Photoacoustic detection of circulating melanoma cells in late stage patients

被引:0
作者
Viator, John A. [1 ]
Hazur, Marc [1 ]
Sajewski, Andrea [2 ]
Tarhini, Ahmad [3 ]
Sanders, Martin E. [4 ]
Edgar, Robert H. [2 ]
机构
[1] Duquesne Univ, Dept Engn, 600 Forbes Ave, Pittsburgh, PA 15282 USA
[2] Univ Pittsburgh, Dept Bioengn, 3700 OHara St, Pittsburgh, PA 15260 USA
[3] Moffitt Comprehens Canc Ctr & Res Inst, 10920 McKinley Dr, Tampa, FL 33612 USA
[4] Acousys Biodevices Inc, 1777 Highland Dr, Ann Arbor, MI 48108 USA
基金
美国国家卫生研究院;
关键词
Diagnosis; metastasis; optoacoustics; MINIMAL RESIDUAL DISEASE; TUMOR-CELLS; PROSTATE-CANCER; CAPTURE; MARKER;
D O I
10.1142/S1793545820500236
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Melanoma is the deadliest skin cancer and is responsible for over 7000 deaths in the US annually. The spread of cancer, or metastasis, is responsible for these deaths, as secondary tumors interrupt normal organ function. Circulating tumor cells, or those cells that spread throughout the body from the primary tumor, are thought to be responsible for metastasis. We developed an optical method, photoacoustic flow cytometry, in order to detect and enumerate circulating melanoma cells (CMCs) from blood samples of patients. We tested the blood of Stage IV melanoma patients to show the ability of the photoacoustic flow cytometer to detect these rare cells in blood. We then tested the system on archived blood samples from Stage III melanoma patients with known outcomes to determine if detection of CMCs can predict future metastasis. We detected between 0 and 66 CMCs in Stage IV patients. For the Stage III study, we found that of those samples with CMCs, two remained disease free and five developed metastasis. Of those without CMCs, six remained disease free and one developed metastasis. We believe that photoacoustic detection of CMCs provides valuable information for the prediction of metastasis and we postulate a system for more accurate prognosis.
引用
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页数:8
相关论文
共 29 条
[1]   Counting particles by means of optoacoustics: Potential limits in real solutions [J].
Autrey, T ;
Egerev, S ;
Foster, NS ;
Fokin, A ;
Ovchinnikov, O .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2003, 74 (01) :628-631
[2]  
Balic M, 2012, EXPERT REV MOL DIAGN, V12, P303, DOI [10.1586/erm.12.12, 10.1586/ERM.12.12]
[3]  
Campana D, 1999, CYTOMETRY, V38, P139, DOI 10.1002/(SICI)1097-0320(19990815)38:4<139::AID-CYTO1>3.0.CO
[4]  
2-H
[5]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791
[6]   Circulating tumor cells in prostate cancer: A potential surrogate marker of survival [J].
Doyen, Jerome ;
Alix-Panabieres, Catherine ;
Hofman, Paul ;
Parks, Scott K. ;
Chamorey, Emmanuel ;
Naman, Herve ;
Hannoun-Levi, Jean-Michel .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2012, 81 (03) :241-256
[7]   Prognostic significance and modalities of flow cytometric minimal residual disease detection in childhood acute lymphoblastic leukemia [J].
Dworzak, MN ;
Fröschl, G ;
Printz, D ;
Mann, G ;
Pötschger, U ;
Mühlegger, N ;
Fritsch, G ;
Gadner, H .
BLOOD, 2002, 99 (06) :1952-1958
[8]  
Gage T., 2010, ANALYSIS, V11, P18
[9]   In vivo liquid biopsy using Cytophone platform for photoacoustic detection of circulating tumor cells in patients with melanoma [J].
Galanzha, Ekaterina I. ;
Menyaev, Yulian A. ;
Yadem, Aayire C. ;
Sarimollaoglu, Mustafa ;
Juratli, Mazen A. ;
Nedosekin, Dmitry A. ;
Foster, Stephen R. ;
Jamshidi-Parsian, Azemat ;
Siegel, Eric R. ;
Makhoul, Issam ;
Hutchins, Laura F. ;
Suen, James Y. ;
Zharov, Vladimir P. .
SCIENCE TRANSLATIONAL MEDICINE, 2019, 11 (496)
[10]  
Garstecki P, 2006, LAB CHIP, V6, P693