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2025/9/28 13:26:57 | Browse: 5 | 下载: 7
Publication Name 世界华人消化杂志
手稿编号 40344
手稿来源省、自治区或特别行政区 浙江省
Received
2025-07-24 03:15
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2025-09-15 10:20
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2025-09-28 13:26
ISSN 1009-3079 (print) and 2219-2859 (online)
开放获取 This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
版权 ©The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
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网址 http://www.wjgnet.com
专业类型 消化内科学
手稿栏目类型 临床研究
文章标题 阿帕替尼通过VEGFR2-PLC-ERK1/2通路抑制结肠癌LS174T细胞增殖的机制研究
手稿来源 自由来稿
所有作者列表 崔亦筱, 余德顺, 张诗琪
ORCID
作者 ORCID Number
崔亦筱 http://orcid.org/0000-0001-7133-4997
基金项目及其编号
通讯作者 崔亦筱, 本科, 主治医师, 310000, 浙江省杭州市拱墅区东新路848号, 树兰(杭州)医院药剂科. songjing79196567@163.com
关键词 结肠癌; 阿帕替尼; 细胞凋亡; 细胞周期; VEGFR2-PLC-ERK1/2通路
核心内容提要 结肠癌(colorectal cancer, CRC)治疗中, 血管内皮生长因子/血管内皮生长因子受体[(vascular endothelial growth factor, VEGF)/(vascular endothelial growth factor receptor, VEGFR)]靶向药物是研究重点. 阿帕替尼作为小分子酪氨酸激酶抑制剂, 通过特异性结合VEGFR-2, 抑制VEGF诱导的内皮细胞增殖及微血管生成. 其机制涉及阻断VEGFR2-PLC-ERK1/2信号通路, 进而抑制肿瘤血管形成和CRC细胞增殖. 体外及裸鼠移植实验证实, 阿帕替尼对胃癌、CRC等实体瘤具有显著抗肿瘤活性, 为晚期CRC治疗提供了新策略.
出版日期 2025-09-28 13:26
引文著录 崔亦筱, 余德顺, 张诗琪. 阿帕替尼通过VEGFR2-PLC-ERK1/2通路抑制结肠癌LS174T细胞增殖的机制研究. 世界华人消化杂志 2025; 33(9): 741-748
URL https://www.wjgnet.com/1009-3079/full/v33/i9/741.htm
DOI https://dx.doi.org/10.11569/wcjd.v33.i9.741
Full Article (PDF) WCJD-33-741-with-cover.pdf
审稿意见 WCJD-40344-Peer-review(s).pdf
科学编辑工作清单 WCJD-40344-Scientific editor work list.pdf