Copyright
©The Author(s) 2021.
World J Clin Cases. Apr 26, 2021; 9(12): 2721-2730
Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2721
Published online Apr 26, 2021. doi: 10.12998/wjcc.v9.i12.2721
Figure 1 Distribution of circulating tumor cells in lung cancer patients and controls.
A: Circulating tumor cells (CTCs) with epithelial markers, CTCs with mesenchymal markers (M-CTCs), and CTCs with both marker (E&M-CTCs) can be identified in one CTC; B: Positive rate of CTCs in lung cancer cases was significantly higher than those in benign or healthy controls; C: The numbers of CTCs, M-CTCs, and E&M-CTCs in lung cancer cases were significantly higher than those in healthy controls (P < 0.05); however, there was no disparity between lung cancer and benign controls; D: The proportions of M-CTCs plus E&M-CTCs increased gradually in healthy controls, benign controls, and lung cancer cases. aP < 0.05; bP < 0.01; cP < 0.001. GGO: Ground-glass opacities.
Figure 2 Receiver operating characteristic curve of all lung cancer patients and ground-glass opacities patients.
A: Area under the receiver operating characteristic curve (AUC) of total circulating tumor cells (CTCs) and CTCs with both markers (E&M-CTCs) for lung cancer diagnosis were 0.828 and 0.7648, respectively; B: AUCs of total CTCs and E&M-CTCs for ground-glass opacity (GGO) diagnosis were 0.7963 and 0.7504, respectively.
- Citation: Jiang SS, Mao CG, Feng YG, Jiang B, Tao SL, Tan QY, Deng B. Circulating tumor cells with epithelial-mesenchymal transition markers as potential biomarkers for the diagnosis of lung cancer. World J Clin Cases 2021; 9(12): 2721-2730
- URL: https://www.wjgnet.com/2307-8960/full/v9/i12/2721.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v9.i12.2721