与未生育的对应者相比,PPBC中SEMA7A蛋白表达增加。此外,有淋巴结受累和淋巴管浸润的PPBC患者的肿瘤平均水平更高,这表明SEMA7A作为一种预后生物标志物具有潜在作用。与这一假设一致,我们确定了肿瘤中SEMA7A的表达水平,其可以预测复发。我们提出SEMA7A作为PPBC患者的潜在生物标志物和治疗靶点,这些患者目前缺乏强有力的预后预测指标和独特的靶向治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec65/7572422/59f52df38a52/41523_2020_198_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec65/7572422/0ec85d427955/41523_2020_198_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec65/7572422/59f52df38a52/41523_2020_198_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec65/7572422/0ec85d427955/41523_2020_198_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec65/7572422/59f52df38a52/41523_2020_198_Fig2_HTML.jpg

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本文引用的文献

1
Postpartum breast cancer progression is driven by semaphorin 7a-mediated invasion and survival.产后乳腺癌的进展是由信号素 7a 介导的侵袭和存活所驱动的。
Oncogene. 2020 Mar;39(13):2772-2785. doi: 10.1038/s41388-020-1192-9. Epub 2020 Feb 4.
2
Association Between Postpartum Breast Cancer Diagnosis and Metastasis and the Clinical Features Underlying Risk.产后乳腺癌诊断与转移的相关性及其潜在风险的临床特征。
JAMA Netw Open. 2019 Jan 4;2(1):e186997. doi: 10.1001/jamanetworkopen.2018.6997.
3
Semaphorin 7A Promotes Macrophage-Mediated Lymphatic Remodeling during Postpartum Mammary Gland Involution and in Breast Cancer.
基质细胞脱离诱导的细胞凋亡抵抗由信号素 7a 介导。
Cell Death Dis. 2021 Sep 24;12(10):872. doi: 10.1038/s41419-021-04133-5.
信号素 7A 促进产后乳腺退化和乳腺癌中巨噬细胞介导的淋巴管重塑。
Cancer Res. 2018 Nov 15;78(22):6473-6485. doi: 10.1158/0008-5472.CAN-18-1642. Epub 2018 Sep 25.
4
Vascular Semaphorin 7A Upregulation by Disturbed Flow Promotes Atherosclerosis Through Endothelial β1 Integrin.血管信号素 7A 通过紊乱流促进动脉粥样硬化形成通过内皮 β1 整合素。
Arterioscler Thromb Vasc Biol. 2018 Feb;38(2):335-343. doi: 10.1161/ATVBAHA.117.310491. Epub 2017 Dec 21.
5
Semaphorin 7a exerts pleiotropic effects to promote breast tumor progression.信号素7a发挥多效性作用以促进乳腺肿瘤进展。
Oncogene. 2016 Sep 29;35(39):5170-8. doi: 10.1038/onc.2016.49. Epub 2016 Apr 11.
6
Management of the patient with postpartum breast cancer.产后乳腺癌患者的管理
Oncology (Williston Park). 2014 Sep;28(9):768-70.
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Wound healing-like immune program facilitates postpartum mammary gland involution and tumor progression.伤口愈合样免疫程序促进产后乳腺退化和肿瘤进展。
Int J Cancer. 2015 Apr 15;136(8):1803-13. doi: 10.1002/ijc.29181. Epub 2014 Sep 15.
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Cyclooxygenase-2-dependent lymphangiogenesis promotes nodal metastasis of postpartum breast cancer.环氧化酶-2依赖性淋巴管生成促进产后乳腺癌的淋巴结转移。
J Clin Invest. 2014 Sep;124(9):3901-12. doi: 10.1172/JCI73777. Epub 2014 Aug 18.
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