Establishment and Characterization of 5-Fluorouracil-Resistant Human Colorectal Cancer Stem-Like Cells: Tumor Dynamics under Selection Pressure

被引:37
|
作者
Francipane, Maria Giovanna [1 ,2 ,3 ]
Bulanin, Denis [4 ]
Lagasse, Eric [1 ,2 ]
机构
[1] Univ Pittsburgh, Sch Med, McGowan Inst Regenerat Med, Pittsburgh, PA 15219 USA
[2] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15219 USA
[3] Ri MED Fdn, I-90133 Palermo, Italy
[4] Nazarbayev Univ, Sch Med, Dept Biomed Sci, Astana 010000, Kazakhstan
关键词
colorectal cancer; chemoresistance; cancer stem cells; SIGNALING PATHWAY; DNA-REPAIR; SURVIVAL; PROLIFERATION; GROWTH; ACTIVATION; EXPRESSION; PROTEIN; DIFFERENTIATION; TUMORIGENICITY;
D O I
10.3390/ijms20081817
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
5-Fluorouracil (5-FU) remains the gold standard of first-line treatment for colorectal cancer (CRC). Although it may initially debulk the tumor mass, relapses frequently occur, indicating the existence of cancer cells that are therapy-resistant and are capable of refueling tumor growth. To identify mechanisms of drug resistance, CRC stem-like cells were subjected to long-term 5-FU selection using either intermittent treatment regimen with the IC50 drug dose or continuous treatment regimen with escalating drug doses. Parental cancer cells were cultivated in parallel. Real-time PCR arrays and bioinformatic tools were used to investigate gene expression changes. We found the first method selected for cancer cells with more aggressive features. We therefore transplanted these cancer cells or parental cells in mice, and again, found that not only did the 5-FU-selected cancer cells generate more aggressive tumors with respect to their parental counterpart, but they also showed a different gene expression pattern as compared to what we had observed in vitro, with ID1 the top upregulated gene. We propose ID1 as a stemness marker pervasively expressed in secondary lesions emerging after completion of chemotherapy.
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页数:23
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