Suppr超能文献

实体瘤中的细胞视黄酸结合蛋白2

Cellular Retinoic-Acid Binding Protein 2 in Solid Tumor.

作者信息

Jiao Xiaoyang, Liu Rang, Huang Jiali, Lu Lichun, Li Zibo, Xu Liyan, Li Enmin

机构信息

Cell biology and genetics department, Shantou University Medical College Shantou, Guangdong, China.

The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College Shantou, Guangdong, China.

出版信息

Curr Protein Pept Sci. 2020;21(5):507-516. doi: 10.2174/1389203721666200203150721.

Abstract

The retinoic acid (RA) signaling pathway is crucial for many biological processes. The RA transporter, Cellular Retinoic-Acid Binding Protein 2 (CRABP2), is abnormally expressed in various tumor types. CRABP2 presents significant effects on tumorous behaviors and functions, including cell proliferation, apoptosis, invasion, migration, metastasis, and angiogenesis. The tumorigenesis mechanism of CRABP2, as both suppressor and promotor, is complicated, therefore, there remains the need for further investigation. Elucidating the regulating mechanisms in a specific stage of the tumor could facilitate CRABP2 to be a biomarker in cancer diagnosis and prognosis. Besides, clarifying the pathways of CRABP2 in cancer development will contribute to the gene-targeted therapy. In this review, we summarized the expression, distribution, and mechanism of CRABP2 in solid tumors. Illuminating the CRABP2 signaling pathway may benefit understanding the retinoid signaling pathway, providing a useful biomarker for future clinical trials.

摘要

维甲酸(RA)信号通路对许多生物学过程至关重要。RA转运蛋白,即细胞视黄酸结合蛋白2(CRABP2),在多种肿瘤类型中异常表达。CRABP2对肿瘤行为和功能具有显著影响,包括细胞增殖、凋亡、侵袭、迁移、转移和血管生成。CRABP2作为抑癌因子和促癌因子的肿瘤发生机制很复杂,因此,仍需要进一步研究。阐明肿瘤特定阶段的调控机制可能有助于CRABP2成为癌症诊断和预后的生物标志物。此外,阐明CRABP2在癌症发展中的途径将有助于基因靶向治疗。在本综述中,我们总结了CRABP2在实体瘤中的表达、分布及机制。阐明CRABP2信号通路可能有助于理解类视黄醇信号通路,为未来的临床试验提供有用的生物标志物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验