Harold C Simmons Comprehensive Cancer Center, UT Southwestern Medical Center, Dallas, TX, USA.
Department of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.
Breast Cancer (Dove Med Press). 2015 Aug 11;7:231-7. doi: 10.2147/BCTT.S87041. eCollection 2015.
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.
Hyperspectral immunologic cell by cell analysis was applied to touch imprint smears obtained from fresh tumors of breast cancer patients.
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.
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.
本研究探讨了三阴性乳腺癌患者体内单个细胞的分子状态,并对这些肿瘤进行了分子鉴定和特征分析,以期考虑潜在的靶向治疗方法。
应用超光谱免疫细胞逐个分析技术对乳腺癌患者新鲜肿瘤的触印涂片进行分析。
逐个细胞分析证实,肿瘤标志物存在显著的肿瘤内分子异质性,与聚合酶链反应标志物报告存在差异。在对单个细胞中的十个分子标志物进行的十组细胞分析中,发现了相邻细胞的个体细胞异质性,其中包括一些被认为具有“干细胞”特征的标志物。此外,这种异质性与原发性肿瘤的大小或分期以及肿瘤内的部位无关。
在三阴性乳腺癌中,当对“相邻细胞”进行检查时,存在非常显著的分子异质性,因此不太可能成功进行靶向治疗。此外,认为这些变化将为肿瘤休眠提供答案也是不合理的。