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GT198 癌蛋白疫苗可延缓 MMTV-PyMT 小鼠肿瘤生长。

Oncoprotein GT198 vaccination delays tumor growth in MMTV-PyMT mice.

机构信息

Georgia Cancer Center, Medical College of Georgia, Augusta University, Augusta, GA, USA; Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta University, Augusta, GA, USA.

Department of General Surgery, The First of Affiliated Hospital of Jinan University, And Institute of Precision Cancer Medicine and Pathology, Jinan University Medical College, Guangzhou, Guangdong, China; Research Center of Translational Medicine, The Second Affiliated Hospital of Shantou University Medical College, Shantou, China.

出版信息

Cancer Lett. 2020 Apr 28;476:57-66. doi: 10.1016/j.canlet.2020.02.005. Epub 2020 Feb 12.

Abstract

Targeting early lesion in breast cancer is more therapeutically effective. We have previously identified an oncoprotein GT198 (PSMC3IP) in human breast cancer. Here we investigated GT198 in MMTV-PyMT mouse mammary gland tumors and found that GT198 is a shared early lesion in both species. Similar to human breast cancer even before a tumor appears, cytoplasmic GT198 is overexpressed in mouse tumor stroma including pericyte stem cells, descendent adipocytes, fibroblasts, and myoepithelial cells. Using recombinant GT198 protein as an antigen, we vaccinated MMTV-PyMT mice and found that the GT198 vaccine delayed mouse tumor growth and reduced lung metastasis. The antitumor effects were linearly correlated with vaccinated mouse serum titers of GT198 antibody, which recognized cell surface GT198 protein on viable tumor cells confirmed by FACS. Furthermore, GT198 tumor cells isolated from MMTV-PyMT tumor induced faster tumor growths than GT198 cells when re-implanted into normal FVB/N mice. Together, this first study of GT198 vaccine in mouse showed its effectiveness in antitumor and anti-metastasis. The finding supports GT198 as a potential target in human immunotherapy since GT198 defect is shared in both human and mouse.

摘要

针对乳腺癌早期病变的治疗效果更佳。我们之前在人类乳腺癌中发现了一种癌蛋白 GT198(PSMC3IP)。在这里,我们研究了 MMTV-PyMT 小鼠乳腺肿瘤中的 GT198,发现 GT198 是两种物种中共同的早期病变。与人类乳腺癌类似,甚至在肿瘤出现之前,细胞质 GT198 在小鼠肿瘤基质中过度表达,包括周细胞干细胞、衍生的脂肪细胞、成纤维细胞和肌上皮细胞。我们使用重组 GT198 蛋白作为抗原对 MMTV-PyMT 小鼠进行了疫苗接种,发现 GT198 疫苗延迟了小鼠肿瘤的生长并减少了肺转移。抗肿瘤作用与接种小鼠血清中 GT198 抗体的效价呈线性相关,该效价通过 FACS 证实可识别活肿瘤细胞表面的 GT198 蛋白。此外,从 MMTV-PyMT 肿瘤中分离的 GT198 肿瘤细胞在重新植入正常 FVB/N 小鼠时比 GT198 细胞引起更快的肿瘤生长。总之,这项关于 GT198 疫苗在小鼠中的首次研究表明,它在抗肿瘤和抗转移方面具有有效性。这一发现支持将 GT198 作为人类免疫治疗的潜在靶点,因为 GT198 缺陷在人类和小鼠中均存在。

相似文献

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Oncoprotein GT198 vaccination delays tumor growth in MMTV-PyMT mice.GT198 癌蛋白疫苗可延缓 MMTV-PyMT 小鼠肿瘤生长。
Cancer Lett. 2020 Apr 28;476:57-66. doi: 10.1016/j.canlet.2020.02.005. Epub 2020 Feb 12.
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GT198 Expression Defines Mutant Tumor Stroma in Human Breast Cancer.GT198表达定义了人类乳腺癌中的突变肿瘤基质。
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本文引用的文献

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Turning the corner on therapeutic cancer vaccines.癌症治疗性疫苗迎来转机。
NPJ Vaccines. 2019 Feb 8;4:7. doi: 10.1038/s41541-019-0103-y. eCollection 2019.
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GT198 Expression Defines Mutant Tumor Stroma in Human Breast Cancer.GT198表达定义了人类乳腺癌中的突变肿瘤基质。
Am J Pathol. 2016 May;186(5):1340-50. doi: 10.1016/j.ajpath.2016.01.006. Epub 2016 Mar 18.

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