期刊文献+

MMTV-PyMT乳腺癌小鼠模型肿瘤发生的特点

Characteristics of Tumorigenesis in MMTV-PyMT Breast Cancer Mouse Model
下载PDF
导出
摘要 以MMTV-PyMT乳腺癌小鼠模型为对象,研究其肿瘤发生特点。观察MMTV-PyMT转基因小鼠,记录乳腺癌小鼠肿瘤的发病时间、发生位置以及肿瘤小鼠的生存时间,并且通过病理学切片观察不同时间段乳腺癌的病理变化。大多数MMTV-PyMT雌性小鼠在出生后的第8周开始发生肿瘤,而雄性小鼠在第19周左右产生肿瘤;雌鼠自发产生肿瘤后最长生存时间为12周,而雄鼠则为28周。不同时间段的MMTV-PyMT雌性小鼠乳腺肿瘤染伊红染色结果有着明显的区别,早期肿瘤均为浸润性导管癌,随着癌症的发展,癌细胞开始突破基底膜,癌细胞扩散至整个乳腺组织中,整体呈现出弥漫性分布、癌巢着色较深,细胞间推挤或重叠。MMTV-PyMT自发性乳腺癌小鼠雌性小鼠和雄性小鼠均可发生乳腺癌,雌性小鼠具有发病时间早,生存时间短,肿瘤时期变化明显等特点。 In MMTV-PyMT mouse model of breast cancer as the object to study the tumorigenesis characteristics.Observe the MMTV-PyMT transgenic mice,record the onset time,location of tumors and survival time of tumor mice in breast cancer mice,and observe the pathological changes of breast cancer in different periods by pathological sectioning.Most MMTV-PyMT female mice begin to develop tumors in the 8th week after birth,while male mice develop tumors around the 19th week;the longest survival time for female mice after spontaneous tumor development is 12 weeks,while for male mice it is 28 weeks.The results of HE staining of breast tumors in MMTV-PyMT female mice at different periods are significantly different.The early tumors were invasive ductal carcinomas.As cancer progressed,the cancer cells began to break through the basement membrane,and the cancer cells spread to the entire breast tissue.Medium,the whole showed a diffuse distribution,the color of the cancer nest was dark,and the cells pushed or overlapped.MMTV-PyMT spontaneous breast cancer mice can occur in both female and male mice.Female mice have the characteristics of early-onset time,short survival time,and obvious changes in tumor stage.
作者 姚祥龙 杨帅 陈芳慧 盛乐 赵曼 阮健 鲁山 李君 蔡亚非 YAO Xiang-long;YANG Shuai;CHEN Fang-hui;SHENG Le;ZHAO Man;RUAN Jian;LU Shan;LI Jun;CAI Ya-fei(Anhui Provincial Key Laboratory of Molecular Enzymology and Mechanism of Major Disease,College of life Sciences,Anhui Normal University,Wuhu 241000,China;College of Animal Science and Technology ,Nanjing Agricultural University,Nanjing 210095,China)
出处 《安徽师范大学学报(自然科学版)》 CAS 2020年第4期348-351,355,共5页 Journal of Anhui Normal University(Natural Science)
基金 安徽省自然科学基金项目(1908085MC83) 国家自然科学基金项目(31970413)。
关键词 乳腺癌小鼠 肿瘤发生 MMTV-PyMT breast cancer mice tumorigenesis MMTV-PyMT
  • 相关文献

参考文献6

二级参考文献73

  • 1余微波,谷俊朝.乳腺癌动物模型的建立[J].国外医学(外科学分册),2005,32(1):63-66. 被引量:18
  • 2杨桂仙,张大方.乳腺癌动物模型的研究现状与评价[J].长春中医药大学学报,2007,23(2):82-83. 被引量:10
  • 3Pritehard KI, Shepherd LE, O' Malley FP, et al. HER2 and responsiveness of breast cancer to adjuvant chemotherapy [ J ]. N Engl J Med,2006,354(20) : 2103 -2111.
  • 4Piechocki MP,Ho YS,Pilon S,et al. Human ErbB-2 (Her-2) transgenic mice: a model system for testing Her-2 based vaccines [ J ]. J Immunol,2003,171 ( 11 ) : 5787 - 5794.
  • 5Finkle D, Quan ZR,Asghari V,et al. HER2-targeted therapy reduces incidence and progression of midlife mammary tumors in female murine mammary tumor virus huHER2-transgenic mice[ J]. Clin Cancer Res,2004,10(7) :2499 -2511.
  • 6Hodgson JG, Malek T, Bornstein S, et al. Copy number aberrations in mouse breast tumors reveal loci and genes important in tumorigenic receptor tyrosine kinase signaling[J]. Cancer Res,2005,65(21 ) :9695 -9704.
  • 7Howe LR, Chang SH,Tolle KC,et al. HER2/neu-induced mammary tumorigenesis and angiogenesis are reduced in cyclooxygenase-2 knockout mice[J]. Cancer Res,2005,65(21 ) :10113 - 10119.
  • 8Dankort D, Maslikowski B, Warner N, et al. Grb2 and Shc adapter proteins play distinct roles in Neu ( ErbB)-2-induced mammary tumorigenesis: implications for human breast cancer[ J]. Mol Cell Biol,2001,21(5) :1540 - 1551.
  • 9Knutson KL,Almand B, Dang Y, et al. Neu antigen-negative variants can be generated after neu-specific antibody therapy in neu transgenic mice [ J ]. Cancer Res ,2004 ,64 ( 3 ) : 1146 - 1151.
  • 10Roh H,Pippin J, Drebin JA. Down-regulation of HER-2/neu expression induces apoptosis in human cancer cells that overexpress HER-2/ neu[ J ]. Cancer Res,2000,60 (3) :560 - 565.

共引文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部