{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["10"],"submitter":["Su Y"],"pubmed_abstract":["Clear cell adenocarcinoma of the cervix (CCAC) is a special type of HPV-independent cervical cancer. It has a low incidence rate, can be difficult to diagnose early, has a poor prognosis. Its peak incidence is in adolescence, which poses a great threat to women's health. Therefore, it is very important to explore the pathogenesis of cervical clear cell adenocarcinoma to guide subsequent treatment and prevention. This study analyzed 3 juvenile patients with CCAC diagnosed at the First Affiliated Hospital of Zhengzhou University. Using next-generation sequencing methods, we analyzed the pathogenesis of the patients and their close relatives by analyzing the genetic alterations of patients. CMTM5 was identified as the only shared mutated gene. Using published literature and comparative analys"],"journal":["Frontiers in medicine"],"pagination":["1211888"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10466801"],"repository":["biostudies-literature"],"pubmed_title":["Genetic alterations in juvenile cervical clear cell adenocarcinoma unrelated to human papillomavirus."],"pmcid":["PMC10466801"],"pubmed_authors":["Zhou M","Cao L","Yuan S","Zhang D","Wang B","Zhang M","Zhang L","Wang H","Zhou Y","Zhang R","Li X","Zhang T","Luo J","Zhang Y","Su Y","Chen S","Zhang C"],"additional_accession":[]},"is_claimable":false,"name":"Genetic alterations in juvenile cervical clear cell adenocarcinoma unrelated to human papillomavirus.","description":"Clear cell adenocarcinoma of the cervix (CCAC) is a special type of HPV-independent cervical cancer. It has a low incidence rate, can be difficult to diagnose early, has a poor prognosis. Its peak incidence is in adolescence, which poses a great threat to women's health. Therefore, it is very important to explore the pathogenesis of cervical clear cell adenocarcinoma to guide subsequent treatment and prevention. This study analyzed 3 juvenile patients with CCAC diagnosed at the First Affiliated Hospital of Zhengzhou University. Using next-generation sequencing methods, we analyzed the pathogenesis of the patients and their close relatives by analyzing the genetic alterations of patients. CMTM5 was identified as the only shared mutated gene. Using published literature and comparative analys","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023","modification":"2025-04-04T11:26:10.523Z","creation":"2025-04-04T11:26:10.523Z"},"accession":"S-EPMC10466801","cross_references":{"pubmed":["37654657"],"doi":["10.3389/fmed.2023.1211888"]}}