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Frequency and genome load of Epstein-Barr virus in 509 breast cancers from different geographical areas
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  • Regular Article
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  • Published: 20 March 2001

Frequency and genome load of Epstein-Barr virus in 509 breast cancers from different geographical areas

  • F Fina1,
  • S Romain1,
  • L'H Ouafik1,
  • J Palmari1,
  • F Ben Ayed2,
  • S Benharkat3,
  • P Bonnier4,
  • F Spyratos5,
  • J A Foekens6,
  • C Rose7,
  • M Buisson8,
  • H Gérard1,
  • M O Reymond1,
  • J M Seigneurin8 &
  • …
  • P M Martin1 

British Journal of Cancer volume 84, pages 783–790 (2001)Cite this article

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Abstract

Since the few data exploring a possible association between Epstein–Barr virus (EBV) and breast cancer are conflicting, we investigated this association together with the influences of geographical areas. 509 breast cancers were sampled from areas with varying risks of nasopharynx carcinoma (NPC) such as North Africa (Algeria and Tunisia, high-risk area); southern France (Marseille, intermediate-risk area); and northern Europe (northern France, the Netherlands and Denmark; low-risk areas). Polymerase chain reaction (PCR) of a subregion of EBV BamHIC encoding the EBERs demonstrated that 31.8% of the tumours contained the viral genome. No significant differences were observed among the geographical areas. However, positive samples showed higher loads of the EBV genome in the NPC high- and intermediate-risk areas than in the low-risk areas. EBV type 1 was the dominant strain. In situ hybridization studies using a35S-labelled riboprobe for EBER1 and a laser capture microdissection, combined with quantitative PCR, showed that EBV localization was restricted to some tumour epithelial cell clusters. EBV could not be detected in the stroma. Considering the whole population covered, the presence of the EBV genome was not correlated with age, menopausal status, tumour, size, nodal status or histological grade. © 2001 Cancer Research Campaign

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Change history

  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Author information

Authors and Affiliations

  1. Assistance Publique-Hôpitaux de Marseille, Laboratoire de Transfert d’Oncologie Biologique, Faculté de Médecine Nord, Boulevard Pierre Dramard, 13916, Marseille, Cedex 20, France

    F Fina, S Romain, L'H Ouafik, J Palmari, H Gérard, M O Reymond & P M Martin

  2. Institut Salah Azaïz, Service d’Hémato-Oncologie, Boulevard du 9 Avril 1938, BP 173, 1006, Tunis, Tunisia

    F Ben Ayed

  3. Centre Hospitalo-Universitaire Ibn Rochd, Laboratoire Central, 23000, Annaba, Algeria

    S Benharkat

  4. Assistance Publique-Hôpitaux de Marseille, Service de Gynécologie et Obstétrique A, Hôpital de la Conception, 147 Boulevard Baille, 13385, Marseille, Cedex 5, France

    P Bonnier

  5. Département de Biologie, Centre René Huguenin, 35 rue Dailly, 92210, St Cloud, France

    F Spyratos

  6. Josephine Nefkens Institute, Dr. Molewaterplein 50, room Be426, 3015, GE Rotterdam, The Netherlands

    J A Foekens

  7. Department of Oncology R, University Hospital, DK-5000 Odense C, Denmark

    C Rose

  8. Faculté de Médecine de Grenoble, Laboratoire de Virologie Médicale Moléculaire, Domaine de la Merci, La Tronche, 38706, France

    M Buisson & J M Seigneurin

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Additional information

Part of this work was presented to the VII Symposium of the International Association for Research on Epstein–Barr Virus and Associated Diseases, Hong-Kong, 13–16 November 1996.

On behalf of: K Rahal, A Gammoudi (Institut Salah Azaïz, Tunis, Tunisia); SHaddad, A Djemaa (Centre Hospitalier Universitaire, Constantine, Algeria); L Piana (Hôpital de la Conception, Marseille, France); JM Brandone, C Bressac (Clinique Bouchard, Marseille, France); C Charpin (Assistance Publique-Hôpitaux de Marseille, Faculté de Médecine Nord, Marseille, France); M Pizzi-Anselme, J Del Grande, J Guidon (Laboratoire d'Anatomie Pathologique et Cytologie, Marseille, France); and the clinicians and pathologists from Centre René Huguenin (St Cloud, France); Dr Daniel den Hoed Cancer Center (Rotterdam, the Netherlands); and the Finsen Institute (Copenhagen, Denmark) who actively participated in the study.

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Fina, F., Romain, S., Ouafik, L. et al. Frequency and genome load of Epstein-Barr virus in 509 breast cancers from different geographical areas. Br J Cancer 84, 783–790 (2001). https://doi.org/10.1054/bjoc.2000.1672

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  • Received: 02 August 2000

  • Revised: 18 December 2000

  • Accepted: 21 December 2000

  • Published: 20 March 2001

  • Issue date: 23 March 2001

  • DOI: https://doi.org/10.1054/bjoc.2000.1672

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Keywords

  • breast cancer
  • Epstein–Barr virus
  • polymerase chain reaction
  • real-time quantitative polymerase chain reaction
  • genotyping
  • in situ hybridization
  • laser capture microdissection

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