Role of PARP inhibitors in prostate cancer
DSB may develop as a result of DNA replication if SSB goes unrepaired [17]. Because replication forks can break when they come into contact with a SSB, homologous recombination is an essential mechanism for repairing replication forks and preventing fork collapse [18]. CURRENT APPLICATIONS AND STUDY...
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Veröffentlicht in: | Central European journal of urology 2024-07, Vol.77 (3), p.424-435 |
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creator | Szczotka, Julia Szpila, Gabriela Hejduk, Michał Mucha, Ewa Rudel, Jolanta Kępiński, Michał Kaletka, Julia Ryszawy, Jakub Zapala, Piotr Tsuboi, Ichiro Matsukawa, Akihiro Miszczyk, Marcin Fazekas, Tamas Zattoni, Fabio Bryniarski, Piotr Rajwa, Paweł |
description | DSB may develop as a result of DNA replication if SSB goes unrepaired [17]. Because replication forks can break when they come into contact with a SSB, homologous recombination is an essential mechanism for repairing replication forks and preventing fork collapse [18]. CURRENT APPLICATIONS AND STUDY RESULTS OF PARP INHIBITORS Olaparib In December 2014, olaparib (Lynparza, Astra Zeneca AB, and Merck) was approved in the European Union and the United States for the treatment of advanced ovarian cancer and breast cancer with BRCA1/2 gene mutations [25]. Patients with deleterious or suspected deleterious gBRCAm, HER2-negative (no human epidermal growth factor receptor type 2) metastatic breast cancer who have received chemotherapy in the neoadjuvant, adjuvant, or metastatic setting are eligible for treatment with Lynparza [26]. [...]the median overall survival (0S) was 18.5 months for patients in the olaparib arm compared to 15.1 months for those in the control group [28]. |
doi_str_mv | 10.5173/ceju.2024.72.R1 |
format | Article |
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[...]the median overall survival (0S) was 18.5 months for patients in the olaparib arm compared to 15.1 months for those in the control group [28].</description><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Cell cycle</subject><subject>Cell death</subject><subject>Chemotherapy</subject><subject>Enzymes</subject><subject>FDA approval</subject><subject>Genes</subject><subject>Literature reviews</subject><subject>Metastasis</subject><subject>Mutation</subject><subject>Ovarian cancer</subject><subject>Prostate cancer</subject><subject>Side effects</subject><issn>2080-4806</issn><issn>2080-4873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNijsLwjAYRT9EwaKdXQNuQmOefYwiimMp7qWWFBNKo0n6_80gzt7lHjgHYEcJlrTgx16ZGTPCBC4YbugCEkZKkomy4Msfk3wNqfeGxOWlyKVM4NDYUSE7oPrU1EhPT_3QwTofEb2c9aELCvXd1Cu3hdXQjV6l39_A_nq5n29Z7N6z8qE1dnZTVC2nQlBesUry_6oPIao3tg</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Szczotka, Julia</creator><creator>Szpila, Gabriela</creator><creator>Hejduk, Michał</creator><creator>Mucha, Ewa</creator><creator>Rudel, Jolanta</creator><creator>Kępiński, Michał</creator><creator>Kaletka, Julia</creator><creator>Ryszawy, Jakub</creator><creator>Zapala, Piotr</creator><creator>Tsuboi, Ichiro</creator><creator>Matsukawa, Akihiro</creator><creator>Miszczyk, Marcin</creator><creator>Fazekas, Tamas</creator><creator>Zattoni, Fabio</creator><creator>Bryniarski, Piotr</creator><creator>Rajwa, Paweł</creator><general>Polish Urological Association</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BYOGL</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20240701</creationdate><title>Role of PARP inhibitors in prostate cancer</title><author>Szczotka, Julia ; 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Because replication forks can break when they come into contact with a SSB, homologous recombination is an essential mechanism for repairing replication forks and preventing fork collapse [18]. CURRENT APPLICATIONS AND STUDY RESULTS OF PARP INHIBITORS Olaparib In December 2014, olaparib (Lynparza, Astra Zeneca AB, and Merck) was approved in the European Union and the United States for the treatment of advanced ovarian cancer and breast cancer with BRCA1/2 gene mutations [25]. Patients with deleterious or suspected deleterious gBRCAm, HER2-negative (no human epidermal growth factor receptor type 2) metastatic breast cancer who have received chemotherapy in the neoadjuvant, adjuvant, or metastatic setting are eligible for treatment with Lynparza [26]. 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subjects | Breast cancer Cancer therapies Cell cycle Cell death Chemotherapy Enzymes FDA approval Genes Literature reviews Metastasis Mutation Ovarian cancer Prostate cancer Side effects |
title | Role of PARP inhibitors in prostate cancer |
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