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Diosgenin inhibits hTERT gene expression in the A549 lung cancer cell line
Rahmati Yamchi Mohammad1, Ghareghomi Somayyeh, Haddadchi Gholamreza
1Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Background:
Diosgenin, a steroidal saponin from a therapeutic herb, fenugreek (Trigonellafoenum-graceum L.), has been recognized to have anticancer properties. Telomerase activity is not detected in typical healthy cells, while in cancer cell telomerase expression is reactivated, therefore providing a promising cancer therapeutic target.
Materials And Methods:
We studied the inhibitory effect of diosgenin on human telomerase reverse transcriptase gene (hTERT) expression which is critical for telomerase activity. MTT- assays and qRT-PCR analysis were conducted to assess cytotoxicity and hTERT gene expression inhibition effects, respectively.
Results:
MTT results showed that IC50 values for 24, 48 and 72h after treatment were 47, 44 and 43μM, respectively. Culturing cells with diosgenin treatment caused down-regulation of hTERT expression.
Discussion:
These results show that diosgenin inhibits telomerase activity by down-regulation of hTERT gene expression in the A549 lung cancer cell line.
Insights
Diosgenin, derived from fenugreek, inhibits cancer cell growth by down-regulating human telomerase reverse transcriptase (hTERT) gene expression, a key target for cancer therapy.
Area of Science:
- Biochemistry
- Molecular Biology
- Pharmacology
Background:
- Diosgenin, a natural compound from fenugreek, exhibits anticancer properties.
- Telomerase is reactivated in cancer cells, making it a therapeutic target.
- Human telomerase reverse transcriptase (hTERT) is crucial for telomerase activity.
Purpose of the Study:
- To investigate diosgenin's inhibitory effect on hTERT gene expression.
- To assess diosgenin's impact on telomerase activity in cancer cells.
Main Methods:
- Cytotoxicity was evaluated using MTT assays.
- hTERT gene expression was analyzed via qRT-PCR.
- A549 lung cancer cell line was used for experiments.
Main Results:
- Diosgenin demonstrated dose-dependent cytotoxicity with IC50 values ranging from 43-47μM.
- Diosgenin treatment led to the down-regulation of hTERT gene expression.
- Inhibition of hTERT expression suggests a mechanism for telomerase activity suppression.
Conclusions:
- Diosgenin effectively inhibits telomerase activity in A549 lung cancer cells.
- The mechanism involves the down-regulation of hTERT gene expression.
- Diosgenin shows potential as a therapeutic agent targeting telomerase in lung cancer.
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