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Updated: Jun 13, 2026

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
Published on: April 13, 2015
[Effects of differentially expressed proteins in hepatocellular carcinoma cell treated by different telomerase
Xiao Wei1, Zhiyong Zhang, Min He
1Key Laboratory of Public Health and Safety,Ministry of Education, School of Public Health, Fudan University, Shanghai 200032, China. wx_smile@126.com
Objective:
To detect differentially expressed proteins in hepatocellular carcinoma cell line SMMC-7721 treated separately by eight telomerase inhibitors including antisense oligodeoxynuclectide of human telomerase RNA (hTR-ASODN), sense oligodeoxynuclectide of hTR (hTR-SODN), ASODN of human telomerase reverse transcriptase (hTERT-ASODN), SODN of hTERT (hTERT-SODN), epigallocatechin gallate (EGCG), 3'-azido-3'-deoxythymidine (AZT), all trans-retinoic acid (ATRA) and adriamycin (ADM) using surface enhanced laser desorption/ionization time of flight-mass spectrom (SELDI-TOF-MS) technology.
Methods:
SELDI-TOF-MS technology and weak cation exchanger (WCX-2) protein chip were used to detect differentially expressed secretory and cytoplasmic proteins of SMMC-7721 cell treated separately by eight telomerase inhibitors. The control group was hepatocellular carcinoma SMMC-7721 cell without any disposal.
Results:
The results of WCX-2 protein chip showed that the secretory and cytoplasmic proteins were differentially expressed in SMMC-7721 cell treated separately by eight telomerase inhibitors. But some proteins were down-regulated or up-regulated together in all experimental groups. The molecular weight of these differential proteins were all less than 10,000 Da.
Conclusion:
Differentially expressed and common changes of proteins in SMMC-7721 cell treated separately by eight telomerase inhibitors would associate with telomerase activity.
Insights
Hepatocellular carcinoma cells treated with eight telomerase inhibitors showed differential protein expression, with some proteins commonly changing across all treatments. These protein alterations are linked to telomerase activity, offering insights into cancer mechanisms.
Area of Science:
- Proteomics
- Cancer Biology
- Molecular Medicine
Context:
- Hepatocellular carcinoma (HCC) is a significant global health concern.
- Telomerase plays a critical role in cancer cell proliferation and immortality.
- Targeting telomerase is a promising strategy for HCC treatment.
Purpose:
- To identify differentially expressed proteins in the SMMC-7721 HCC cell line upon treatment with eight distinct telomerase inhibitors.
- To analyze common protein expression changes across various telomerase inhibition strategies.
- To investigate the association between protein expression alterations and telomerase activity.
Summary:
- Surface-enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) with a weak cation exchanger (WCX-2) protein chip was employed to analyze protein expression in SMMC-7721 cells.
- Cells were treated with eight telomerase inhibitors: human telomerase RNA (hTR) antisense oligodeoxynucleotide (ASODN), hTR sense oligodeoxynucleotide (SODN), human telomerase reverse transcriptase (hTERT) ASODN, hTERT SODN, epigallocatechin gallate (EGCG), 3'-azido-3'-deoxythymidine (AZT), all-trans-retinoic acid (ATRA), and adriamycin (ADM).
- Differential expression of secretory and cytoplasmic proteins was observed, with many having a molecular weight under 10,000 Da. Some proteins exhibited coordinated down-regulation or up-regulation across all treatment groups.
Impact:
- This study reveals specific protein expression profiles associated with telomerase inhibition in HCC cells.
- The findings contribute to understanding the molecular mechanisms underlying telomerase-targeted therapies for hepatocellular carcinoma.
- Identified protein changes may serve as potential biomarkers for treatment response or novel therapeutic targets.
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