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整合素β1在食管鳞状细胞癌进展和化疗耐药中的作用。

Role of Integrin β1 in the progression and chemo-resistance of esophageal squamous cell carcinoma.

作者信息

Xie Ying-Hua, Ran Li-Qiang, Wu Zhi-Yong, Sun Chun, Xu Xiu-E, Zou Hai-Ying, Fang Wang-Kai, Xie Jian-Jun

机构信息

Department of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou, China.

Department of Surgical Oncology, Shantou Central Hospital, Affiliated Shantou Hospital of Sun Yat-sen University, Shantou, China.

出版信息

J Cancer. 2022 Mar 28;13(7):2074-2085. doi: 10.7150/jca.68647. eCollection 2022.

Abstract

Integrins have been shown to play an important role in the tumorigenesis of many cancers. In this work, we aimed to explore the expression and clinical value of Integrin α5β1 in esophageal squamous cell carcinoma (ESCC), and the effect of integrin β1 on the development and chemo-resistance of ESCC cells. The expression profiling of integrins was analyzed in the mRNA expression dataset of ESCC. The expression of Integrin α5β1 in 278 cases of ESCC tissues and 62 cases of paracancerous tissues was detected by immunohistochemistry (IHC). The association between the expression of Integrin α5β1 and the survival of ESCC patients was analyzed by Kaplan-Meier analysis. The effect of Integrin β1 on the proliferation, migration, and invasion of ESCC cells was examined by MTS, Transwell migration, and Transwell invasion assay. The effect of Integrin β1 and L1 cell adhesion molecule (L1CAM) on cisplatin resistance was detected by MTS and the signal pathways involved were analyzed by Western blotting. Integrin β1 and Integrin α5 were significantly up-regulated in ESCC. High expression of Integrin β1 was also related to worse overall survival of ESCC patients and patients with low levels of both Integrin β1 and Integrin α5 showed the shortest survival. Results of IHC revealed that Integrin α5β1 was up-regulated in ESCC and its high expression was associated with poor prognosis and could serve as an independent prognostic factor. siRNA-mediated Integrin β1 silencing or antibody blocking restrained the proliferation, migration, and invasion of ESCC cells. Simultaneous knockdown of Integrin β1 and L1CAM reduced the cisplatin resistance of ESCC cells. Further studies showed that knockdown of Integrin β1 and L1CAM suppressed the activity of Akt signaling with or without cisplatin treatment. Moreover, dual high expression of Integrin β1 and L1CAM was related to worse overall survival of ESCC patients treated with preoperative chemotherapy. Integrin α5β1 was up-regulated in ESCC and could be used as a new prognostic indicator for ESCC patients. In addition, Integrin β1 was involved in the proliferation, invasion, and chemo-resistance of ESCC cells.

摘要

整合素已被证明在多种癌症的肿瘤发生中起重要作用。在本研究中,我们旨在探讨整合素α5β1在食管鳞状细胞癌(ESCC)中的表达及临床价值,以及整合素β1对ESCC细胞发育和化疗耐药性的影响。在ESCC的mRNA表达数据集中分析了整合素的表达谱。采用免疫组织化学(IHC)检测278例ESCC组织和62例癌旁组织中整合素α5β1的表达。通过Kaplan-Meier分析整合素α5β1的表达与ESCC患者生存率之间的关系。采用MTS法、Transwell迁移实验和Transwell侵袭实验检测整合素β1对ESCC细胞增殖、迁移和侵袭的影响。采用MTS法检测整合素β1和L1细胞粘附分子(L1CAM)对顺铂耐药性的影响,并通过蛋白质免疫印迹法分析相关信号通路。整合素β1和整合素α5在ESCC中显著上调。整合素β1的高表达也与ESCC患者较差的总生存率相关,且整合素β1和整合素α5水平均低的患者生存期最短。免疫组织化学结果显示,整合素α5β1在ESCC中上调,其高表达与预后不良相关,可作为独立的预后因素。siRNA介导的整合素β1沉默或抗体阻断可抑制ESCC细胞的增殖、迁移和侵袭。同时敲低整合素β1和L1CAM可降低ESCC细胞的顺铂耐药性。进一步研究表明,无论是否进行顺铂治疗,敲低整合素β1和L1CAM均可抑制Akt信号通路的活性。此外,整合素β1和L1CAM的双高表达与接受术前化疗的ESCC患者较差的总生存率相关。整合素α5β1在ESCC中上调,可作为ESCC患者的新预后指标。此外,整合素β1参与了ESCC细胞的增殖、侵袭和化疗耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb10/9066195/caaa429f47b9/jcav13p2074g001.jpg

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