国际肿瘤学杂志 ›› 2025, Vol. 52 ›› Issue (9): 583-586.doi: 10.3760/cma.j.cn371439-20250331-00098

• 综述 • 上一篇    下一篇

SHCBP1在恶性肿瘤中的作用机制及临床研究进展

刘美1, 胡玉崇1,2(), 李凤桐1, 朝乐门1, 柳檬1, 亢琳琳3   

  1. 1内蒙古医科大学内蒙古临床学院,呼和浩特 010017
    2内蒙古自治区人民医院妇产科,呼和浩特 010017
    3内蒙古科技大学包头医学院,包头 014040
  • 收稿日期:2025-03-31 修回日期:2025-05-22 出版日期:2025-09-08 发布日期:2025-10-21
  • 通讯作者: 胡玉崇 E-mail:bigbear2002.student@sina.com

Mechanism of action of SHCBP1 in malignant tumors and progress in clinical research

Liu Mei1, Hu Yuchong1,2(), Li Fengtong1, Chao Lemen1, Liu Meng1, Kang Linlin3   

  1. 1Affiliated Inner Mongolia Clinical College of Inner Mongolia Medical University, Hohhot 010017, China
    2Department of Gynecology and Obstetrics, Inner Mongolia People's Hospital, Hohhot 010017, China
    3Baotou Medical College, Inner Mongolia University of Science & Technology, Baotou 014040, China
  • Received:2025-03-31 Revised:2025-05-22 Online:2025-09-08 Published:2025-10-21
  • Contact: Hu Yuchong E-mail:bigbear2002.student@sina.com

摘要:

SHCBP1是一种可特异性结合SH2结构域的Src同源胶原蛋白,可作为关键调控蛋白,在多种恶性肿瘤中呈异常高表达,通过影响细胞周期、增殖和侵袭等过程,参与肿瘤的发生与发展。此外,SHCBP1高表达与多种恶性肿瘤化疗耐药及不良预后密切相关,靶向抑制可增强化疗敏感性,为多种实体瘤提供新的治疗策略,是重要的预后评估生物标志物和潜在治疗靶点。

关键词: 肿瘤, 含Src同源结构域2转化蛋白质1, 细胞增殖, 细胞运动, 肿瘤微环境, 预后

Abstract:

SHCBP1 is a type of Src homologous collagen that can specifically bind to the SH2 structural domain. It can act as a key regulatory protein, and exhibits abnormally high expression in a variety of malignant tumors. Through affecting the processes such as cell cycle, proliferation, and invasion, it participates in tumor genesis and development. In addition, high expression of SHCBP1 is closely related to chemotherapy resistance and poor prognosis of many malignant tumors, and its targeted inhibition can enhance the sensitivity of chemotherapy and provide new therapeutic strategies for a variety of solid tumors, making it an important biomarker for prognostic assessment and a potential therapeutic target.

Key words: Neoplasms, Src homology 2 domain-containing, transforming protein 1, Cell proliferation, Cell movement, Tumor microenvironment, Prognosis