Research Papers:

CD133+CD54+CD44+ circulating tumor cells as a biomarker of treatment selection and liver metastasis in patients with colorectal cancer

Chao Fang, Chuanwen Fan, Cun Wang, Qiaorong Huang, Wentong Meng, Yongyang Yu, Lie Yang, Zhihai Peng, Jiankun Hu, Yuan Li, Xianming Mo and Zongguang Zhou _

PDF  |  HTML  |  Supplementary Files  |  Order a Reprint

Oncotarget. 2016; 7:77389-77403. https://doi.org/10.18632/oncotarget.12675

Metrics: PDF 1157 views  |   HTML 786 views  |   ?  


Chao Fang1,2,*, Chuanwen Fan1,2,*, Cun Wang1, Qiaorong Huang3, Wentong Meng3, Yongyang Yu1, Lie Yang1, Zhihai Peng4, Jiankun Hu1, Yuan Li2, Xianming Mo3, Zongguang Zhou1,2

1Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, China

2Institute of Digestive Surgery, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China

3Laboratory of Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China

4Department of General Surgery, Shanghai First People’s Hospital, Shanghai Jiaotong University, Shanghai, China

*These authors have contributed equally to this work

Correspondence to:

Zongguang Zhou, email: zhou767@163.com

Xianming Mo, email: xmingmo@scu.edu.cn

Keywords: colorectal cancer, circulating tumor cells, CD133+CD54+CD44+ cellular subpopulation, liver metastasis, predictive biomarker

Received: February 25, 2016    Accepted: September 20, 2016    Published: October 15, 2016


Introduction: Liver is the most common site of distant metastasis in colorectal cancer (CRC). Early diagnosis and appropriate treatment selection decides overall prognosis of patients. However, current diagnostic measures were basically imaging but not functional. Circulating tumor cells (CTCs) known as hold the key to understand the biology of metastatic mechanism provide a novel and auxiliary diagnostic strategy for CRC with liver metastasis (CRC-LM).

Results: The expression of CD133+ and CD133+CD54+CD44+ cellular subpopulations were higher in the peripheral blood of CRC-LM patients when compared with those without metastasis (P<0.001). Multivariate analysis proved the association between the expression of CD133+CD44+CD54+ cellular subpopulation and the existence of CRC-LM (P<0.001). The combination of abdominal CT/MRI, CEA and the CD133+CD44+CD54+ cellular subpopulation showed increased detection and discrimination rate for liver metastasis, with a sensitivity of 88.2% and a specificity of 92.4%. Meanwhile, it also show accurate predictive value for liver metastasis (OR=2.898, 95% C.I.1.374–6.110).

Materials and Method: Flow cytometry and multivariate analysis was performed to detect the expression of cancer initiating cells the correlation between cellular subpopulations and liver metastasis in patients with CRC. The receiver operating characteristic curves combined with the area under the curve were generated to compare the predictive ability of the cellular subpopulation for liver metastasis with current CT and MRI images.

Conclusions: The identification, expression and application of CTC subpopulations will provide an ideal cellular predictive marker for CRC liver metastasis and a potential marker for further investigation.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 12675