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甘薯 SPG-56 通过促进细胞凋亡和抑制转移抑制 MCF-7 荷瘤小鼠体内乳腺癌的生长

Anti-breast Cancer Activity of SPG-56 from Sweet Potato in MCF-7 Bearing Mice in Situ through Promoting Apoptosis and Inhibiting Metastasis.

机构信息

School of Pharmaceutical Sciences, Southwest University, Chongqing, 400716, China.

McLean Hospital, Harvard Medical School, Belmont, 02478, MA, USA.

出版信息

Sci Rep. 2019 Jan 16;9(1):146. doi: 10.1038/s41598-018-29099-x.

DOI:10.1038/s41598-018-29099-x
PMID:30651572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6335419/
Abstract

SPG-56 is a newly isolated glycoprotein from sweet potatoes (Zhongshu NO. 1), but its value for suppressing breast cancer progression remains unknown. This study was designed to investigate the potential anti-cancer effects of SPG-56, which consists of 2.9% sugar and 97.1% protein. The effects of SPG-56 on the proliferation and apoptosis of breast cancer cells were determined using CCK-8 and Hoechst 33342 assays and flow cytometry, after staining with Annexin V and PI respectively. The activities of SPG-56 against breast cancer were examined using female BALB/c nude mice orthotopically implanted with human breast carcinoma cells of the types MCF-7 and 4T1-Luc. The cellular experiments showed that SPG-56 inhibited proliferation and promoted apoptosis of MCF-7 cells dose- and time-dependently. Oral administration of SPG-56 significantly suppressed the development of MCF-7 tumor cells (P < 0.01) as compared with an untreated group. The serum tumor markers CEA, CA125 and CA153 in a 240 mg/kg/d SPG-56 decreased by 54.8%, 91.8%, and 90.3%, respectively. The experiments further demonstrated that SPG-56 inhibited the metastasis of breast cancer in MCF-7 and 4T1-bearing mice by altering the expression of MMP2, MMP9, VEGF, Occludin and Claudin. It is concluded that SPG-56 may have potential as a novel anti-tumor candidate for breast cancer.

摘要

SPG-56 是从甘薯(中薯 1 号)中分离得到的一种新的糖蛋白,但它抑制乳腺癌进展的价值尚不清楚。本研究旨在探讨 SPG-56 的潜在抗癌作用,SPG-56 由 2.9%的糖和 97.1%的蛋白质组成。分别用 Annexin V 和 PI 染色后,通过 CCK-8 和 Hoechst 33342 测定法和流式细胞术测定 SPG-56 对乳腺癌细胞增殖和凋亡的影响。通过将人乳腺癌细胞 MCF-7 和 4T1-Luc 原位植入雌性 BALB/c 裸鼠来检查 SPG-56 对乳腺癌的作用。细胞实验表明,SPG-56 呈剂量和时间依赖性地抑制 MCF-7 细胞的增殖并促进其凋亡。与未治疗组相比,SPG-56 的口服给药显著抑制 MCF-7 肿瘤细胞的发展(P<0.01)。SPG-56(240mg/kg/d)治疗组的血清肿瘤标志物 CEA、CA125 和 CA153 分别降低了 54.8%、91.8%和 90.3%。实验进一步表明,SPG-56 通过改变 MMP2、MMP9、VEGF、Occludin 和 Claudin 的表达抑制 MCF-7 和 4T1 荷瘤小鼠的乳腺癌转移。综上所述,SPG-56 可能是一种新型的乳腺癌抗肿瘤候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97f/6335419/3dab5c7151b0/41598_2018_29099_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97f/6335419/f94188ea018b/41598_2018_29099_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97f/6335419/3dab5c7151b0/41598_2018_29099_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97f/6335419/f94188ea018b/41598_2018_29099_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e97f/6335419/3dab5c7151b0/41598_2018_29099_Fig10_HTML.jpg

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