[HTML][HTML] Chemotherapy reduces PARP1 in cancers of the ovary: implications for future clinical trials involving PARP inhibitors
BMC medicine, 2015•Springer
Background PARP inhibitors have shown promising clinical results in cancer patients
carrying BRCA1/2 mutations. Their clinical efficacy could logically be influenced by PARP1
protein levels in patient tumors. Methods We screened three cohorts of patients with ovarian
cancer, totaling 313 samples, and evaluated PARP1 protein expression by
immunohistochemistry with further validation by western blotting. Results We observed that
up to 60% of tumors showed little PARP1 protein expression. In serous ovarian tumors …
carrying BRCA1/2 mutations. Their clinical efficacy could logically be influenced by PARP1
protein levels in patient tumors. Methods We screened three cohorts of patients with ovarian
cancer, totaling 313 samples, and evaluated PARP1 protein expression by
immunohistochemistry with further validation by western blotting. Results We observed that
up to 60% of tumors showed little PARP1 protein expression. In serous ovarian tumors …
Background
PARP inhibitors have shown promising clinical results in cancer patients carrying BRCA1/2 mutations. Their clinical efficacy could logically be influenced by PARP1 protein levels in patient tumors.
Methods
We screened three cohorts of patients with ovarian cancer, totaling 313 samples, and evaluated PARP1 protein expression by immunohistochemistry with further validation by western blotting.
Results
We observed that up to 60 % of tumors showed little PARP1 protein expression. In serous ovarian tumors, comparing intratumoral PARP1 expression between chemo-naïve and post-chemotherapy patients revealed a decrease in intratumoral PARP1 following chemotherapy in all three cohorts (immunohistochemistry: p < 0.001, n = 239; western blot: p = 0.012, n = 74). The findings were further confirmed in a selection of matched samples from the same patients before and after chemotherapy.
Conclusion
Our data suggest that patients should be screened for PARP1 expression prior to therapy with PARP inhibitors. Further, the observed reduction of intratumoral PARP1 post-chemotherapy suggests that treating chemo-naïve patients with PARP inhibitors prior to the administration of chemotherapy, or concurrently, might increase the responsiveness to PARP1 inhibition. Thus, a change in the timing of PARP inhibitor administration may be warranted for future clinical trials.
Springer
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