Enrichment and Molecular Analysis of Breast Cancer Disseminated Tumor Cells from Bone Marrow Using Microfiltration

• Published in: PloS one 2017-01, Vol.12 (1), p.e0170761-e0170761
• Main Authors: Pillai, Sreeraj G, Zhu, Peixuan, Siddappa, Chidananda M, Adams, Daniel L, Li, Shuhong, Makarova, Olga V, Amstutz, Pete, Nunley, Ryan, Tang, Cha-Mei, Watson, Mark A, Aft, Rebecca L
• Format: Article
• Language: English
• Subjects: Adult; Aged; Antigens; Automation; Biology and Life Sciences; Biomarkers; Bone cancer; Bone marrow; Bone Marrow Cells - metabolism; Bone Marrow Cells - pathology; Bone surgery; Breast cancer; Breast Neoplasms - genetics; Breast Neoplasms - pathology; Cancer; Cancer cells; Cancer metastasis; CD45 antigen; Cell Separation - methods; Cell Size; Cytokeratin; Deoxyribonucleic acid; DNA; Enrichment; ErbB-2 protein; Female; Filtration; Filtration - methods; Finite element method; Gene amplification; Gene expression; Gene Expression Regulation, Neoplastic; Genetic aspects; Health aspects; Humans; Immunocytochemistry; In Situ Hybridization; Medical research; Medicine; Medicine and Health Sciences; Metastasis; Microfiltration; Middle Aged; Neoplasm Proteins - biosynthesis; Neoplasm Proteins - genetics; Neoplastic Cells, Circulating - metabolism; Neoplastic Cells, Circulating - pathology; Oncology; Patients; Polymerase chain reaction; Receptor, ErbB-2 - biosynthesis; Receptor, ErbB-2 - genetics; Research and Analysis Methods; Ribonucleic acid; RNA; RNA, Messenger - genetics; Tumor cells
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0170761

Molecular characterization of disseminated tumor cells (DTCs) in the bone marrow (BM) of breast cancer (BC) patients has been hindered by their rarity. To enrich for these cells using an antigen-independent methodology, we have evaluated a size-based microfiltration device in combination with several downstream biomarker assays. BM aspirates were collected from healthy volunteers or BC patients. Healthy BM was mixed with a specified number of BC cells to calculate recovery and fold enrichment by microfiltration. Specimens were pre-filtered using a 70 μm mesh sieve and the effluent filtered through CellSieve microfilters. Captured cells were analyzed by immunocytochemistry (ICC), FISH for HER-2/neu gene amplification status, and RNA in situ hybridization (RISH). Cells eluted from the filter were used for RNA isolation and subsequent qRT-PCR analysis for DTC biomarker gene expression. Filtering an average of 14×106 nucleated BM cells yielded approximately 17-21×103 residual BM cells. In the BC cell spiking experiments, an average of 87% (range 84-92%) of tumor cells were recovered with approximately 170- to 400-fold enrichment. Captured BC cells from patients co-stained for cytokeratin and EpCAM, but not CD45 by ICC. RNA yields from 4 ml of patient BM after filtration averaged 135ng per 10 million BM cells filtered with an average RNA Integrity Number (RIN) of 5.3. DTC-associated gene expression was detected by both qRT-PCR and RISH in filtered spiked or BC patient specimens but, not in control filtered normal BM. We have tested a microfiltration technique for enrichment of BM DTCs. DTC capture efficiency was shown to range from 84.3% to 92.1% with up to 400-fold enrichment using model BC cell lines. In patients, recovered DTCs can be identified and distinguished from normal BM cells using multiple antibody-, DNA-, and RNA-based biomarker assays.