Literature DB >> 17695489

Germline NBS1 mutations in families with aggregation of Breast and/or ovarian cancer from north-east Poland.

Celina Kanka1, Izabela Brozek, Beata Skalska, Anna Siemiatkowska, Janusz Limon.   

Abstract

BACKGROUND: NBS1 gene, which product participates in DNA repair, has been postulated to be a susceptibility factor for a number of types of cancer, including breast cancer. The carrier frequency of the 657del5 and I171V NBS1 gene mutations among Polish patients with familial breast and/or ovarian cancer was compared with that of randomly selected newborns. PATIENTS AND METHODS: Using allele-specific amplification-polymerase chain reaction (ASAPCR) and restriction fragment length polymorphismpolymerase chain reaction (RFLP-PCR) techniques, blood samples were analysed from 250 patients with breast or/and ovarian cancer and a total number of 4,000 for 657del5 mutation and 1,300 for I1171V mutation controls.
RESULTS: Although an increased frequency of both mutations in cancer cases - 0.8% of 657del5 and 2.4% of I171V, compared to controls - 0.52% and 1.38%, respectively, was found, the differences were not statistically significant.
CONCLUSION: Our results indicate that NBS1 mutations do not contribute significantly to breast or ovarian cancer development.

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Year:  2007        PMID: 17695489

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  8 in total

1.  Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation.

Authors:  Haeyoung Kim; Dae-Yeon Cho; Doo Ho Choi; Gee Hue Jung; Inkyung Shin; Won Park; Seung Jae Huh; Sung-Won Kim; Sue K Park; Jong Won Lee; Seok Jin Nam; Jeong Eon Lee; Won Ho Gil; Seok Won Kim
Journal:  Fam Cancer       Date:  2015-09       Impact factor: 2.375

2.  The frequency of NBN molecular variants in pediatric astrocytic tumors.

Authors:  Dorota Piekutowska-Abramczuk; Elzbieta Ciara; Ewa Popowska; Wiesława Grajkowska; Bozenna Dembowska-Bagińska; Ewa Kowalewska; Aneta Czajńska; Marta Perek-Polnik; Marcin Roszkowski; Małgorzata Syczewska; Małgorzata Krajewska-Walasek; Danuta Perek; Krystyna H Chrzanowska
Journal:  J Neurooncol       Date:  2009-07-22       Impact factor: 4.130

3.  Significant association between Nijmegen breakage syndrome 1 657del5 polymorphism and breast cancer risk.

Authors:  Guofeng Zhang; Yu Zeng; Zhongyan Liu; Weiwei Wei
Journal:  Tumour Biol       Date:  2013-06-14

4.  Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers.

Authors:  Timothy R Rebbeck; Nandita Mitra; Susan M Domchek; Fei Wan; Shannon Chuai; Tara M Friebel; Saarene Panossian; Amanda Spurdle; Georgia Chenevix-Trench; Christian F Singer; Georg Pfeiler; Susan L Neuhausen; Henry T Lynch; Judy E Garber; Jeffrey N Weitzel; Claudine Isaacs; Fergus Couch; Steven A Narod; Wendy S Rubinstein; Gail E Tomlinson; Patricia A Ganz; Olufunmilayo I Olopade; Nadine Tung; Joanne L Blum; Roger Greenberg; Katherine L Nathanson; Mary B Daly
Journal:  Cancer Res       Date:  2009-07-07       Impact factor: 12.701

Review 5.  Mystery of DNA repair: the role of the MRN complex and ATM kinase in DNA damage repair.

Authors:  Kamila Czornak; Sanaullah Chughtai; Krystyna H Chrzanowska
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240

6.  The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?

Authors:  Eva Seemanova; Raymonda Varon; Jan Vejvalka; Petr Jarolim; Pavel Seeman; Krystyna H Chrzanowska; Martin Digweed; Igor Resnick; Ivo Kremensky; Kathrin Saar; Katrin Hoffmann; Véronique Dutrannoy; Mohsen Karbasiyan; Mehdi Ghani; Ivo Barić; Mustafa Tekin; Peter Kovacs; Michael Krawczak; André Reis; Karl Sperling; Michael Nothnagel
Journal:  PLoS One       Date:  2016-12-09       Impact factor: 3.240

7.  Prospective study of high-risk, BRCA1/2-mutation negative women: the 'negative study'.

Authors:  Joanne Kotsopoulos; Kelly Metcalfe; Jill Alston; Dina Nikitina; Ophira Ginsburg; Andrea Eisen; Rochelle Demsky; Mohammad Akbari; Kevin Zbuk; Steven A Narod
Journal:  BMC Cancer       Date:  2014-03-25       Impact factor: 4.430

8.  NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations.

Authors:  Keita Tomioka; Tatsuo Miyamoto; Silvia Natsuko Akutsu; Hiromi Yanagihara; Kazumasa Fujita; Ekaterina Royba; Hiroshi Tauchi; Takashi Yamamoto; Iemasa Koh; Eiji Hirata; Yoshiki Kudo; Masao Kobayashi; Satoshi Okada; Shinya Matsuura
Journal:  Sci Rep       Date:  2021-10-04       Impact factor: 4.379

  8 in total

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