Musashi-1在妇科恶性肿瘤发生发展中的作用
作者: |
1常红霞,
2张三元,
2李风艳
1 山西医科大学,山西 太原 030001 2 山西医科大学第一医院妇科,山西 太原 030001 |
通讯: |
张三元
Email: zsyprofessor@aliyun.com |
DOI: | 10.3978/j.issn.2095-6959.2021.04.024 |
基金: | 山西省重点研发计划项目(201803D31111)。 |
摘要
妇科恶性肿瘤严重威胁女性健康,尽管目前治疗策略相对有效,但复发及耐药仍是影响整体生存率的重要因素。研究表明肿瘤的复发及耐药与具有自我更新、无限增殖、多向分化潜能及高致瘤性的肿瘤干细胞(cancer stem cells,CSCs)亚群密切相关。Musashi-1是一种最新研究报道的CSCs标志物,多数研究认为其通过Notch、Wnt等信号通路发挥作用,在多种肿瘤组织中异常表达,在妇科恶性肿瘤中高表达,且与肿瘤的分期、分化、血管浸润及化学药物治疗耐药等密切相关。深入研究其在妇科恶性肿瘤中的作用机制,可为妇科恶性肿瘤的临床治疗提供新思路。现就Musashi-1在妇科恶性肿瘤中的表达情况及作用机制进行综述。
关键词:
Musashi-1;妇科恶性肿瘤;信号通路
Role of Musashi-1 in the development of gynecological malignancies
CorrespondingAuthor: ZHANG Sanyuan Email: zsyprofessor@aliyun.com
DOI: 10.3978/j.issn.2095-6959.2021.04.024
Foundation: This work was supported by the Key Research and Development Project of Shanxi Province, China (201803D31111).
Abstract
Gynecological malignancies seriously threaten women’s health. Although current treatment strategies are relatively effective, relapse and drug resistance are still important factors affecting the overall survival rate of malignancies. Studies have shown that tumor recurrence and drug resistance are closely related to cancer stem cells (CSCs) subpopulations with self-renewal, infinite proliferation, multi-directional differentiation potential, and high tumorigenicity. Musashi-1 is a CSCs marker reported by the latest research. Most studies believe that it plays a role through signaling pathways such as Notch and Wnt. It is abnormally expressed in a variety of tumor tissues and highly expressed in gynecological malignant tumors. Besides, Musashi-1 is closely related to tumor stage, differentiation, vascular invasion and chemotherapy resistance. The in-depth study of its action mechanism in gynecological malignant tumors can provide new ideas for the clinical treatment of gynecological malignant tumors. This manuscript reviews the expression and action mechanism of Musashi-1 in gynecological malignant tumors.
Keywords:
Musashi-1; gynecological malignancy; signal pathway