In Vivo Long-Term Monitoring of Circulating Tumor Cells Fluctuation during Medical Interventions

• Published in: PloS one Vol. 10; no. 9; p. e0137613
• Main Authors: Juratli, Mazen A., Siegel, Eric R., Nedosekin, Dmitry A., Sarimollaoglu, Mustafa, Jamshidi-Parsian, Azemat, Cai, Chengzhong, Menyaev, Yulian A., Suen, James Y., Galanzha, Ekaterina I., Zharov, Vladimir P.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 14.09.2015; Public Library of Science (PLoS)
• Subjects: Animals; Biopsy; Biopsy - adverse effects; Biopsy - methods; Blood circulation; Breast cancer; Breast Neoplasms - pathology; Breast Neoplasms - surgery; Breast Neoplasms - therapy; Colorectal cancer; Compression; Cytometry; Dynamics; Flow Cytometry; Fluorescence; Heterografts; Inoculation; Intervention; Laboratory animals; Lasers; Mammary gland; Mammography; Mammography - adverse effects; Medical research; Melanoma; Metastasis; Mice; Mice, Nude; Neoplasm Metastasis - pathology; Neoplastic Cells, Circulating; Otolaryngology; Peripheral blood; Side effects; Surgery; Tumor cells; Tumors; Variation; United States > US; Arkansas
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0137613

The goal of this research was to study the long-term impact of medical interventions on circulating tumor cell (CTC) dynamics. We have explored whether tumor compression, punch biopsy or tumor resection cause dissemination of CTCs into peripheral blood circulation using in vivo fluorescent flow cytometry and breast cancer-bearing mouse model inoculated with MDA-MB-231-Luc2-GFP cells in the mammary gland. Two weeks after tumor inoculation, three groups of mice were the subject of the following interventions: (1) tumor compression for 15 minutes using 400 g weight to approximate the pressure during mammography; (2) punch biopsy; or (3) surgery. The CTC dynamics were determined before, during and six weeks after these interventions. An additional group of tumor-bearing mice was used as control and did not receive an intervention. The CTC dynamics in all mice were monitored weekly for eight weeks after tumor inoculation. We determined that tumor compression did not significantly affect CTC dynamics, either during the procedure itself (P = 0.28), or during the 6-week follow-up. In the punch biopsy group, we observed a significant increase in CTC immediately after the biopsy (P = 0.02), and the rate stayed elevated up to six weeks after the procedure in comparison to the tumor control group. The CTCs in the group of mice that received a tumor resection disappeared immediately after the surgery (P = 0.03). However, CTC recurrence in small numbers was detected during six weeks after the surgery. In the future, to prevent these side effects of medical interventions, the defined dynamics of intervention-induced CTCs may be used as a basis for initiation of aggressive anti-CTC therapy at time-points of increasing CTC number.