中国癌症杂志 ›› 2024, Vol. 34 ›› Issue (6): 590-597.doi: 10.19401/j.cnki.1007-3639.2024.06.007

• 综述 • 上一篇    下一篇

人源胰腺癌类器官模型的构建及应用新进展

陈虹1,2,3(), 曹治云1,2,3()()   

  1. 1.福建中医药大学中西医结合研究院,福建 福州 350122
    2.福建省中西医结合老年性疾病重点实验室,福建 福州 350122
    3.福建省高校中西医结合基础重点实验室,福建 福州 350122
  • 收稿日期:2024-01-03 修回日期:2024-04-11 出版日期:2024-06-30 发布日期:2024-07-16
  • 通信作者: 曹治云(ORCID:0000-0002-4873-149X),研究员,博士研究生导师。E-mail: caozhiyun@fjtcm.edu.cn。
  • 作者简介:陈 虹(ORCID:0009-0005-6889-077X),硕士。
  • 基金资助:
    漳州片仔癀药业股份有限公司横向联合项目(YHT-21104)

Recent progress in the construction and application of patient-derived pancreatic cancer organoid models

CHEN Hong1,2,3(), CAO Zhiyun1,2,3()()   

  1. 1. Institute of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou 350122, Fujian Province, China
    2. Key Laboratory of Integrative Medicine for Geriatric Diseases of Fujian Province, Fuzhou 350122, Fujian Province, China
    3. Fujian Key Laboratory of Integrative Medicine, Fujian University, Fuzhou 350122, Fujian Province, China
  • Received:2024-01-03 Revised:2024-04-11 Published:2024-06-30 Online:2024-07-16

摘要:

胰腺癌严重威胁人类健康,其高度异质性和恶性表型使患者的5年生存率仅为7.2%。胰腺癌的发病机制及药物开发研究常依赖于传统的二维培养模型(细胞系)和患者来源异种移植瘤模型,但因细胞系缺乏肿瘤的三维环境和异质性特征,而异种移植瘤模型则存在培养时间长、成功率低、难以开展高通量药物筛选等问题,急需开发可高度反映胰腺癌特征和分子变异的三维培养模型。人源胰腺癌类器官作为近年发展起来的三维培养模型,是从组织样本中提取的多细胞单位,在机械和酶消化后嵌入细胞外基质凝胶中,可再现原患者的组织学特征及器官特点,甚至具有原器官的功能。随着胰腺癌类器官培养体系的不断发展及完善,其简便、经济及稳定的培养技术已经逐步建立,推动人源胰腺癌类器官的应用扩展到药物高通量筛选、个体化精准治疗、更深入的发病机制及针对性的药物开发研究。同时,人源胰腺癌类器官亦是胰腺癌临床分子分型研究的优势全新半体内模型,特别在针对研究高突变及高异质性患者的病因、分子特征、组织形态及体细胞突变负荷方面表现优越。大样本量人源胰腺癌类器官生物样本库的构建,将成为生物学、基础医学和临床肿瘤学研究的全新平台,有助于胰腺癌发病机制的深入研究及治疗策略的优化。人源胰腺癌类器官可再现临床患者特征的实验室模型的应用,将使药物筛选、发病机制研究、个体化治疗的实现成为可能。本文综述人源胰腺癌类器官的最新研究进展,希望该文为从事相关人源胰腺癌类器官研究的人员提供借鉴。

关键词: 胰腺癌, 人源类器官, 发病机制, 药物筛选, 精准治疗

Abstract:

Pancreatic cancer is a worldwide medical and health problem. Due to its high heterogeneity and malignant phenotype, the 5-year survival rate of pancreatic cancer is only 7.2%, which is a serious threat to human health. The biological mechanism and drug development research of pancreatic cancer often rely on the traditional two-dimensional culture models (cell lines) and patient-derived xenograft models. However, cell lines lack the three-dimensional environment and heterogeneity of the tumor, while xenograft models have the disadvantages of long culture time, low success rate and difficulty in carrying out high-throughput drug screening. There is an urgent need to develop three-dimensional culture models that can highly reflect the characteristics and molecular variation of pancreatic cancer. As a three-dimensional culture model developed in recent years, human-derived pancreatic cancer organoids are multicellular units extracted from tissue samples and embedded in extracellular matrix gels after mechanical and enzymatic digestion, which can reproduce the histological characteristics and organ characteristics of the original patient, and even have the functions of the original organ. With the continuous development and improvement of pancreatic cancer organoids culture system, its simple, economical and stable culture technology has been gradually established, which promotes the application of human pancreatic cancer organoids to high-throughput drug screening, individualized precision treatment and deeper pathogenesis and targeted drug development research. At the same time, human-derived pancreatic cancer organoids are also a novel semi-in vivo model for the study of clinical molecular typing of pancreatic cancer, especially for the study of etiology, molecular characteristics, histomorphology and somatic mutation burden of patients with high mutation rate and high heterogeneity. The construction of human pancreatic cancer organoid biobank with large sample size is a new platform for biology, basic medicine and clinical science oncology research, which provides a reliable resource for the in-depth study of the pathogenesis of pancreatic cancer and the development of treatment strategies. In summary, the research progress of human pancreatic cancer organoids promotes the application of laboratory models that recapitulate the characteristics of clinical patients, improves the connection between basic laboratory research and clinical patients, and provides clinical sources for drug screening, pathogenesis research, individualized treatment strategies and the construction of biobanks. Therefore, this article reviewed the latest research progress of human pancreatic cancer organoids, in order to provide reference for researchers engaged in the research of human pancreatic cancer organoids.

Key words: Pancreatic cancer, Patient-derived organoids, Pathogenesis, Drug screening, Precision treatment

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