<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Widjaja AO</submitter><funding>Sjöbergstiftelsen</funding><funding>Nilsson-Ehle Endowments</funding><funding>Kungliga vetenskaps och vitterhets-samhället</funding><funding>Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement</funding><funding>Stiftelsen Assar Gabrielssons Fond</funding><funding>Gunvor and Ivan Svensson foundation</funding><funding>Sweden innovation agency</funding><funding>Cancera foundation</funding><funding>Lions Cancerfond väst</funding><funding>Cancerfonden</funding><pagination>2043-2050</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12922644</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>158(8)</volume><pubmed_abstract>High-grade serous ovarian carcinoma (HGSC) is the most lethal form of ovarian carcinoma, often diagnosed at advanced stages due to non-specific symptoms and the lack of reliable screening methods. This proof-of-concept study aimed to develop a robust TP53 mutation panel for detecting HGSC through targeted DNA sequencing in both liquid and solid biopsies. We constructed a custom TP53 gene panel and utilized a PCR-based unique molecular identifier approach for next-generation sequencing to analyze 94 samples from 11 patients diagnosed with HGSC, including primary tumor, plasma, ascites, ovarian cyst fluid, vaginal, endocervical and endometrial samples. Detected TP53 mutations were analyzed, categorized, and their frequencies calculated. Pathogenic TP53 mutations were identified in all patien</pubmed_abstract><journal>International journal of cancer</journal><pubmed_title>Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma.</pubmed_title><pmcid>PMC12922644</pmcid><funding_grant_id>965065</funding_grant_id><funding_grant_id>21‐1848</funding_grant_id><funding_grant_id>FB23‐118</funding_grant_id><funding_grant_id>2021‐01145</funding_grant_id><funding_grant_id>FB23-118</funding_grant_id><funding_grant_id>965552</funding_grant_id><funding_grant_id>22‐2080</funding_grant_id><funding_grant_id>FB22‐79</funding_grant_id><funding_grant_id>FB22‐67</funding_grant_id><funding_grant_id>FB23‐66</funding_grant_id><funding_grant_id>22-2080</funding_grant_id><funding_grant_id>FB23-66</funding_grant_id><funding_grant_id>FB22-67</funding_grant_id><funding_grant_id>21-1848</funding_grant_id><funding_grant_id>2021-01145</funding_grant_id><funding_grant_id>FB22-79</funding_grant_id><funding_grant_id>2020-0414</funding_grant_id><pubmed_authors>Lindberg JH</pubmed_authors><pubmed_authors>Gyllensten U</pubmed_authors><pubmed_authors>Ulfenborg B</pubmed_authors><pubmed_authors>Lycke M</pubmed_authors><pubmed_authors>Widjaja AO</pubmed_authors><pubmed_authors>Santamaria ML</pubmed_authors><pubmed_authors>Carlsson T</pubmed_authors><pubmed_authors>Sundfeldt K</pubmed_authors><pubmed_authors>Stahlberg A</pubmed_authors><pubmed_authors>Linder A</pubmed_authors><pubmed_authors>Micallef P</pubmed_authors><pubmed_authors>Osterlund T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detecting TP53 mutations in paired liquid and tissue biopsies from patients with high-grade serous ovarian carcinoma.</name><description>High-grade serous ovarian carcinoma (HGSC) is the most lethal form of ovarian carcinoma, often diagnosed at advanced stages due to non-specific symptoms and the lack of reliable screening methods. This proof-of-concept study aimed to develop a robust TP53 mutation panel for detecting HGSC through targeted DNA sequencing in both liquid and solid biopsies. We constructed a custom TP53 gene panel and utilized a PCR-based unique molecular identifier approach for next-generation sequencing to analyze 94 samples from 11 patients diagnosed with HGSC, including primary tumor, plasma, ascites, ovarian cyst fluid, vaginal, endocervical and endometrial samples. Detected TP53 mutations were analyzed, categorized, and their frequencies calculated. Pathogenic TP53 mutations were identified in all patien</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Apr</publication><modification>2026-07-09T11:39:42.022Z</modification><creation>2026-07-09T10:54:15.722Z</creation></dates><accession>S-EPMC12922644</accession><cross_references><pubmed>41363274</pubmed><doi>10.1002/ijc.70277</doi></cross_references></HashMap>