Effect of cyp1a1, cyp1b1 and cyp2c gene polymorphisms on doxorubicin and paclitaxel

The genes encoding metabolizing cytochrome P450 enzyme are studied for their importance in cancer susceptibility. Therefore, it is of interest to identify the correlation of CYP1A, CYP1B and CYP2C gene polymorphisms on drug response (DG-RS) and toxicity reactions in Indian population. Hence, 200 breast cancer patients received doxorubicin (DXR) and paclitaxel (PCX) chemotherapy. Further, chemotherapy induced hematological (HEM) and none (N)-HEM toxicity reactions were recorded. We found that, the Univariate Logistic Regression analysis showed negative association of CYP1B1 (4326 C>G) gene polymorphisms with microsites (OR=0.14, 95% CI: 0.03-0.54; p=0.004) in breast cancer patients treated with Doxorubicin. Thus, protective effect of CYP1B1-polymorphisms with doxorubicin and paclitaxel based chemotherapy induced N-HEM toxicity and CYP2C9- polymorphisms with paclitaxel induced body ache and CYP1A1-polymorphisms with peripheral neuropathy in breast cancer patients.

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Bioinformation
Published
2024-10-31
DOI
https://doi.org/10.6026/9732063002001244
Citations
1
Primary Topic
Cancer Treatment and Pharmacology
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article
Field-Weighted Citation Impact
0.28
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article

Effect of cyp1a1, cyp1b1 and cyp2c gene polymorphisms on doxorubicin and paclitaxel

Anand Gudur, Rashmi Gudur, Kailas D. Datkhile, Suresh Bhosale
1 citations
Bioinformation
Cancer Treatment and Pharmacology
0.28
article

Effect of cyp1a1, cyp1b1 and cyp2c gene polymorphisms on doxorubicin and paclitaxel

Anand Gudur, Rashmi Gudur, Kailas D. Datkhile, Suresh Bhosale
article en
1 citations

Abstract

The genes encoding metabolizing cytochrome P450 enzyme are studied for their importance in cancer susceptibility. Therefore, it is of interest to identify the correlation of CYP1A, CYP1B and CYP2C gene polymorphisms on drug response (DG-RS) and toxicity reactions in Indian population. Hence, 200 breast cancer patients received doxorubicin (DXR) and paclitaxel (PCX) chemotherapy. Further, chemotherapy induced hematological (HEM) and none (N)-HEM toxicity reactions were recorded. We found that, the Univariate Logistic Regression analysis showed negative association of CYP1B1 (4326 C>G) gene polymorphisms with microsites (OR=0.14, 95% CI: 0.03-0.54; p=0.004) in breast cancer patients treated with Doxorubicin. Thus, protective effect of CYP1B1-polymorphisms with doxorubicin and paclitaxel based chemotherapy induced N-HEM toxicity and CYP2C9- polymorphisms with paclitaxel induced body ache and CYP1A1-polymorphisms with peripheral neuropathy in breast cancer patients.

BioinformationVol. 20(10)
Krishna Institute of Medical Sciences (IN)
Good health and well-being
Openalex Percentile: Top 32%
Cancer Treatment and Pharmacology
0.28
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