論文

査読有り 国際誌
2020年1月2日

TP53 and PTEN mutations were shared in concurrent germ cell tumor and acute megakaryoblastic leukemia

BMC Cancer
  • Akizuki K
  • Sekine M
  • Kogure Y
  • Kameda T
  • Shide K
  • Koya J
  • Kamiunten A
  • Kubuki Y
  • Tahira Y
  • Hidaka T
  • Kiwaki T
  • Tanaka H
  • Sato Y
  • Kataoka H
  • Kataoka K
  • Shimoda K
  • 全て表示

20
1
開始ページ
5
終了ページ
5
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1186/s12885-019-6497-0
出版者・発行元
BMC Cancer

Background: The occurrence of a mediastinal germ cell tumor (GCT) and hematological malignancy in the same patient is very rare. Due to its rarity, there have been only two reports of the concurrent cases undergoing detailed genetic analysis with whole-exome sequencing (WES), and the possible clonal relationship between the both tumors remained not fully elucidated. Methods: We performed whole-exome sequencing analysis of mediastinal GCT and acute myeloid leukemia (AML) samples obtained from one young Japanese male adult patient with concurrent both tumors, and investigated the possible clonal relationship between them. Results: Sixteen somatic mutations were detected in the mediastinal GCT sample and 18 somatic mutations in the AML sample. Mutations in nine genes, including TP53 and PTEN both known as tumor suppressor genes, were shared in both tumors. Conclusions: All in our case and in the previous two cases with concurrent mediastinal GCT and AML undergoing with whole-exome sequencing analysis, TP53 and PTEN mutations were commonly shared in both tumors. These data not only suggest that these tumors share a common founding clone, but also indicate that associated mediastinal GC

リンク情報
DOI
https://doi.org/10.1186/s12885-019-6497-0
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31898539
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941398
URL
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85077393148&origin=inward
ID情報
  • DOI : 10.1186/s12885-019-6497-0
  • PubMed ID : 31898539
  • PubMed Central 記事ID : PMC6941398

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