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Authors He T, Qiu T, Wang X, Gui H, Wang X, Hu Q, Xia H, Qi G, Wu J, Ma H
Received 3 August 2016
Accepted for publication 30 November 2016
Published 4 January 2017 Volume 2017:10 Pages 195—203
DOI https://doi.org/10.2147/OTT.S118834
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Akshita Wason
Peer reviewer comments 3
Editor who approved publication: Dr Faris Farassati
Objective: This study investigated the correlation between choline/creatine
(Cho/Cr) ratios determined by multivoxel proton magnetic resonance spectroscopy
(1H-MRS) and the distribution of cancer stem-like
cells (CSLCs) in high-grade gliomas.
Patients and methods: Sixteen patients with high-grade gliomas were
recruited and underwent 1H-MRS examination before surgery to identify
distinct tumor regions with variable Cho/Cr ratios. Using intraoperative
neuronavigation, tumor tissues were accurately sampled from regions with high
and low Cho/Cr ratios within each tumor. The distribution of CSLCs in samples
from glioma tissue regions with different Cho/Cr ratios was quantified by
neurosphere culture, immunohistochemistry, and Western blot.
Results: The mean neurosphere formation rate in tissues with
high Cho/Cr ratios was significantly increased compared with that in low Cho/Cr
ratio tissues (13.94±5.94 per 100 cells vs 8.04±3.99 per 100 cells, P <0.001).
Immunohistochemistry indicated that tissues with high Cho/Cr ratios had
elevated expression of CD133, nestin, and CD15, relative to low Cho/Cr ratio
tissue samples (23.6%±3.8% vs 18.3%±3.3%, 25.2%±4.5% vs 19.8%±2.8%, 24.5%±3.8%
vs 17.8%±2.2%, respectively; all P <0.001). Western blot
demonstrated that relative CD133 and nestin protein expression in high Cho/Cr
ratio regions was significantly higher than that in low Cho/Cr ratio tissue
samples (0.50±0.17 vs 0.30±0.08, 0.45±0.13 vs 0.27±0.07, respectively; both P <0.001). The
protein expression levels of CD133 and nestin were highly correlated with
Cho/Cr ratios (r =0.897 and r =0.861,
respectively).
Conclusion: Cho/Cr ratios correlate with the distribution of CSLCs
in high-grade gliomas, and this may assist in identifying foci enriched with
CSLCs and thus improve the management of high-grade gliomas.
Keywords: high-grade glioma, 1H-MRS, cancer
stem-like cells, choline, creatine, Cho/Cr