4.7 Article

Subclassification of prostate cancer circulating tumor cells by nuclear size reveals very small nuclear circulating tumor cells in patients with visceral metastases

期刊

CANCER
卷 121, 期 18, 页码 3240-3251

出版社

WILEY
DOI: 10.1002/cncr.29455

关键词

prostate cancer; circulating tumor cells; visceral metastasis; NanoVelcro Chips; nuclear size

类别

资金

  1. Department of Defense Idea Award [W81XWH-11-1-0422]
  2. Steven Spielberg Discovery Fund in Prostate Cancer Research
  3. Prostate Cancer Foundation
  4. St. Anthony Prostate Cancer Research Fund
  5. CD McKinnon Memorial Fund for Neuroendocrine Prostate Cancer
  6. Berns Family Fund
  7. UCLA Prostate Cancer SPORE Program
  8. National Institutes of Health/National Cancer Institute Innovative Molecular Analysis Technologies Program [R21 CA151159, R33 CA157396]
  9. National Natural Science Foundation of China [30900650/H1615, 81372501/H1615]

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BACKGROUNDAlthough enumeration of circulating tumor cells (CTCs) has shown some clinical value, the pool of CTCs contains a mixture of cells that contains additional information that can be extracted. The authors subclassified CTCs by shape features focusing on nuclear size and related this with clinical information. METHODSA total of 148 blood samples were obtained from 57 patients with prostate cancer across the spectrum of metastatic states: no metastasis, nonvisceral metastasis, and visceral metastasis. CTCs captured and enumerated on NanoVelcro Chips (CytoLumina, Los Angeles, Calif) were subjected to pathologic review including nuclear size. The distribution of nuclear size was analyzed using a Gaussian mixture model. Correlations were made between CTC subpopulations and metastatic status. RESULTSStatistical modeling of nuclear size distribution revealed 3 distinct subpopulations: large nuclear CTCs, small nuclear CTCs, and very small nuclear CTCs (vsnCTCs). Small nuclear CTCs and vsnCTC identified those patients with metastatic disease. However, vsnCTC counts alone were found to be elevated in patients with visceral metastases when compared with those without (0.360.69 vs 1.953.77 cells/mL blood; P<.001). Serial enumeration studies suggested the emergence of vsnCTCs occurred before the detection of visceral metastases. CONCLUSIONSThere are morphologic subsets of CTCs that can be identified by fundamental pathologic approaches, such as nuclear size measurement. The results of this observational study strongly suggest that CTCs contain relevant information regarding disease status. In particular, the detection of vsnCTCs was found to be correlated with the presence of visceral metastases and should be formally explored as a putative blood-borne biomarker to identify patients at risk of developing this clinical evolution of prostate cancer. Cancer 2015;121:3240-3251. (c) 2015 American Cancer Society. In this observational study, the authors use NanoVelcro chips to isolate circulating tumor cells (CTCs) from patients with prostate cancer and generate cell images appropriate for histopathological analysis and nuclear size measurement. In doing so, the authors identify a CTC subset of very small nuclear CTCs that exhibits significant correlation with the presence of visceral metastases and can be explored as a potential biomarker for this lethal progression in patients with prostate cancer.

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