{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T13:33:03Z","timestamp":1792157583703,"version":"4.4.0"},"reference-count":58,"publisher":"The Endocrine Society","issue":"7","license":[{"start":{"date-parts":[[2023,1,6]],"date-time":"2023-01-06T00:00:00Z","timestamp":1672963200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100012166","name":"National Key R&D Program of China","doi-asserted-by":"publisher","award":["2018YFA0800801"],"award-info":[{"award-number":["2018YFA0800801"]}],"id":[{"id":"10.13039\/501100012166","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81770874"],"award-info":[{"award-number":["81770874"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["81974126"],"award-info":[{"award-number":["81974126"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["61803360"],"award-info":[{"award-number":["61803360"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Clinical Science and Technology Innovation Project of Shanghai Shenkang Hospital Development Center","award":["SHDC12018120"],"award-info":[{"award-number":["SHDC12018120"]}]},{"name":"Shanghai Municipal Key Clinical Specialty","award":["2017ZZ01013"],"award-info":[{"award-number":["2017ZZ01013"]}]},{"DOI":"10.13039\/501100004921","name":"Shanghai Jiao Tong University Affiliated Sixth People\u2019s Hospital Basic Scientific Research","doi-asserted-by":"publisher","award":["ynms202118"],"award-info":[{"award-number":["ynms202118"]}],"id":[{"id":"10.13039\/501100004921","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,6,16]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Objective<\/jats:title>\n                  <jats:p>To define somatic variants of parathyroid adenoma (PA) and to provide novel insights into the underlying molecular mechanism of sporadic PA.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Basic clinical characteristics and biochemical indices of 73 patients with PA were collected. Whole-exome sequencing was performed on matched tumor-constitutional DNA pairs to detect somatic alterations. Functional annotation was carried out by ingenuity pathway analysis afterward. The protein expression of the variant gene was confirmed by immunohistochemistry, and the relationship between genotype and phenotype was analyzed.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Somatic variants were identified in 1549 genes, with an average of 69 variants per tumor (range, 13-2109; total, 9083). Several novel recurrent somatic variants were detected, such as KMT2D (15\/73), MUC4 (14\/73), POTEH (13\/73), CD22 (12\/73), HSPA2 (12\/73), HCFC1 (11\/73), MAGEA1 (11\/73), and SLC4A3 (11\/73), besides the previously reported PA-related genes, including MEN1 (11\/73), CASR (6\/73), MTOR (4\/73), ASXL3 (3\/73), FAT1 (3\/73), ZFX (5\/73), EZH1 (2\/73), POT1 (2\/73), and EZH2 (1\/73). Among them, KMT2D might be the candidate driver gene of PA. Crucially, 5 patients carried somatic mutations in CDC73, showed an aggressive phenotype similar to that of parathyroid carcinoma (PC), and had a decreased expression of parafibromin. Pathway analysis of recurrent potential PA-associated driver variant genes revealed functional enrichments in the signaling pathway of Notch.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>Our study expanded the pathogenic variant spectrum of PA and indicated that KMT2D might be a novel candidate driver gene and be considered as a diagnostic biomarker for PA. Meanwhile, CDC73 mutations might be an early developmental event from PA to PC. The results provided insights into elucidating the pathogenesis of parathyroid tumorigenesis and a certain basis for clinical diagnosis and treatment.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1210\/clinem\/dgad002","type":"journal-article","created":{"date-parts":[[2023,1,8]],"date-time":"2023-01-08T04:50:06Z","timestamp":1673153406000},"page":"1768-1775","source":"Crossref","is-referenced-by-count":18,"title":["Genomic Profiling Reveals the Variant Landscape of Sporadic Parathyroid Adenomas in Chinese Population"],"prefix":"10.1210","volume":"108","author":[{"given":"Xiaohui","family":"Tao","sequence":"first","affiliation":[{"name":"Shanghai Clinical Research Center of Bone Diseases, Department of Osteoporosis and Bone Diseases, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine , Shanghai 200233 , 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