Unknown

Dataset Information

0

Label-free quantitative proteomics of CD133-positive liver cancer stem cells.


ABSTRACT:

Unlabelled

Background

CD133-positive liver cancer stem cells, which are characterized by their resistance to conventional chemotherapy and their tumor initiation ability at limited dilutions, have been recognized as a critical target in liver cancer therapeutics. In the current work, we developed a label-free quantitative method to investigate the proteome of CD133-positive liver cancer stem cells for the purpose of identifying unique biomarkers that can be utilized for targeting liver cancer stem cells. Label-free quantitation was performed in combination with ID-based Elution time Alignment by Linear regression Quantitation (IDEAL-Q) and MaxQuant.

Results

Initially, IDEAL-Q analysis revealed that 151 proteins were differentially expressed in the CD133-positive hepatoma cells when compared with CD133-negative cells. We then analyzed these 151 differentially expressed proteins by MaxQuant software and identified 10 significantly up-regulated proteins. The results were further validated by RT-PCR, western blot, flow cytometry or immunofluorescent staining which revealed that prominin-1, annexin A1, annexin A3, transgelin, creatine kinase B, vimentin, and EpCAM were indeed highly expressed in the CD133-positive hepatoma cells.

Conclusions

These findings confirmed that mass spectrometry-based label-free quantitative proteomics can be used to gain insights into liver cancer stem cells.

SUBMITTER: Tsai ST 

PROVIDER: S-EPMC3576254 | biostudies-literature | 2012 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Label-free quantitative proteomics of CD133-positive liver cancer stem cells.

Tsai Sheng-Ta ST   Tsou Chih-Chiang CC   Mao Wan-Yu WY   Chang Wei-Chao WC   Han Hsin-Ying HY   Hsu Wen-Lian WL   Li Chung-Leung CL   Shen Chia-Ning CN   Chen Chung-Hsuan CH  

Proteome science 20121121 1


<h4>Unlabelled</h4><h4>Background</h4>CD133-positive liver cancer stem cells, which are characterized by their resistance to conventional chemotherapy and their tumor initiation ability at limited dilutions, have been recognized as a critical target in liver cancer therapeutics. In the current work, we developed a label-free quantitative method to investigate the proteome of CD133-positive liver cancer stem cells for the purpose of identifying unique biomarkers that can be utilized for targeting  ...[more]

Similar Datasets

| S-EPMC4086339 | biostudies-literature
| S-EPMC9599763 | biostudies-literature
| S-EPMC7859943 | biostudies-literature
| S-EPMC2577209 | biostudies-literature
| S-EPMC3092194 | biostudies-literature
| S-EPMC3436780 | biostudies-literature
| S-EPMC7247262 | biostudies-literature
| S-EPMC4730314 | biostudies-literature
| S-EPMC4934060 | biostudies-literature
2017-02-09 | GSE62905 | GEO