Molecular heterogeneity in adjacent cells in triple-negative breast cancer

被引:0
|
作者
Huebschman, Michael L. [1 ]
Lane, Nancy L. [1 ]
Liu, Huaying [1 ]
Sarode, Venetia R. [2 ]
Devlin, Judith L. [1 ]
Frenkel, Eugene P. [1 ,3 ]
机构
[1] UT Southwestern Med Ctr, Harold C Simmons Comprehens Canc Ctr, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
[2] UT Southwestern Med Ctr, Dept Pathol, Dallas, TX 75390 USA
[3] UT Southwestern Med Ctr, Dept Internal Med, Div Hematol Med Oncol, Dallas, TX 75390 USA
来源
关键词
hyperspectral; cancer stem cells; CSC; CD44; CD24; ALDH1; uPAR; CD133;
D O I
10.2147/BCTT.5.67041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study interrogates the molecular status of individual cells in patients with triple-negative breast cancers and explores the molecular identification and characterization of these tumors to consider the exploitation of a potential-targeted therapeutic approach. Patients and methods: Hyperspectral immunologic cell by cell analysis was applied to touch imprint smears obtained from fresh tumors of breast cancer patients. Results: Cell by cell analysis confirms significant intratumoral molecular heterogeneity in cancer markers with differences from polymerase chain reaction marker reporting. The individual cell heterogeneity was recognized in adjacent cells examined with panels of ten molecular markers in each single cell and included some markers that are considered to express "stem-cell" character. In addition, heterogeneity did not relate either to the size or stage of the primary tumor or to the site from within the cancer. Conclusion: There is a very significant molecular heterogeneity when "adjacent cells" are examined in triple-negative breast cancer, thereby making a successful targeted approach unlikely. In addition, it is not reasonable to consider that these changes will provide an answer to tumor dormancy.
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页数:7
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