{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T21:14:48Z","timestamp":1777670088491,"version":"3.51.4"},"reference-count":71,"publisher":"SAGE Publications","issue":"15-16","license":[{"start":{"date-parts":[[2020,8,1]],"date-time":"2020-08-01T00:00:00Z","timestamp":1596240000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Human Gene Therapy"],"published-print":{"date-parts":[[2020,8]]},"abstract":"<jats:p>\n                    The aim is to investigate the genomic characterization of uterine sarcoma for rAd-\n                    <jats:italic toggle=\"yes\">p53<\/jats:italic>\n                    (Gendicine\n                    <jats:sup>\u00ae<\/jats:sup>\n                    ) combined with chemotherapy treatment. We recently published an article on 12 cases of uterine sarcomas, which were treated with rAd-\n                    <jats:italic toggle=\"yes\">p53<\/jats:italic>\n                    combined with chemotherapy. We found that rAd-\n                    <jats:italic toggle=\"yes\">p53<\/jats:italic>\n                    combined with chemotherapy is effective for various uterine sarcomas. Pretreatment pathological specimens of four uterine sarcoma patients were collected from the above recent clinical research and numbered 1\u20134A\/B. Tumor samples were subjected to targeted sequencing by using a 416 genes panel. We profiled the mutation spectrum and tumor mutation burden in the tumors, identified mutated genes, and explored their gene function. We also verified the p53 protein expression using immunohistochemistry. We identified a total of 30 mutated genes that were found from the next-generation sequencing test results. The average number of mutated genes was up to seven in the five samples.\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    gene was mutated in two of the four patients, No. 1 and No. 4B. They are c.C833G (p.P278R) missense mutation and a point mutation (C141*) that result in a premature stop codon. We did not find a mutated\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    gene in the other two cases, but we identified mutated genes, including\n                    <jats:italic toggle=\"yes\">CREBBP<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">LYN<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">CDKN2A<\/jats:italic>\n                    , and\n                    <jats:italic toggle=\"yes\">JAK2,<\/jats:italic>\n                    which were located upstream of the\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    gene; they may have an impact on\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    . We also identified 11 additional genes which are involved in\n                    <jats:italic toggle=\"yes\">p53<\/jats:italic>\n                    -related signaling pathways or have interaction with p53. Compared to solid tumor mutational burden (TMB) distribution, none of their TMB was ranking in the top 25%. Mutant p53 protein expression was positive in two specimens. Our results demonstrated that the\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    signaling pathway plays an important role in uterine sarcoma tumorigenesis.\n                    <jats:italic toggle=\"yes\">TP53<\/jats:italic>\n                    and the upstream genes such as\n                    <jats:italic toggle=\"yes\">CREBBP<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">LYN<\/jats:italic>\n                    ,\n                    <jats:italic toggle=\"yes\">CDKN2A<\/jats:italic>\n                    , and\n                    <jats:italic toggle=\"yes\">JAK2<\/jats:italic>\n                    may be involved in the genomic characterization for rAd-\n                    <jats:italic toggle=\"yes\">p53<\/jats:italic>\n                    (Gendicine) combined with chemotherapy in uterine sarcoma. Besides, the average amount of mutated genes from every patient is large.\n                  <\/jats:p>","DOI":"10.1089\/hum.2019.305","type":"journal-article","created":{"date-parts":[[2020,2,4]],"date-time":"2020-02-04T07:39:28Z","timestamp":1580801968000},"page":"881-890","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":6,"title":["Investigation on the Genomic Characterization of Uterine Sarcoma for rAd-\n                    <i>p53<\/i>\n                    Combined with Chemotherapy Treatment"],"prefix":"10.1177","volume":"31","author":[{"given":"Yu","family":"Xia","sequence":"first","affiliation":[{"name":"Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lei","family":"Wang","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiaolin","family":"Ma","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China."}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiuqin","family":"Li","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2020,8,17]]},"reference":[{"key":"e_1_3_5_2_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.1226344"},{"key":"e_1_3_5_3_2","doi-asserted-by":"publisher","DOI":"10.1001\/jama.2014.3741"},{"key":"e_1_3_5_4_2","doi-asserted-by":"publisher","DOI":"10.1093\/annonc\/mdy054"},{"key":"e_1_3_5_5_2","doi-asserted-by":"publisher","DOI":"10.1089\/hum.2017.238"},{"key":"e_1_3_5_6_2","doi-asserted-by":"publisher","DOI":"10.1089\/hum.2017.218"},{"key":"e_1_3_5_7_2","doi-asserted-by":"publisher","DOI":"10.1158\/1078-0432.CCR-09-1296"},{"key":"e_1_3_5_8_2","doi-asserted-by":"publisher","DOI":"10.1186\/1741-7015-12-16"},{"key":"e_1_3_5_9_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymthe.2006.08.061"},{"key":"e_1_3_5_10_2","doi-asserted-by":"publisher","DOI":"10.1089\/hum.2017.206"},{"key":"e_1_3_5_11_2","doi-asserted-by":"publisher","DOI":"10.1093\/bioinformatics\/btu170"},{"key":"e_1_3_5_12_2","doi-asserted-by":"publisher","DOI":"10.1093\/bioinformatics\/btp324"},{"key":"e_1_3_5_13_2","doi-asserted-by":"publisher","DOI":"10.1101\/gr.107524.110"},{"key":"e_1_3_5_14_2","doi-asserted-by":"crossref","unstructured":"Van der Auwera GA Carneiro MO Hartl C et al. 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