Literature DB >> 28413668

PALB2 mutation in a woman with bilateral breast cancer: A case report.

Hiroshi Nakagomi1, Yosuke Hirotsu2, Kenichiro Okimoto2,3, Ikuko Sakamoto4, Kenji Amemiya2, Satoko Nakagomi5, Takeo Kubota6, Hitoshi Mochizuki2, Masao Omata2,7.   

Abstract

Partner and localizer of breast cancer 2 (PALB2) was identified as a moderate-risk gene of breast and pancreas cancer. The present authors previously reported that no PALB2 germline mutations with a deleterious frameshift or stop codons were identified in 155 Japanese patients with breast and/or ovarian cancer who were estimated to be at risk of hereditary cancer, according to the National Comprehensive Cancer Network (NCCN) criteria. In the present study, one patient with a deleterious mutation of PALB2 (c. 2834+2 T>C) has been identified from a study of an additional 128 cases. Therefore, the prevalence of PALB2 among Japanese patients is now estimated to be 0.35% (1/283). The proband was a 63-year-old woman with bilateral breast cancer, although she had experienced no other cancers. The proband had two elder sisters, the eldest of whom died from pancreatic cancer at 60 years of age. The proband's 40-year-old daughter was affected, but did not show any malignancies. There are only a few reports concerning PALB2 mutations in Japan. To the best of our knowledge, this is the first case study to reveal the significance of DNA-repair genes in the development of malignancies in Japanese patients with breast cancer.

Entities:  

Keywords:  Japanese; PALB2; breast cancer; case report; pancreas cancer

Year:  2017        PMID: 28413668      PMCID: PMC5374944          DOI: 10.3892/mco.2017.1189

Source DB:  PubMed          Journal:  Mol Clin Oncol        ISSN: 2049-9450


  39 in total

1.  Novel germline PALB2 truncating mutations in African American breast cancer patients.

Authors:  Yonglan Zheng; Jing Zhang; Qun Niu; Dezheng Huo; Olufunmilayo I Olopade
Journal:  Cancer       Date:  2011-08-26       Impact factor: 6.860

2.  PALB2 mutations 1592delT and 229delT are not present in Korean breast cancer patients negative for BRCA1 and BRCA2 mutations.

Authors:  Jin Ho Kim; Doo Ho Choi; Dae Yeon Cho; Sei Hyun Ahn; Byung Ho Son; Bruce G Haffty
Journal:  Breast Cancer Res Treat       Date:  2010-03-06       Impact factor: 4.872

3.  Intrinsic HER2 V777L mutation mediates resistance to trastuzumab in a breast cancer patient.

Authors:  Yosuke Hirotsu; Hiroshi Nakagomi; Kenji Amemiya; Toshio Oyama; Masayuki Inoue; Hitoshi Mochizuki; Masao Omata
Journal:  Med Oncol       Date:  2016-11-29       Impact factor: 3.064

4.  PALB2 mutations in European familial pancreatic cancer families.

Authors:  E P Slater; P Langer; E Niemczyk; K Strauch; J Butler; N Habbe; J P Neoptolemos; W Greenhalf; D K Bartsch
Journal:  Clin Genet       Date:  2010-11       Impact factor: 4.438

5.  A recurrent mutation in PALB2 in Finnish cancer families.

Authors:  Hannele Erkko; Bing Xia; Jenni Nikkilä; Johanna Schleutker; Kirsi Syrjäkoski; Arto Mannermaa; Anne Kallioniemi; Katri Pylkäs; Sanna-Maria Karppinen; Katrin Rapakko; Alexander Miron; Qing Sheng; Guilan Li; Henna Mattila; Daphne W Bell; Daniel A Haber; Mervi Grip; Mervi Reiman; Arja Jukkola-Vuorinen; Aki Mustonen; Juha Kere; Lauri A Aaltonen; Veli-Matti Kosma; Vesa Kataja; Ylermi Soini; Ronny I Drapkin; David M Livingston; Robert Winqvist
Journal:  Nature       Date:  2007-02-07       Impact factor: 49.962

Review 6.  The complex genetic landscape of familial breast cancer.

Authors:  Lorenzo Melchor; Javier Benítez
Journal:  Hum Genet       Date:  2013-04-05       Impact factor: 4.132

7.  PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.

Authors:  Nazneen Rahman; Sheila Seal; Deborah Thompson; Patrick Kelly; Anthony Renwick; Anna Elliott; Sarah Reid; Katarina Spanova; Rita Barfoot; Tasnim Chagtai; Hiran Jayatilake; Lesley McGuffog; Sandra Hanks; D Gareth Evans; Diana Eccles; Douglas F Easton; Michael R Stratton
Journal:  Nat Genet       Date:  2006-12-31       Impact factor: 38.330

8.  PALB2 mutations in German and Russian patients with bilateral breast cancer.

Authors:  Natalia Bogdanova; Anna P Sokolenko; Aglaya G Iyevleva; Svetlana N Abysheva; Magda Blaut; Michael Bremer; Hans Christiansen; Margret Rave-Fränk; Thilo Dörk; Evgeny N Imyanitov
Journal:  Breast Cancer Res Treat       Date:  2010-12-17       Impact factor: 4.872

9.  Comparison between two amplicon-based sequencing panels of different scales in the detection of somatic mutations associated with gastric cancer.

Authors:  Yosuke Hirotsu; Yuichiro Kojima; Kenichiro Okimoto; Kenji Amemiya; Hitoshi Mochizuki; Masao Omata
Journal:  BMC Genomics       Date:  2016-10-26       Impact factor: 3.969

10.  Rapid Changes in Circulating Tumor DNA in Serially Sampled Plasma During Treatment of Breast Cancer: A Case Report.

Authors:  Hiroshi Nakagomi; Yosuke Hirotsu; Kenji Amemiya; Haruka Nakada; Masayuki Inoue; Hitoshi Mochizuki; Toshio Oyama; Masao Omata
Journal:  Am J Case Rep       Date:  2017-01-09
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  3 in total

1.  Mutation status of RAD51C, PALB2 and BRIP1 in 100 Japanese familial breast cancer cases without BRCA1 and BRCA2 mutations.

Authors:  Katsutoshi Sato; Mio Koyasu; Sachio Nomura; Yuri Sato; Mizuho Kita; Yuumi Ashihara; Yasue Adachi; Shinji Ohno; Takuji Iwase; Dai Kitagawa; Eri Nakashima; Reiko Yoshida; Yoshio Miki; Masami Arai
Journal:  Cancer Sci       Date:  2017-09-18       Impact factor: 6.716

2.  Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.

Authors:  Minako Mori; Asuka Hira; Kenichi Yoshida; Hideki Muramatsu; Yusuke Okuno; Yuichi Shiraishi; Michiko Anmae; Jun Yasuda; Shu Tadaka; Kengo Kinoshita; Tomoo Osumi; Yasushi Noguchi; Souichi Adachi; Ryoji Kobayashi; Hiroshi Kawabata; Kohsuke Imai; Tomohiro Morio; Kazuo Tamura; Akifumi Takaori-Kondo; Masayuki Yamamoto; Satoru Miyano; Seiji Kojima; Etsuro Ito; Seishi Ogawa; Keitaro Matsuo; Hiromasa Yabe; Miharu Yabe; Minoru Takata
Journal:  Haematologica       Date:  2019-02-21       Impact factor: 9.941

3.  Exon splicing analysis of intronic variants in multigene cancer panel testing for hereditary breast/ovarian cancer.

Authors:  Jin-Sun Ryu; Hye-Young Lee; Eun Hae Cho; Kyong-Ah Yoon; Min-Kyeong Kim; Jungnam Joo; Eun-Sook Lee; Han-Sung Kang; Seeyoun Lee; Dong Ock Lee; Myong Cheol Lim; Sun-Young Kong
Journal:  Cancer Sci       Date:  2020-09-02       Impact factor: 6.716

  3 in total

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