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软骨寡聚基质蛋白通过激活PI3K/AKT/Bcl-2信号通路影响甲状腺乳头状癌细胞的生物学行为。

Cartilage oligomeric matrix protein affects the biological behavior of papillary thyroid carcinoma cells by activating the PI3K/AKT/Bcl-2 pathway.

作者信息

Zhang Jirong, Wang Hongzhi, Lv Chunpeng, Han Jun, Hao Mingyu, Li Jingjing, Qiao Hong

机构信息

Department of Geriatrics, The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, Heilongjiang Province, China.

Epidemiology and Health Statistics, Harbin Medical University, Harbin 150086, Heilongjiang Province, China.

出版信息

J Cancer. 2021 Jan 15;12(6):1623-1633. doi: 10.7150/jca.49144. eCollection 2021.

Abstract

To explore the effect of cartilage oligomeric matrix protein (COMP) on papillary thyroid carcinoma (PTC). COMP expression levels in PTC tissues and matched adjacent normal tissues were measured using tissue microarrays. Human PTC cells were cultured and transduced with lentiviral short hairpin RNA against COMP (COMP-shRNA), a negative control (NC) shRNA, or mock transfected (Control). We used the Cell Counting Kit-8, performed colony formation assays, wound healing assays, Transwell invasion assays, flow cytometry, and measured the expression of apoptosis-related proteins at the mRNA and protein levels to explore the effects of COMP on the biological behavior of PTC cells and to discover the specific signaling pathway involved in these processes. COMP expression was significantly higher in PTC tissues than in adjacent normal tissues. At the cellular level, COMP promoted cell migration, increased the invasiveness of PTC cells, and inhibited apoptosis. However, differences in cell proliferation were only observed within 72 hours. At the same time, colony formation assays showed that silencing COMP inhibited the proliferation of PTC cells. We also found that COMP regulated the behavior of PTC cells by activating the PI3K/AKT/Bcl-2 pathway. COMP is upregulated in PTC, which enhances cancer cell invasion and inhibits apoptosis, contributing to the development and progression of PTC. Thus, COMP may serve as a new biomarker for PTC.

摘要

探讨软骨寡聚基质蛋白(COMP)对甲状腺乳头状癌(PTC)的影响。使用组织芯片检测PTC组织及配对的癌旁正常组织中COMP的表达水平。培养人PTC细胞,并用针对COMP的慢病毒短发夹RNA(COMP-shRNA)、阴性对照(NC)shRNA转导,或进行空载体转染(对照)。我们使用细胞计数试剂盒-8、进行集落形成试验、伤口愈合试验、Transwell侵袭试验、流式细胞术,并在mRNA和蛋白质水平检测凋亡相关蛋白的表达,以探讨COMP对PTC细胞生物学行为的影响,并发现这些过程中涉及的特定信号通路。COMP在PTC组织中的表达明显高于癌旁正常组织。在细胞水平上,COMP促进细胞迁移,增加PTC细胞的侵袭性,并抑制细胞凋亡。然而,仅在72小时内观察到细胞增殖的差异。同时,集落形成试验表明,沉默COMP可抑制PTC细胞的增殖。我们还发现COMP通过激活PI3K/AKT/Bcl-2信号通路来调节PTC细胞的行为。COMP在PTC中上调,增强癌细胞侵袭并抑制凋亡,促进PTC的发生和发展。因此,COMP可能作为PTC的一种新的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d5f/7890313/f45160d9fc0a/jcav12p1623g001.jpg

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