奥希替尼通过抑制 MAPK 通路提高宫颈癌化疗疗效

IF 1.8 4区 医学 Q3 ONCOLOGY
Cancer Investigation Pub Date : 2024-05-01 Epub Date: 2024-05-31 DOI:10.1080/07357907.2024.2359987
Yue Hu, Chao Hu
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引用次数: 0

摘要

治疗复发性宫颈癌是一项巨大的挑战。Osimertinib是美国食品及药物管理局批准的表皮生长因子受体(EGFR)抑制剂,是一种很有前景的选择。我们的研究考察了奥希替尼增强紫杉醇对宫颈癌疗效的潜力。奥希替尼能有效抑制癌细胞的生长,并诱导多种细胞系的细胞凋亡。奥西美替尼与紫杉醇联用,可在抑制宫颈癌细胞方面发挥协同作用。重要的是,奥希替尼的抑制作用不依赖于表皮生长因子受体;它以 Mnk 磷酸化为靶点,降低了 eIF4E 的活性。在小鼠体内,奥西替尼-紫杉醇联合疗法在抑制癌症生长方面超过了单个药物。这些临床前研究结果表明,osimertinib可以作为提高紫杉醇在宫颈癌治疗中有效性的一种手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancement of Chemotherapy Efficacy in Cervical Cancer via MAPK Pathway Inhibition by Osimertinib.

Addressing recurrent cervical cancer poses a substantial challenge. Osimertinib, an FDA-approved EGFR inhibitor, has emerged as a promising option. Our study examined its potential to enhance paclitaxel's efficacy against cervical cancer. Osimertinib effectively hindered cancer cell growth and induced apoptosis across multiple cell lines. Combined with paclitaxel, it exhibited synergy in suppressing cervical cancer cells. Importantly, osimertinib's inhibitory effect was EGFR-independent; it targeted Mnk phosphorylation, reducing eIF4E activity. In mice, the combined osimertinib-paclitaxel treatment surpassed individual drugs in inhibiting cancer growth. These preclinical findings suggest osimertinib's repurposing as a means to improve paclitaxel's effectiveness in cervical cancer treatment.

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来源期刊
Cancer Investigation
Cancer Investigation 医学-肿瘤学
CiteScore
3.80
自引率
4.20%
发文量
71
审稿时长
8.5 months
期刊介绍: Cancer Investigation is one of the most highly regarded and recognized journals in the field of basic and clinical oncology. It is designed to give physicians a comprehensive resource on the current state of progress in the cancer field as well as a broad background of reliable information necessary for effective decision making. In addition to presenting original papers of fundamental significance, it also publishes reviews, essays, specialized presentations of controversies, considerations of new technologies and their applications to specific laboratory problems, discussions of public issues, miniseries on major topics, new and experimental drugs and therapies, and an innovative letters to the editor section. One of the unique features of the journal is its departmentalized editorial sections reporting on more than 30 subject categories covering the broad spectrum of specialized areas that together comprise the field of oncology. Edited by leading physicians and research scientists, these sections make Cancer Investigation the prime resource for clinicians seeking to make sense of the sometimes-overwhelming amount of information available throughout the field. In addition to its peer-reviewed clinical research, the journal also features translational studies that bridge the gap between the laboratory and the clinic.
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