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壳寡糖通过抑制 CEMIP 通路抑制 PI3K/AKT/mTOR 抑制骨肉瘤恶性进展。

Chitosan oligosaccharide suppresses osteosarcoma malignancy by inhibiting CEMIP via the PI3K/AKT/mTOR pathway.

机构信息

Department of Orthopedics, The Second Affiliated Hospital of Zhejiang University School of Medicine, Jiefang Campus, 88 Jiefang Road, Shangcheng District, Hangzhou, 310009, China.

Zhejiang University School of Medicine, Zhejiang University Huajiachi Campus, 268 Kaixuan Road, Jianggan District, Hangzhou, 310029, China.

出版信息

Med Oncol. 2023 Sep 5;40(10):294. doi: 10.1007/s12032-023-02165-9.


DOI:10.1007/s12032-023-02165-9
PMID:37668818
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10480286/
Abstract

Osteosarcoma is a malignant bone tumor that is prone to metastasize early and primarily affects children and adolescents. Cell migration-inducing protein (CEMIP) plays a crucial role in the progression and malignancy of various tumor diseases, including osteosarcoma. Chitosan oligosaccharide (COS), an oligomer isolated from chitin, has been found to have significant anti-tumor activity in various cancers. This study investigates the effects of COS on CEMIP expression in osteosarcoma and explores the underlying mechanism. In present study, in vitro experiments were conducted to confirm the inhibitory activity of COS on human osteosarcoma cells. Our results demonstrate that COS possesses inhibitory effects against human osteosarcoma cells and significantly suppresses CEMIP expression in vitro. Next, we studied the inhibition of the expression of CEMIP by COS and then performed bioinformatics analysis to explore the potential inhibitory mechanism of COS against signaling pathways involved in regulating CEMIP expression. Bioinformatics analysis predicted a close association between the PI3K signaling pathway and CEMIP expression and that the inhibitory effect of COS on CEMIP expression may be related to PI3K signaling pathway regulation. The results of this study show that COS treatment significantly inhibits CEMIP expression and the PI3K/AKT/mTOR signaling pathway, as observed both in vitro and in vivo. This study demonstrates that COS could inhibit the expression of CEMIP, which is closely related to osteosarcoma malignancy. This inhibitory effect may be attributed to the inhibition of the PI3K/AKT/mTOR signaling pathway in vitro and in vivo.

摘要

骨肉瘤是一种恶性骨肿瘤,易早期转移,主要影响儿童和青少年。细胞迁移诱导蛋白(CEMIP)在多种肿瘤疾病的进展和恶性转化中发挥着关键作用,包括骨肉瘤。壳聚糖寡糖(COS)是从甲壳素中分离得到的一种低聚物,已被发现对多种癌症具有显著的抗肿瘤活性。本研究探讨了 COS 对骨肉瘤中 CEMIP 表达的影响,并探讨了其潜在的作用机制。在本研究中,进行了体外实验以确认 COS 对人骨肉瘤细胞的抑制活性。结果表明,COS 对人骨肉瘤细胞具有抑制作用,并显著抑制 CEMIP 的体外表达。接下来,我们研究了 COS 对 CEMIP 表达的抑制作用,并进行了生物信息学分析,以探讨 COS 对调节 CEMIP 表达的信号通路的潜在抑制机制。生物信息学分析预测 PI3K 信号通路与 CEMIP 表达密切相关,COS 对 CEMIP 表达的抑制作用可能与 PI3K 信号通路的调节有关。本研究结果表明,COS 处理可显著抑制 CEMIP 表达和 PI3K/AKT/mTOR 信号通路,无论是在体外还是体内。本研究表明,COS 可以抑制与骨肉瘤恶性程度密切相关的 CEMIP 表达。这种抑制作用可能归因于体外和体内 PI3K/AKT/mTOR 信号通路的抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/8d13c980a72e/12032_2023_2165_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/29bc36dd1d34/12032_2023_2165_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/bb76a923ee12/12032_2023_2165_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/c48803cff712/12032_2023_2165_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/dd5fdc70a5ad/12032_2023_2165_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/42de50c161c9/12032_2023_2165_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/7bde47aec38e/12032_2023_2165_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/f70810e5df67/12032_2023_2165_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/8d13c980a72e/12032_2023_2165_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/29bc36dd1d34/12032_2023_2165_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/bb76a923ee12/12032_2023_2165_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/c48803cff712/12032_2023_2165_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/dd5fdc70a5ad/12032_2023_2165_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/42de50c161c9/12032_2023_2165_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/7bde47aec38e/12032_2023_2165_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/f70810e5df67/12032_2023_2165_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b20b/10480286/8d13c980a72e/12032_2023_2165_Fig8_HTML.jpg

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引用本文的文献

[1]
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Discov Oncol. 2025-6-7

[2]
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Oncol Res. 2025-3-19

本文引用的文献

[1]
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J Alzheimers Dis. 2023

[2]
Evolution of Natural Product Scaffolds as Potential Proteasome Inhibitors in Developing Cancer Therapeutics.

Metabolites. 2023-3-31

[3]
Osteosarcoma: Current Concepts and Evolutions in Management Principles.

J Clin Med. 2023-4-9

[4]
Potential mechanisms of osthole against bladder cancer cells based on network pharmacology, molecular docking, and experimental validation.

BMC Complement Med Ther. 2023-4-17

[5]
CEMIP, acting as a scaffold protein for bridging GRAF1 and MIB1, promotes colorectal cancer metastasis via activating CDC42/MAPK pathway.

Cell Death Dis. 2023-2-27

[6]
Inhibition of CEMIP potentiates the effect of sorafenib on metastatic hepatocellular carcinoma by reducing the stiffness of lung metastases.

Cell Death Dis. 2023-1-13

[7]
KIAA1199 Correlates With Tumor Microenvironment and Immune Infiltration in Lung Adenocarcinoma as a Potential Prognostic Biomarker.

Pathol Oncol Res. 2022

[8]
CEMIP, a Promising Biomarker That Promotes the Progression and Metastasis of Colorectal and Other Types of Cancer.

Cancers (Basel). 2022-10-18

[9]
CEMIP Promotes Osteosarcoma Progression and Metastasis Through Activating Notch Signaling Pathway.

Front Oncol. 2022-7-26

[10]
Cell migration inducing hyaluronidase 1 promotes growth and metastasis of papillary thyroid carcinoma.

Bioengineered. 2022-5

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