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Evaluating the Relationship between Cathepsins and Papillary Thyroid Carcinoma: A Mendelian Randomization Study
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Background:
Papillary Thyroid Carcinoma (PTC) is the most common thyroid cancer,
with an etiology and progression that are not fully understood. Research suggests a link between
cathepsins and PTC, but the causal nature of this link is unclear. This study uses Mendelian Randomization
(MR) to investigate if cathepsins causally influence PTC risk.
Methods:
We applied univariable and multivariable MR analyses using genetic variants as proxies
for cathepsin levels. Genetic data for cathepsins were sourced from the INTERVAL study, while
PTC data came from the Finnish Genome-Wide Association Study database. Our analysis employed
several MR methods, including the Inverse Variance Weighted (IVW) approach, MR-Egger,
and the Weighted Median method, to provide comprehensive insights and address possible
pleiotropy.
Results:
MR findings suggest a significant causal association between higher cathepsin levels and
increased PTC risk. Notably, genetic variants indicating higher cathepsin Z expression were positively
causal associated with PTC risk (OR:1.1190, 95% CI: 1.0029-1.2486), multivariable analysis
confirmed significant carcinogenesis role of cathepsin Z in PTC (OR: 1.1593, 95% CI:
1.0137-1.3258), with results consistent across various tests, indicating a robust relationship.
Conclusion:
This study established a causal link between cathepsin levels and PTC risk, emphasizing
the roles of cathepsin Z in its progression. These insights could lead to new therapeutic strategies
targeting these enzymes. Further research is necessary to understand the underlying biological
mechanisms and their clinical implications.
Bentham Science Publishers Ltd.
Title: Evaluating the Relationship between Cathepsins and Papillary Thyroid Carcinoma: A Mendelian Randomization Study
Description:
Background:
Papillary Thyroid Carcinoma (PTC) is the most common thyroid cancer,
with an etiology and progression that are not fully understood.
Research suggests a link between
cathepsins and PTC, but the causal nature of this link is unclear.
This study uses Mendelian Randomization
(MR) to investigate if cathepsins causally influence PTC risk.
Methods:
We applied univariable and multivariable MR analyses using genetic variants as proxies
for cathepsin levels.
Genetic data for cathepsins were sourced from the INTERVAL study, while
PTC data came from the Finnish Genome-Wide Association Study database.
Our analysis employed
several MR methods, including the Inverse Variance Weighted (IVW) approach, MR-Egger,
and the Weighted Median method, to provide comprehensive insights and address possible
pleiotropy.
Results:
MR findings suggest a significant causal association between higher cathepsin levels and
increased PTC risk.
Notably, genetic variants indicating higher cathepsin Z expression were positively
causal associated with PTC risk (OR:1.
1190, 95% CI: 1.
0029-1.
2486), multivariable analysis
confirmed significant carcinogenesis role of cathepsin Z in PTC (OR: 1.
1593, 95% CI:
1.
0137-1.
3258), with results consistent across various tests, indicating a robust relationship.
Conclusion:
This study established a causal link between cathepsin levels and PTC risk, emphasizing
the roles of cathepsin Z in its progression.
These insights could lead to new therapeutic strategies
targeting these enzymes.
Further research is necessary to understand the underlying biological
mechanisms and their clinical implications.
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