Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney-Reference-Cited by-同舟云学术

Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney

Published:2021-05-04 Issue:8 Volume:60 Page:546-558
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Haruta Masayuki¹,Arai Yasuhito²,Okita Hajime³,Tanaka Yukichi⁴,Takimoto Tetsuya⁵,Kamijo Takehiko¹,Oue Takaharu⁶,Souzaki Ryota⁷,Taguchi Tomoaki⁷,Kuwahara Yasumichi⁸,Chin Motoaki⁹,Nakadate Hisaya¹⁰,Hiyama Eiso¹¹,Ishida Yasushi¹²,Koshinaga Tsugumichi¹³,Kaneko Yasuhiko¹^ORCID

Affiliation:

1. Research Institute for Clinical Oncology Saitama Cancer Center Saitama Japan

2. Cancer Genomics Division National Cancer Center Research Institute Tokyo Japan

3. Division of Diagnostic Pathology Keio University School of Medicine Tokyo Japan

4. Department of Pathology Kanagawa Children's Medical Center Yokohama Kanagawa Japan

5. Department of Childhood Cancer Data Management Childhood Cancer Center, National Center for Child Health and Development Tokyo Japan

6. Department of Pediatric Surgery Hyogo College of Medicine Nishinomiya Hyogo Japan

7. Department of Pediatric Surgery, Faculty of Medical Sciences Kyushu University Fukuoka Japan

8. Department of Biochemistry and Molecular Biology, Graduate School of Medical Science Kyoto Prefectural University of Medicine Kyoto Japan

9. Department of Pediatrics Nihon University School of Medicine Tokyo Japan

10. Division of Hematology National Center for Child Health and Development Tokyo Japan

11. Department of Pediatric Surgery Hiroshima University Hospital Hiroshima Japan

12. Pediatric Medical Center Ehime Prefectural Central Hospital Matsuyama Ehime Japan

13. Department of Pediatric Surgery Nihon University School of Medicine Tokyo Japan

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22952

Reference41 articles.

1. Biology and Treatment of Rhabdoid Tumor

2. Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

3. A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers

4. Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis

5. Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes