TY - JOUR
T1 - Characteristics of Li-Fraumeni syndrome in Japan
T2 - A review study by the special committee of JSHT
AU - for the Li-Fraumeni syndrome special committee of the Japanese Society for Hereditary Tumors (JSHT)
AU - Funato, Michinori
AU - Tsunematsu, Yukiko
AU - Yamazaki, Fumito
AU - Tamura, Chieko
AU - Kumamoto, Tadashi
AU - Takagi, Masatoshi
AU - Kato, Shunsuke
AU - Sugimura, Haruhiko
AU - Tamura, Kazuo
N1 - Funding Information:
This study was supported in part by a grant from the Japanese Ministry of Education, Science, Sports and Culture (19K07763), the Health and Labor Sciences Research Grants of Research on Measures for Intractable Diseases (H23‐nanchi‐ippan‐069), and Research on Cancer Control (H29‐gantaisaku‐ippan‐002) from the Ministry of Health, Labor, and Welfare.
Funding Information:
This study was supported in part by a grant from the Japanese Ministry of Education, Science, Sports and Culture (19K07763), the Health and Labor Sciences Research Grants of Research on Measures for Intractable Diseases (H23-nanchi-ippan-069), and Research on Cancer Control (H29-gantaisaku-ippan-002) from the Ministry of Health, Labor, and Welfare. Professor Hiroshi Yagata (Saitama Medical University), who passed away before this paper was submitted, made a great contribution to the research on breast cancer occurring in Li-Fraumeni syndrome and its surveillance. We would like to express our deep appreciation for him. In addition, we greatly appreciate the patients and their families who cooperated with us for this study. We also thank Dr J. Toguchida (Kyoto University), Dr T. Oka (Asahikawa Medical University), Dr M. Tokunaga (Kagoshima Municipal Hospital), Dr T. Kawaguchi (Kumamoto University), Dr M. Tsurusawa (Aichi Medical University), Dr T. Yonemoto (Chiba Cancer Center), Dr M. Yano (Akita University), Dr H. Tsuchiya (Kanazawa University), Dr R. Fukano (Kyusyu Cancer Center), Dr M. Kouroki (Kumamoto University), Dr K. Ishiguro (Tottori University), Dr H. Ogi (Kumamoto University), Dr T. Matsubara (Mie University), Dr A. Matsumine (Mie University), Dr J. Yoshimura (Niigata University), Dr T. Iwai (Kagawa Children Hospital), Dr H. Maeda (Fukui University), Dr N. Kagawa (Osaka University), Dr H. Uchida (Kagoshima University), Dr T. Yoshikawa (Fujita Medical University), Dr S. Sugihara (Shikoku Cancer Center), Dr. S. Nakamura (Showa University), Dr. H. Yamagami (Sapporo-Kosei General Hospital), Dr. M. Yanagimachi (Yokohama City University), Dr. M. Yamauchi (St. Luke’s International Hospital) for providing the clinical information and Dr S. Kojima (Nagoya University), Dr S. Mizutani (Tokyo Medical Dental University), Dr M. Tsurusawa (Aichi Medical University), Dr K. Osafune (Kyoto University), and Dr H. Kaneko (Nagara Medical Center) for providing advice on this study. We also thank the Japanese Society of Hereditary Tumors (JSHT) for their strong support as the backbone of our Li-Fraumeni Working Group. We would like to thank Editage (www.editage.com) for English language editing.
Publisher Copyright:
© 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2021/7
Y1 - 2021/7
N2 - Li-Fraumeni syndrome (LFS) is a hereditary cancer predisposition syndrome, and the majority of patients with LFS have been identified with germline variants in the p53 tumor suppressor (TP53) gene. In the past three decades, considerable case reports of TP53 germline variants have been published in Japan. To the best of our knowledge, there have been no large-scale studies of Japanese patients with LFS. In this study, we aimed to identify Japanese patients with TP53 germline variants and to reveal the characteristics of LFS in Japan. We collected reported cases by reviewing the medical literature and cases diagnosed at the institutions of the authors. We identified 68 individuals from 48 families with TP53 germline pathogenic or likely pathogenic variants. Of the 48 families, 35 (72.9%) had missense variants, most of which were located within the DNA-binding loop. A total of 128 tumors were identified in the 68 affected individuals. The 128 tumor sites were as follows: breast, 25; bones, 16; brain, 12; hematological, 11; soft tissues, 10; stomach, 10; lung, 10; colorectum, 10; adrenal gland, 9; liver, 4; and others, 11. Unique phenotype patterns of LFS were shown in Japan in comparison with those in a large national LFS cohort study in France. Above all, a higher frequency of patients with stomach cancer was observed in Japanese TP53 germline variant carriers. These results may provide useful information for the clinical management of LFS in Japan.
AB - Li-Fraumeni syndrome (LFS) is a hereditary cancer predisposition syndrome, and the majority of patients with LFS have been identified with germline variants in the p53 tumor suppressor (TP53) gene. In the past three decades, considerable case reports of TP53 germline variants have been published in Japan. To the best of our knowledge, there have been no large-scale studies of Japanese patients with LFS. In this study, we aimed to identify Japanese patients with TP53 germline variants and to reveal the characteristics of LFS in Japan. We collected reported cases by reviewing the medical literature and cases diagnosed at the institutions of the authors. We identified 68 individuals from 48 families with TP53 germline pathogenic or likely pathogenic variants. Of the 48 families, 35 (72.9%) had missense variants, most of which were located within the DNA-binding loop. A total of 128 tumors were identified in the 68 affected individuals. The 128 tumor sites were as follows: breast, 25; bones, 16; brain, 12; hematological, 11; soft tissues, 10; stomach, 10; lung, 10; colorectum, 10; adrenal gland, 9; liver, 4; and others, 11. Unique phenotype patterns of LFS were shown in Japan in comparison with those in a large national LFS cohort study in France. Above all, a higher frequency of patients with stomach cancer was observed in Japanese TP53 germline variant carriers. These results may provide useful information for the clinical management of LFS in Japan.
KW - Japan
KW - Li-Fraumeni syndrome
KW - TP53 germline pathogenic variant
KW - phenocopy
KW - stomach cancer
UR - http://www.scopus.com/inward/record.url?scp=85106258350&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85106258350&partnerID=8YFLogxK
U2 - 10.1111/cas.14919
DO - 10.1111/cas.14919
M3 - Article
C2 - 33932062
AN - SCOPUS:85106258350
SN - 1347-9032
VL - 112
SP - 2821
EP - 2834
JO - Cancer Science
JF - Cancer Science
IS - 7
ER -